embryonic/larval tracheal system
}
REF
{
REFM|FBrf0067338
|BDGP Project Members
|1994-1999
REFM|FBrf0083714
|Meister and Braun
|1995.10
REFM|FBrf0102844
|Harvie et al.
|1998
REFM|FBrf0103143
|Jackle and Janning
|1998.8.10
}
ALESR
{
ASYM|FBal0137262==eyc04012b
REFDSR
{
RDID|FBrf0141505
|Sang and Ready
|2002
PHP|FBal0137262==eyc04012b homozygotes and
| FBal0137262==eyc04012b/FBab0002027==Df(2R)Px2 animals show
|disturbances in rhabdomere topology similar to the
| FBal0137261==eyc1 phenotype.
|FBal0137262==eyc04012b animals show mild fusion of the abdominal tergites.
PHM|(with Df(2R)Px2) rhabdomere
|rhabdomere
|abdominal tergite
}
REF
{
REFM|FBrf0141505
|Sang and Ready
|2002
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0019536 ICL 1 1360 SYM 1 1360{}17 ASTR 1 - CLOC 1 2B1-2B1 REF 1 2 DT 1 21 Aug 2003 RESZ 345
ID|FBti0019536
SYM|1360{}17
SYN|TE19536
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}17
CLOC|2B1-2B1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003421.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019546 ICL 1 1360 SYM 1 1360{}27 ASTR 1 - CLOC 1 3B1-3B2 REF 1 2 DT 1 21 Aug 2003 RESZ 345
ID|FBti0019546
SYM|1360{}27
SYN|TE19546
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}27
CLOC|3B1-3B2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003425.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019595 ICL 1 1360 SYM 1 1360{}76 ASTR 1 - CLOC 1 6C12-6C12 REF 1 2 DT 1 21 Aug 2003 RESZ 347
ID|FBti0019595
SYM|1360{}76
SYN|TE19595
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}76
CLOC|6C12-6C12
LOCB|genomic location inferred from flanking sequence
DBAF|AE003438.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019613 ICL 1 1360 SYM 1 1360{}94 ASTR 1 - CLOC 1 9B1-9B1 REF 1 2 DT 1 21 Aug 2003 RESZ 345
ID|FBti0019613
SYM|1360{}94
SYN|TE19613
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}94
CLOC|9B1-9B1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003449.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019634 ICL 1 1360 SYM 1 1360{}115 ASTR 1 - CLOC 1 11C1-11C1 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019634
SYM|1360{}115
SYN|TE19634
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}115
CLOC|11C1-11C1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003490.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019637 ICL 1 1360 SYM 1 1360{}136 ASTR 1 - CLOC 1 13B4-13B4 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019637
SYM|1360{}136
SYN|TE19637
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}136
CLOC|13B4-13B4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003498.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019639 ICL 1 1360 SYM 1 1360{}154 ASTR 1 - CLOC 1 16F7-16F7 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019639
SYM|1360{}154
SYN|TE19639
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}154
CLOC|16F7-16F7
LOCB|genomic location inferred from flanking sequence
DBAF|AE003507.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019662 ICL 1 1360 SYM 1 1360{}190 ASTR 1 - CLOC 1 19E7-19E7 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019662
SYM|1360{}190
SYN|TE19662
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}190
CLOC|19E7-19E7
LOCB|genomic location inferred from flanking sequence
DBAF|AE003569.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019709 ICL 1 1360 SYM 1 1360{}237 ASTR 1 - CLOC 1 20A5-20A5 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019709
SYM|1360{}237
SYN|TE19709
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}237
CLOC|20A5-20A5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003122.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019717 ICL 1 1360 SYM 1 1360{}245 ASTR 1 - CLOC 1 20B1-20B1 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019717
SYM|1360{}245
SYN|TE19717
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}245
CLOC|20B1-20B1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003574.5
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019770 ICL 1 1360 SYM 1 1360{}389 ASTR 1 - CLOC 1 35F1-35F1 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019770
SYM|1360{}389
SYN|TE19770
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}389
CLOC|35F1-35F1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003650.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019771 ICL 1 1360 SYM 1 1360{}396 ASTR 1 - CLOC 1 36C6-36C6 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019771
SYM|1360{}396
SYN|TE19771
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}396
CLOC|36C6-36C6
LOCB|genomic location inferred from flanking sequence
DBAF|AE003654.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019780 ICL 1 1360 SYM 1 1360{}420 ASTR 1 - CLOC 1 38A3-38A3 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019780
SYM|1360{}420
SYN|TE19780
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}420
CLOC|38A3-38A3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003664.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019799 ICL 1 1360 SYM 1 1360{}441 ASTR 1 - CLOC 1 38C2-38C2 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019799
SYM|1360{}441
SYN|TE19799
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}441
CLOC|38C2-38C2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003666.5
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019825 ICL 1 1360 SYM 1 1360{}478 ASTR 1 - CLOC 1 38F4-38F4 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019825
SYM|1360{}478
SYN|TE19825
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}478
CLOC|38F4-38F4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003668.5
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019828 ICL 1 1360 SYM 1 1360{}483 ASTR 1 - CLOC 1 39A5-39A5 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019828
SYM|1360{}483
SYN|TE19828
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}483
CLOC|39A5-39A5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003669.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019831 ICL 1 1360 SYM 1 1360{}493 ASTR 1 - CLOC 1 39D5-39D5 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019831
SYM|1360{}493
SYN|TE19831
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}493
CLOC|39D5-39D5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003670.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019839 ICL 1 1360 SYM 1 1360{}502 ASTR 1 - CLOC 1 39E2-39E2 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019839
SYM|1360{}502
SYN|TE19839
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}502
CLOC|39E2-39E2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003781.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019840 ICL 1 1360 SYM 1 1360{}503 ASTR 1 - CLOC 1 39E2-39E2 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019840
SYM|1360{}503
SYN|TE19840
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}503
CLOC|39E2-39E2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003781.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019841 ICL 1 1360 SYM 1 1360{}504 ASTR 1 - CLOC 1 39E2-39E2 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019841
SYM|1360{}504
SYN|TE19841
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}504
CLOC|39E2-39E2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003781.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019842 ICL 1 1360 SYM 1 1360{}505 ASTR 1 - CLOC 1 39E2-39E2 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019842
SYM|1360{}505
SYN|TE19842
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}505
CLOC|39E2-39E2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003781.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019847 ICL 1 1360 SYM 1 1360{}517 ASTR 1 - CLOC 1 39F3-39F3 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019847
SYM|1360{}517
SYN|TE19847
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}517
CLOC|39F3-39F3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003781.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019243 ICL 1 1360 SYM 1 1360{}528 ASTR 1 - CLOC 1 40E3-40E3 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019243
SYM|1360{}528
SYN|TE19243
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}528
CLOC|40E3-40E3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003782.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019857 ICL 1 1360 SYM 1 1360{}542 ASTR 1 - CLOC 1 40F4-40F4 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019857
SYM|1360{}542
SYN|TE19857
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}542
CLOC|40F4-40F4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003783.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019861 ICL 1 1360 SYM 1 1360{}548 ASTR 1 - CLOC 1 40F6-40F6 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019861
SYM|1360{}548
SYN|TE19861
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}548
CLOC|40F6-40F6
LOCB|genomic location inferred from flanking sequence
DBAF|AE003783.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019864 ICL 1 1360 SYM 1 1360{}551 ASTR 1 - CLOC 1 40F7-40F7 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019864
SYM|1360{}551
SYN|TE19864
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}551
CLOC|40F7-40F7
LOCB|genomic location inferred from flanking sequence
DBAF|AE003783.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019876 ICL 1 1360 SYM 1 1360{}569 ASTR 1 - CLOC 1 40F7-40F7 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019876
SYM|1360{}569
SYN|TE19876
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}569
CLOC|40F7-40F7
LOCB|genomic location inferred from flanking sequence
DBAF|AE002603.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019262 ICL 1 1360 SYM 1 1360{}573 ASTR 1 - CLOC 1 40F7-40F7 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019262
SYM|1360{}573
SYN|TE19262
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}573
CLOC|40F7-40F7
LOCB|genomic location inferred from flanking sequence
DBAF|AE002603.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019895 ICL 1 1360 SYM 1 1360{}608 ASTR 1 - CLOC 1 41E5-41E5 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019895
SYM|1360{}608
SYN|TE19895
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}608
CLOC|41E5-41E5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003788.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019896 ICL 1 1360 SYM 1 1360{}610 ASTR 1 - CLOC 1 41E5-41E5 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019896
SYM|1360{}610
SYN|TE19896
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}610
CLOC|41E5-41E5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003788.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019902 ICL 1 1360 SYM 1 1360{}636 ASTR 1 - CLOC 1 41F2-41F2 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019902
SYM|1360{}636
SYN|TE19902
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}636
CLOC|41F2-41F2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003787.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019905 ICL 1 1360 SYM 1 1360{}644 ASTR 1 - CLOC 1 41F2-41F2 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019905
SYM|1360{}644
SYN|TE19905
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}644
CLOC|41F2-41F2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003787.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019916 ICL 1 1360 SYM 1 1360{}661 ASTR 1 - CLOC 1 41F3-41F3 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019916
SYM|1360{}661
SYN|TE19916
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}661
CLOC|41F3-41F3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003786.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019917 ICL 1 1360 SYM 1 1360{}666 ASTR 1 - CLOC 1 41F3-41F3 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019917
SYM|1360{}666
SYN|TE19917
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}666
CLOC|41F3-41F3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003786.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019920 ICL 1 1360 SYM 1 1360{}676 ASTR 1 - CLOC 1 41F5-41F5 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019920
SYM|1360{}676
SYN|TE19920
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}676
CLOC|41F5-41F5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003786.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019922 ICL 1 1360 SYM 1 1360{}680 ASTR 1 - CLOC 1 41F5-41F5 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019922
SYM|1360{}680
SYN|TE19922
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}680
CLOC|41F5-41F5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003786.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019937 ICL 1 1360 SYM 1 1360{}700 ASTR 1 - CLOC 1 41F6-41F6 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019937
SYM|1360{}700
SYN|TE19937
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}700
CLOC|41F6-41F6
LOCB|genomic location inferred from flanking sequence
DBAF|AE003786.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019939 ICL 1 1360 SYM 1 1360{}702 ASTR 1 - CLOC 1 41F6-41F6 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019939
SYM|1360{}702
SYN|TE19939
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}702
CLOC|41F6-41F6
LOCB|genomic location inferred from flanking sequence
DBAF|AE003786.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019275 ICL 1 1360 SYM 1 1360{}709 ASTR 1 - CLOC 1 42A15-42A15 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0019275
SYM|1360{}709
SYN|TE19275
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}709
CLOC|42A15-42A15
LOCB|genomic location inferred from flanking sequence
DBAF|AE003789.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019969 ICL 1 1360 SYM 1 1360{}747 ASTR 1 - CLOC 1 42B1-42B2 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019969
SYM|1360{}747
SYN|TE19969
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}747
CLOC|42B1-42B2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003789.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019978 ICL 1 1360 SYM 1 1360{}780 ASTR 1 - CLOC 1 44D3-44D3 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019978
SYM|1360{}780
SYN|TE19978
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}780
CLOC|44D3-44D3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003836.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019279 ICL 1 1360 SYM 1 1360{}795 ASTR 1 - CLOC 1 46D1-46D2 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019279
SYM|1360{}795
SYN|TE19279
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}795
CLOC|46D1-46D2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003831.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019992 ICL 1 1360 SYM 1 1360{}829 ASTR 1 - CLOC 1 51A4-51A4 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019992
SYM|1360{}829
SYN|TE19992
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}829
CLOC|51A4-51A4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003814.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019993 ICL 1 1360 SYM 1 1360{}835 ASTR 1 - CLOC 1 51F11-51F11 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0019993
SYM|1360{}835
SYN|TE19993
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}835
CLOC|51F11-51F11
LOCB|genomic location inferred from flanking sequence
DBAF|AE003811.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020017 ICL 1 1360 SYM 1 1360{}906 ASTR 1 - CLOC 1 62A2-62A2 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0020017
SYM|1360{}906
SYN|TE20017
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}906
CLOC|62A2-62A2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003471.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020018 ICL 1 1360 SYM 1 1360{}907 ASTR 1 - CLOC 1 62A2-62A2 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0020018
SYM|1360{}907
SYN|TE20018
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}907
CLOC|62A2-62A2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003471.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020116 ICL 1 1360 SYM 1 1360{}1005 ASTR 1 - CLOC 1 71B4-71B4 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020116
SYM|1360{}1005
SYN|TE20116
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1005
CLOC|71B4-71B4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003532.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020143 ICL 1 1360 SYM 1 1360{}1032 ASTR 1 - CLOC 1 75A8-75A8 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020143
SYM|1360{}1032
SYN|TE20143
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1032
CLOC|75A8-75A8
LOCB|genomic location inferred from flanking sequence
DBAF|AE003522.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020155 ICL 1 1360 SYM 1 1360{}1044 ASTR 1 - CLOC 1 75E1-75E2 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020155
SYM|1360{}1044
SYN|TE20155
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1044
CLOC|75E1-75E2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003519.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020193 ICL 1 1360 SYM 1 1360{}1082 ASTR 1 - CLOC 1 78D4-78D4 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020193
SYM|1360{}1082
SYN|TE20193
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1082
CLOC|78D4-78D4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003594.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020194 ICL 1 1360 SYM 1 1360{}1083 ASTR 1 - CLOC 1 78D4-78D4 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020194
SYM|1360{}1083
SYN|TE20194
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1083
CLOC|78D4-78D4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003594.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020207 ICL 1 1360 SYM 1 1360{}1096 ASTR 1 - CLOC 1 80A1-80A1 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020207
SYM|1360{}1096
SYN|TE20207
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1096
CLOC|80A1-80A1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003598.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020224 ICL 1 1360 SYM 1 1360{}1113 ASTR 1 - CLOC 1 80C5-80C5 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020224
SYM|1360{}1113
SYN|TE20224
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1113
CLOC|80C5-80C5
LOCB|genomic location inferred from flanking sequence
DBAF|AE002786.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020225 ICL 1 1360 SYM 1 1360{}1114 ASTR 1 - CLOC 1 80C5-80C5 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020225
SYM|1360{}1114
SYN|TE20225
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1114
CLOC|80C5-80C5
LOCB|genomic location inferred from flanking sequence
DBAF|AE002786.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020229 ICL 1 1360 SYM 1 1360{}1118 ASTR 1 - CLOC 1 80D1-80D1 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020229
SYM|1360{}1118
SYN|TE20229
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1118
CLOC|80D1-80D1
LOCB|genomic location inferred from flanking sequence
DBAF|AE002786.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020230 ICL 1 1360 SYM 1 1360{}1119 ASTR 1 - CLOC 1 80D1-80D1 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020230
SYM|1360{}1119
SYN|TE20230
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1119
CLOC|80D1-80D1
LOCB|genomic location inferred from flanking sequence
DBAF|AE002786.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020240 ICL 1 1360 SYM 1 1360{}1129 ASTR 1 - CLOC 1 80D3-80D3 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020240
SYM|1360{}1129
SYN|TE20240
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1129
CLOC|80D3-80D3
LOCB|genomic location inferred from flanking sequence
DBAF|AE002786.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020243 ICL 1 1360 SYM 1 1360{}1132 ASTR 1 - CLOC 1 80D3-80D3 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020243
SYM|1360{}1132
SYN|TE20243
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1132
CLOC|80D3-80D3
LOCB|genomic location inferred from flanking sequence
DBAF|AE002786.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020244 ICL 1 1360 SYM 1 1360{}1133 ASTR 1 - CLOC 1 80D3-80D3 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020244
SYM|1360{}1133
SYN|TE20244
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1133
CLOC|80D3-80D3
LOCB|genomic location inferred from flanking sequence
DBAF|AE002656.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020249 ICL 1 1360 SYM 1 1360{}1138 ASTR 1 - CLOC 1 80D5-80D5 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020249
SYM|1360{}1138
SYN|TE20249
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1138
CLOC|80D5-80D5
LOCB|genomic location inferred from flanking sequence
DBAF|AE002656.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020271 ICL 1 1360 SYM 1 1360{}1160 ASTR 1 - CLOC 1 80E2-80E2 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020271
SYM|1360{}1160
SYN|TE20271
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1160
CLOC|80E2-80E2
LOCB|genomic location inferred from flanking sequence
DBAF|AE002656.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020273 ICL 1 1360 SYM 1 1360{}1162 ASTR 1 - CLOC 1 80E3-80E3 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020273
SYM|1360{}1162
SYN|TE20273
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1162
CLOC|80E3-80E3
LOCB|genomic location inferred from flanking sequence
DBAF|AE002656.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020282 ICL 1 1360 SYM 1 1360{}1171 ASTR 1 - CLOC 1 80F3-80F3 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020282
SYM|1360{}1171
SYN|TE20282
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1171
CLOC|80F3-80F3
LOCB|genomic location inferred from flanking sequence
DBAF|AE002665.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020291 ICL 1 1360 SYM 1 1360{}1180 ASTR 1 - CLOC 1 80F5-80F5 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020291
SYM|1360{}1180
SYN|TE20291
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1180
CLOC|80F5-80F5
LOCB|genomic location inferred from flanking sequence
DBAF|AE002665.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020301 ICL 1 1360 SYM 1 1360{}1198 ASTR 1 - CLOC 1 82C2-82C2 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020301
SYM|1360{}1198
SYN|TE20301
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1198
CLOC|82C2-82C2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003606.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019290 ICL 1 1360 SYM 1 1360{}1201 ASTR 1 - CLOC 1 82C3-82C3 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0019290
SYM|1360{}1201
SYN|TE19290
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1201
CLOC|82C3-82C3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003606.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020305 ICL 1 1360 SYM 1 1360{}1206 ASTR 1 - CLOC 1 82C4-82C4 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020305
SYM|1360{}1206
SYN|TE20305
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1206
CLOC|82C4-82C4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003605.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019309 ICL 1 1360 SYM 1 1360{}1226 ASTR 1 - CLOC 1 83C4-83C4 REF 1 3 DT 1 21 Aug 2003 RESZ 450
ID|FBti0019309
SYM|1360{}1226
SYN|CR31553
|TE19309
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0104946
|FlyBase
|1996-
SYN|CR31553
}
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1226
CLOC|83C4-83C4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003601.3
}
REF
{
REFM|FBrf0104946
|FlyBase
|1996-
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020322 ICL 1 1360 SYM 1 1360{}1257 ASTR 1 - CLOC 1 84E2-84E2 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020322
SYM|1360{}1257
SYN|TE20322
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1257
CLOC|84E2-84E2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003676.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019330 ICL 1 1360 SYM 1 1360{}1258 ASTR 1 - CLOC 1 84E6-84E6 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0019330
SYM|1360{}1258
SYN|TE19330
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1258
CLOC|84E6-84E6
LOCB|genomic location inferred from flanking sequence
DBAF|AE003677.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020323 ICL 1 1360 SYM 1 1360{}1270 ASTR 1 - CLOC 1 85B4-85B4 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020323
SYM|1360{}1270
SYN|TE20323
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1270
CLOC|85B4-85B4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003680.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019361 ICL 1 1360 SYM 1 1360{}1299 ASTR 1 - CLOC 1 87B12-87B13 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019361
SYM|1360{}1299
SYN|TE19361
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1299
CLOC|87B12-87B13
LOCB|genomic location inferred from flanking sequence
DBAF|AE003696.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019418 ICL 1 1360 SYM 1 1360{}1408 ASTR 1 - CLOC 1 95A1-95A1 REF 1 3 DT 1 21 Aug 2003 RESZ 768
ID|FBti0019418
SYM|1360{}1408
SYN|CR31276
|TE19418
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
CLOC|95A1-95A1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003743.3
}
REFDSR
{
RDID|FBrf0166453
|FlyBase Genome Annotators
|2004
SYN|1360{}1408
CLOC|95A1-95A1
LOCB|genomic location inferred from flanking sequence
CC|"CR31276" was annotated as a "miscellaneous curator's observation" in
| release 3.1 of the genome annotation, but has been deleted in release 3.2
| as it corresponded to the FBti0019418==1360{}1408 insertion.
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
REFM|FBrf0166453
|FlyBase Genome Annotators
|2004
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019460 ICL 1 1360 SYM 1 1360{}1457 ASTR 1 - CLOC 1 99E3-99E3 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0019460
SYM|1360{}1457
SYN|TE19460
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1457
CLOC|99E3-99E3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003773.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020393 ICL 1 1360 SYM 1 1360{}1463 ASTR 1 - CLOC 1 100A6-100A6 REF 1 3 DT 1 21 Aug 2003 RESZ 452
ID|FBti0020393
SYM|1360{}1463
SYN|CR31011
|TE20393
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0104946
|FlyBase
|1996-
SYN|CR31011
}
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1463
CLOC|100A6-100A6
LOCB|genomic location inferred from flanking sequence
DBAF|AE003775.2
}
REF
{
REFM|FBrf0104946
|FlyBase
|1996-
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020400 ICL 1 1360 SYM 1 1360{}1476 ASTR 1 - CLOC 1 102A1-102A1 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020400
SYM|1360{}1476
SYN|TE20400
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1476
CLOC|102A1-102A1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003845.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020403 ICL 1 1360 SYM 1 1360{}1479 ASTR 1 - CLOC 1 102A3-102A3 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020403
SYM|1360{}1479
SYN|TE20403
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1479
CLOC|102A3-102A3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003845.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020404 ICL 1 1360 SYM 1 1360{}1480 ASTR 1 - CLOC 1 102A3-102A3 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020404
SYM|1360{}1480
SYN|TE20404
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1480
CLOC|102A3-102A3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003845.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020405 ICL 1 1360 SYM 1 1360{}1481 ASTR 1 - CLOC 1 102A3-102A3 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020405
SYM|1360{}1481
SYN|TE20405
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1481
CLOC|102A3-102A3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003845.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019472 ICL 1 1360 SYM 1 1360{}1482 ASTR 1 - CLOC 1 102A4-102A4 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019472
SYM|1360{}1482
SYN|TE19472
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1482
CLOC|102A4-102A4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003845.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019477 ICL 1 1360 SYM 1 1360{}1488 ASTR 1 - CLOC 1 102B1-102B1 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019477
SYM|1360{}1488
SYN|TE19477
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1488
CLOC|102B1-102B1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003844.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019479 ICL 1 1360 SYM 1 1360{}1491 ASTR 1 - CLOC 1 102B1-102B1 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019479
SYM|1360{}1491
SYN|TE19479
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1491
CLOC|102B1-102B1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003844.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019484 ICL 1 1360 SYM 1 1360{}1498 ASTR 1 - CLOC 1 102B5-102B5 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019484
SYM|1360{}1498
SYN|TE19484
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1498
CLOC|102B5-102B5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003844.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020414 ICL 1 1360 SYM 1 1360{}1502 ASTR 1 - CLOC 1 102B5-102B5 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020414
SYM|1360{}1502
SYN|TE20414
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1502
CLOC|102B5-102B5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003844.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020415 ICL 1 1360 SYM 1 1360{}1503 ASTR 1 - CLOC 1 102B5-102B5 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020415
SYM|1360{}1503
SYN|TE20415
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1503
CLOC|102B5-102B5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003844.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019485 ICL 1 1360 SYM 1 1360{}1504 ASTR 1 - CLOC 1 102B5-102B5 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019485
SYM|1360{}1504
SYN|TE19485
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1504
CLOC|102B5-102B5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003844.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020418 ICL 1 1360 SYM 1 1360{}1507 ASTR 1 - CLOC 1 102B6-102B7 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020418
SYM|1360{}1507
SYN|TE20418
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1507
CLOC|102B6-102B7
LOCB|genomic location inferred from flanking sequence
DBAF|AE003844.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020419 ICL 1 1360 SYM 1 1360{}1508 ASTR 1 - CLOC 1 102B7-102B7 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020419
SYM|1360{}1508
SYN|TE20419
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1508
CLOC|102B7-102B7
LOCB|genomic location inferred from flanking sequence
DBAF|AE003844.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019488 ICL 1 1360 SYM 1 1360{}1512 ASTR 1 - CLOC 1 102B8-102B8 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019488
SYM|1360{}1512
SYN|TE19488
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1512
CLOC|102B8-102B8
LOCB|genomic location inferred from flanking sequence
DBAF|AE003844.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020422 ICL 1 1360 SYM 1 1360{}1514 ASTR 1 - CLOC 1 102C1-102C1 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020422
SYM|1360{}1514
SYN|TE20422
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1514
CLOC|102C1-102C1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003844.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020423 ICL 1 1360 SYM 1 1360{}1515 ASTR 1 - CLOC 1 102C1-102C1 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020423
SYM|1360{}1515
SYN|TE20423
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1515
CLOC|102C1-102C1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003844.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019494 ICL 1 1360 SYM 1 1360{}1520 ASTR 1 - CLOC 1 102D1-102D1 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019494
SYM|1360{}1520
SYN|TE19494
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1520
CLOC|102D1-102D1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003843.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019496 ICL 1 1360 SYM 1 1360{}1525 ASTR 1 - CLOC 1 102D5-102D5 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019496
SYM|1360{}1525
SYN|TE19496
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1525
CLOC|102D5-102D5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003843.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020432 ICL 1 1360 SYM 1 1360{}1530 ASTR 1 - CLOC 1 102E5-102E5 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020432
SYM|1360{}1530
SYN|TE20432
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1530
CLOC|102E5-102E5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003843.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020434 ICL 1 1360 SYM 1 1360{}1533 ASTR 1 - CLOC 1 102E5-102E5 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020434
SYM|1360{}1533
SYN|TE20434
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1533
CLOC|102E5-102E5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003843.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019500 ICL 1 1360 SYM 1 1360{}1536 ASTR 1 - CLOC 1 102F2-102F2 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019500
SYM|1360{}1536
SYN|TE19500
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1536
CLOC|102F2-102F2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003847.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019502 ICL 1 1360 SYM 1 1360{}1539 ASTR 1 - CLOC 1 102F3-102F3 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019502
SYM|1360{}1539
SYN|TE19502
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1539
CLOC|102F3-102F3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003846.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019507 ICL 1 1360 SYM 1 1360{}1543 ASTR 1 - CLOC 1 102F4-102F4 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019507
SYM|1360{}1543
SYN|TE19507
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1543
CLOC|102F4-102F4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003846.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020437 ICL 1 1360 SYM 1 1360{}1545 ASTR 1 - CLOC 1 102F4-102F4 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020437
SYM|1360{}1545
SYN|TE20437
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1545
CLOC|102F4-102F4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003846.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020438 ICL 1 1360 SYM 1 1360{}1546 ASTR 1 - CLOC 1 102F4-102F4 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020438
SYM|1360{}1546
SYN|TE20438
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1546
CLOC|102F4-102F4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003846.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019516 ICL 1 1360 SYM 1 1360{}1558 ASTR 1 - CLOC 1 102F8-102F8 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019516
SYM|1360{}1558
SYN|TE19516
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1558
CLOC|102F8-102F8
LOCB|genomic location inferred from flanking sequence
DBAF|AE003846.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019518 ICL 1 1360 SYM 1 1360{}1561 ASTR 1 - CLOC 1 102F8-102F8 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019518
SYM|1360{}1561
SYN|TE19518
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1561
CLOC|102F8-102F8
LOCB|genomic location inferred from flanking sequence
DBAF|AE003846.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020446 ICL 1 1360 SYM 1 1360{}1565 ASTR 1 - CLOC 1 102F8-102F8 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020446
SYM|1360{}1565
SYN|TE20446
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1565
CLOC|102F8-102F8
LOCB|genomic location inferred from flanking sequence
DBAF|AE003846.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020451 ICL 1 1360 SYM 1 1360{}1570 ASTR 1 - CLOC 1 102F8-102F8 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020451
SYM|1360{}1570
SYN|TE20451
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1570
CLOC|102F8-102F8
LOCB|genomic location inferred from flanking sequence
DBAF|AE003846.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020452 ICL 1 1360 SYM 1 1360{}1571 ASTR 1 - CLOC 1 102F8-102F8 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020452
SYM|1360{}1571
SYN|TE20452
ASTP|FBtp0011398==1360
DT|21 Aug 2003
|21 Aug 2003
ICL|1360
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1360{}1571
CLOC|102F8-102F8
LOCB|genomic location inferred from flanking sequence
DBAF|AE003846.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014399 ICL 1 ? SYM 1 1360{}da1 ASTR 1 - CLOC 1 31D11--E1 REF 1 5 DT 1 26 Mar 2002 RESZ 862
ID|FBti0014399
SYM|1360{}da1
SYN|?{}da1
ASTP|FBtp0011398==1360
DT|26 Mar 2002
|6 Jan 2000
ICL|?
ASGN|FBgn0000413==da
REFDSR
{
RDID|FBrf0055585
|Keyes et al.
|1992
PHC|lethal | maternal effect | conditional ts
}
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}da1
ASAL|FBal0002214==da1
MU|spontaneous
CLOC|31D11--E1
|Insertion site
LOCB|Proximity to gene: FBgn0000413==da
}
REFDSR
{
RDID|FBrf0068461
|Cummings and Cronmiller
|1994
PHC|(with da2) lethal
}
REFDSR
{
RDID|FBrf0138569
|Castanon et al.
|2001
PHC|lethal | conditional ts
}
REF
{
REFM|FBrf0055585
|Keyes et al.
|1992
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0068461
|Cummings and Cronmiller
|1994
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0138569
|Castanon et al.
|2001
}
ALESR
{
ASYM|FBal0002214==da1
REFDSR
{
RDID|FBrf0041411
|Uenoyama
|1984
PHP|FBal0016680==Sxlf1 heterozygous female progeny derived from
| heterozygous FBal0002214==da1
|mothers have reduced viability. The viability is increased if the
|FBal0016680==Sxlf1/+ progeny are also carrying
| FBal0012357==msl-31, and is decreased
|if the FBal0002214==da1/+ mothers are also carrying
| FBal0012357==msl-31. The frequency
|of sex transformation in FBal0016680==Sxlf1/+ female progeny
| derived from FBal0002214==da1/+
|mothers is increased if either the mothers or the progeny are homozygous
|for FBal0012357==msl-31. The frequency of morphological
| abnormalities seen
|... (see FBal0002214==da1 report)
}
REFDSR
{
RDID|FBrf0054060
|Bopp et al.
|1991
PHP|At the restrictive temperature (25oC) less than 1% of females derived
|from homozygous mothers eclose. At the permissive temperature (18oC)
|the viability of these females derived from homozygous mothers is 100%.
}
REFDSR
{
RDID|FBrf0078360
|Estes et al.
|1995
PHP|Homozygous females have no female offspring due to failure to properly
|regulate the FBgn0003659==Sxl gene in the zygote.
}
REFDSR
{
RDID|FBrf0094140
|Bell
|1954
PHP|Homozygous females when mated to any male produce normal sons but no
|daughters. Otherwise, FBgn0000413==da mutant cannot be distinguished from wild
|type.
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|(=da); viable; temperature-sensitive hypomorph; strong
|daughterless maternal effect above 22oC; lethal
|with Df or amorphic alleles; lethal at 29oC
}
REFDSR
{
RDID|FBrf0106007
|Anand et al.
|1998
PHP|Does not interact with FBal0094602==Sxldlf,
| FBal0094543==fl(1)3535 or FBal0094542==fl(1)3546.
}
REFDSR
{
RDID|FBrf0138569
|Castanon et al.
|2001
PHP|Homozygotes survive at 18oC and die at 25oC.
|FBal0002214==da1 homozygous embryos lacking maternal and zygotic
| FBgn0000413==da have defects
|in mesodermal development. The mesoderm migrates properly, however,
|further mesodermal development is impaired. Somatic muscle development
|is severely suppressed, embryos have reduced numbers of aberrantly
|placed syncitial muscles. Heart development is also repressed.
PHM|embryonic/larval somatic muscle
|mesoderm
|embryonic/larval heart
}
REF
{
REFM|FBrf0041411
|Uenoyama
|1984
REFM|FBrf0054060
|Bopp et al.
|1991
REFM|FBrf0078360
|Estes et al.
|1995
REFM|FBrf0094140
|Bell
|1954
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0106007
|Anand et al.
|1998
REFM|FBrf0138569
|Castanon et al.
|2001
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0019679 ICL 1 1731 SYM 1 1731{}207 ASTR 1 - CLOC 1 20A1-20A1 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019679
SYM|1731{}207
SYN|TE19679
ASTP|FBtp0011400==1731
DT|21 Aug 2003
|21 Aug 2003
ICL|1731
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1731{}207
CLOC|20A1-20A1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003568.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020325 ICL 1 1731 SYM 1 1731{}1272 ASTR 1 - CLOC 1 85B4-85B4 REF 1 2 DT 1 21 Aug 2003 RESZ 351
ID|FBti0020325
SYM|1731{}1272
SYN|TE20325
ASTP|FBtp0011400==1731
DT|21 Aug 2003
|21 Aug 2003
ICL|1731
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|1731{}1272
CLOC|85B4-85B4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003680.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0015144 ICL 1 ? SYM 1 ?{}anon-4Caverzwickt ASTR 1 - CLOC 1 4C REF 1 2 DT 1 6 Jan 2000 RESZ 431
ID|FBti0015144
SYM|?{}anon-4Caverzwickt
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0014102==anon-4Ca
REFDSR
{
RDID|FBrf0064240
|Poeck et al.
|1991
SYN|?{}anon-4Caverzwickt
ASAL|FBal0065901==anon-4Caverzwickt
CLOC|4C
|Insertion site
LOCB|Proximity to gene: FBgn0014102==anon-4Ca
}
REF
{
REFM|FBrf0064240
|Poeck et al.
|1991
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0002824 ICL 1 ? SYM 1 ?{}Antp72j ASTR 1 - CLOC 1 84B1--2 REF 1 2 DT 1 5 Feb 1999 RESZ 512
ID|FBti0002824
SYM|?{}Antp72j
DT|5 Feb 1999
|24 Jun 1997
ICL|?
ASGN|FBgn0000095==Antp
REFDSR
{
RDID|FBrf0039012
|Scott et al.
|1983
ASAL|FBal0000572==Antp72j
MU|spontaneous
CLOC|84B1--2
|Insertion site
LOCB|Proximity to gene: FBgn0000095==Antp
PHC|viable
CC|Insertion determined to be repetitive; approximately 8.3kb; not shown to
| coorelate with mutant phenotype.
}
REF
{
REFM|FBrf0039012
|Scott et al.
|1983
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0000572==Antp72j
REFDSR
{
RDID|FBrf0039012
|Scott et al.
|1983
PHP|Antennae to leg transformations.
PHM|leg | ectopic
|antenna
}
REF
{
REFM|FBrf0039012
|Scott et al.
|1983
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0002825 ICL 1 ? SYM 1 ?{}AntpScx ASTR 1 - CLOC 1 84B1--2 REF 1 5 DT 1 5 Feb 1999 RESZ 1078
ID|FBti0002825
SYM|?{}AntpScx
DT|5 Feb 1999
|24 Jun 1997
ICL|?
ASGN|FBgn0000095==Antp
|FBgn0003339==Scr
REFDSR
{
RDID|FBrf0027527
|Duncan and Kaufman
|1975
PHC|lethal | recessive
}
REFDSR
{
RDID|FBrf0034841
|Kaufman et al.
|1980
PHC|lethal | recessive
}
REFDSR
{
RDID|FBrf0039012
|Scott et al.
|1983
ASAL|FBal0000617==AntpScx
MU|spontaneous
CLOC|84B1--2
|Insertion site
LOCB|Proximity to gene: FBgn0000095==Antp
PHC|lethal | recessive
CC|Insertion determined to be repetitive; approximately 3kb; not shown to
| coorelate with mutant phenotype.
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHC|lethal | recessive
}
REFDSR
{
RDID|FBrf0149025
|Southworth and Kennison
|2002
ASAL|FBal0138396==ScrScx
PHC|(with Antp1) lethal
|(with Antp23) lethal
}
REF
{
REFM|FBrf0027527
|Duncan and Kaufman
|1975
REFM|FBrf0034841
|Kaufman et al.
|1980
REFM|FBrf0039012
|Scott et al.
|1983
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0149025
|Southworth and Kennison
|2002
}
ALESR
{
ASYM|FBal0138396==ScrScx
REFDSR
{
RDID|FBrf0149025
|Southworth and Kennison
|2002
PHP|Heterozygous males have an average of 2.7 ectopic sex comb teeth per
|second leg. The number of sex comb teeth on the first leg is normal.
|FBal0138396==ScrScx/FBal0015280==Scr4 males have the
| same average number of sex comb
|teeth per first leg as FBal0015280==Scr4/+ males.
|Heterozygous males have an average of 0.1 ectopic sex comb teeth per
|third leg.
|FBal0138396==ScrScx/FBal0015278==Scr2 males have an
| average of 1.3 ectopic sex comb teeth
|... (see FBal0138396==ScrScx report)
PHM|mesothoracic leg & sex comb | ectopic
|metathoracic leg & sex comb | ectopic
|(with Scr2) mesothoracic leg & sex comb | ectopic
|(with Scr4) mesothoracic leg & sex comb | ectopic
|(with Scr4) metathoracic leg & sex comb | ectopic
|(with Scr4, Dp(3;Y)77ab) mesothoracic leg & sex comb | ectopic
|(with Scr4, Dp(3;Y)77ab) metathoracic leg & sex comb | ectopic
|(with ScrTpl9) mesothoracic leg & sex comb | ectopic
|(with ScrTpl9) metathoracic leg & sex comb | ectopic
}
REF
{
REFM|FBrf0149025
|Southworth and Kennison
|2002
}
}
# EO ALESR
ALESR
{
ASYM|FBal0000617==AntpScx
REFDSR
{
RDID|FBrf0027527
|Duncan and Kaufman
|1975
PHP|Sex combs are present on all male legs.
PHM|sex comb | ectopic
}
REFDSR
{
RDID|FBrf0034841
|Kaufman et al.
|1980
PHP|Sex comb teeth are produced on the basitarsus of all six legs (transformation
|of meso- and metathoracic into prothoracic legs).
PHM|sex comb
|mesothoracic leg
|metathoracic leg
}
REFDSR
{
RDID|FBrf0034853
|Lewis et al.
|1980
PHP|Transformation of meso- and metathoracic legs to prothoracic leg identity.
PHM|mesothoracic leg
|metathoracic leg
}
REFDSR
{
RDID|FBrf0039012
|Scott et al.
|1983
PHP|Partial transformation of second and third legs into first legs.
PHM|mesothoracic leg
|metathoracic leg
}
REFDSR
{
RDID|FBrf0043249
|Dura et al.
|1985
PHP|Enhanced by FBal0013723==ph-d2.
}
REFDSR
{
RDID|FBrf0046404
|Kennison and Russell
|1987
PHP|Suppressed by a duplication carrying FBgn0003042==Pc+.
}
REFDSR
{
RDID|FBrf0073734
|Lewis et al.
|1980
PHP|Transformation of meso- and metathoracic leg to prothoracic leg identity.
PHM|mesothoracic leg
|metathoracic leg
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Sex combs may be present on all six legs of male. At least
|one extra sex comb present in 75-90% of males. Third pair of
|legs less often affected than second.
|RK2.
PHM|sex comb
|mesothoracic leg
|metathoracic leg
}
REFDSR
{
RDID|FBrf0110811
|Sinclair et al.
|1984
PHP|Between 44.4% and 61.5% of heterozygous males have an extra sex combs
|phenotype.
PHM|leg
|sex comb | ectopic
}
REF
{
REFM|FBrf0027527
|Duncan and Kaufman
|1975
REFM|FBrf0034841
|Kaufman et al.
|1980
REFM|FBrf0034853
|Lewis et al.
|1980
REFM|FBrf0039012
|Scott et al.
|1983
REFM|FBrf0043249
|Dura et al.
|1985
REFM|FBrf0046404
|Kennison and Russell
|1987
REFM|FBrf0073734
|Lewis et al.
|1980
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0110811
|Sinclair et al.
|1984
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014268 ICL 1 ? SYM 1 ?{}btl-a ASTR 1 - CLOC 1 102C2--3 REF 1 4 DT 1 6 Jan 2000 RESZ 762
ID|FBti0014268
SYM|?{}btl-a
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0005666==bt
REFDSR
{
RDID|FBrf0016176
|Hochman et al.
|1964
PHC|lethal | recessive
}
REFDSR
{
RDID|FBrf0022724
|Hochman
|1971
PHC|lethal
}
REFDSR
{
RDID|FBrf0079869
|Ayme-Southgate et al.
|1995
SYN|?{}btl-a
ASAL|FBal0027983==btl-a
CLOC|102C2--3
|Insertion site
LOCB|Proximity to gene: FBgn0005666==bt
PHC|lethal | embryonic | recessive
|(with btD) lethal | embryonic
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHC|lethal | embryonic | recessive
}
REF
{
REFM|FBrf0016176
|Hochman et al.
|1964
REFM|FBrf0022724
|Hochman
|1971
REFM|FBrf0079869
|Ayme-Southgate et al.
|1995
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0027983==btl-a
REFDSR
{
RDID|FBrf0079869
|Ayme-Southgate et al.
|1995
PHP|Homozygotes die as late embryos and do not have spontaneous muscle
|contractions. FBal0001328==btD/FBal0027983==btl-a
| transheterozygotes die as embryos.
}
REF
{
REFM|FBrf0079869
|Ayme-Southgate et al.
|1995
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014101 ICL 1 ? SYM 1 ?{}BxM ASTR 1 - CLOC 1 17C3--4 REF 1 2 DT 1 6 Jan 2000 RESZ 407
ID|FBti0014101
SYM|?{}BxM
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0000242==Bx
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}BxM
ASAL|FBal0001443==BxM
MU|spontaneous
CLOC|17C3--4
|Insertion site
LOCB|Proximity to gene: FBgn0000242==Bx
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014994 ICL 1 P SYM 1 ?{}can8 ASTR 1 - CLOC 1 67D12 REF 1 3 DT 1 23 Jul 2001 RESZ 537
ID|FBti0014994
SYM|?{}can8
SYN|P{}can8
DT|23 Jul 2001
|6 Jan 2000
ICL|P
ASGN|FBgn0011569==can
REFDSR
{
RDID|FBrf0087570
|Lin et al.
|1996
SYN|P{}can8
ASAL|FBal0049380==can8
CLOC|67D12
|Insertion site
LOCB|Proximity to gene: FBgn0011569==can
PHC|male sterile | recessive
}
REFDSR
{
RDID|FBrf0135773
|Hiller et al.
|2001
PHC|male sterile
}
REF
{
REFM|FBrf0087570
|Lin et al.
|1996
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135773
|Hiller et al.
|2001
}
ALESR
{
ASYM|FBal0049380==can8
REFDSR
{
RDID|FBrf0087570
|Lin et al.
|1996
PHP|Early stages of spermatogenesis up through mature primary spermatocytes
|are present and normal. Postmeiotic stages are completely absent.
|Mutant testes have an abundance of mature primary spermatocytes with
|large, round nuclei and prominent nucleoli.
|Spermatocytes arrest in the G2/M transition of meiosis I with partial
|chromosome condensation.
PHM|testis
|spermatocyte
}
REF
{
REFM|FBrf0087570
|Lin et al.
|1996
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014995 ICL 1 P SYM 1 ?{}can9 ASTR 1 - CLOC 1 67D12 REF 1 3 DT 1 23 Jul 2001 RESZ 537
ID|FBti0014995
SYM|?{}can9
SYN|P{}can9
DT|23 Jul 2001
|6 Jan 2000
ICL|P
ASGN|FBgn0011569==can
REFDSR
{
RDID|FBrf0087570
|Lin et al.
|1996
SYN|P{}can9
ASAL|FBal0049381==can9
CLOC|67D12
|Insertion site
LOCB|Proximity to gene: FBgn0011569==can
PHC|male sterile | recessive
}
REFDSR
{
RDID|FBrf0135773
|Hiller et al.
|2001
PHC|male sterile
}
REF
{
REFM|FBrf0087570
|Lin et al.
|1996
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135773
|Hiller et al.
|2001
}
ALESR
{
ASYM|FBal0049381==can9
REFDSR
{
RDID|FBrf0087570
|Lin et al.
|1996
PHP|Early stages of spermatogenesis up through mature primary spermatocytes
|are present and normal. Postmeiotic stages are completely absent.
|Mutant testes have an abundance of mature primary spermatocytes with
|large, round nuclei and prominent nucleoli. Early stages of spermatogenesis
|up through mature primary spermatocytes are present and normal. Postmeiotic
|stages are completely absent. Mutant testes have an abundance of mature
|primary spermatocytes with large, round nuclei and prominent nucleoli.
|... (see FBal0049381==can9 report)
PHM|testis
|spermatocyte
}
REF
{
REFM|FBrf0087570
|Lin et al.
|1996
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0016955 ICL 1 ? SYM 1 ?{}cg1 ASTR 1 - CLOC 1 50E1 REF 1 2 DT 1 25 Dec 2000 RESZ 478
ID|FBti0016955
SYM|?{}cg1
DT|25 Dec 2000
|25 Dec 2000
ICL|?
ASGN|FBgn0000289==cg
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHC|female sterile | recessive
}
REFDSR
{
RDID|FBrf0130102
|Svendsen et al.
|2000
SYN|?{}cg1
ASAL|FBal0001596==cg1
MU|spontaneous
CLOC|50E1
|Insertion site
LOCB|Proximity to gene: FBgn0000289==cg
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0130102
|Svendsen et al.
|2000
}
ALESR
{
ASYM|FBal0001596==cg1
REFDSR
{
RDID|FBrf0007527
|Beatty
|1949
PHP|Oogenesis highly irregular.
}
REFDSR
{
RDID|FBrf0052918
|Diaz-Benjumea and Garcia-Bellido
|1990
PHP|Terminal gaps in wing vein L4 and homozygotes have intercalary gaps in wing
| vein L5.
|Also abnormalities in legs and in oogenesis.
PHM|wing vein L4
|wing vein L5
|leg
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Sex combs of male extremely large. Number of sex comb teeth increased
|from 10 to 18; number of bractless bristles increased; width of distal
|portion of basitarsus increased 1.6 fold; total number of bristles on
|basitarsus increased in both sexes (FBrf0065640; FBrf0063395). Some
|distortion and shortening of legs. Wings show gap in vein L4 between
|posterior crossvein and margin. Wings slightly curved. Effects result from
|a combination of overgrowth and irregular folding of imaginal rudiments
|... (see FBal0001596==cg1 report)
PHM|sex comb
|wing vein L4
|wing
}
REFDSR
{
RDID|FBrf0129753
|Campbell and Tomlinson
|2000
PHP|Homozygous and FBal0001596==cg1/FBal0008129==cg07659
| flies have gaps in wing vein L4.
|Homozygous and FBal0001596==cg1/FBal0008129==cg07659
| males have extra sex comb teeth.
PHM|wing vein L4
|(with cg07659) wing vein L4
|sex comb | supernumerary
|(with cg07659) sex comb | supernumerary
}
REFDSR
{
RDID|FBrf0130102
|Svendsen et al.
|2000
PHP|Homozygotes have phenotypes in the wing, leg and antenna.
|Approximately 10% of
| FBal0001596==cg1/FBal0008129==cg07659 and 50% of FBal0001596==cg1/FBal0119302==cg3
|animals eclose to adult stages, with most of the remaining animals
|dying as pharate adults.
|FBal0001596==cg1/FBal0001596==cg1,
| FBal0001596==cg1/FBal0008129==cg07659 and
| FBal0001596==cg1/FBal0119302==cg3 flies have
|defects in some combination of the posterior compartment longitudinal
|veins L4 and L5. Defects in vein L4, ranging from a slight thinning
|... (see FBal0001596==cg1 report)
PHM|wing
|leg
|antenna
|wing vein L4
|wing vein L5
|(with cg07659) wing vein L4
|(with cg07659) wing vein L5
|(with cg3) wing vein L4
|(with cg3) wing vein L5
|(with cg07659) wing vein L2
|wing margin | anterior
|(with cg3) wing margin | anterior
|(with cg07659) wing margin | anterior
|sex comb | supernumerary
|mesothoracic leg
|(with cg07659) ventral thoracic disc
|(with cg07659) sex comb | supernumerary
|(with cg07659) prothoracic tibial transverse bristle row | supernumerary
|(with cg3) wing | posterior compartment
|(with cg07659) wing | posterior compartment
}
REFDSR
{
RDID|FBrf0131401
|Song et al.
|2000
PHP|FBal0001596==cg1/FBal0125097==cgk11504
| transheterozygotes show pleiotropic defects in
|bristle number, wing venation and oogenesis.
PHM|(with cgk11504) wing vein
|(with cgk11504) macrochaeta
}
REF
{
REFM|FBrf0007527
|Beatty
|1949
REFM|FBrf0052918
|Diaz-Benjumea and Garcia-Bellido
|1990
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0129753
|Campbell and Tomlinson
|2000
REFM|FBrf0130102
|Svendsen et al.
|2000
REFM|FBrf0131401
|Song et al.
|2000
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0016968 ICL 1 ? SYM 1 ?{}cg3 ASTR 1 - CLOC 1 50E1 REF 1 2 DT 1 25 Dec 2000 RESZ 410
ID|FBti0016968
SYM|?{}cg3
DT|25 Dec 2000
|25 Dec 2000
ICL|?
ASGN|FBgn0000289==cg
REFDSR
{
RDID|FBrf0130102
|Svendsen et al.
|2000
SYN|?{}cg3
ASAL|FBal0119302==cg3
CLOC|50E1
|Insertion site
LOCB|Proximity to gene: FBgn0000289==cg
PHC|lethal | recessive
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0130102
|Svendsen et al.
|2000
}
ALESR
{
ASYM|FBal0119302==cg3
REFDSR
{
RDID|FBrf0130102
|Svendsen et al.
|2000
PHP|Most homozygotes survive until the pharate adult stage.
|Approximately 50% of FBal0001596==cg1/FBal0119302==cg3
| animals eclose to adult stages,
|with most of the remaining animals dying as pharate adults. FBal0001596==cg1/FBal0119302==cg3
|flies have defects in some combination of the posterior compartment
|longitudinal veins L4 and L5. Defects in vein L4, ranging from a slight
|thinning of the vein to gaps of increasing size are seen in 100% of
|wings. Defects in wing vein L5 are seen in less than 25% of flies.
|... (see FBal0119302==cg3 report)
PHM|(with cg1) wing vein L4
|(with cg1) wing vein L5
|(with cg1) wing margin | anterior
|(with cg07659) prothoracic tibial preapical bristle | supernumerary
|(with cg07659) sex comb | supernumerary
|(with cg1) wing | posterior compartment
|(with cg07659) wing | anterior compartment
|(with cg07659) ventral thoracic disc | anterior compartment
}
REF
{
REFM|FBrf0130102
|Svendsen et al.
|2000
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014281 ICL 1 ? SYM 1 ?{}ci36 ASTR 1 - CLOC 1 102A1--3 REF 1 2 DT 1 6 Jan 2000 RESZ 411
ID|FBti0014281
SYM|?{}ci36
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0004859==ci
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}ci36
ASAL|FBal0001645==ci36
MU|spontaneous
CLOC|102A1--3
|Insertion site
LOCB|Proximity to gene: FBgn0004859==ci
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0001645==ci36
REFDSR
{
RDID|FBrf0073755
|Locke and Tartof
|1994
PHP|Homozygous viable.
}
REFDSR
{
RDID|FBrf0092613
|Locke and Hanna
|1996
PHM|wing vein
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Less extreme than FBal0001644==ci1. Ranges from appearance of a plexus
|in L4 between crossveins to gaps in L4 and L5 posterior
|to crossveins.
|RK3.
}
REF
{
REFM|FBrf0073755
|Locke and Tartof
|1994
REFM|FBrf0092613
|Locke and Hanna
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0016967 ICL 1 ? SYM 1 ?{}cin ASTR 1 - CLOC 1 102A1--3 REF 1 2 DT 1 25 Dec 2000 RESZ 481
ID|FBti0016967
SYM|?{}cin
DT|25 Dec 2000
|25 Dec 2000
ICL|?
ASGN|FBgn0004859==ci
REFDSR
{
RDID|FBrf0129753
|Campbell and Tomlinson
|2000
SYN|?{}cin
ASAL|FBal0119295==cin
CLOC|102A1--3
|Insertion site
LOCB|Proximity to gene: FBgn0004859==ci
PHC|(with ciD) lethal | pupal
|(with ci94) lethal | pupal
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0129753
|Campbell and Tomlinson
|2000
}
ALESR
{
ASYM|FBal0119295==cin
REFDSR
{
RDID|FBrf0129753
|Campbell and Tomlinson
|2000
PHP|A small percentage of flies have wing duplications and most flies have
|enlarged antennae.
|FBal0119295==cin/FBal0045443==ci94 imaginal discs show overgrowth.
PHM|wing
|antenna
|(with ci94) ventral thoracic disc
|(with ci94) dorsal mesothoracic disc
}
REF
{
REFM|FBrf0129753
|Campbell and Tomlinson
|2000
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014283 ICL 1 ? SYM 1 ?{}ciW ASTR 1 - CLOC 1 102A1--3 REF 1 2 DT 1 6 Jan 2000 RESZ 408
ID|FBti0014283
SYM|?{}ciW
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0004859==ci
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}ciW
ASAL|FBal0001653==ciW
MU|spontaneous
CLOC|102A1--3
|Insertion site
LOCB|Proximity to gene: FBgn0004859==ci
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0001653==ciW
REFDSR
{
RDID|FBrf0052918
|Diaz-Benjumea and Garcia-Bellido
|1990
PHP|Lack all longitudinal and transverse veins and affect morphogenesis
|of legs and eyes.
}
REFDSR
{
RDID|FBrf0073755
|Locke and Tartof
|1994
PHP|Homozygous viable.
}
REFDSR
{
RDID|FBrf0087686
|Sanchez-Herrero et al.
|1996
PHP|Homozygotes occasionally show overgrowth in the anterior compartment
|of the wing. FBal0001651==ciD/FBal0001653==ciW flies
| have abnormal legs.
PHM|wing | anterior compartment
|(with ciD) leg
}
REFDSR
{
RDID|FBrf0088080
|Dominguez et al.
|1996
PHP|Wings from homozygotes have, at low penetrance, a mirror symmetrical
|outgrowth composed of anterior wing material, resembling duplications
|caused by ectopic FBgn0000490==dpp expression.
PHM|wing
}
REFDSR
{
RDID|FBrf0092613
|Locke and Hanna
|1996
PHM|wing vein
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Homozygote is extreme ci type. Wings sometimes almost
|twice normal width, arclike, and virtually lack veins.
|Often present is a well-organized pattern of venation
|in which the posterior crossvein flows smoothly into
|L5. Legs lumpy, sex combs larger than normal, antennae
|enlarged, eyes smaller and extra bristles present.
|Heterozygote shows gap in L4 in 80% of flies. FBal0001653==ciW
|... (see FBal0001653==ciW report)
}
REFDSR
{
RDID|FBrf0108513
|Dominguez
|1999
PHP|When analyzed in large clones in the developing eye the packing in
|the ommatidial clusters is disrupted.
PHM|ommatidial cluster
}
REFDSR
{
RDID|FBrf0129753
|Campbell and Tomlinson
|2000
PHP|Heterozygotes show variable loss of vein L4 tissue.
PHM|wing vein L4
}
REFDSR
{
RDID|FBrf0130102
|Svendsen et al.
|2000
PHP|Heterozygotes show wing vein L4 defects.
PHM|wing vein L4
}
REF
{
REFM|FBrf0052918
|Diaz-Benjumea and Garcia-Bellido
|1990
REFM|FBrf0073755
|Locke and Tartof
|1994
REFM|FBrf0087686
|Sanchez-Herrero et al.
|1996
REFM|FBrf0088080
|Dominguez et al.
|1996
REFM|FBrf0092613
|Locke and Hanna
|1996
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0108513
|Dominguez
|1999
REFM|FBrf0129753
|Campbell and Tomlinson
|2000
REFM|FBrf0130102
|Svendsen et al.
|2000
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014284 ICL 1 ? SYM 1 ?{}cm1 ASTR 1 - CLOC 1 6E4 REF 1 2 DT 1 6 Jan 2000 RESZ 397
ID|FBti0014284
SYM|?{}cm1
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0000330==cm
REFDSR
{
RDID|FBrf0112254
|Mullins et al.
|1999
SYN|?{}cm1
ASAL|FBal0001720==cm1
MU|spontaneous
CLOC|6E4
|Insertion site
LOCB|Proximity to gene: FBgn0000330==cm
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0112254
|Mullins et al.
|1999
}
ALESR
{
ASYM|FBal0001720==cm1
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye color: translucent dark ruby.
|Eye color: deep orange, with FBal0016127==st1.
|Eye color: lighter than FBal0001342==bw1, with FBal0001342==bw1.
|Malpighian tubule color: very pale yellow.
|RK1.
PHM|pigment cell
|Malpighian tubule
}
REFDSR
{
RDID|FBrf0112254
|Mullins et al.
|1999
PHP|Eye color: darker than wild type.
|Dramatic reduction in number of secondary and tertiary pigment granules
|surrounding the ommatidium. Outer rhabdomeres are also occasionally
|missing.
PHM|pigment cell
|secondary pigment cell pigment granule
|tertiary pigment cell pigment granule
|rhabdomere
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0112254
|Mullins et al.
|1999
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014285 ICL 1 ? SYM 1 ?{}cm4 ASTR 1 - CLOC 1 6E4 REF 1 2 DT 1 6 Jan 2000 RESZ 388
ID|FBti0014285
SYM|?{}cm4
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0000330==cm
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}cm4
ASAL|FBal0001723==cm4
CLOC|6E4
|Insertion site
LOCB|Proximity to gene: FBgn0000330==cm
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0001723==cm4
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|reverts spontaneously
|unstable
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014286 ICL 1 ? SYM 1 ?{}cosV1 ASTR 1 - CLOC 1 43B1--2 REF 1 2 DT 1 6 Jan 2000 RESZ 410
ID|FBti0014286
SYM|?{}cosV1
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0000352==cos
REFDSR
{
RDID|FBrf0096304
|Sisson et al.
|1997
SYN|?{}cosV1
ASAL|FBal0001778==cosV1
MU|spontaneous \?
CLOC|43B1--2
|Insertion site
LOCB|Proximity to gene: FBgn0000352==cos
}
REF
{
REFM|FBrf0096304
|Sisson et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0001778==cosV1
REFDSR
{
RDID|FBrf0065539
|Preat et al.
|1993
PHP|Phenotypic interactions when in combination with FBgn0000352==cos.
}
REFDSR
{
RDID|FBrf0076434
|Capdevila and Guerrero
|1994
PHP|Viable mutation. Wing phenotype is similar to the phenotype resulting
|from ectopic expression of FBal0039403==hhScer\UAS.cCa, induction
| of overgrowth with
|a mirror image duplication of structures of the anterior and posterior
|compartments.
PHM|wing | posterior compartment
|wing | anterior compartment
}
REFDSR
{
RDID|FBrf0087686
|Sanchez-Herrero et al.
|1996
PHP|FBal0001784==Cos2
| FBal0001778==cosV1/FBal0001782==cosV5 flies have
| abnormal legs. FBal0031366==fuJ; FBal0001784==Cos2
|FBal0001778==cosV1/FBal0001782==cosV5 flies show a
| FBgn0000352==cos phenotype in the thorax and
|legs.
PHM|leg
}
REFDSR
{
RDID|FBrf0096304
|Sisson et al.
|1997
PHP|Displays adult pattern duplications in the presence of semidominant
|alleles of FBgn0000353==Cos.
}
REFDSR
{
RDID|FBrf0098968
|Sanchez et al.
|1997
PHP|FBal0001778==cosV1/FBal0001782==cosV5 females show
| duplication of the dorsal vaginal
|plate with an increment in the number of sensilla trichodea and loss
|of the ventral vaginal plate. The eighth tergite and vulva are reduced.
|Anal plates are abnormal.
|FBal0001778==cosV1/FBal0001782==cosV5 males show
| fusion of the lateral plates and the
|claspers. The hypandrium phragma is reduced.
PHM|female gonopod | dorsal
|female gonopod | ventral
|genital arch
|vulva
|epiproct
|hypoproct
|lateral plate
|clasper
|hypandrial process
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|class III allele
|FBal0001782==cosV5 >= FBal0001781==cosV4 =
| FBal0001778==cosV1 >= FBal0001779==cosV2 >= FBal0001780==cosV3
}
REF
{
REFM|FBrf0065539
|Preat et al.
|1993
REFM|FBrf0076434
|Capdevila and Guerrero
|1994
REFM|FBrf0087686
|Sanchez-Herrero et al.
|1996
REFM|FBrf0096304
|Sisson et al.
|1997
REFM|FBrf0098968
|Sanchez et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0024409 ICL 1 ? SYM 1 ?{}Cyp6g1PSU-R ASTR 1 - CLOC 1 48E7 REF 1 2 DT 1 3 Apr 2003 RESZ 373
ID|FBti0024409
SYM|?{}Cyp6g1PSU-R
DT|3 Apr 2003
|3 Apr 2003
ICL|?
ASGN|FBgn0025454==Cyp6g1
REFDSR
{
RDID|FBrf0155239
SYN|?{}Cyp6g1PSU-R
ASAL|FBal0141853==Cyp6g1PSU-R
CLOC|48E7
|Insertion site
LOCB|Proximity to gene: FBgn0025454==Cyp6g1
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155239
}
ALESR
{
ASYM|FBal0141853==Cyp6g1PSU-R
REFDSR
{
RDID|FBrf0155239
PHP|The "PSU-R" strain shows dominant complete resistance to DDT.
}
REF
{
REFM|FBrf0155239
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014881 ICL 1 ? SYM 1 ?{}Dfd1 ASTR 1 - CLOC 1 84A5 REF 1 2 DT 1 6 Jan 2000 RESZ 405
ID|FBti0014881
SYM|?{}Dfd1
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0000439==Dfd
REFDSR
{
RDID|FBrf0051400
|McGinnis et al.
|1990
SYN|?{}Dfd1
ASAL|FBal0002374==Dfd1
MU|spontaneous
CLOC|84A5
|Insertion site
LOCB|Proximity to gene: FBgn0000439==Dfd
}
REF
{
REFM|FBrf0051400
|McGinnis et al.
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0002374==Dfd1
REFDSR
{
RDID|FBrf0046135
|Regulski et al.
|1987
PHP|Adult head defects.
}
REFDSR
{
RDID|FBrf0051116
|McGinnis et al.
|1990
PHP|Adults have ventral eye and orbital tissue missing.
}
REFDSR
{
RDID|FBrf0051400
|McGinnis et al.
|1990
PHP|Loss of ventral eye and orbital regions in the adult head. Head defects
|phenocopied by FBal0038716==Dfdhs.PK constructs and heat-shock
| constructs of the
|human Hox4.2 in cells of the eye disc during third larval instar development.
PHM|ocellus | adult
}
REFDSR
{
RDID|FBrf0051503
|Chadwick et al.
|1990
PHP|Adult head deformations: lower eye and orbital structures are absent.
|Homozygotes have bulbous growths in the place of missing eye tissue,
|these may be duplications of the second antennal segment.
}
REFDSR
{
RDID|FBrf0103357
|Saget et al.
|1998
PHP|Heterozygous males have ectopic antero-ventral bristles on the head.
PHM|head bristle | ectopic
|adult head
|head bristle
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|dominant
|Eyes reduced ventrally and anteriorly, or furrowed. Vibrissae tufted.
|Extremely variable, often overlapping wild type, but usually
|excellent character with Ly or at 19oC. Classifiable in
|single dose in triploids (Schultz, 1934).
|Muller reported an occasional homozygote as extreme dwarf with flimsy wings.
|RK2.
}
REF
{
REFM|FBrf0046135
|Regulski et al.
|1987
REFM|FBrf0051116
|McGinnis et al.
|1990
REFM|FBrf0051400
|McGinnis et al.
|1990
REFM|FBrf0051503
|Chadwick et al.
|1990
REFM|FBrf0103357
|Saget et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014401 ICL 1 ? SYM 1 ?{}dlg12 ASTR 1 - CLOC 1 10B6--10 REF 1 5 DT 1 6 Jan 2000 RESZ 832
ID|FBti0014401
SYM|?{}dlg12
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0001624==dlg1
REFDSR
{
RDID|FBrf0049482
|Woods and Bryant
|1989
SYN|?{}dlg12
ASAL|FBal0002671==dlg12
MU|X ray
CLOC|10B6--10
|Insertion site
LOCB|Proximity to gene: FBgn0001624==dlg1
PHC|lethal | recessive | conditional ts
}
REFDSR
{
RDID|FBrf0049894
|Perrimon et al.
|1989
PHC|lethal | conditional ts
}
REFDSR
{
RDID|FBrf0088171
|Guan et al.
|1996
PHC|lethal | recessive | conditional ts
}
REFDSR
{
RDID|FBrf0098920
|Goode and Perrimon
|1997
PHC|lethal | recessive | conditional ts
}
REF
{
REFM|FBrf0049482
|Woods and Bryant
|1989
REFM|FBrf0049894
|Perrimon et al.
|1989
REFM|FBrf0088171
|Guan et al.
|1996
REFM|FBrf0098920
|Goode and Perrimon
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0002671==dlg12
REFDSR
{
RDID|FBrf0049482
|Woods and Bryant
|1989
PHP|Completely lethal at 25oC, homozygotes show 75% viability at 18oC.
|Females exhibit a maternal-effect embryonic lethality when fertilized
|by FBal0002671==dlg12 sperm even at the permissive temperature.
| This lethality
|can be rescued by wild-type sperm.
}
REFDSR
{
RDID|FBrf0049894
|Perrimon et al.
|1989
PHP|Embryos exhibit defects associated with dorsal closure and head involution.
}
REFDSR
{
RDID|FBrf0088171
|Guan et al.
|1996
PHP|Temperature-sensitive allele. At the permissive temperature (18oC),
|hemizygotes show a hypomorphic phenotype, developing small imaginal
|disc tumors. Type I boutons appear similar to wild-type in these
|animals. At the restrictive temperature (29oC), hemizygotes show
|a similar phenotype to FBal0002675==dlg16 or
| FBal0002683==dlg114 hemizygotes, developing
|large tumors in the brain and imaginal discs. The subsynaptic reticulum
|at type I boutons is poorly developed in these animals.
|... (see FBal0002671==dlg12 report)
PHM|imaginal disc | conditional ts
|larval brain | conditional ts
|postsynaptic membrane
}
REFDSR
{
RDID|FBrf0098920
|Goode and Perrimon
|1997
PHP|FBal0002671==dlg12/FBal0002674==dlg15 animals are
| viable and have completely normal egg
|chambers at 18oC. After 6 hours at 25oC, follicle cells
| exit the
|follicular epithelium and intermingle with germ cells at the anterior
|and posterior poles of the egg chamber. Cells that remain in the epithelium
|retain their polarized characteristics, whereas those that have exited
|the epithelium have an apolar morphology. Nurse cells extend processes
|to meet the invasive follicle cells. Follicle cells at the anterior
|... (see FBal0002671==dlg12 report)
PHM|follicle cell | conditional ts
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Homozygotes fail to survive when raised at 25oC;
|when raised at 18oC however, 37% survival attained;
|hemizygous females show 65-70% survival at 18oC,
|but are also lethal at 25oC. Survival at 18oC
|nearly complete in heterozygotes with FBal0002674==dlg15 and
|FBal0002687==dlg118 and survival at 25oC is 4% and 95%
|respectively. Embryos produced by matings between
|... (see FBal0002671==dlg12 report)
}
REF
{
REFM|FBrf0049482
|Woods and Bryant
|1989
REFM|FBrf0049894
|Perrimon et al.
|1989
REFM|FBrf0088171
|Guan et al.
|1996
REFM|FBrf0098920
|Goode and Perrimon
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0002861 ICL 1 ? SYM 1 ?{}Dll10 ASTR 1 - CLOC 1 60E2 REF 1 2 DT 1 5 Feb 1999 RESZ 641
ID|FBti0002861
SYM|?{}Dll10
DT|5 Feb 1999
|24 Jun 1997
ICL|?
ASGN|FBgn0000157==Dll
REFDSR
{
RDID|FBrf0050642
|Cohen et al.
|1989
ASAL|FBal0001007==Dll10
MU|PM hybrid dysgenesis
CLOC|60E2
|Insertion site
LOCB|Proximity to gene: FBgn0000157==Dll
CC|8kb insertion, unidentified; within 13kb intron. See also FBti0002860==P{}60E.a, a
| P-element insertion also on the FBal0001007==Dll10 chromosome,
| 70kb 3' of the FBgn0000157==Dll transcript.
}
REF
{
REFM|FBrf0050642
|Cohen et al.
|1989
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0001007==Dll10
REFDSR
{
RDID|FBrf0050642
|Cohen et al.
|1989
PHP|Fails to develop limbs.
}
REF
{
REFM|FBrf0050642
|Cohen et al.
|1989
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015265 ICL 1 ? SYM 1 ?{}Dsim\lzL ASTR 1 - CLOC 1 - REF 1 2 DT 1 6 Jan 2000 RESZ 410
ID|FBti0015265
SYM|?{}Dsim\lzL
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0018267==Dsim\lz
REFDSR
{
RDID|FBrf0105876
|Loreto et al.
|1998
SYN|?{}Dsim\lzL
ASAL|FBal0095813==Dsim\lzL
LOCB|Proximity to gene: FBgn0018267==Dsim\lz
PHC|female sterile | recessive
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0105876
|Loreto et al.
|1998
}
ALESR
{
ASYM|FBal0095813==Dsim\lzL
REFDSR
{
RDID|FBrf0105876
|Loreto et al.
|1998
PHP|The eyes are reduced in size in mutant flies and the surface of the
|eye has a glistening appearance and altered pigmentation. The tarsal
|claws are reduced. Homozygous females are sterile; the spermathecae
|and parovaria are absent.
|Eye color: brown.
PHM|eye
|tarsus
|spermathecal duct
|female accessory gland
}
REF
{
REFM|FBrf0105876
|Loreto et al.
|1998
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015255 ICL 1 ? SYM 1 ?{}Dsp11 ASTR 1 - CLOC 1 14B14--15 REF 1 2 DT 1 1 May 2001 RESZ 526
ID|FBti0015255
SYM|?{}Dsp11
SYN|?{}Dsp15101
|?{}bss5101
DT|1 May 2001
|6 Jan 2000
ICL|?
ASGN|FBgn0011764==Dsp1
REFDSR
{
RDID|FBrf0105889
|Mosrin-Huaman et al.
|1998
SYN|?{}bss5101
ASAL|FBal0094567==Dsp11
CLOC|14B14--15
|Insertion site
LOCB|Proximity to gene: FBgn0011764==Dsp1
PHC|lethal | recessive | partially
|sterile | recessive | partially
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0105889
|Mosrin-Huaman et al.
|1998
}
ALESR
{
ASYM|FBal0094567==Dsp11
REFDSR
{
RDID|FBrf0105889
|Mosrin-Huaman et al.
|1998
PHP|Few hemizygous males survive to adulthood. They have severe morphological
|and physiological defects; they walk with difficulty, can hardly fly
|and have severely impaired fertility. These flies die prematurely
|(50% die within 5 days of eclosion).
|Few homozygous females survive to adulthood. They have the same phenotypical
|characteristics as hemizygous males. The females achieve complete
|oogenesis but lay few eggs. At 26oC these eggs do not hatch into
|... (see FBal0094567==Dsp11 report)
PHM|egg
|abdominal 5 ventral denticle belt
|abdominal 4 ventral denticle belt
|embryonic/first instar larval cuticle
}
REFDSR
{
RDID|FBrf0127514
|Decoville et al.
|2000
PHP|Homozygotes are poorly fertile and only 50% of eggs lead to viable
|larvae. Embryos which do not give rise to larvae stop development
|before the cellular blastoderm stage.
}
REFDSR
{
RDID|FBrf0132331
|Decoville et al.
|2001
PHP|Homozygous adults do not show paralysis after vibration of the culture
|vial.
|Homozygotes and hemizygotes die prematurely, show very low fertility
|and have various homeotic transformations.
|The first type of transformation corresponds to a T1 to T2 transformation;
|hemizygous males have reduced sex combs, with an average of 6 teeth
|(compared to the 11 seen in wild type). The size of the sex comb never
|... (see FBal0094567==Dsp11 report)
PHM|sex comb
|haltere
|wing | ectopic
|metathoracic laterotergite
|scutum | ectopic
|adult abdominal segment 6
|adult abdominal segment 5 | ectopic
|adult abdominal segment 4
|abdominal sternite bristle | ectopic
|metathoracic segment | anterior compartment
}
REF
{
REFM|FBrf0105889
|Mosrin-Huaman et al.
|1998
REFM|FBrf0127514
|Decoville et al.
|2000
REFM|FBrf0132331
|Decoville et al.
|2001
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014410 ICL 1 ? SYM 1 ?{}dsxT ASTR 1 - CLOC 1 84E5--6 REF 1 3 DT 1 6 Jan 2000 RESZ 454
ID|FBti0014410
SYM|?{}dsxT
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0000504==dsx
REFDSR
{
RDID|FBrf0051864
|Nagoshi and Baker
|1990
SYN|?{}dsxT
ASAL|FBal0003205==dsxT
MU|spontaneous
CLOC|84E5--6
|Insertion site
LOCB|Proximity to gene: FBgn0000504==dsx
}
REF
{
REFM|FBrf0051864
|Nagoshi and Baker
|1990
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0003205==dsxT
REFDSR
{
RDID|FBrf0046300
|Nothiger et al.
|1987
PHP|Only affects XX flies: the terminalia of XX heterozygous flies carry
|abnormal male and female elements, with the female genitalia anterior
|to the male genitalia. The male genitalia are well developed, but
|the penis apparatus is reduced, the hypandrium is mostly absent and
|many bristles are abnormal. The female vaginal plate is always present,
|but is reduced in size with abnormal bristles. There is often a mass
|of yellow, chitinized material between the vaginal plates, which is
|... (see FBal0003205==dsxT report)
PHM|female terminalia
|female genitalia
|female gonopod
|prothoracic leg | female
|female analia
|anal plate | female
|genitalia
}
REFDSR
{
RDID|FBrf0076142
|Nagoshi et al.
|1995
PHP|No more than 26% of XX
| FBal0003205==dsxT/FBal0003154==dsx1 mutant
| pseudomales produce
|gonads with the most severe group 1 pseudotestes phenotype. The remaining
|pseudomales have a less severe phenotype, with viable germ cells.
|FBal0013357==otu10 and Df(1)otu-P&Dgr;1 cause an increase in
| severity of
|this phenotype: over 70% of the resulting gonads were of group 1.
PHM|germ cell
}
REF
{
REFM|FBrf0046300
|Nothiger et al.
|1987
REFM|FBrf0076142
|Nagoshi et al.
|1995
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014444 ICL 1 ? SYM 1 ?{}en1 ASTR 1 - CLOC 1 47F17--48A1 REF 1 3 DT 1 6 Jan 2000 RESZ 508
ID|FBti0014444
SYM|?{}en1
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0000577==en
REFDSR
{
RDID|FBrf0042028
|Poole et al.
|1985
PHC|lethal
}
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}en1
ASAL|FBal0003716==en1
MU|spontaneous
CLOC|47F17--48A1
|Insertion site
LOCB|Proximity to gene: FBgn0000577==en
}
REF
{
REFM|FBrf0042028
|Poole et al.
|1985
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0003716==en1
REFDSR
{
RDID|FBrf0005419
|Brasted
|1941
PHP|In males, extra sex comb often present smaller than normal and in
|mirror-image position in posterior compartment.
PHM|sex comb | ectopic
}
REFDSR
{
RDID|FBrf0013911
|Tokunaga
|1961
PHM|prothoracic tarsal segment | posterior compartment
}
REFDSR
{
RDID|FBrf0024005
|Garcia-Bellido and Santamaria
|1972
PHP|Duplications of transverse rows in female prothoracic leg, extra
|bristles in mesothoracic and metathoracic tarsi.
PHM|mesothoracic tibial transverse bristle row
|metathoracic tibial transverse bristle row
}
REFDSR
{
RDID|FBrf0027996
|Morata and Lawrence
|1975
PHP|Clones of FBal0003716==en1 cells of posterior compartment origin
| fail to
|respect anterior-posterior compartment border in wing disc as do
|FBal0012675==mwh1 clones in wing discs of
| FBal0003716==en1 homozygotes.
PHM|dorsal mesothoracic disc | posterior compartment | somatic clone
|dorsal mesothoracic disc | anterior/posterior compartment boundary | somatic clone
}
REFDSR
{
RDID|FBrf0028554
|Lawrence and Morata
|1976
PHP|Clones of FBal0003716==en1 cells of posterior compartment origin
| fail to
|respect anterior-posterior compartment border in wing disc as do
|FBal0012675==mwh1 clones in wing discs of
| FBal0003716==en1 homozygotes.
PHM|dorsal mesothoracic disc | posterior compartment | somatic clone
|dorsal mesothoracic disc | anterior/posterior compartment boundary | somatic clone
}
REFDSR
{
RDID|FBrf0033468
|Lawrence et al.
|1979
PHP|Duplications of transverse rows in female prothoracic leg, extra
|bristles in mesothoracic and metathoracic tarsi.
PHM|mesothoracic tibial transverse bristle row
|metathoracic tibial transverse bristle row
}
REFDSR
{
RDID|FBrf0037911
|Lawrence and Struhl
|1982
PHP|Homozygous clones in the wing are frequently lost in the posterior
|but not the anterior compartment.
PHM|wing | posterior compartment | somatic clone
}
REFDSR
{
RDID|FBrf0039205
|Morata et al.
|1983
PHP|At 29oC the third segment of the antenna is larger than wild-type
|in homozygous flies, and a bristle close to the border is often enlarged.
|This phenotype is enhanced by the FBgn0005562==M(3)65F mutation. FBal0003716==en1/FBal0003717==en2
|transheterozygotes have abnormal antennae, the phenotype increasing
|at higher temperatures (25 or 29oC). At 29oC the posterior compartment
|of the second segment is almost always abnormal, having extra anterior-like
|bristles which are often arranged in a mirror-image symmetry with respect
|... (see FBal0003716==en1 report)
PHM|antenna
|antennal segment 3
|(with en2) antennal segment 2 | posterior compartment
}
REFDSR
{
RDID|FBrf0039215
|Epper and Sanchez
|1983
PHP|Male FBal0003716==en1 homozygotes have abnormal genitalia, with a reduction
|in the number of clasper teeth, rudimentary dorsal parameres of the
|penis apparatus, and often incomplete rotation of the penis apparatus.
|Viable heteroallelic combinations with other FBgn0000577==en alleles show a more
|extreme phenotype, with a reduction in the genital arch process, hypandrium
|and hypandrial phragma as well. Extra genital arch and anal plate
|bristles are sometimes seen.
|... (see FBal0003716==en1 report)
PHM|hypandrium
|penis
|genital arch
|clasper
|female gonopod
}
REFDSR
{
RDID|FBrf0041008
|Eberlein
|1984
PHP|Shows wing to haltere transformation in FBal0003716==en1/FBal0003743==en28.
PHM|(with en28) wing
}
REFDSR
{
RDID|FBrf0042022
|Kuner et al.
|1985
PHP|Severe thoracic morphological defects.
}
REFDSR
{
RDID|FBrf0043525
|Gubb
|1985
PHP|The posterior wing is an abnormal shape in homozygous flies. The posterior
|wing veins have a variable disrupted pattern, with the anterior crossvein
|(ACV) often being absent or reduced and vein III often appearing slightly
|thickened. The campaniform sensillum associated with the ACV is often
|absent, while the campaniform sensilla of vein III may be increased
|in number. Campaniform sensilla are often found in the posterior wing,
|where they may or may not be associated with vein tissue. Many posterior
|... (see FBal0003716==en1 report)
PHM|wing | posterior
|anterior crossvein
|wing vein L3
|sensillum campaniformium of anterior crossvein
|sensillum campaniformium
|posterior hair
|alar lobe
|scutellum
|prothoracic leg
}
REFDSR
{
RDID|FBrf0046012
|Grau and Simpson
|1987
PHP|In FBal0001792==Cos10, FBal0003716==en1 double mutants
| the duplications characteristic
|of FBal0001792==Cos10 only occur in the original anterior
| compartment, and not
|in the transformed posterior compartment, indicating that the FBal0001792==Cos10
|duplications develop as a position response.
}
REFDSR
{
RDID|FBrf0049488
|Condie and Brower
|1989
PHP|Homozygous adults have abnormal wings, with a posterior to anterior
|transformation. The sex comb on the male prothoracic leg is partially
|duplicated posteriorly. The posterior wing is grossly disrupted in
|FBal0003716==en1/FBal0003717==en2 transheterozygotes,
| rarely having an organized fourth
|or fifth vein. The sex comb on the male prothoracic leg is duplicated
|posteriorly, more distal leg segments are fused and terminal claws
|are sometimes missing. The arista and other anterior elements of the
|... (see FBal0003716==en1 report)
PHM|wing
|wing vein L4
|wing vein L5
|sex comb
}
REFDSR
{
RDID|FBrf0051823
|Hama et al.
|1990
PHP|Heterozygotes with FBal0034516==enXho23 and
| FBal0034515==enSac27 display wing vein abnormalities.
}
REFDSR
{
RDID|FBrf0058044
|Held
|1993
PHP|Additional bristles in the second leg.
PHM|mesothoracic tarsal bristle longitudinal row 2
|mesothoracic tarsal bristle longitudinal row 2.5
}
REFDSR
{
RDID|FBrf0076129
|Felsenfeld and Kennison
|1995
PHP|Mutation has no effect on the FBal0005484==hhMrt phenotype.
}
REFDSR
{
RDID|FBrf0076146
|Sturtevant and Bier
|1995
PHP|Coordinate mutant.
}
REFDSR
{
RDID|FBrf0079370
|Schwartz et al.
|1995
PHP|Viable.
}
REFDSR
{
RDID|FBrf0079938
|Chase and Baker
|1995
PHP|Heterozygotes with FBal0016052==enspt display the FBgn0000577==en and
| spermatheca phenotypes
|at 25oC.
}
REFDSR
{
RDID|FBrf0080091
|Hidalgo
|1994
PHP|FBal0031487==hhbar3 in combination with
| FBab0022271==Df(2R)enE/FBal0003716==en1 causes a phenotype
|reminiscent of a weak FBgn0000490==dpp mutation is produced, narrowing of the
|space between wing veins 3 and 4. Posterior wing clones affect adjacent
|cells of the anterior compartment and cause an overall reduction in
|wing size.
}
REFDSR
{
RDID|FBrf0092613
|Locke and Hanna
|1996
PHP|Homozygotes exhibit a variety of wing vein alterations in the posterior
|compartment of the wing.
|Transheterozygotes with FBal0034506==enEnci have a posterior
| specific wing phenotype:
|bristles characteristic of the anterior wing margin are present on
|the posterior wing margin. Males have duplicated sex combs on the
|prothoracic legs.
PHM|wing & macrochaeta
|sex comb
|wing vein
|wing | posterior compartment
}
REFDSR
{
RDID|FBrf0103326
|Maschat et al.
|1998
PHP|2% of homozygotes and 5% of
| FBal0003716==en1/FBal0003769==en54 flies have a gap
| in the
|fourth wing vein at 25oC.
PHM|wing vein L4
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|viable
}
REF
{
REFM|FBrf0005419
|Brasted
|1941
REFM|FBrf0013911
|Tokunaga
|1961
REFM|FBrf0024005
|Garcia-Bellido and Santamaria
|1972
REFM|FBrf0027996
|Morata and Lawrence
|1975
REFM|FBrf0028554
|Lawrence and Morata
|1976
REFM|FBrf0033468
|Lawrence et al.
|1979
REFM|FBrf0037911
|Lawrence and Struhl
|1982
REFM|FBrf0039205
|Morata et al.
|1983
REFM|FBrf0039215
|Epper and Sanchez
|1983
REFM|FBrf0041008
|Eberlein
|1984
REFM|FBrf0042022
|Kuner et al.
|1985
REFM|FBrf0043525
|Gubb
|1985
REFM|FBrf0046012
|Grau and Simpson
|1987
REFM|FBrf0049488
|Condie and Brower
|1989
REFM|FBrf0051823
|Hama et al.
|1990
REFM|FBrf0058044
|Held
|1993
REFM|FBrf0076129
|Felsenfeld and Kennison
|1995
REFM|FBrf0076146
|Sturtevant and Bier
|1995
REFM|FBrf0079370
|Schwartz et al.
|1995
REFM|FBrf0079938
|Chase and Baker
|1995
REFM|FBrf0080091
|Hidalgo
|1994
REFM|FBrf0092613
|Locke and Hanna
|1996
REFM|FBrf0103326
|Maschat et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015054 ICL 1 ? SYM 1 ?{}Est-6unspecified ASTR 1 - CLOC 1 69A1 REF 1 2 DT 1 6 Jan 2000 RESZ 424
ID|FBti0015054
SYM|?{}Est-6unspecified
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0000592==Est-6
REFDSR
{
RDID|FBrf0052539
|Brady et al.
|1990
SYN|?{}Est-6unspecified
ASAL|FBal0058970==Est-6unspecified
CLOC|69A1
|Insertion site
LOCB|Proximity to gene: FBgn0000592==Est-6
}
REF
{
REFM|FBrf0052539
|Brady et al.
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014459 ICL 1 ? SYM 1 ?{}fliI2:19B ASTR 1 - CLOC 1 19F5 REF 1 3 DT 1 31 May 2000 RESZ 549
ID|FBti0014459
SYM|?{}fliI2:19B
SYN|?{}fliI2/19B
DT|31 May 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0000709==fliI
REFDSR
{
RDID|FBrf0064390
|Campbell et al.
|1993
PHC|lethal | recessive
}
REFDSR
{
RDID|FBrf0083951
|de Couet et al.
|1995
SYN|?{}fliI2/19B
ASAL|FBal0031278==fliI2:19B
CLOC|19F5
|Insertion site
LOCB|Proximity to gene: FBgn0000709==fliI
}
REF
{
REFM|FBrf0064390
|Campbell et al.
|1993
REFM|FBrf0083951
|de Couet et al.
|1995
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0002826 ICL 1 ? SYM 1 ?{}ftz11 ASTR 1 - CLOC 1 84A6 REF 1 5 DT 1 5 Sep 2000 RESZ 1143
ID|FBti0002826
SYM|?{}ftz11
SYN|?{}ftzW20
|?{}ftzw20
DT|5 Sep 2000
|24 Jun 1997
ICL|?
ASGN|FBgn0001077==ftz
REFDSR
{
RDID|FBrf0039012
|Scott et al.
|1983
SYN|?{}ftz11
ASAL|FBal0004816==ftz11
MU|ethyl methanesulfonate
CLOC|84A6
|Insertion site
LOCB|Proximity to gene: FBgn0001077==ftz
PHC|lethal | recessive
CC|Insertion determined to be repetitive; approximately 3kb; not shown to
| coorelate with mutant phenotype.
|Insertion determined to be repetitive element of appoximately 3kb;
| correlation with the mutant phenotype asssumed but not proven.
}
REFDSR
{
RDID|FBrf0040502
|Weiner et al.
|1984
ASAL|FBal0004816==ftz11
MU|ethyl methanesulfonate
PHC|lethal | embryonic | pair rule
}
REFDSR
{
RDID|FBrf0040715
|Wakimoto et al.
|1984
PHC|lethal | embryonic
}
REFDSR
{
RDID|FBrf0073734
|Lewis et al.
|1980
PHC|lethal | recessive
}
REF
{
REFM|FBrf0039012
|Scott et al.
|1983
REFM|FBrf0040502
|Weiner et al.
|1984
REFM|FBrf0040715
|Wakimoto et al.
|1984
REFM|FBrf0073734
|Lewis et al.
|1980
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0004816==ftz11
REFDSR
{
RDID|FBrf0040502
|Weiner et al.
|1984
PHM|embryonic epidermis
|denticle belt
}
REFDSR
{
RDID|FBrf0040715
|Wakimoto et al.
|1984
PHP|FBal0004816==ftz11/FBab0002646==Df(3R)Scr show abnormal
| segmentation of the germ band,
|with at least half the segments missing. The segmentation of the ventral
|nerve cord is also affected. The labial lobe cannot be seen, and the
|H piece of the larval mouthparts is missing in late embryos. Dorsal
|closure is disrupted.
PHM|contracted germ band stage
|central nervous system | embryonic
|hypostomal sclerite
}
REFDSR
{
RDID|FBrf0046027
|Bender et al.
|1987
PHM|epidermis | embryonic
|embryonic nervous system
}
REFDSR
{
RDID|FBrf0048119
|Jack et al.
|1988
PHP|Odd numbered denticle bands missing.
}
REFDSR
{
RDID|FBrf0049007
|Doe et al.
|1988
PHP|FBtp0005207==P{ftzK}; FBal0004816==ftz11/FBal0004818==ftz13
| individuals die as embryos or larvae.
|66% of FBtp0000074==P{ftzG};
| FBal0004816==ftz11/FBal0004818==ftz13 individuals
| survive to adulthood.
|FBtp0005207==P{ftzK}; FBal0004816==ftz11/FBal0004818==ftz13
| embryos are identified by weak segmentation
|defects in the CNS.
}
REFDSR
{
RDID|FBrf0049576
|Lawrence and Johnston
|1989
PHP|The eve stripes mature as wild-type.
}
REFDSR
{
RDID|FBrf0054059
|Parkhurst and Ish-Horowicz
|1991
PHP|Interacts with FBal0030148==RpII140wimp maternal effect.
}
REFDSR
{
RDID|FBrf0055876
|Panzer et al.
|1992
PHP|Parasegments 1 and 2 are fused and the salivary gland placodes occupy
|the posterior half of the fused parasegment in the FBgn0003339==Scr expression
|domain.
PHM|parasegment 1
|parasegment 2
}
REFDSR
{
RDID|FBrf0056133
|Tabata et al.
|1992
PHP|ftz embryos lack even-numbered hh stripes.
}
REFDSR
{
RDID|FBrf0084489
|Welte et al.
|1995
PHP|Heterozygotes with FBal0004823==ftzUal1 exhibit a higher
| frequency of heat shock
|induced transformation of abdominal segment 1 than those embryos carrying
|three wild type copies of FBgn0001077==ftz (FBab0003681==Dp(3;3)D1/+). An addition of another
|wild type FBgn0001077==ftz to these embryos results in another modest increase
|in frequency of transformation.
}
REFDSR
{
RDID|FBrf0086468
|Hyduk and Percival-Smith
|1996
PHP|Mutant embryos are deficient for cuticular structures derived from
|the even numbered parasegments.
PHM|parasegment 2
|parasegment 10
|parasegment 12
|parasegment 14
|parasegment 4
|parasegment 10
|parasegment 12
|parasegment 14
|parasegment 6
|parasegment 10
|parasegment 12
|parasegment 14
|parasegment 8
|parasegment 10
|parasegment 12
|parasegment 14
|epidermis | embryonic
}
REFDSR
{
RDID|FBrf0130058
|Rusch and Kaufman
|2000
PHP|The maxillary and labial lobes are fused in mutant embryos.
PHM|embryonic labial segment
|embryonic maxillary segment
}
REF
{
REFM|FBrf0040502
|Weiner et al.
|1984
REFM|FBrf0040715
|Wakimoto et al.
|1984
REFM|FBrf0046027
|Bender et al.
|1987
REFM|FBrf0048119
|Jack et al.
|1988
REFM|FBrf0049007
|Doe et al.
|1988
REFM|FBrf0049576
|Lawrence and Johnston
|1989
REFM|FBrf0054059
|Parkhurst and Ish-Horowicz
|1991
REFM|FBrf0055876
|Panzer et al.
|1992
REFM|FBrf0056133
|Tabata et al.
|1992
REFM|FBrf0084489
|Welte et al.
|1995
REFM|FBrf0086468
|Hyduk and Percival-Smith
|1996
REFM|FBrf0130058
|Rusch and Kaufman
|2000
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0016757 ICL 1 ? SYM 1 ?{}ftz12 ASTR 1 - CLOC 1 - REF 1 3 DT 1 4 Dec 2000 RESZ 464
ID|FBti0016757
SYM|?{}ftz12
DT|4 Dec 2000
|16 Nov 2000
ICL|?
ASGN|FBgn0001077==ftz
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
ASAL|FBal0004817==ftz12
MU|ethyl methanesulfonate
CC|Unattributed statement that this allele is associated with a 5-kb insertion
| in the transcribed region.
}
REF
{
REFM|FBrf0039012
|Scott et al.
|1983
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014467 ICL 1 ? SYM 1 ?{}fw34e ASTR 1 - CLOC 1 11A1 REF 1 2 DT 1 6 Jan 2000 RESZ 459
ID|FBti0014467
SYM|?{}fw34e
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0001083==fw
REFDSR
{
RDID|FBrf0091112
|Leshko-Lindsay and Corces
|1997
SYN|?{}fw34e
ASAL|FBal0004903==fw34e
CLOC|11A1
|Insertion site
LOCB|Proximity to gene: FBgn0001083==fw
PHC|lethal | partially
|lethal | female | pupal
}
REF
{
REFM|FBrf0091112
|Leshko-Lindsay and Corces
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0004903==fw34e
REFDSR
{
RDID|FBrf0091112
|Leshko-Lindsay and Corces
|1997
PHP|Mild defects in eye morphology. Defects in the development of the
|mechanosensory bristles including the macrochaetae, microchaetae and
|bristles surrounding the eye. Shortened head and scutellum.
|FBal0004903==fw34e/FBab0000482==Df(1)KA10 transheterozygotes do
| not produce any viable
|adult females, female lethal phase occurs in the pupal stages.
PHM|retina
|macrochaeta
|microchaeta
|eye & macrochaeta
|adult head
|scutellum
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Originally showed eye surface medium folded; bristles
|much gnarled. Schultz and Curry report that stock in
|1940 showed gnarled bristles and eye small but no
|vertical fold.
|RK2.
}
REF
{
REFM|FBrf0091112
|Leshko-Lindsay and Corces
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015044 ICL 1 ? SYM 1 ?{}fwU2 ASTR 1 - CLOC 1 11A1 REF 1 2 DT 1 6 Jan 2000 RESZ 431
ID|FBti0015044
SYM|?{}fwU2
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0001083==fw
REFDSR
{
RDID|FBrf0091112
|Leshko-Lindsay and Corces
|1997
SYN|?{}fwU2
ASAL|FBal0057359==fwU2
CLOC|11A1
|Insertion site
LOCB|Proximity to gene: FBgn0001083==fw
PHC|lethal | partially
}
REF
{
REFM|FBrf0091112
|Leshko-Lindsay and Corces
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0057359==fwU2
REFDSR
{
RDID|FBrf0091112
|Leshko-Lindsay and Corces
|1997
PHP|Eyes are reduced in size and exhibit deep penetrating furrows in the
|retina that reach the basement membrane. Adjacent to the furrows the
|lamina has depressions. Ommatidial pattern is severely disorganized
|(appear as bent not straight columns and ommatidia are often missing
|in the retinal epithelium producing large gaps between the columns)
|and the ommatidia show altered morphology (lose hexagonal shape and
|appear flattened or rounded, number and spacing of photoreceptors is
|... (see FBal0057359==fwU2 report)
PHM|retina
|ommatidium
|lamina
|interommatidial bristle
|photoreceptor cell
|cone cell
|pigment cell
|macrochaeta
|microchaeta
|eye & macrochaeta
|adult head
|scutellum
}
REF
{
REFM|FBrf0091112
|Leshko-Lindsay and Corces
|1997
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015043 ICL 1 ? SYM 1 ?{}fwU3 ASTR 1 - CLOC 1 11A1 REF 1 2 DT 1 6 Jan 2000 RESZ 408
ID|FBti0015043
SYM|?{}fwU3
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0001083==fw
REFDSR
{
RDID|FBrf0091112
|Leshko-Lindsay and Corces
|1997
SYN|?{}fwU3
ASAL|FBal0057358==fwU3
CLOC|11A1
|Insertion site
LOCB|Proximity to gene: FBgn0001083==fw
}
REF
{
REFM|FBrf0091112
|Leshko-Lindsay and Corces
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014468 ICL 1 ? SYM 1 ?{}fz28 ASTR 1 - CLOC 1 70D4--5 REF 1 2 DT 1 6 Jan 2000 RESZ 398
ID|FBti0014468
SYM|?{}fz28
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0001085==fz
REFDSR
{
RDID|FBrf0051945
|Adler et al.
|1990
SYN|?{}fz28
ASAL|FBal0004944==fz28
MU|&ggr; ray
CLOC|70D4--5
|Insertion site
LOCB|Proximity to gene: FBgn0001085==fz
}
REF
{
REFM|FBrf0051945
|Adler et al.
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0004944==fz28
REFDSR
{
RDID|FBrf0051945
|Adler et al.
|1990
PHP|Moderate phenotype.
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Moderate thoracic bristle phenotype; moderate wing-hair disorientation.
PHM|macrochaeta & thorax | adult
|wing hair
}
REF
{
REFM|FBrf0051945
|Adler et al.
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014996 ICL 1 ? SYM 1 ?{}fzGD4b ASTR 1 - CLOC 1 70D4--5 REF 1 2 DT 1 6 Jan 2000 RESZ 391
ID|FBti0014996
SYM|?{}fzGD4b
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0001085==fz
REFDSR
{
RDID|FBrf0051945
|Adler et al.
|1990
SYN|?{}fzGD4b
ASAL|FBal0049583==fzGD4b
CLOC|70D4--5
|Insertion site
LOCB|Proximity to gene: FBgn0001085==fz
}
REF
{
REFM|FBrf0051945
|Adler et al.
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0049583==fzGD4b
REFDSR
{
RDID|FBrf0051945
|Adler et al.
|1990
PHP|Moderate phenotype.
}
REF
{
REFM|FBrf0051945
|Adler et al.
|1990
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014997 ICL 1 ? SYM 1 ?{}fzGL3a ASTR 1 - CLOC 1 70D4--5 REF 1 2 DT 1 6 Jan 2000 RESZ 391
ID|FBti0014997
SYM|?{}fzGL3a
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0001085==fz
REFDSR
{
RDID|FBrf0051945
|Adler et al.
|1990
SYN|?{}fzGL3a
ASAL|FBal0049586==fzGL3a
CLOC|70D4--5
|Insertion site
LOCB|Proximity to gene: FBgn0001085==fz
}
REF
{
REFM|FBrf0051945
|Adler et al.
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0049586==fzGL3a
REFDSR
{
RDID|FBrf0051945
|Adler et al.
|1990
PHP|Moderate phenotype.
}
REF
{
REFM|FBrf0051945
|Adler et al.
|1990
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015598 ICL 1 ? SYM 1 ?{}g1 ASTR 1 - CLOC 1 12B4--6 REF 1 2 DT 1 31 May 2000 RESZ 394
ID|FBti0015598
SYM|?{}g1
DT|31 May 2000
|31 May 2000
ICL|?
ASGN|FBgn0001087==g
REFDSR
{
RDID|FBrf0125153
|Lloyd et al.
|1999
SYN|?{}g1
ASAL|FBal0004957==g1
MU|spontaneous
CLOC|12B4--6
|Insertion site
LOCB|Proximity to gene: FBgn0001087==g
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0125153
|Lloyd et al.
|1999
}
ALESR
{
ASYM|FBal0004957==g1
REFDSR
{
RDID|FBrf0054090
|Tearle
|1991
PHP|Lightly pigmented eyes and some pigment deposition in the ocelli.
PHM|pigment cell
}
REFDSR
{
RDID|FBrf0125153
|Lloyd et al.
|1999
PHP|Eye color: red pigments are reduced to 57 +/- 2% of wild-type levels,
|brown pigments are reduced to 25 +/- 3% of wild-type levels in females.
|Red pigments are reduced to 72 +/- 4% of wild-type levels, brown pigments
|are reduced to 66 +/- 1% of wild-type levels in males.
|Malpighian tubule color: colorless (wild-type color is orange).
|Testis color: pale yellow (wild-type color is bright yellow).
PHM|pigment cell
|Malpighian tubule
|testis sheath
}
REFDSR
{
RDID|FBrf0127175
|Kretzschmar et al.
|2000
PHP|Eye color: the drosopterin (red pigment) content of
| FBal0004957==g1 flies is
|reduced compared to wild type.
|Eye color: the drosopterin (red pigment) content of
| FBal0004957==g1 FBal0014434==rb1
|double mutant flies is reduced to 18% of wild type.
|Eye color: the xanthommatin (brown pigment) content of
| FBal0004957==g1 flies
|is reduced to 58% of wild type.
|Eye color: the xanthommatin (brown pigment) content of
| FBal0004957==g1 FBal0014434==rb1
|... (see FBal0004957==g1 report)
PHM|pigment cell
}
REF
{
REFM|FBrf0054090
|Tearle
|1991
REFM|FBrf0125153
|Lloyd et al.
|1999
REFM|FBrf0127175
|Kretzschmar et al.
|2000
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015599 ICL 1 ? SYM 1 ?{}g3 ASTR 1 - CLOC 1 12B4--6 REF 1 2 DT 1 31 May 2000 RESZ 394
ID|FBti0015599
SYM|?{}g3
DT|31 May 2000
|31 May 2000
ICL|?
ASGN|FBgn0001087==g
REFDSR
{
RDID|FBrf0125153
|Lloyd et al.
|1999
SYN|?{}g3
ASAL|FBal0004960==g3
MU|spontaneous
CLOC|12B4--6
|Insertion site
LOCB|Proximity to gene: FBgn0001087==g
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0125153
|Lloyd et al.
|1999
}
ALESR
{
ASYM|FBal0004960==g3
REFDSR
{
RDID|FBrf0093727
|Simpson et al.
|1997
PHP|Eye color: dull brownish.
|Flies have reduced pigmentation throughout the body; pigment granules
|are still visible in the ommatidia but contain less pigment than
|wild-type.
PHM|pigment granule
}
REFDSR
{
RDID|FBrf0095986
|Ooi et al.
|1997
PHP|Eyes exhibit pigmentation defects and reduced number of pigment granules.
PHM|pigment cell
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Like FBal0004957==g1, but gives lighter orange in combination with
|FBgn0003965==v. Has 21% normal red pigment and 47% normal brown pigment
|(Nolte, 1959). Malpighian tubes extremely
|pale yellow (Brehme and Demerec, 1942).
|RK1.
}
REFDSR
{
RDID|FBrf0125153
|Lloyd et al.
|1999
PHP|Eye color: red pigments are reduced to 45 +/- 1% of wild-type levels,
|brown pigments are reduced to 70 +/- 8% of wild-type levels in females.
|Red pigments are reduced to 50 +/- 3% of wild-type levels, brown pigments
|are reduced to 52 +/- 5% of wild-type levels in males.
|Malpighian tubule color: colorless (wild-type color is orange).
|Testis color: yellow (wild-type color is bright yellow).
PHM|pigment cell
|Malpighian tubule
|testis sheath
}
REFDSR
{
RDID|FBrf0129983
|Mullins et al.
|2000
PHP|In an assay for larval motility, FBal0004960==g3 mutants
| performed as well as
|wild-type larvae. In locomotor assays testing olfactory response to
|propionic acid, FBal0004960==g3 mutants perform significantly
| less well than
|wild-type larvae.
}
REF
{
REFM|FBrf0093727
|Simpson et al.
|1997
REFM|FBrf0095986
|Ooi et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0125153
|Lloyd et al.
|1999
REFM|FBrf0129983
|Mullins et al.
|2000
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015600 ICL 1 ? SYM 1 ?{}g4 ASTR 1 - CLOC 1 12B4--6 REF 1 2 DT 1 31 May 2000 RESZ 388
ID|FBti0015600
SYM|?{}g4
DT|31 May 2000
|31 May 2000
ICL|?
ASGN|FBgn0001087==g
REFDSR
{
RDID|FBrf0125153
|Lloyd et al.
|1999
SYN|?{}g4
ASAL|FBal0004961==g4
MU|X ray
CLOC|12B4--6
|Insertion site
LOCB|Proximity to gene: FBgn0001087==g
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0125153
|Lloyd et al.
|1999
}
ALESR
{
ASYM|FBal0004961==g4
REFDSR
{
RDID|FBrf0005752
|Brehme and Demerec
|1942
PHP|Malpighian tubule color: extremely pale yellow.
PHM|Malpighian tubule
}
REFDSR
{
RDID|FBrf0012680
|Nolte
|1959
PHP|22% normal red pigment and 23% normal brown pigment.
PHM|pigment cell
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye color: like FBal0004958==g2.
|RK1.
PHM|pigment cell
}
REFDSR
{
RDID|FBrf0125153
|Lloyd et al.
|1999
PHP|Eye color: red pigments are reduced to 25 +/- 1% of wild-type levels,
|brown pigments are reduced to 28 +/- 5% of wild-type levels in females.
|Red pigments are reduced to 38 +/- 3% of wild-type levels, brown pigments
|are reduced to 37 +/- 3% of wild-type levels in males.
|Malpighian tubule color: very pale-clear (wild-type color is orange).
|Testis color: yellow (wild-type color is bright yellow).
PHM|pigment cell
|Malpighian tubule
|testis sheath
}
REF
{
REFM|FBrf0005752
|Brehme and Demerec
|1942
REFM|FBrf0012680
|Nolte
|1959
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0125153
|Lloyd et al.
|1999
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015610 ICL 1 ? SYM 1 ?{}g61 ASTR 1 - CLOC 1 12B4--6 REF 1 2 DT 1 31 May 2000 RESZ 382
ID|FBti0015610
SYM|?{}g61
DT|31 May 2000
|31 May 2000
ICL|?
ASGN|FBgn0001087==g
REFDSR
{
RDID|FBrf0125153
|Lloyd et al.
|1999
SYN|?{}g61
ASAL|FBal0095411==g61
CLOC|12B4--6
|Insertion site
LOCB|Proximity to gene: FBgn0001087==g
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0125153
|Lloyd et al.
|1999
}
}
# EOR
TIR
{
RETE|ID 1 FBti0015601 ICL 1 ? SYM 1 ?{}gEMS ASTR 1 - CLOC 1 12B4--6 REF 1 2 DT 1 31 May 2000 RESZ 385
ID|FBti0015601
SYM|?{}gEMS
DT|31 May 2000
|31 May 2000
ICL|?
ASGN|FBgn0001087==g
REFDSR
{
RDID|FBrf0125153
|Lloyd et al.
|1999
SYN|?{}gEMS
ASAL|FBal0004992==gEMS
CLOC|12B4--6
|Insertion site
LOCB|Proximity to gene: FBgn0001087==g
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0125153
|Lloyd et al.
|1999
}
}
# EOR
TIR
{
RETE|ID 1 FBti0015602 ICL 1 ? SYM 1 ?{}gim ASTR 1 - CLOC 1 12B4--6 REF 1 2 DT 1 31 May 2000 RESZ 382
ID|FBti0015602
SYM|?{}gim
DT|31 May 2000
|31 May 2000
ICL|?
ASGN|FBgn0001087==g
REFDSR
{
RDID|FBrf0125153
|Lloyd et al.
|1999
SYN|?{}gim
ASAL|FBal0004994==gim
CLOC|12B4--6
|Insertion site
LOCB|Proximity to gene: FBgn0001087==g
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0125153
|Lloyd et al.
|1999
}
}
# EOR
TIR
{
RETE|ID 1 FBti0022289 ICL 1 ? SYM 1 ?{}gish1 ASTR 1 - CLOC 1 89B9--12 REF 1 2 DT 1 26 Mar 2002 RESZ 349
ID|FBti0022289
SYM|?{}gish1
DT|26 Mar 2002
|26 Mar 2002
ICL|?
ASGN|FBgn0011253==gish
REFDSR
{
RDID|FBrf0145174
|Hummel et al.
|2002
SYN|?{}gish1
CLOC|89B9--12
|Insertion site
LOCB|Proximity to gene: FBgn0011253==gish
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0145174
|Hummel et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014470 ICL 1 ? SYM 1 ?{}gro1 ASTR 1 - CLOC 1 96F10 REF 1 2 DT 1 6 Jan 2000 RESZ 410
ID|FBti0014470
SYM|?{}gro1
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0001139==gro
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}gro1
ASAL|FBal0005217==gro1
MU|spontaneous
CLOC|96F10
|Insertion site
LOCB|Proximity to gene: FBgn0001139==gro
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0005217==gro1
REFDSR
{
RDID|FBrf0046015
|Knust et al.
|1987
PHP|Low penetrance bushes of bristles over compound eyes of homozygous
|flies. FBal0005217==gro1, FBgn0000591==E(spl)- transheterozygotes
| are viable and exhibit
|a large number of bristles on thorax, head and wings.
}
REFDSR
{
RDID|FBrf0055903
|Fischer-Vize et al.
|1992
PHP|FBal0045820==groBFP2/FBal0005217==gro1
| transheterozygotes have wild-type eyes.
}
REFDSR
{
RDID|FBrf0084542
|de Celis and Ruiz-Gomez
|1995
PHP|The wing phenotype of FBal0005217==gro1 heterozygous with
| deletions for FBgn0001139==gro
|is of overgrowth and pattern duplications in regions close to the D/V
|compartment boundary in the anterior compartment. Weak phenotypes
|include distal bifurcation of vein LIII and thickening of the proximal
|costa. Extreme phenotypes consist of overgrowth and pattern duplications
|in proximal or distal regions of the anterior wing margin, including
|duplication and triplication of LIII and loss of LII. Sensory elements
|... (see FBal0005217==gro1 report)
PHM|wing vein L1
|wing vein L2
|wing vein L3
|wing | anterior compartment
|wing | dorsal/ventral compartment boundary
|macrochaeta & head
|macrochaeta & thorax
|macrochaeta & abdominal tergite
|microchaeta & head
|microchaeta & thorax
|microchaeta & abdominal tergite
}
REFDSR
{
RDID|FBrf0099460
|Price et al.
|1997
PHP|FBal0082904==groC105/FBal0005217==gro1 mutants display
| enlarged and fused ocelli, and
|an increased number of fronto-orbital microchaetae.
PHM|ocellus
|microchaeta & head | adult
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Homozygotes have clumps of extra bristles above each
|eye which give impression of bushy eyebrows; also
|extra bristles on the humerus. Top of head tends to be
|malformed; ocelli often enlarged and run together. In
|selected stocks, penetrance approaches 100%, but is
|low in unselected stocks. Concluded to be an allele of
|E(spl) on the basis of the visible phenotype of
|... (see FBal0005217==gro1 report)
}
REF
{
REFM|FBrf0046015
|Knust et al.
|1987
REFM|FBrf0055903
|Fischer-Vize et al.
|1992
REFM|FBrf0084542
|de Celis and Ruiz-Gomez
|1995
REFM|FBrf0099460
|Price et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0025340 ICL 1 ? SYM 1 ?{}gt1a ASTR 1 - CLOC 1 3A3 REF 1 2 DT 1 7 Jul 2003 RESZ 593
ID|FBti0025340
SYM|?{}gt1a
SYN|?{}?{}gt1
DT|7 Jul 2003
|7 Jul 2003
ICL|?
ID2|FBti0014474
ASGN|FBgn0001150==gt
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}gt1a
ASAL|FBal0005233==gt1
MU|spontaneous
CLOC|3A3
|Insertion site
LOCB|Proximity to gene: FBgn0001150==gt
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
CC|One of two insertions associated with this allele; see FBti0025341==?{}gt1b.
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0005233==gt1
REFDSR
{
RDID|FBrf0003150
|Bridges
|1935
PHP|Salivary gland chromosomes are double normal thickness in some cells.
PHM|larval salivary gland | embryonic & chromosome
}
REFDSR
{
RDID|FBrf0043261
|Narachi and Boyd
|1985
PHP|FBal0005252==gtQ292/FBal0005233==gt1 larvae show a
| reduction in the normal inhibition
|of DNA synthesis following treatment with N-acetoxy-2-acetylaminofluorene.
|FBal0005234==gt13z/FBal0005233==gt1 larvae do not have
| a defect in the repair of X-ray
|induced DNA breaks.
}
REFDSR
{
RDID|FBrf0049604
|Mohler et al.
|1989
PHP|Delayed pupariation and enlarged larvae, pupae and adults.
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Larval development is 4 days longer than normal, resulting in giant
|larvae, pupae, and imagos. Adult weight is 1.7 times normal. Not all
|genetically FBgn0001150==gt flies show the giant character, the rest have normal
|size. The distribution is sharply bimodal. The percentage of
|phenotypically giant animals is greatest in well-fed cultures, and is
|also raised by the modifying action of FBal0001034==bb11.
|RK3.
}
REF
{
REFM|FBrf0003150
|Bridges
|1935
REFM|FBrf0043261
|Narachi and Boyd
|1985
REFM|FBrf0049604
|Mohler et al.
|1989
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0025341 ICL 1 ? SYM 1 ?{}gt1b ASTR 1 - CLOC 1 3A3 REF 1 2 DT 1 7 Jul 2003 RESZ 593
ID|FBti0025341
SYM|?{}gt1b
SYN|?{}?{}gt1
DT|7 Jul 2003
|7 Jul 2003
ICL|?
ID2|FBti0014474
ASGN|FBgn0001150==gt
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}gt1b
ASAL|FBal0005233==gt1
MU|spontaneous
CLOC|3A3
|Insertion site
LOCB|Proximity to gene: FBgn0001150==gt
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
CC|One of two insertions associated with this allele; see FBti0025340==?{}gt1a.
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0005233==gt1
REFDSR
{
RDID|FBrf0003150
|Bridges
|1935
PHP|Salivary gland chromosomes are double normal thickness in some cells.
PHM|larval salivary gland | embryonic & chromosome
}
REFDSR
{
RDID|FBrf0043261
|Narachi and Boyd
|1985
PHP|FBal0005252==gtQ292/FBal0005233==gt1 larvae show a
| reduction in the normal inhibition
|of DNA synthesis following treatment with N-acetoxy-2-acetylaminofluorene.
|FBal0005234==gt13z/FBal0005233==gt1 larvae do not have
| a defect in the repair of X-ray
|induced DNA breaks.
}
REFDSR
{
RDID|FBrf0049604
|Mohler et al.
|1989
PHP|Delayed pupariation and enlarged larvae, pupae and adults.
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Larval development is 4 days longer than normal, resulting in giant
|larvae, pupae, and imagos. Adult weight is 1.7 times normal. Not all
|genetically FBgn0001150==gt flies show the giant character, the rest have normal
|size. The distribution is sharply bimodal. The percentage of
|phenotypically giant animals is greatest in well-fed cultures, and is
|also raised by the modifying action of FBal0001034==bb11.
|RK3.
}
REF
{
REFM|FBrf0003150
|Bridges
|1935
REFM|FBrf0043261
|Narachi and Boyd
|1985
REFM|FBrf0049604
|Mohler et al.
|1989
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014520 ICL 1 ? SYM 1 ?{}Lim32 ASTR 1 - CLOC 1 37B13--C1 REF 1 3 DT 1 6 Jan 2000 RESZ 561
ID|FBti0014520
SYM|?{}Lim32
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0002023==Lim3
REFDSR
{
RDID|FBrf0046993
|Black et al.
|1987
PHC|lethal | larval | recessive
}
REFDSR
{
RDID|FBrf0084402
|Stathakis et al.
|1995
SYN|?{}Lim32
ASAL|FBal0008649==Lim32
MU|ethyl methanesulfonate + formaldehyde
CLOC|37B13--C1
|Insertion site
LOCB|Proximity to gene: FBgn0002023==Lim3
}
REF
{
REFM|FBrf0046993
|Black et al.
|1987
REFM|FBrf0084402
|Stathakis et al.
|1995
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0008649==Lim32
REFDSR
{
RDID|FBrf0089206
|Wright
|1996
PHP|Most hemizygotes do not pupariate, remaining as second or third instar
|larvae up to 8 or 9 days after egg laying. A few hemizygotes do pupariate
|8 to 11 days after egg laying, and these pupae generally develop into
|pharate adults that do not eclose. These pharate adults show a complete
|lack of differentiated cuticle on the abdomen, and have reduced cuticle
|formation on the thorax and head.
PHM|cuticle & abdomen | pharate adult
|cuticle & thorax | pharate adult
|cuticle & head | pharate adult
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|strong allele in which second and third instar larvae
|persist until days eight and nine; few survive to
|pharate-adult stage with incomplete sclerotization.
}
REF
{
REFM|FBrf0089206
|Wright
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014535 ICL 1 ? SYM 1 ?{}lz34 ASTR 1 - CLOC 1 8D12 REF 1 2 DT 1 6 Jan 2000 RESZ 395
ID|FBti0014535
SYM|?{}lz34
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0002576==lz
REFDSR
{
RDID|FBrf0093407
|Crew et al.
|1997
SYN|?{}lz34
ASAL|FBal0011773==lz34
MU|spontaneous
CLOC|8D12
|Insertion site
LOCB|Proximity to gene: FBgn0002576==lz
}
REF
{
REFM|FBrf0093407
|Crew et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0011773==lz34
REFDSR
{
RDID|FBrf0011129
|Green and Green
|1956
PHP|Homozygotes have rough eyes which are reduced in size. Red eye pigment
|is distributed over the entire eye. The tarsal claws are reduced.
|The spermathecae and pars ovariae are absent in homozygous females.
PHM|eye
|spermathecum
|tarsus
|ovary
}
REFDSR
{
RDID|FBrf0068701
|Stocker et al.
|1993
PHP|The antennal funiculus is reduced in size in hemizygous males. All
|large and small basiconic sensilla on the antennal funiculus are missing,
|and the number of trichoid sensilla on the antennal funiculus is reduced.
|The number of coeloconic sensilla on the antennal funiculus is normal.
PHM|antennal segment 3
|sensillum basiconicum of antennal segment 3
|sensillum trichodeum of antennal segment 3
}
REFDSR
{
RDID|FBrf0083505
|Vosshall and Young
|1995
PHP|Displays locomotor activity rhythm with an approximately 24h period.
}
REFDSR
{
RDID|FBrf0086985
|Daga et al.
|1996
PHP|R7 cells are converted to outer receptor cells.
PHM|photoreceptor cell R7
}
REFDSR
{
RDID|FBrf0090446
|Batterham et al.
|1996
PHP|Homozygotes show disruption of the ommatidial array and fusion of ommatidia
|across the posterior half of the eye. Black pock marks are visible
|on the surface of the eye. The retina is moderately disorganized,
|particularly in the posterior region. The underlying lamina is also
|disorganized in the posterior region. The fenestrated membrane is
|abnormal. Rhabdomeric bundles are found in the cortex of the lamina.
|The number and type of photoreceptors in each ommatidium are sometimes
|... (see FBal0011773==lz34 report)
PHM|eye | posterior
|ommatidium
|eye
|lamina cortex
|retina
|lamina
}
REFDSR
{
RDID|FBrf0093407
|Crew et al.
|1997
PHP|Rough eye phenotype. Some secondary pigment cells are absent. Photoreceptor
|neuron recruitment is perturbed. Some facets have only six cells,
|R7 appears to be transformed to R1-6-like photoreceptor cell. An R7-like
|cell is missing in some facets.
PHM|photoreceptor cell R7
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye phenotype intermediate between lz and FBal0011764==lz3.
|Surface of eye has large areas of fused facets with a
|few normal facets (Clayton, 1957);
|eye color dark red with small yellowish spots. Larval
|Malpighian tubes slightly lighter than normal;
|variable (Brehme and Demerec, 1942).
|Tarsal claws reduced. Spermathecae and parovaria
|... (see FBal0011773==lz34 report)
}
REFDSR
{
RDID|FBrf0158867
|Siddall et al.
|2003
PHP|FBal0011773==lz34 adults have a severe mutant eye phenotype.
| Ectopic cell
|death is seen in third larval instar eye discs.
PHM|eye
|eye disc
}
REF
{
REFM|FBrf0011129
|Green and Green
|1956
REFM|FBrf0068701
|Stocker et al.
|1993
REFM|FBrf0083505
|Vosshall and Young
|1995
REFM|FBrf0086985
|Daga et al.
|1996
REFM|FBrf0090446
|Batterham et al.
|1996
REFM|FBrf0093407
|Crew et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0158867
|Siddall et al.
|2003
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014537 ICL 1 ? SYM 1 ?{}lzK ASTR 1 - CLOC 1 8D12 REF 1 2 DT 1 6 Jan 2000 RESZ 377
ID|FBti0014537
SYM|?{}lzK
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0002576==lz
REFDSR
{
RDID|FBrf0093407
|Crew et al.
|1997
SYN|?{}lzK
ASAL|FBal0011825==lzK
CLOC|8D12
|Insertion site
LOCB|Proximity to gene: FBgn0002576==lz
}
REF
{
REFM|FBrf0093407
|Crew et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0011825==lzK
REFDSR
{
RDID|FBrf0049495
|Renfranz and Benzer
|1989
PHP|A weak lz allele. Adult eye slightly rough, irregular facets shapes,
|eye disc appears normal.
}
REFDSR
{
RDID|FBrf0063599
|Krivshenko
|1956
PHP|Homozygous males have slightly narrow eyes, with uneven fused facets.
|Males are viable and fertile, homozygous females have not been obtained.
|Heterozygous females are phenotypically normal.
PHM|eye
|ommatidium
}
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
PHP|RK1.
|Tarsal claws normal. Spermathecae and parovaria present.
}
REFDSR
{
RDID|FBrf0068701
|Stocker et al.
|1993
PHP|The antennal funiculus is reduced in size in hemizygous males. The
|number of large and small basiconic sensilla is reduced. The density
|of the coeloconic sensilla on the antennal funiculus is increased and
|the density of the large basiconic sensilla on the antennal funiculus
|is decreased compared to wild-type.
PHM|antennal segment 3
|sensillum basiconicum of antennal segment 3
}
REFDSR
{
RDID|FBrf0086985
|Daga et al.
|1996
PHP|Some ommatidia have a supernumerary R7 photoreceptor cell, and some
|have extra outer photoreceptor cells.
PHM|photoreceptor cell
}
REFDSR
{
RDID|FBrf0090446
|Batterham et al.
|1996
PHP|Homozygous females have normal eyes. Hemizygous males have a mild
|rough eye phenotype, with disruption of the ommatidial array at the
|posterior rim of the eye. Black pock marks are visible on the surface
|of the eye.
PHM|eye | posterior
|ommatidium
|eye
}
REFDSR
{
RDID|FBrf0093407
|Crew et al.
|1997
PHP|Mild eye phenotype. Defects in photoreceptor neuron recruitment.
|Some facets have seven cells with larger, R1 to R6 like rhabdomeres,
|an R7-like cell is absent. Facets may have a duplicated R7 cells.
|Other facets have normal looking R7 cells but incorrect numbers of
|outer photoreceptor cells.
PHM|photoreceptor cell R1
|photoreceptor cell R2
|photoreceptor cell R3
|photoreceptor cell R4
|photoreceptor cell R5
|photoreceptor cell R6
|photoreceptor cell R7
}
REFDSR
{
RDID|FBrf0158867
|Siddall et al.
|2003
PHP|FBal0011825==lzK adults have a mild mutant eye phenotype. Ectopic
| cell death
|is seen in third larval instar eye discs.
PHM|eye
|eye disc
}
REF
{
REFM|FBrf0049495
|Renfranz and Benzer
|1989
REFM|FBrf0063599
|Krivshenko
|1956
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0068701
|Stocker et al.
|1993
REFM|FBrf0086985
|Daga et al.
|1996
REFM|FBrf0090446
|Batterham et al.
|1996
REFM|FBrf0093407
|Crew et al.
|1997
REFM|FBrf0158867
|Siddall et al.
|2003
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0037935 ICL 1 ? SYM 1 ?{}lzL ASTR 1 - CLOC 1 8D12 REF 1 2 DT 1 21 Oct 2003 RESZ 385
ID|FBti0037935
SYM|?{}lzL
DT|21 Oct 2003
|21 Oct 2003
ICL|?
ASGN|FBgn0002576==lz
REFDSR
{
RDID|FBrf0158867
|Siddall et al.
|2003
SYN|?{}lzL
ASAL|FBal0061066==lzL
CLOC|8D12
|Insertion site
LOCB|Proximity to gene: FBgn0002576==lz
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0158867
|Siddall et al.
|2003
}
ALESR
{
ASYM|FBal0061066==lzL
REFDSR
{
RDID|FBrf0068701
|Stocker et al.
|1993
PHP|The antennal funiculus is reduced in size in hemizygous males. All
|large and small basiconic sensilla on the antennal funiculus are missing,
|and the number of trichoid sensilla on the antennal funiculus is reduced.
|The number of coeloconic sensilla on the antennal funiculus is normal.
|The density of the coeloconic sensilla on the antennal funiculus is
|increased and the density of the trichoid sensilla on the antennal
|funiculus is decreased compared to wild-type.
|... (see FBal0061066==lzL report)
PHM|antennal segment 3
|sensillum basiconicum of antennal segment 3
|sensillum trichodeum of antennal segment 3
|maxillary palp sensillum basiconicum
}
REFDSR
{
RDID|FBrf0090446
|Batterham et al.
|1996
PHP|Homozygotes have a total lack of ommatidial structure in the eye.
|Pigment is dispersed as a ring around the edge of the eye ("spectacle"
|phenotype). Few, if any lenses form, and the eye is covered by a cuticle
|scar. The 'retina' appears to lack pigment cells. Photoreceptor cell
|orientation is random, and the fenestrated membrane is absent.
PHM|eye
|ommatidium
|lens
|photoreceptor cell
|pigment cell
}
REFDSR
{
RDID|FBrf0093407
|Crew et al.
|1997
PHP|15% of photoreceptor cell clusters are abnormal, cells R1 and R6 are
|not recruited properly. Uniform sheet of unorganized cone cells is
|found. The periphery of the retina contains cells in loosely organized
|clusters including cones as well as primary and secondary pigment cells,
|the darker pigment produces the 'spectacle' phenotype.
PHM|photoreceptor cell R1
|photoreceptor cell R6
|cone cell
}
REFDSR
{
RDID|FBrf0158867
|Siddall et al.
|2003
PHP|FBal0061066==lzL adults have a "spectacle" eye phenotype.
| Ommatidial clusters
|are rarely detectable in FBal0061066==lzL eyes. Ectopic cell
| death is seen
|in third larval instar eye discs, between rows 3 an 7 posterior to
|the morphogenetic furrow.
PHM|ommatidium
|eye disc
|eye
}
REF
{
REFM|FBrf0068701
|Stocker et al.
|1993
REFM|FBrf0090446
|Batterham et al.
|1996
REFM|FBrf0093407
|Crew et al.
|1997
REFM|FBrf0158867
|Siddall et al.
|2003
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014543 ICL 1 ? SYM 1 ?{}mei-W681 ASTR 1 - CLOC 1 56D9--11 REF 1 2 DT 1 6 Jan 2000 RESZ 453
ID|FBti0014543
SYM|?{}mei-W681
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0002716==mei-W68
ARGS|FBgn0002716
REFDSR
{
RDID|FBrf0104768
|McKim and Hayashi-Hagihara
|1998
SYN|?{}mei-W681
ASAL|FBal0012191==mei-W681
CLOC|56D9--11
|Insertion site
LOCB|Proximity to gene: FBgn0002716==mei-W68
}
REF
{
REFM|FBrf0104768
|McKim and Hayashi-Hagihara
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0012191==mei-W681
REFDSR
{
RDID|FBrf0059133
|McKim et al.
|1993
PHP|Metaphase arrest prevented.
}
REFDSR
{
RDID|FBrf0093814
|Carpenter
|1997.5.12
PHP|Ultrastructural studies of pachytene reveal synaptonemal complex that is
|normal in structure and length and which undergoes the same changes in
|length as is observed in wild type as the cells progress through
|pachytene; chromocentral organization and chromatin condensation are also
|normal. However, no late recombination nodules were observed in the nine
|nuclei reconstructed which were between the developmental landmarks which
|demark their presence in wild type.
}
REFDSR
{
RDID|FBrf0100602
|McKim et al.
|1998
PHP|Severe mutation.
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Females homozygous for mei-W68 show a complete absence
|of meiotic recombination (Baker, unpublished data).
|A less severe allele (mei-W68L1-Lindsley) reduces
|exchange to approximately 60% of control levels and
|also alters the distribution of residual exchanges.
|Analysis of mitotic chromosome behavior (Baker et al.,
|1978) suggests that the FBgn0002716==mei-W68+ gene product is
|... (see FBal0012191==mei-W681 report)
}
REFDSR
{
RDID|FBrf0158977
|Carpenter
|2003
PHP|Crossing over is reduced in
| FBal0090228==mei-W68L1/FBal0012191==mei-W681 females.
|Homozygotes lack meiotic crossing over. Premeiotic exchanges occur
|in homozygous females.
|FBal0012191==mei-W681 is recessive to wild type when
| nondisjunction frequencies
|are examined but has dominant effects on crossing over.
|Homozygous and
| FBal0090228==mei-W68L1/FBal0012191==mei-W681 females
| show normal dynamics
|of germ-line mitotic divisions. The dynamics of entry into meiosis
|... (see FBal0012191==mei-W681 report)
PHM|late recombination nodule
|early recombination nodule
}
REF
{
REFM|FBrf0059133
|McKim et al.
|1993
REFM|FBrf0093814
|Carpenter
|1997.5.12
REFM|FBrf0100602
|McKim et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0158977
|Carpenter
|2003
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014164 ICL 1 ? SYM 1 ?{}N55e11 ASTR 1 - CLOC 1 3C7--9 REF 1 6 DT 1 6 Jan 2000 RESZ 737
ID|FBti0014164
SYM|?{}N55e11
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0004647==N
REFDSR
{
RDID|FBrf0040185
|Lehmann et al.
|1983
PHC|lethal | embryonic | neurogenic | recessive
}
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}N55e11
ASAL|FBal0012701==N55e11
MU|spontaneous
CLOC|3C7--9
|Insertion site
LOCB|Proximity to gene: FBgn0004647==N
}
REFDSR
{
RDID|FBrf0091115
|Long et al.
|1996
PHC|lethal | recessive
}
REF
{
REFM|FBrf0040185
|Lehmann et al.
|1983
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0091115
|Long et al.
|1996
REFM|FBrf0098202
|Brennan et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0112013
|Rauskolb et al.
|1999
}
ALESR
{
ASYM|FBal0012701==N55e11
REFDSR
{
RDID|FBrf0027480
|Shellenbarger and Mohler
|1975
PHP|Lethal in combination with FBal0012887==Nl1N-ts1 or
| FBal0012861==NAx-tsl at 29oC.
}
REFDSR
{
RDID|FBrf0038108
|Poulson and Lefevre
|1982
PHP|Male flies carrying FBab0003125==Dp(1;2)51bV76e show wing-notching and lateral
|incisions, leg defects and tarsal reductions, missing or multiple bristles,
|missing or fused ocelli and variegated or roughened eyes, at varying
|frequencies.
}
REFDSR
{
RDID|FBrf0040181
|Campos-Ortega
|1983
PHP|The presence of the FBal0012701==N55e11 did not affect the
| epidermal pattern in
|the thoracic and abdominal segments of hemizygotes derived from FBal0002643==dl1/FBal0002643==dl1
|hemizygotes. Double mutants FBal0012701==N55e11 and
| FBal0002644==dl2 had neuralization of
|additional ectodermal cells in the thoracic and abdominal segments.
|Double mutants FBal0012701==N55e11 and Tl had neuralization of
| the entire ectoderm,
|a huge CNS and no epidermis as it had been substituted for by neural
|tissue.
}
REFDSR
{
RDID|FBrf0040185
|Lehmann et al.
|1983
PHP|Extreme embryonic neurogenic phenotype.
PHM|epidermis | embryonic
}
REFDSR
{
RDID|FBrf0043047
|Vassin et al.
|1985
PHP|Notching of the tips and/or edges of the wing. Veins are frequently
|broadened at the marginal junctions, forming delta-like thickenings.
PHM|wing
|wing vein
}
REFDSR
{
RDID|FBrf0048995
|Brand and Campos-Ortega
|1988
PHP|The amount of maternally derived gene product does not modify the phenotype
|of double neurogenic mutants. FBal0012701==N55e11 expression was
| modified by
|the presence of ASC loss-of-function mutations. All embryonic cells
|initiate neural development but later in development some cells switch
|their fate either to epidermogenesis or cell death.
}
REFDSR
{
RDID|FBrf0051582
|Cabrera
|1990
PHP|Post-transcriptional control of AS-C expression is suppressed, all
|cells expressing RNA accumulate protein.
}
REFDSR
{
RDID|FBrf0053344
|Heitzler and Simpson
|1991
PHP|Neural hyperplasia of cells within a mutant clone. Mutant clones fail
|to form bristles.
}
REFDSR
{
RDID|FBrf0053362
|Corbin et al.
|1991
PHP|FBal0012701==N55e11 shows severe neural hypertrophy, a 6--9 fold
| increase in nau
|expressing cells per cluster relative to wild type. Embryos show a
|disrupted CNS pattern. When heterozygous with FBab0000974==Df(1)svr the CNS ladder
|structure is apparent, hypertrophy is seen in the nau expressing cells
|and the medial superclusters arise in a disrupted pattern compared
|to wildtype.
}
REFDSR
{
RDID|FBrf0053769
|Goriely et al.
|1991
PHP|Increase in SMCs per cluster in embryos lacking the maternal product.
}
REFDSR
{
RDID|FBrf0054994
|de Celis et al.
|1991
PHP|Homozygous clones produced during the last stages of the formation
|of the adult sensory organs develop into sensory organ mother cells
|when induced early, or its neural sublineage later.
}
REFDSR
{
RDID|FBrf0055911
|Skeath and Carroll
|1992
PHP|ac protein distribution in FBal0012701==N55e11 embryos show ac
| expression is not
|restricted to a single cell of an ectodermal cell cluster, instead
|most cells of the cluster retain ac expression at a high level, enlarge,
|delaminate and become neuroblasts.
}
REFDSR
{
RDID|FBrf0059323
|Bodmer et al.
|1993
PHP|Hyperplasia of replicating sensory precursors: due to an increased
|number of ectodermal cells being recruited as sensory precursor cells.
|Extra precursor cells are recruited beyond the normal time window
|for neurogenesis in the PNS.
PHM|ectoderm
}
REFDSR
{
RDID|FBrf0068598
|Menne and Klambt
|1994
PHP|Mutant embryos rarely form commissural or longitudinal connections.
|Although the first axons grow out at the same time as wild-type axons,
|they are never oriented towards the midline, and even fail to form
|connections on the ipsilateral side. Both anterior and middle pairs
|of midline glia are absent, and the posterior pair are duplicated but
|found at ectopic positions. There are 4-8 additional neuronal midline
|cells per segment.
PHM|central nervous system | embryonic
|midline glial cell
|midline glial cell | ectopic
}
REFDSR
{
RDID|FBrf0072582
|Bate et al.
|1993
PHP|Embryos exhibit few, if any, fused muscles. The unfused, birefringent
|fibers, have a random pattern of fine fibers apparently radiating out
|from small fragments of dorsal cuticle. The birefringent is clearly
|correlated with the expansion of the CNS and PNS, and the loss of epidermis
|and the degree to which myoblast fusion occurs. Where myoblast fusion
|fails conspicuous clusters of mesodermal cells are formed and if epidermal
|territories are expanded cells in these clusters may be recruited to
|... (see FBal0012701==N55e11 report)
PHM|embryonic/larval somatic muscle
|embryonic nervous system
|epidermis | embryonic
|myoblast | embryonic
}
REFDSR
{
RDID|FBrf0072959
|Diaz-Benjumea and Hafen
|1994
PHP|FBal0014587==rl1/FBab0002207==Df(2R)rl10a strongly enhances the
| wing phenotype of FBal0012701==N55e11/+.
}
REFDSR
{
RDID|FBrf0074921
|de Celis and Garcia-Bellido
|1994
PHP|Clones running along the veins differentiate broad stretches of cells
|with vein histotype, to differentiate cells must be within 10-15 normal
|cell diameters from the vein. Clones can also affect vein differentiation
|on the other wing surface. Clones can also reduce the intervein distance.
|Clones in the dorso-ventral compartment border can induce scalloping
|indicating non-autonomous effects in wing margin loss.
|Clonal behavior of FBgn0004647==N clones in the wing does not result from abnormal
|... (see FBal0012701==N55e11 report)
PHM|wing
|wing | dorsal/ventral compartment boundary
}
REFDSR
{
RDID|FBrf0074922
|de Celis et al.
|1991
PHP|Cause a complex pleiotropic syndrome including perturbations of the
|chaetae pattern.
}
REFDSR
{
RDID|FBrf0075100
|Hoch et al.
|1994
PHP|Embryos derived from germline clones show supernumerary Malpighian
|tubule tip cells segregating from the tubule primordial cells. The
|tubules of these embryos do not go on to secrete uric acid.
PHM|Malpighian tubule primordium | germ-line clone
|Malpighian tubule tip cell | germ-line clone
}
REFDSR
{
RDID|FBrf0076037
|Couso and Martinez Arias
|1994
PHP|FBal0012701==N55e11/FBal0012887==Nl1N-ts1 animals
| reared at 17oC and exposed to 29oC
|for 24 hrs in the second larval instar give rise to adults with duplicated
|(sometimes triplicated) legs, with ventral branch points, and reduced
|or absent wings with accompanying wing to notum transformation. This
|phenotype is identical to that produced by loss of FBgn0004009==wg during second
|and early third larval instar. Heterozygosity for
| FBal0012701==N55e11 reduces
|viability and increases penetrance of wing/haltere phenotypes of FBal0018482==wg1.
|... (see FBal0012701==N55e11 report)
}
REFDSR
{
RDID|FBrf0076146
|Sturtevant and Bier
|1995
PHP|Thickened vein mutant.
PHM|wing vein
}
REFDSR
{
RDID|FBrf0083156
|Gonzalez-Gaitan and Jaeckle
|1995
PHP|Instead of forming distinct invagination folds, the FBgn0004647==N mutant stomodeal
|nervous system anlage invaginates en masse.
PHM|stomatogastric nervous system primordium
}
REFDSR
{
RDID|FBrf0084329
|Rulifson and Blair
|1995
PHP|SMC differentiation and proneural activation in
| FBal0012701==N55e11 wing margin
|clones display dual phenotypes. Clones that do not substantially disrupt
|FBgn0004009==wg expression have neurogenic phenotypes and clones that disrupt
|FBgn0004009==wg expression have a mixture of antiproneural and neurogenic phenotypes.
}
REFDSR
{
RDID|FBrf0089977
|Guo et al.
|1996
PHP|Heterozygotes exhibit no obvious hair or socket abnormalities. Heterozygotes
|carrying one copy of FBtp0003391==P{hs-numb} in the absence of heat shock have
|double hairs without sockets at the anterior wing margin. This phenotype
|is enhanced with two copies of FBtp0003391==P{hs-numb}.
}
REFDSR
{
RDID|FBrf0090023
|de Celis et al.
|1996
PHP|Clones in the thorax produce patches of naked cuticle, due to the differentiation
|of the ectopic SOPs into neurons.
|Clones in the wing that reach the wing margin show a loss of margin
|and blade tissue due to the requirement for FBgn0004647==N at the D/V boundary.
|Wing veins also appear thicker.
PHM|sensillum precursor | ectopic
|macrochaeta
|wing
|dorsal double row
|ventral double row
|wing vein
}
REFDSR
{
RDID|FBrf0090425
|Abu-Issa and Cavicchi
|1996
PHP|Heterozygotes show thickening of the wing veins, occasional terminal
|nicking of the wing, and 1-4 ectopic bristles on the wing surface.
PHM|wing
|wing vein
|wing sensillum | ectopic
}
REFDSR
{
RDID|FBrf0090560
|Frise et al.
|1996
PHP|FBal0012701==N55e11/+ flies have a notched wing phenotype.
| Homozygous clones
|induced in the sensory organ precursor daughter IIa cells of the
|adult external sense organs, when FBal0058958==Scer\FLP1Scer\UAS.cBa
|expression is driven by FBal0052395==Scer\GAL4sca-109-68, produce
| a twinned
|hair phenotype.
PHM|wing
|external sensory organ | somatic clone
}
REFDSR
{
RDID|FBrf0091115
|Long et al.
|1996
PHP|Wing nicking phenotype.
}
REFDSR
{
RDID|FBrf0091127
|Murata et al.
|1996
PHP|Heterozygotes have a triangular expansion of the veins at the wing
|margin, and approximately 25% of flies have notched wings.
PHM|wing
|wing vein
}
REFDSR
{
RDID|FBrf0093461
|Giebel et al.
|1997
PHP|FBal0042573==Scer\GAL4da.G32-mediated coexpression of
| FBal0045936==l(1)scScer\UAS.cHa and FBal0061468==daScer\UAS.cGa
|cause increase of cells in the CNS: brain lobes are enlarged (protruding
|through the holes in the cephalic epidermis), the ventral cord shows
|regional enlargement and sensory organs contain a large number of neurons.
|Neural hyperplasia is also increased, epidermis, fore- and hindgut,
|tracheal tree and salivary glands are completely neuralized.
PHM|embryonic nervous system
|larval brain | embryonic
|ventral nerve cord
|epidermis
|larval foregut | embryonic
|larval hindgut | embryonic
|embryonic/larval tracheal system
|larval salivary gland | embryonic
}
REFDSR
{
RDID|FBrf0093711
|Seugnet et al.
|1997
PHP|Segregation of neuroblasts 5-2 and 7-4 is normal at early stages.
|Late embryos are strongly neuralized.
|Embryos derived from germline clones exhibit disturbed segmentation
|in some segments and some 5-2 equivalence groups are fused. Segregation
|of the 5-2 and 7-4 neuroblast occurs in an irregular manner at later
|stages.
PHM|neuroblast NB5-2 | germ-line clone
|neuroblast NB7-4 | germ-line clone
|central nervous system | larval | germ-line clone
|peripheral nervous system | larval | germ-line clone
}
REFDSR
{
RDID|FBrf0097687
|Vervoort et al.
|1997
PHP|Embryos exhibit supernumerary md neurons that derive from ASC precursors.
PHM|multidendritic neuron
}
REFDSR
{
RDID|FBrf0098202
|Brennan et al.
|1997
PHP|Hemizygous lethal. Heterozygotes have a neurogenic phenotype and have
|a marked increase in the number of bristles on the notum.
PHM|adult thoracic sensillum
}
REFDSR
{
RDID|FBrf0098359
|Stuttem and Campos-Ortega
|1997
PHP|Transplantation of single cells from FBal0012701==N55e11 embryos
| into the ventral
|neurogenic region of wild-type host embryos reveals non-autonomous
|behavior of these cells; the cells can give rise to both neural and
|epidermal offspring. Single cells from FBal0012701==N55e11
| embryos transplanted
|into the ventral neurogenic region of FBal0012701==N55e11 host
| embryos give
|rise to only neural cells. Single cells from FBal0012701==N55e11
| embryos transplanted
|into the procephalic neuroectoderm or the proctodeal anlage of wild-type
|... (see FBal0012701==N55e11 report)
}
REFDSR
{
RDID|FBrf0098813
|Jagla et al.
|1997
PHP|Homozygous embryos have an increased number of cardiac precursor cells.
PHM|embryonic/larval dorsal vessel | precursor
}
REFDSR
{
RDID|FBrf0099033
|Doherty et al.
|1997
PHM|epidermis | embryonic
}
REFDSR
{
RDID|FBrf0099460
|Price et al.
|1997
PHM|wing
}
REFDSR
{
RDID|FBrf0099884
|Sotillos et al.
|1997
PHP|Heterozygotes show scalloping of the wing margin and thickening of
|the wing veins.
PHM|wing
|wing vein
}
REFDSR
{
RDID|FBrf0101998
|Rottgen et al.
|1998
PHP|FBal0012701==N55e11/FBab0000579==Df(1)N-8 transheterozygotes
| exhibit ectopic bristles on
|the notum.
PHM|(with Df(1)N-8) scutum & macrochaeta | ectopic
}
REFDSR
{
RDID|FBrf0102423
|Zeng et al.
|1998
PHP|Homozygous clones on the central region of the adult scutum are devoid
|of any external bristle structures, such as shafts and sockets.
|Homozygous clones induced in the sensory organ lineage frequently have
|bristles with double shafts (approximately 39% of homozygous macrochaetae
|have double shafts).
PHM|socket & scutum | somatic clone
|macrochaeta & scutum | somatic clone
|macrochaeta | somatic clone
|sensillum precursor | somatic clone
}
REFDSR
{
RDID|FBrf0102699
|Martinez Arias
|1998
PHP|The cuticle of a
| FBal0012887==Nl1N-ts1/FBal0012701==N55e11 larva grown
| at 17oC until
|early stage 11 and then shifted to 30oC is shorter than wild-type
|and shows segment fusions.
PHM|embryonic/first instar larval cuticle
}
REFDSR
{
RDID|FBrf0102708
|Boube et al.
|1998
PHP|FBal0013509==pb5/FBal0013517==pb13 flies show a slight
| distal transformation of labium
|to antennal arista. If the flies are also heterozygous for FBal0012701==N55e11
|the number of pseudotracheal rows is reduced and a region of apparent
|ectoderm forms between the remaining pseudotracheal rows and the transformed
|antennal structures.
}
REFDSR
{
RDID|FBrf0102828
|Roch et al.
|1998
PHP|Wing veins are thickened.
PHM|wing vein
}
REFDSR
{
RDID|FBrf0104758
|Jagla et al.
|1998
PHP|The segmental border muscle progenitors do not segregate at all or
|do not divide properly.
PHM|segment border muscle | precursor
}
REFDSR
{
RDID|FBrf0104911
|Hoch and Jackle
|1998
PHP|Multiple Malpighian tubule tip cells develop in homozygous embryos.
PHM|Malpighian tubule tip cell
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|A weak Notch. Deltas on wing veins are most reliable
|character for classification. Lethal when heterozygous
|with FBal0012892==Nnd-3, FBal0012703==N60g11 and
| FBal0012759==NCo. In homozygotes and
|hemizygotes hyperplasia of central nervous system
|extreme; embryonic peripheral nervous system abnormal
|with sensilla undifferentiated (Hartenstein and
|Campos-Ortega, 1986).
}
REFDSR
{
RDID|FBrf0106041
|Rusconi and Corbin
|1998
PHP|The number of cells in the FBgn0002922==nau-expressing muscle precursor clusters
|is increased compared to wild-type in homozygous embryos. The number
|of cells in the FBgn0002922==nau-expressing muscle precursor clusters is increased
|to more than twice the number in homozygous embryos (lacking zygotic
|function) in homozygous embryos derived from homozygous female germline
|clones (lacking both maternal and zygotic function).
PHM|embryonic/larval somatic muscle
|embryonic/larval somatic muscle | germ-line clone
}
REFDSR
{
RDID|FBrf0107900
|Nagaraj et al.
|1999
PHP|FBal0012887==Nl1N-ts1/FBal0012701==N55e11 wing discs
| show a reduction in the size of
|the pouch.
|Heterozygotes show mild notching of the distal wing margin.
PHM|wing margin
|dorsal mesothoracic disc
}
REFDSR
{
RDID|FBrf0108514
|Llimargas
|1999
PHP|Mutants show a rudimentary tracheal tree, ectopic fusions between adjacent
|branches and absence of terminal branches. The number of tracheal cells
|is reduced, resulting in reduced branching. Temperature shifts of
|heterozygotes of
| FBal0012701==N55e11/FBal0012887==Nl1N-ts1 suggest
| that in addition to
|its early role in tracheal specification, FBgn0004647==N acts later in both fusion
|and terminal branching programs.
|Cell markers indicate a transformation of presumptive terminal or antifusion
|... (see FBal0012701==N55e11 report)
PHM|trachea | embryonic
}
REFDSR
{
RDID|FBrf0108607
|Bishop et al.
|1999
PHP|FBal0012887==Nl1N-ts1/FBal0012701==N55e11 flies
| exposed to the restrictive temperature
|during the third larval instar and pupal phases show a marked reduction
|in leg length with all areas of the leg segments (joint and interjoint
|tissue) being affected. Joints are completely lost, and also often
|apical bristles.
PHM|leg | conditional ts
|prothoracic tibial apical bristle | conditional ts
|mesothoracic tibial apical bristle | conditional ts
|metathoracic tibial apical bristle | conditional ts
}
REFDSR
{
RDID|FBrf0109019
|Rauskolb and Irvine
|1999
PHP|Homozygous clones in the leg form patches of naked cuticle. The clones
|fail to form joint structures in all regions of the leg (resulting
|in fusion of leg segments) and leg growth is reduced. Fusions are
|seen along the length of the tibia and femur, while end-to-end fusions
|are seen in other leg segments. In most cases, the failure to form
|joints is an autonomous property of the mutant cells in the clone,
|although occasionally joint formation is also inhibited in wild-type
|... (see FBal0012701==N55e11 report)
PHM|joint | somatic clone | cell autonomous
|joint | somatic clone | cell non-autonomous
|leg sensillum | somatic clone
|leg | somatic clone
|tibia | somatic clone
|femur | somatic clone
}
REFDSR
{
RDID|FBrf0109184
|zur Lage and Jarman
|1999
PHP|Leg discs of FBal0012887==Nl1N-ts1/FBal0012701==N55e11
| larvae reared at the restrictive
|temperature for 4-16 hours show a large, disorganized mass of sensory
|organ precursor cells below the epithelium where the SOP cells of the
|femoral chordotonal organ normally form.
PHM|ventral thoracic disc
}
REFDSR
{
RDID|FBrf0111977
|Micchelli and Blair
|1999
PHP|In somatic clones in the wing disc, the majority of
| FBal0012701==N55e11 clones
|that are in contact with the FBgn0000099==ap boundary, disrupt the Dorsal/ventral
|(D/V) lineage restriction. In the most extreme class, clones straddle
|or cross the normal site of the D/V boundary from either side, with
|most or all of the cells being in the wrong compartment. In some cases
|milder distortions lead to "bulging" clones and some clones do approximately
|respect the boundary. Disruptions are not always limited to the mutant
|... (see FBal0012701==N55e11 report)
PHM|dorsal mesothoracic disc | dorsal/ventral compartment boundary | somatic clone
}
REFDSR
{
RDID|FBrf0112013
|Rauskolb et al.
|1999
PHP|Homozygous mutant clones in the wing disc fail to respect the dorsal
|ventral boundary.
PHM|dorsal mesothoracic disc | somatic clone
}
REFDSR
{
RDID|FBrf0112024
|Rusconi and Corbin
|1999
PHP|The number of FBgn0001077==ftz expressing MP2 neurons increases compared to wild-type
|(About 30 on each side of the midline, as compared to 2 in wild-type)
|in homozygous embryos derived from homozygous female germ-line clones
|(lacking both maternal and zygotic function). The extra MP2 clusters
|extend further laterally than seen in FBgn0000463==Dl and FBgn0004837==Su(H). alleles. No
|segmentation defects are seen.
|In homozygous embryos derived from homozygous female germ-line clones
|... (see FBal0012701==N55e11 report)
PHM|dMP2 neuron | ectopic | germ-line clone
|vMP2 neuron | ectopic | germ-line clone
|RP2 neuron | ectopic | germ-line clone
}
REFDSR
{
RDID|FBrf0125167
|de Celis and Bray
|2000
PHP|Wing veins L3 and L5 are thicker than wild-type veins in heterozygous
|flies, and the thickened veins have smooth borders. The wings show
|moderate scalloping of the wing margin.
PHM|wing vein L3
|wing vein L5
|wing vein L3 | ectopic
|wing vein L5 | ectopic
|wing
}
REFDSR
{
RDID|FBrf0135724
|Udolph et al.
|2001
PHP|Glial cells in the central nervous system of embryos are not entirely
|absent.
|In clones of FBal0012701==N55e11 cells in a wild type background
| the pCC is
|transformed into aCC, SPGs are lost and neuronal cells are concomitantly
|gained within the NB1-1 lineage.
PHM|subperineurial glial cell | somatic clone
|neuron | supernumerary | somatic clone
|pCC neuron | somatic clone
|aCC neuron | supernumerary | somatic clone
}
REFDSR
{
RDID|FBrf0136942
|Lopez-Schier and St. Johnston
|2001
PHP|Homozygous somatic clones in the follicle cells do not differentiate
|as polar cells, but block the differentiation of epithelial follicle
|cells and causes them to remain as undifferentiated precursors. When
|a clone falls in a region where the follicle cells normally undergo
|morphogenetic movement, these movements do not occur. The stretched
|follicle cells fail to move over the nurse cells; the centripetal cells
|do not migrate between the oocyte and the nurse cells; and the more
|... (see FBal0012701==N55e11 report)
PHM|follicle cell | somatic clone
|centripetally migrating follicle cell | somatic clone
|interfollicle cell | somatic clone
|polar follicle cell | somatic clone
|mitotic cycle | somatic clone
}
REFDSR
{
RDID|FBrf0137222
|Grammont and Irvine
|2001
PHP|Follicles containing permanent somatic clones for
| FBal0012701==N55e11 are not
|recoverable. In egg chambers with transient somatic clones at either
|end of the follicle polar cells are absent. Where one of the polar-stalk
|precursors is mutant for FBal0012701==N55e11 long stalks (average
| 15 cells)
|develop.
PHM|egg chamber | somatic clone
|polar follicle cell | somatic clone | cell autonomous
|interfollicle cell | somatic clone | cell non-autonomous
}
REFDSR
{
RDID|FBrf0141471
|Lopez-Schier and St. Johnston
|2002
PHP|In mutant clones in the follicle cells the organization of the spectrin
|cytoskeleton is normal.
}
REFDSR
{
RDID|FBrf0141493
|Deng et al.
|2001
PHP|Cells in homozygous follicle cell clones have smaller nuclei than their
|wild-type neighbors (which probably indicates a lack of endocycles
|in the mutant cells). The mutant clones contain more cells than their
|wild-type twin spot sister clones, indicating additional mitoses.
|The mean ratio of the number of cells in the mutant clone/number of
|cells in the wild-type sister clone is 1.8 and the ratio does not change
|as a function of clone size. The DNA content is higher in wild-type
|... (see FBal0012701==N55e11 report)
PHM|follicle cell & nucleus | somatic clone
}
REFDSR
{
RDID|FBrf0144843
|Sudarsan et al.
|2002
PHP|FBgn0004647==N mutant embryos have about 89 cells in each Malpighian tubule cell
|(as opposed to about 125 in wild-type). The tubules are are shorter
|than wild-type which results from a dramatic reduction in cell division
|from Mitosis 17.
|FBgn0004647==N mutant embryos made as germ-line clones have about 89 cells in
|each Malpighian tubule cell (as opposed to about 125 in wild-type).
PHM|Malpighian tubule
|Malpighian tubule | germ-line clone
}
REFDSR
{
RDID|FBrf0146991
|Umesono et al.
|2002
PHP|At the earliest stage of the dorsal bipolar dendritic (dbd) sensory
|organ precursor (SOP) division excess FBgn0002970==nub-positive cells are located
|at the correct position in mutant embryos, suggesting that supernumerary
|dbd SOPs are produced. At stage 12, the dbd support glial cell (DBDG)
|is absent. Supernumerary PG3 glial cells and chordotonal organ ligament
|cells of the are present.
PHM|support cell of the dorsal bipolar dendritic cell
|peripheral glial cell 3 | supernumerary
|scolopidial ligament cell | supernumerary
}
REFDSR
{
RDID|FBrf0147142
|Iwaki and Lengyel
|2002
PHP|Mutant embryos completely lack hindgut boundary cell rows and rings.
PHM|embryonic hindgut
}
REFDSR
{
RDID|FBrf0150723
|Riede
|2001
PHP|Pupal lethal when heterozygous with the MBT chromosome.
}
REFDSR
{
RDID|FBrf0151253
|Glise et al.
|2002
PHP|Heterozygotes lack vein and sensory bristle tissue at the most distal
|tip of the wing.
PHM|wing | distal
|wing vein
|wing margin bristle
}
REFDSR
{
RDID|FBrf0151813
|Tsuda et al.
|2002
PHM|wing
}
REFDSR
{
RDID|FBrf0151928
|Orgogozo et al.
|2002
PHP|FBal0012701==N55e11/FBal0012887==Nl1N-ts1 flies form
| ectopic abdominal ventral multidendritic
|neurons and pI external sensory organ precursor cells, even when raised
|at 19oC.
PHM|(with Nl1N-ts1) abdominal ventral multidendritic neuron | ectopic
|(with Nl1N-ts1) external sensory organ precursor cell | ectopic
}
REFDSR
{
RDID|FBrf0155787
|Lebestky et al.
|2003
PHP|The number of crystal cell precursors seen in mutant lymph glands is
|significantly reduced.
PHM|procrystal cell
}
REFDSR
{
RDID|FBrf0160464
|Crozatier et al.
|2003
PHP|In heterozygous mutants, wing veins are wider than in wild-type, but
|selection of sensory organ precursors (SOP) is not affected. However,
|the campaniform sensillae are still overlapping the posterior-most
|L3 vein cells. The position of SOPs relative to the anterior posterior
|border is not changed in mutant discs, indicating that in the adult
|the position of L3 vein is shifted anteriorly by one or two rows of
|cells.
PHM|wing vein
|sensillum precursor
}
REFDSR
{
RDID|FBrf0167516
|Escudero et al.
|2003
PHP|Heterozygotes show a slight increase in the density of microchaetae
|on the notum.
}
REFDSR
{
RDID|FBrf0179042
|Le Gall
|2004
PHP|Mutant embryos show severe hyperplasia of the central and peripheral
|nervous systems.
PHM|embryonic central nervous system
|embryonic peripheral nervous system
}
REF
{
REFM|FBrf0027480
|Shellenbarger and Mohler
|1975
REFM|FBrf0038108
|Poulson and Lefevre
|1982
REFM|FBrf0040181
|Campos-Ortega
|1983
REFM|FBrf0040185
|Lehmann et al.
|1983
REFM|FBrf0043047
|Vassin et al.
|1985
REFM|FBrf0048995
|Brand and Campos-Ortega
|1988
REFM|FBrf0051582
|Cabrera
|1990
REFM|FBrf0053344
|Heitzler and Simpson
|1991
REFM|FBrf0053362
|Corbin et al.
|1991
REFM|FBrf0053769
|Goriely et al.
|1991
REFM|FBrf0054994
|de Celis et al.
|1991
REFM|FBrf0055911
|Skeath and Carroll
|1992
REFM|FBrf0059323
|Bodmer et al.
|1993
REFM|FBrf0068598
|Menne and Klambt
|1994
REFM|FBrf0072582
|Bate et al.
|1993
REFM|FBrf0072959
|Diaz-Benjumea and Hafen
|1994
REFM|FBrf0074921
|de Celis and Garcia-Bellido
|1994
REFM|FBrf0074922
|de Celis et al.
|1991
REFM|FBrf0075100
|Hoch et al.
|1994
REFM|FBrf0076037
|Couso and Martinez Arias
|1994
REFM|FBrf0076146
|Sturtevant and Bier
|1995
REFM|FBrf0083156
|Gonzalez-Gaitan and Jaeckle
|1995
REFM|FBrf0084329
|Rulifson and Blair
|1995
REFM|FBrf0089977
|Guo et al.
|1996
REFM|FBrf0090023
|de Celis et al.
|1996
REFM|FBrf0090425
|Abu-Issa and Cavicchi
|1996
REFM|FBrf0090560
|Frise et al.
|1996
REFM|FBrf0091115
|Long et al.
|1996
REFM|FBrf0091127
|Murata et al.
|1996
REFM|FBrf0093461
|Giebel et al.
|1997
REFM|FBrf0093711
|Seugnet et al.
|1997
REFM|FBrf0097687
|Vervoort et al.
|1997
REFM|FBrf0098202
|Brennan et al.
|1997
REFM|FBrf0098359
|Stuttem and Campos-Ortega
|1997
REFM|FBrf0098813
|Jagla et al.
|1997
REFM|FBrf0099033
|Doherty et al.
|1997
REFM|FBrf0099460
|Price et al.
|1997
REFM|FBrf0099884
|Sotillos et al.
|1997
REFM|FBrf0101998
|Rottgen et al.
|1998
REFM|FBrf0102423
|Zeng et al.
|1998
REFM|FBrf0102699
|Martinez Arias
|1998
REFM|FBrf0102708
|Boube et al.
|1998
REFM|FBrf0102828
|Roch et al.
|1998
REFM|FBrf0104758
|Jagla et al.
|1998
REFM|FBrf0104911
|Hoch and Jackle
|1998
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0106041
|Rusconi and Corbin
|1998
REFM|FBrf0107900
|Nagaraj et al.
|1999
REFM|FBrf0108514
|Llimargas
|1999
REFM|FBrf0108607
|Bishop et al.
|1999
REFM|FBrf0109019
|Rauskolb and Irvine
|1999
REFM|FBrf0109184
|zur Lage and Jarman
|1999
REFM|FBrf0111977
|Micchelli and Blair
|1999
REFM|FBrf0112013
|Rauskolb et al.
|1999
REFM|FBrf0112024
|Rusconi and Corbin
|1999
REFM|FBrf0125167
|de Celis and Bray
|2000
REFM|FBrf0135724
|Udolph et al.
|2001
REFM|FBrf0136942
|Lopez-Schier and St. Johnston
|2001
REFM|FBrf0137222
|Grammont and Irvine
|2001
REFM|FBrf0141471
|Lopez-Schier and St. Johnston
|2002
REFM|FBrf0141493
|Deng et al.
|2001
REFM|FBrf0144843
|Sudarsan et al.
|2002
REFM|FBrf0146991
|Umesono et al.
|2002
REFM|FBrf0147142
|Iwaki and Lengyel
|2002
REFM|FBrf0150723
|Riede
|2001
REFM|FBrf0151253
|Glise et al.
|2002
REFM|FBrf0151813
|Tsuda et al.
|2002
REFM|FBrf0151928
|Orgogozo et al.
|2002
REFM|FBrf0155787
|Lebestky et al.
|2003
REFM|FBrf0160464
|Crozatier et al.
|2003
REFM|FBrf0167516
|Escudero et al.
|2003
REFM|FBrf0179042
|Le Gall
|2004
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015595 ICL 1 ? SYM 1 ?{}N264-40 ASTR 1 - CLOC 1 3C7--9 REF 1 7 DT 1 31 May 2000 RESZ 992
ID|FBti0015595
SYM|?{}N264-40
DT|31 May 2000
|31 May 2000
ICL|?
ASGN|FBgn0004647==N
REFDSR
{
RDID|FBrf0005044
|Demerec
|1940
PHC|lethal | recessive
}
REFDSR
{
RDID|FBrf0024896
|Foster
|1973
PHC|lethal | recessive
}
REFDSR
{
RDID|FBrf0027480
|Shellenbarger and Mohler
|1975
PHC|lethal | recessive
}
REFDSR
{
RDID|FBrf0040185
|Lehmann et al.
|1983
PHC|lethal | embryonic | neurogenic | recessive
}
REFDSR
{
RDID|FBrf0046957
|Kelley et al.
|1987
SYN|?{}N264-40
ASAL|FBal0012749==N264-40
MU|X ray
CLOC|3C7--9
|Insertion site
LOCB|Proximity to gene: FBgn0004647==N
}
REFDSR
{
RDID|FBrf0051558
|Palka et al.
|1990
PHC|lethal | embryonic | recessive
}
REF
{
REFM|FBrf0005044
|Demerec
|1940
REFM|FBrf0024896
|Foster
|1973
REFM|FBrf0027480
|Shellenbarger and Mohler
|1975
REFM|FBrf0040185
|Lehmann et al.
|1983
REFM|FBrf0046957
|Kelley et al.
|1987
REFM|FBrf0051558
|Palka et al.
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0012749==N264-40
REFDSR
{
RDID|FBrf0005044
|Demerec
|1940
PHP|Lethality is not covered by FBab0009529==Dp(1;3)N264-58.
}
REFDSR
{
RDID|FBrf0024896
|Foster
|1973
PHP|Heterozygotes have a nicked wing phenotype.
|FBal0012852==NAx-16/FBal0012749==N264-40 females show
| temperature sensitive lethality.
|The temperature sensitive period for lethality is during the second
|larval instar stage.
PHM|wing
}
REFDSR
{
RDID|FBrf0027480
|Shellenbarger and Mohler
|1975
PHP|Lethal in combination with FBal0012887==Nl1N-ts1 or
| FBal0012861==NAx-tsl at 29oC.
|Homozygous lethal at 29oC.
}
REFDSR
{
RDID|FBrf0038108
|Poulson and Lefevre
|1982
PHP|Male flies carrying FBab0003125==Dp(1;2)51bV76e show wing-notching and lateral
|incisions, leg defects and tarsal reductions, missing or multiple bristles,
|missing or fused ocelli and variegated or roughened eyes, at varying
|frequencies.
}
REFDSR
{
RDID|FBrf0040185
|Lehmann et al.
|1983
PHP|Extreme embryonic neurogenic phenotype.
PHM|epidermis | embryonic
}
REFDSR
{
RDID|FBrf0051558
|Palka et al.
|1990
PHP|Heterozygotes have slightly elevated numbers of sensilla on the wing.
PHM|wing sensillum
}
REFDSR
{
RDID|FBrf0056217
|Jack and DeLotto
|1992
PHP|Homozygotes exhibit hypertrophy of the nervous system and a gap in
|the tip of the wing margin.
PHM|central nervous system
|wing
}
REFDSR
{
RDID|FBrf0104706
|Park et al.
|1998
PHP|FBgn0000606==eve-expressing pericardial cells fail to form in embryos derived
|from homozygous female germline clones.
PHM|embryonic/larval pericardial cell | germ-line clone
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Typical Notch. Male embryos show developmental
|abnormalities like those of FBab0000579==Df(1)N-8 (Poulson, 1939).
|Lethal with FBal0012892==Nnd-3.
}
REF
{
REFM|FBrf0005044
|Demerec
|1940
REFM|FBrf0024896
|Foster
|1973
REFM|FBrf0027480
|Shellenbarger and Mohler
|1975
REFM|FBrf0038108
|Poulson and Lefevre
|1982
REFM|FBrf0040185
|Lehmann et al.
|1983
REFM|FBrf0051558
|Palka et al.
|1990
REFM|FBrf0056217
|Jack and DeLotto
|1992
REFM|FBrf0104706
|Park et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015594 ICL 1 ? SYM 1 ?{}N264-109 ASTR 1 - CLOC 1 3C7--9 REF 1 2 DT 1 31 May 2000 RESZ 480
ID|FBti0015594
SYM|?{}N264-109
DT|31 May 2000
|31 May 2000
ICL|?
ASGN|FBgn0004647==N
REFDSR
{
RDID|FBrf0046957
|Kelley et al.
|1987
SYN|?{}N264-109
ASAL|FBal0012756==N264-109
MU|X ray
CLOC|3C7--9
|Insertion site
LOCB|Proximity to gene: FBgn0004647==N
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHC|semi-lethal | recessive
}
REF
{
REFM|FBrf0046957
|Kelley et al.
|1987
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0012756==N264-109
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Typical Notch except for semi-lethality with FBal0012892==Nnd-3.
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014176 ICL 1 ? SYM 1 ?{}Nfa-g88 ASTR 1 - CLOC 1 3C7--9 REF 1 2 DT 1 6 Jan 2000 RESZ 416
ID|FBti0014176
SYM|?{}Nfa-g88
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0004647==N
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}Nfa-g88
ASAL|FBal0012871==Nfa-g88
MU|spontaneous
CLOC|3C7--9
|Insertion site
LOCB|Proximity to gene: FBgn0004647==N
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0012871==Nfa-g88
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Phenotype like FBal0012868==Nfa-g.
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014180 ICL 1 ? SYM 1 ?{}Nl1N-1 ASTR 1 - CLOC 1 3C7--9 REF 1 2 DT 1 6 Jan 2000 RESZ 481
ID|FBti0014180
SYM|?{}Nl1N-1
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0004647==N
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}Nl1N-1
ASAL|FBal0012876==Nl1N-1
MU|spontaneous
CLOC|3C7--9
|Insertion site
LOCB|Proximity to gene: FBgn0004647==N
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHC|lethal | recessive
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0012876==Nl1N-1
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|FBal0012876==Nl1N-1/+ females are wild type;
| FBal0012876==Nl1N-1/N females
|and FBal0012876==Nl1N-1/Y males are lethal; l(1)N/Y;FBab0009100==Dp(1;2)51b
|males are Co-like. Heterozygotes with recessive
|visibles at Notch are wild type. Developmental defects
|in FBal0012876==Nl1N-1/Y males are more limited than in N/Y males
|and the defects are confined to the anterior ectoderm
|(Poulson, 1967; Poulson, 1968). Like N mutants, FBal0012876==Nl1N-1
|... (see FBal0012876==Nl1N-1 report)
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014169 ICL 1 ? SYM 1 ?{}NS ASTR 1 - CLOC 1 3C7--9 REF 1 4 DT 1 6 Jan 2000 RESZ 613
ID|FBti0014169
SYM|?{}NS
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0004647==N
REFDSR
{
RDID|FBrf0039985
|Kramers et al.
|1983
PHC|lethal | recessive
}
REFDSR
{
RDID|FBrf0045066
|Schalet
|1986
PHC|lethal | recessive
}
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}NS
ASAL|FBal0012785==NS
MU|spontaneous
CLOC|3C7--9
|Insertion site
LOCB|Proximity to gene: FBgn0004647==N
}
REF
{
REFM|FBrf0039985
|Kramers et al.
|1983
REFM|FBrf0045066
|Schalet
|1986
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0012785==NS
REFDSR
{
RDID|FBrf0045066
|Schalet
|1986
PHP|Heterozygotes display a weak notched wing phenotype.
PHM|wing
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Weak Notch. FBal0012785==NS/FBal0012860==NAx-S is lethal.
}
REF
{
REFM|FBrf0045066
|Schalet
|1986
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0016277 ICL 1 ? SYM 1 ?{}ossisC-1 ASTR 1 - CLOC 1 17A5 REF 1 2 DT 1 17 Aug 2000 RESZ 347
ID|FBti0016277
SYM|?{}ossisC-1
DT|17 Aug 2000
|17 Aug 2000
ICL|?
ASGN|FBgn0004956==os
REFDSR
{
RDID|FBrf0128638
|Sefton et al.
|2000
SYN|?{}ossisC-1
CLOC|17A5
|Insertion site
LOCB|Proximity to gene: FBgn0004956==os
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0128638
|Sefton et al.
|2000
}
}
# EOR
TIR
{
RETE|ID 1 FBti0004662 ICL 1 ? SYM 1 ?{}ovoD1r38D ASTR 1 - CLOC 1 4E2 REF 1 2 DT 1 5 Feb 1999 RESZ 381
ID|FBti0004662
SYM|?{}ovoD1r38D
DT|5 Feb 1999
|29 Dec 1997
ICL|?
ASGN|FBgn0003028==ovo
REFDSR
{
RDID|FBrf0056260
|Garfinkel et al.
|1992
ASAL|FBal0050230==ovoD1r38D
CLOC|4E2
|Insertion site
LOCB|Proximity to gene: FBgn0003028==ovo
}
REF
{
REFM|FBrf0056260
|Garfinkel et al.
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0050230==ovoD1r38D
REFDSR
{
RDID|FBrf0056260
|Garfinkel et al.
|1992
PHP|Phenotypic category: ovo- svb-
}
REF
{
REFM|FBrf0056260
|Garfinkel et al.
|1992
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0004663 ICL 1 ? SYM 1 ?{}ovoD1r47j ASTR 1 - CLOC 1 4E2 REF 1 2 DT 1 5 Feb 1999 RESZ 381
ID|FBti0004663
SYM|?{}ovoD1r47j
DT|5 Feb 1999
|29 Dec 1997
ICL|?
ASGN|FBgn0003028==ovo
REFDSR
{
RDID|FBrf0056260
|Garfinkel et al.
|1992
ASAL|FBal0050231==ovoD1r47j
CLOC|4E2
|Insertion site
LOCB|Proximity to gene: FBgn0003028==ovo
}
REF
{
REFM|FBrf0056260
|Garfinkel et al.
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0050231==ovoD1r47j
REFDSR
{
RDID|FBrf0056260
|Garfinkel et al.
|1992
PHP|Phenotypic category: ovo- svb-
}
REF
{
REFM|FBrf0056260
|Garfinkel et al.
|1992
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0004664 ICL 1 ? SYM 1 ?{}ovoD1rOL ASTR 1 - CLOC 1 4E2 REF 1 2 DT 1 5 Feb 1999 RESZ 379
ID|FBti0004664
SYM|?{}ovoD1rOL
DT|5 Feb 1999
|29 Dec 1997
ICL|?
ASGN|FBgn0003028==ovo
REFDSR
{
RDID|FBrf0056260
|Garfinkel et al.
|1992
ASAL|FBal0050232==ovoD1rOL
CLOC|4E2
|Insertion site
LOCB|Proximity to gene: FBgn0003028==ovo
}
REF
{
REFM|FBrf0056260
|Garfinkel et al.
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0050232==ovoD1rOL
REFDSR
{
RDID|FBrf0056260
|Garfinkel et al.
|1992
PHP|Phenotypic category: ovo- svb-
}
REF
{
REFM|FBrf0056260
|Garfinkel et al.
|1992
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0004661 ICL 1 ? SYM 1 ?{}ovoD1rP1 ASTR 1 - CLOC 1 4E2 REF 1 2 DT 1 5 Feb 1999 RESZ 379
ID|FBti0004661
SYM|?{}ovoD1rP1
DT|5 Feb 1999
|29 Dec 1997
ICL|?
ASGN|FBgn0003028==ovo
REFDSR
{
RDID|FBrf0056260
|Garfinkel et al.
|1992
ASAL|FBal0050233==ovoD1rP1
CLOC|4E2
|Insertion site
LOCB|Proximity to gene: FBgn0003028==ovo
}
REF
{
REFM|FBrf0056260
|Garfinkel et al.
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0050233==ovoD1rP1
REFDSR
{
RDID|FBrf0056260
|Garfinkel et al.
|1992
PHP|Phenotypic category: ovo-, svb+ phenotype.
}
REF
{
REFM|FBrf0056260
|Garfinkel et al.
|1992
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014575 ICL 1 ? SYM 1 ?{}parahd9 ASTR 1 - CLOC 1 14D1--E1 REF 1 2 DT 1 6 Jan 2000 RESZ 409
ID|FBti0014575
SYM|?{}parahd9
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003036==para
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}parahd9
ASAL|FBal0013478==parahd9
CLOC|14D1--E1
|Insertion site
LOCB|Proximity to gene: FBgn0003036==para
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0013478==parahd9
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
PHP|Temperature-sensitive.
|Hybrid dysgenesis gives no wild-type revertants.
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014577 ICL 1 ? SYM 1 ?{}parats115 ASTR 1 - CLOC 1 14D1--E1 REF 1 2 DT 1 6 Jan 2000 RESZ 415
ID|FBti0014577
SYM|?{}parats115
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003036==para
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}parats115
ASAL|FBal0013495==parats115
CLOC|14D1--E1
|Insertion site
LOCB|Proximity to gene: FBgn0003036==para
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0013495==parats115
REFDSR
{
RDID|FBrf0040979
|Ganetzky
|1984
PHP|Viability of double mutant males with FBal0023798==mlenap-ts1 is significantly
|reduced, even at permissive temperatures. Double mutant males at 25oC
|die at or near eclosion.
}
REFDSR
{
RDID|FBrf0099841
|Pittendrigh et al.
|1997
PHP|Homozygous flies do not show significant resistance to
|dichloro-diphenyl-trichloro ethane (DDT) compared to wild-type flies.
}
REF
{
REFM|FBrf0040979
|Ganetzky
|1984
REFM|FBrf0099841
|Pittendrigh et al.
|1997
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014581 ICL 1 ? SYM 1 ?{}pn3 ASTR 1 - CLOC 1 2E1 REF 1 3 DT 1 6 Jan 2000 RESZ 436
ID|FBti0014581
SYM|?{}pn3
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003116==pn
ARGS|FBgn0003116
REFDSR
{
RDID|FBrf0054781
|Teng et al.
|1991
SYN|?{}pn3
ASAL|FBal0013875==pn3
CLOC|2E1
|Insertion site
LOCB|Proximity to gene: FBgn0003116==pn
}
REF
{
REFM|FBrf0054781
|Teng et al.
|1991
REFM|FBrf0091186
|Timmons and Shearn
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0013875==pn3
REFDSR
{
RDID|FBrf0054148
|Teng et al.
|1991
PHM|pigment cell
}
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
PHP|Brownish-red eye.
|RK1.
PHM|pigment cell
}
REFDSR
{
RDID|FBrf0091186
|Timmons and Shearn
|1996
PHM|pigment cell
}
REF
{
REFM|FBrf0054148
|Teng et al.
|1991
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0091186
|Timmons and Shearn
|1996
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015556 ICL 1 ? SYM 1 ?{}Rab6D6E ASTR 1 - CLOC 1 33C4 REF 1 2 DT 1 4 Feb 2000 RESZ 454
ID|FBti0015556
SYM|?{}Rab6D6E
DT|4 Feb 2000
|4 Feb 2000
ICL|?
ASGN|FBgn0015797==Rab6
REFDSR
{
RDID|FBrf0111465
|Purcell and Artavanis-Tsakonas
|1999
SYN|?{}Rab6D6E
ASAL|FBal0102875==Rab6D6E
CLOC|33C4
|Insertion site
LOCB|Proximity to gene: FBgn0015797==Rab6
PHC|lethal | recessive
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0111465
|Purcell and Artavanis-Tsakonas
|1999
}
}
# EOR
TIR
{
RETE|ID 1 FBti0015560 ICL 1 ? SYM 1 ?{}Rab6D24A ASTR 1 - CLOC 1 33C4 REF 1 2 DT 1 4 Feb 2000 RESZ 457
ID|FBti0015560
SYM|?{}Rab6D24A
DT|4 Feb 2000
|4 Feb 2000
ICL|?
ASGN|FBgn0015797==Rab6
REFDSR
{
RDID|FBrf0111465
|Purcell and Artavanis-Tsakonas
|1999
SYN|?{}Rab6D24A
ASAL|FBal0102896==Rab6D24A
CLOC|33C4
|Insertion site
LOCB|Proximity to gene: FBgn0015797==Rab6
PHC|lethal | recessive
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0111465
|Purcell and Artavanis-Tsakonas
|1999
}
}
# EOR
TIR
{
RETE|ID 1 FBti0015559 ICL 1 ? SYM 1 ?{}Rab6D29D ASTR 1 - CLOC 1 33C4 REF 1 2 DT 1 4 Feb 2000 RESZ 457
ID|FBti0015559
SYM|?{}Rab6D29D
DT|4 Feb 2000
|4 Feb 2000
ICL|?
ASGN|FBgn0015797==Rab6
REFDSR
{
RDID|FBrf0111465
|Purcell and Artavanis-Tsakonas
|1999
SYN|?{}Rab6D29D
ASAL|FBal0102892==Rab6D29D
CLOC|33C4
|Insertion site
LOCB|Proximity to gene: FBgn0015797==Rab6
PHC|lethal | recessive
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0111465
|Purcell and Artavanis-Tsakonas
|1999
}
}
# EOR
TIR
{
RETE|ID 1 FBti0016272 ICL 1 ? SYM 1 ?{}rb10 ASTR 1 - CLOC 1 4C7 REF 1 2 DT 1 17 Aug 2000 RESZ 395
ID|FBti0016272
SYM|?{}rb10
DT|17 Aug 2000
|17 Aug 2000
ICL|?
ASGN|FBgn0003210==rb
REFDSR
{
RDID|FBrf0127175
|Kretzschmar et al.
|2000
SYN|?{}rb10
ASAL|FBal0044308==rb10
CLOC|4C7
|Insertion site
LOCB|Proximity to gene: FBgn0003210==rb
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0127175
|Kretzschmar et al.
|2000
}
ALESR
{
ASYM|FBal0044308==rb10
REFDSR
{
RDID|FBrf0127175
|Kretzschmar et al.
|2000
PHP|FBal0044308==rb10/FBal0117392==rbS1 flies have a
| normal landing and optomotor response
|and respond normally to stationary visual stimulation. They show abnormal
|behavior in Buridan's paradigm, a test for alternating pattern fixation.
|FBab0000894==Df(1)rb1/FBal0044308==rb10 flies have a normal landing and
| optomotor response
|and respond normally to stationary visual stimulation. They show abnormal
|behavior in Buridan's paradigm, a test for alternating pattern fixation;
|fixation of visual landmarks is significantly impaired and there is
|... (see FBal0044308==rb10 report)
}
REF
{
REFM|FBrf0127175
|Kretzschmar et al.
|2000
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015321 ICL 1 ? SYM 1 ?{}rod29D ASTR 1 - CLOC 1 100C6--7 REF 1 2 DT 1 6 Jan 2000 RESZ 398
ID|FBti0015321
SYM|?{}rod29D
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003268==rod
REFDSR
{
RDID|FBrf0112029
|Scaerou et al.
|1999
SYN|?{}rod29D
ASAL|FBal0101175==rod29D
CLOC|100C6--7
|Insertion site
LOCB|Proximity to gene: FBgn0003268==rod
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0112029
|Scaerou et al.
|1999
}
}
# EOR
TIR
{
RETE|ID 1 FBti0015320 ICL 1 ? SYM 1 ?{}rodRP153 ASTR 1 - CLOC 1 100C6--7 REF 1 2 DT 1 6 Jan 2000 RESZ 404
ID|FBti0015320
SYM|?{}rodRP153
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003268==rod
REFDSR
{
RDID|FBrf0112029
|Scaerou et al.
|1999
SYN|?{}rodRP153
ASAL|FBal0101174==rodRP153
CLOC|100C6--7
|Insertion site
LOCB|Proximity to gene: FBgn0003268==rod
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0112029
|Scaerou et al.
|1999
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014609 ICL 1 ? SYM 1 ?{}rt2 ASTR 1 - CLOC 1 68C13 REF 1 2 DT 1 6 Jan 2000 RESZ 435
ID|FBti0014609
SYM|?{}rt2
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003292==rt
REFDSR
{
RDID|FBrf0088507
|Martin-Blanco and Garcia-Bellido
|1996
SYN|?{}rt2
ASAL|FBal0014814==rt2
MU|spontaneous
CLOC|68C13
|Insertion site
LOCB|Proximity to gene: FBgn0003292==rt
}
REF
{
REFM|FBrf0088507
|Martin-Blanco and Garcia-Bellido
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0014814==rt2
REFDSR
{
RDID|FBrf0088507
|Martin-Blanco and Garcia-Bellido
|1996
PHP|The bodies of first instar larvae are rotated around the long axis,
|forcing the animals to move in a clockwise circle as they crawl. The
|larval cuticle presents a perfect segmental alignment of landmarks
|but the adult abdominal cuticle segments appear staggered relative
|to each other.
|Embryos show a variable but fully penetrant mutant phenotype. Common
|phenotypes include the lack of some muscles or the presence of very
|... (see FBal0014814==rt2 report)
PHM|cuticle | adult
|embryonic/larval somatic muscle
|embryonic/larval somatic muscle | lateral
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Abdomen twisted, as is rt. Viability erratic, usually
|about 50% wild type. Male fertile; female not tested.
|RK2.
}
REF
{
REFM|FBrf0088507
|Martin-Blanco and Garcia-Bellido
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014518 ICL 1 ? SYM 1 ?{}SamDCc ASTR 1 - CLOC 1 31D9 REF 1 3 DT 1 6 Jan 2000 RESZ 556
ID|FBti0014518
SYM|?{}SamDCc
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0019932==SamDC
ARGS|FBgn0019932
REFDSR
{
RDID|FBrf0058585
|Clegg et al.
|1993
PHC|lethal | recessive
}
REFDSR
{
RDID|FBrf0099842
|Larsson and Rasmuson-Lestander
|1997
SYN|?{}SamDCc
ASAL|FBal0034916==SamDCc
CLOC|31D9
|Insertion site
LOCB|Proximity to gene: FBgn0019932==SamDC
}
REF
{
REFM|FBrf0058585
|Clegg et al.
|1993
REFM|FBrf0099842
|Larsson and Rasmuson-Lestander
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0034916==SamDCc
REFDSR
{
RDID|FBrf0099842
|Larsson and Rasmuson-Lestander
|1997
PHP|Eclosion is delayed by 3 days in homozygous flies, and the adults have
|a Minute-like bristle phenotype.
|FBal0034916==SamDCc is lethal in combination with
| FBal0034918==SamDCe, if FBal0034918==SamDCe
|is maternally inherited.
| FBal0034916==SamDCc/FBal0034918==SamDCe flies in
| which FBal0034918==SamDCe
|is paternally inherited show a 3 day delay in eclosion and the adults
|have a Minute-like bristle phenotype.
|Homozygous, heterozygous,
| FBal0034916==SamDCc/FBal0034917==SamDCd, FBal0034916==SamDCc/FBal0034918==SamDCe
|... (see FBal0034916==SamDCc report)
PHM|macrochaeta
}
REF
{
REFM|FBrf0099842
|Larsson and Rasmuson-Lestander
|1997
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014618 ICL 1 ? SYM 1 ?{}sas796 ASTR 1 - CLOC 1 84C8--D1 REF 1 2 DT 1 6 Jan 2000 RESZ 469
ID|FBti0014618
SYM|?{}sas796
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0002306==sas
ARGS|FBgn0002306
REFDSR
{
RDID|FBrf0055816
|Schonbaum et al.
|1992
SYN|?{}sas796
ASAL|FBal0015137==sas796
CLOC|84C8--D1
|Insertion site
LOCB|Proximity to gene: FBgn0002306==sas
PHC|lethal | larval | polyphasic | conditional cs
}
REF
{
REFM|FBrf0055816
|Schonbaum et al.
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0015137==sas796
REFDSR
{
RDID|FBrf0055816
|Schonbaum et al.
|1992
PHP|Larval lethality is polyphasic, and occasionally viable, fertile adults
|are seen. The progeny of these adults have a variable phenotype ranging
|from severe FBgn0002306==sas defects, to normal, fertile flies. Abnormal tanned
|spots are found between the 4th and 5th, and 1st and 2nd rows of the
|setal belts in second instar larvae.
PHM|larval cuticle
}
REF
{
REFM|FBrf0055816
|Schonbaum et al.
|1992
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014619 ICL 1 ? SYM 1 ?{}sas828 ASTR 1 - CLOC 1 84C8--D1 REF 1 2 DT 1 6 Jan 2000 RESZ 439
ID|FBti0014619
SYM|?{}sas828
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0002306==sas
ARGS|FBgn0002306
REFDSR
{
RDID|FBrf0055816
|Schonbaum et al.
|1992
SYN|?{}sas828
ASAL|FBal0015138==sas828
CLOC|84C8--D1
|Insertion site
LOCB|Proximity to gene: FBgn0002306==sas
PHC|lethal | larval
}
REF
{
REFM|FBrf0055816
|Schonbaum et al.
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0015138==sas828
REFDSR
{
RDID|FBrf0055816
|Schonbaum et al.
|1992
PHP|Larvae die during the first instar moult or as small second instar
|larvae.
}
REF
{
REFM|FBrf0055816
|Schonbaum et al.
|1992
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014621 ICL 1 ? SYM 1 ?{}sc1744 ASTR 1 - CLOC 1 1A8 REF 1 3 DT 1 6 Jan 2000 RESZ 437
ID|FBti0014621
SYM|?{}sc1744
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0004170==sc
REFDSR
{
RDID|FBrf0042024
|Campuzano et al.
|1985
SYN|?{}sc1744
ASAL|FBal0015224==sc1744
CLOC|1A8
|Insertion site
LOCB|Proximity to gene: FBgn0004170==sc
}
REF
{
REFM|FBrf0042024
|Campuzano et al.
|1985
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014622 ICL 1 ? SYM 1 ?{}scAc ASTR 1 - CLOC 1 1A8 REF 1 3 DT 1 6 Jan 2000 RESZ 431
ID|FBti0014622
SYM|?{}scAc
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0004170==sc
REFDSR
{
RDID|FBrf0042024
|Campuzano et al.
|1985
SYN|?{}scAc
ASAL|FBal0015226==scAc
CLOC|1A8
|Insertion site
LOCB|Proximity to gene: FBgn0004170==sc
}
REF
{
REFM|FBrf0042024
|Campuzano et al.
|1985
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014205 ICL 1 ? SYM 1 ?{}Ser1 ASTR 1 - CLOC 1 97E6--8 REF 1 2 DT 1 6 Jan 2000 RESZ 397
ID|FBti0014205
SYM|?{}Ser1
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0004197==Ser
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}Ser1
ASAL|FBal0015427==Ser1
CLOC|97E6--8
|Insertion site
LOCB|Proximity to gene: FBgn0004197==Ser
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0015427==Ser1
REFDSR
{
RDID|FBrf0022273
|Belt
|1971
PHP|FBal0015427==Ser1 is homozygous viable; initially thought to be homozygous
|lethal, but lethality removable by recombination; the closely linked
|lethal persists in many FBal0015427==Ser1-bearing chromosomes. Homozygous
|FBal0015427==Ser1 produces extreme incision of wing margins
| especially in second
|posterior cell.
}
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
PHP|Wings of FBal0015427==Ser1/+ and hemizygous
| FBal0015427==Ser1 notched at tip; deepest
|notch at second posterior cell. In triploids, one dose of FBal0015427==Ser1
|overlaps wild type. As with other FBgn0004197==Ser alleles expression suppressed
|by FBgn0001169==H and FBgn0004647==N. Dominant wing phenotype; homozygous viable.
PHM|wing
}
REFDSR
{
RDID|FBrf0105825
|Fostier et al.
|1998
PHP|Wing margin phenotype not affected by FBal0039064==Su(dx)sp.
}
REF
{
REFM|FBrf0022273
|Belt
|1971
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105825
|Fostier et al.
|1998
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014210 ICL 1 ? SYM 1 ?{}Sh16 ASTR 1 - CLOC 1 16F3--5 REF 1 2 DT 1 6 Jan 2000 RESZ 412
ID|FBti0014210
SYM|?{}Sh16
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003380==Sh
REFDSR
{
RDID|FBrf0052684
|Gautam and Tanouye
|1990
SYN|?{}Sh16
ASAL|FBal0015556==Sh16
MU|spontaneous
CLOC|16F3--5
|Insertion site
LOCB|Proximity to gene: FBgn0003380==Sh
}
REF
{
REFM|FBrf0052684
|Gautam and Tanouye
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0015556==Sh16
REFDSR
{
RDID|FBrf0038065
|Ganetzky and Wu
|1982
PHP|Ether-dependent leg shaking and wing scissoring. Chloroform, ethyl
|acetate and carbon dioxide etherization does not elicit shaking behavior,
|though nitrogen and triethylkamine etherization does. Unetherized,
|older flies show uncoordinated walking behavior, and stand quivering
|on the bottom of the culture bottle.
}
REFDSR
{
RDID|FBrf0049615
|Gisselmann et al.
|1989
PHP|A-type current is completely absent.
}
REFDSR
{
RDID|FBrf0052397
|Haugland and Wu
|1990
PHP|IA is completely eliminated in homozygous third larval instar muscles.
}
REFDSR
{
RDID|FBrf0080515
|Zhao et al.
|1995
PHP|"Giant" neurons derived from flies carrying
| FBal0061621==Sh29-4.hs in a FBal0015556==Sh16
|background show a heat shock inducible A-type K+ current. This current
|shows slow recovery from inactivation compared to wild-type.
}
REFDSR
{
RDID|FBrf0084181
|Megumi et al.
|1995
PHP|More sensitive than the wild-type to the knock-down effect of acute
|&ggr;-irradiation.
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|abnormal leg shaking under ether anesthesia; abnormal A-type
|potassium currents in larval muscle and/or pupal flight muscle;
|abnormal action potentials in the adult cervical giant fiber; abnormal
|synaptic transmission at the larval neuromuscular junction and multiple
|firing of larval motoneurons.
}
REF
{
REFM|FBrf0038065
|Ganetzky and Wu
|1982
REFM|FBrf0049615
|Gisselmann et al.
|1989
REFM|FBrf0052397
|Haugland and Wu
|1990
REFM|FBrf0080515
|Zhao et al.
|1995
REFM|FBrf0084181
|Megumi et al.
|1995
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014637 ICL 1 ? SYM 1 ?{}sn5S ASTR 1 - CLOC 1 7D1--2 REF 1 3 DT 1 6 Jan 2000 RESZ 514
ID|FBti0014637
SYM|?{}sn5S
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003447==sn
REFDSR
{
RDID|FBrf0048245
|Roiha et al.
|1988
PHC|female sterile
}
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}sn5S
ASAL|FBal0015777==sn5S
MU|spontaneous
CLOC|7D1--2
|Insertion site
LOCB|Proximity to gene: FBgn0003447==sn
}
REF
{
REFM|FBrf0048245
|Roiha et al.
|1988
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0015777==sn5S
REFDSR
{
RDID|FBrf0048245
|Roiha et al.
|1988
PHP|Extreme bristle phenotype, female sterile.
PHM|macrochaeta
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|class 1 - female sterile with gnarled macrochaetae and kinky microchaetae
}
REF
{
REFM|FBrf0048245
|Roiha et al.
|1988
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014636 ICL 1 ? SYM 1 ?{}sn36a ASTR 1 - CLOC 1 7D1--2 REF 1 4 DT 1 6 Jan 2000 RESZ 617
ID|FBti0014636
SYM|?{}sn36a
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003447==sn
REFDSR
{
RDID|FBrf0048245
|Roiha et al.
|1988
PHC|female sterile
}
REFDSR
{
RDID|FBrf0054119
|Paterson and O'Hare
|1991
SYN|?{}sn36a
ASAL|FBal0015801==sn36a
MU|spontaneous
CLOC|7D1--2
|Insertion site
LOCB|Proximity to gene: FBgn0003447==sn
}
REFDSR
{
RDID|FBrf0072754
|Cant et al.
|1994
PHC|sterile
}
REF
{
REFM|FBrf0048245
|Roiha et al.
|1988
REFM|FBrf0054119
|Paterson and O'Hare
|1991
REFM|FBrf0072754
|Cant et al.
|1994
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0015801==sn36a
REFDSR
{
RDID|FBrf0048245
|Roiha et al.
|1988
PHP|Extreme bristle phenotype, female sterile.
PHM|macrochaeta
}
REFDSR
{
RDID|FBrf0072754
|Cant et al.
|1994
PHP|Bristles are gnarled due to disrupted actin filament bundles.
|Nurse cell cytoplasmic actin filaments are absent.
PHM|macrochaeta
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Macrochaetae gnarled in a fairly extreme manner.
|Microchaetae wild type. FBal0015801==sn36a is only allele to
|cause pronounced reduction in replication of oocyte
|nurse cell DNA (King and Burnett, 1957). Also causes more extreme retardation
|of vitellogenesis than other female-sterile sn alleles
|(Bender, 1960). FBal0015801==sn36a FBal0015774==sn4
| homozygote has nearly normal
|bristles and is sterile.
|... (see FBal0015801==sn36a report)
}
REF
{
REFM|FBrf0048245
|Roiha et al.
|1988
REFM|FBrf0072754
|Cant et al.
|1994
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015161 ICL 1 ? SYM 1 ?{}stghwy ASTR 1 - CLOC 1 99A5 REF 1 2 DT 1 6 Jan 2000 RESZ 416
ID|FBti0015161
SYM|?{}stghwy
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003525==stg
REFDSR
{
RDID|FBrf0111437
|Mozer and Easwarachandran
|1999
SYN|?{}stghwy
ASAL|FBal0086318==stghwy
CLOC|99A5
|Insertion site
LOCB|Proximity to gene: FBgn0003525==stg
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0111437
|Mozer and Easwarachandran
|1999
}
ALESR
{
ASYM|FBal0086318==stghwy
REFDSR
{
RDID|FBrf0101687
|Stocker and Hafen
|1998
PHP|Homozygotes have bristle and eye defects. Eye discs contain ectopic
|photoreceptors that are predominantly of the R2/R5 type.
PHM|photoreceptor cell | ectopic
|photoreceptor cell R2 | ectopic
|photoreceptor cell R5 | ectopic
|eye
|macrochaeta
|eye disc
}
REFDSR
{
RDID|FBrf0111437
|Mozer and Easwarachandran
|1999
PHP|Eye of adults are slightly rough and slightly smaller than those of
|wild type. The macrochaetae of the notum are missing. Ommatidia have
|one or more extra photoreceptor cells which may be of any of the inner
|or outer photoreceptor cell types. This phenotype is seen when heterozygous
|with FBal0099818==stgDr-mr21, FBal0099821==stgDr-FA30,
| FBal0035718==stgAR2 or FBal0035719==stgRXT13 or
|FBab0024883==Df(3R)Ptp99AR3.
|When FBal0086318==stghwy is heterozygous with
| FBal0016176==stg4 or FBal0016174==stg2 there
|... (see FBal0086318==stghwy report)
PHM|eye
|macrochaeta
|ommatidium
|photoreceptor cell
|eye disc
}
REF
{
REFM|FBrf0101687
|Stocker and Hafen
|1998
REFM|FBrf0111437
|Mozer and Easwarachandran
|1999
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014695 ICL 1 ? SYM 1 ?{}su(f)25 ASTR 1 - CLOC 1 20E REF 1 2 DT 1 6 Jan 2000 RESZ 421
ID|FBti0014695
SYM|?{}su(f)25
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003559==su(f)
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}su(f)25
ASAL|FBal0016289==su(f)25
MU|spontaneous
CLOC|20E
|Insertion site
LOCB|Proximity to gene: FBgn0003559==su(f)
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014692 ICL 1 ? SYM 1 ?{}su(Hw)2 ASTR 1 - CLOC 1 88B3 REF 1 3 DT 1 6 Jan 2000 RESZ 519
ID|FBti0014692
SYM|?{}su(Hw)2
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003567==su(Hw)
REFDSR
{
RDID|FBrf0058581
|Dorsett
|1993
PHC|female sterile
}
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}su(Hw)2
ASAL|FBal0016319==su(Hw)2
MU|spontaneous
CLOC|88B3
|Insertion site
LOCB|Proximity to gene: FBgn0003567==su(Hw)
}
REF
{
REFM|FBrf0058581
|Dorsett
|1993
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0016319==su(Hw)2
REFDSR
{
RDID|FBrf0043905
|Campuzano et al.
|1986
PHP|FBal0016319==su(Hw)2/FBal0016324==su(Hw)7
| heterozygotes almost completely suppress the "Hw"
|phenotype FBal0000170==acHw-1+R5, extra macrochaetae are seen on
| the pleura and
|postnotum. This was accompanied by a 2--3 fold reduction of ac RNA,
|sc RNA levels were unchanged. A positive correlation can be seen between
|increased levels of ac transcripts and the appearance of the "Hw" phenotype.
}
REFDSR
{
RDID|FBrf0048095
|Parkhurst et al.
|1988
PHP|Low viability.
}
REFDSR
{
RDID|FBrf0053795
|Sanchez-Herrero
|1991
PHP|Phenotype of FBal0000090==abd-Aiab2-K is suppressed.
}
REFDSR
{
RDID|FBrf0057275
|Zerges et al.
|1992
PHP|Suppresses oblique truncated wing of FBal0014357==rsP1 and FBal0014358==rsP2.
}
REFDSR
{
RDID|FBrf0082023
|Georgiev and Corces
|1995
PHP|FBal0016319==su(Hw)2 cancels the effect of
| FBal0032166==mod(mdg4)ul on trans repression
|of FBgn0004034==y gene expression.
}
REF
{
REFM|FBrf0043905
|Campuzano et al.
|1986
REFM|FBrf0048095
|Parkhurst et al.
|1988
REFM|FBrf0053795
|Sanchez-Herrero
|1991
REFM|FBrf0057275
|Zerges et al.
|1992
REFM|FBrf0082023
|Georgiev and Corces
|1995
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014087 ICL 1 ? SYM 1 ?{}Su(z)2Arp1.mod ASTR 1 - CLOC 1 49E7 REF 1 2 DT 1 6 Jan 2000 RESZ 426
ID|FBti0014087
SYM|?{}Su(z)2Arp1.mod
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0008654==Su(z)2
REFDSR
{
RDID|FBrf0051927
|Brunk and Adler
|1990
SYN|?{}Su(z)2Arp1.mod
ASAL|FBal0029000==Su(z)2Arp1.mod
CLOC|49E7
|Insertion site
LOCB|Proximity to gene: FBgn0008654==Su(z)2
}
REF
{
REFM|FBrf0051927
|Brunk and Adler
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0029000==Su(z)2Arp1.mod
REFDSR
{
RDID|FBrf0051927
|Brunk and Adler
|1990
PHP|Dominant FBal0034079==Su(z)2Arp1 phenotype unmodified, despite molecular
|modification of P element in FBal0034079==Su(z)2Arp1.
}
REF
{
REFM|FBrf0051927
|Brunk and Adler
|1990
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014086 ICL 1 ? SYM 1 ?{}Su(z)2DI41 ASTR 1 - CLOC 1 49E7 REF 1 2 DT 1 6 Jan 2000 RESZ 414
ID|FBti0014086
SYM|?{}Su(z)2DI41
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0008654==Su(z)2
REFDSR
{
RDID|FBrf0051927
|Brunk and Adler
|1990
SYN|?{}Su(z)2DI41
ASAL|FBal0028998==Su(z)2DI41
CLOC|49E7
|Insertion site
LOCB|Proximity to gene: FBgn0008654==Su(z)2
}
REF
{
REFM|FBrf0051927
|Brunk and Adler
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0023617 ICL 1 ? SYM 1 ?{}SuURES ASTR 1 - CLOC 1 68A4 REF 1 2 DT 1 18 Jul 2002 RESZ 398
ID|FBti0023617
SYM|?{}SuURES
DT|18 Jul 2002
|18 Jul 2002
ICL|?
ASGN|FBgn0025355==SuUR
REFDSR
{
RDID|FBrf0147054
|Makunin et al.
|2002
SYN|?{}SuURES
ASAL|FBal0091620==SuURES
CLOC|68A4
|Insertion site
LOCB|Proximity to gene: FBgn0025355==SuUR
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0147054
|Makunin et al.
|2002
}
ALESR
{
ASYM|FBal0091620==SuURES
REFDSR
{
RDID|FBrf0102893
|Belyaeva et al.
|1998
PHP|The weak points found in wild-type larval polytene chromosomes are
|missing in all intercalary heterochromatin (IH) regions in homozygous
|larvae. The frequency of ectopic pairing between IH regions and between
|telomeres and pericentric heterochromatin (PH) is greatly decreased.
|Clear bands are seen in regions that form net-like &bgr;-heterochromatin
|in the basements of chromosome arms adjoining the chromocenters in
|wild-type animals. Additional material appears to be present in PH,
|... (see FBal0091620==SuURES report)
PHM|weak point
|heterochromatin
|beta-heterochromatin
|alpha-heterochromatin
|intercalary heterochromatin
}
REFDSR
{
RDID|FBrf0104733
|Belyaeva et al.
|1998
PHP|FBal0091620==SuURES flies lack the "weak" points in the
| intercalary heterochromatin
|of the salivary gland chromosomes, lack ectopic contacts between chromosome
|regions and have additional intercalary heterochromatin in the centromeric
|regions. The intercalary heterochromatin region in 39E does not show
|DNA underreplication. The phenotype is semidominant.
PHM|weak point
|intercalary heterochromatin
}
REFDSR
{
RDID|FBrf0144771
|Semeshin et al.
|2001
PHP|In FBal0091620==SuURES mutants new bands appear in the 20BF
| region in polytene
|chromosome squashes. The banding pattern at the base of the chromosome
|2 arms is more clear-cut in FBal0091620==SuURES mutants. A new
| well structured
|block of chromosome material named "Plato Atlantis", containing a total
|of 25 bands, is formed in the 80C3-81F1-2 interval in
| FBal0091620==SuURES mutant
|polytene chromosome squashes. The 101E region of chromosome 4 has
|no banding pattern and has the appearance of &agr;-heterochromatin in
|... (see FBal0091620==SuURES report)
PHM|band
|polytene chromosome
|intercalary heterochromatin
|heterochromatin
}
REFDSR
{
RDID|FBrf0150705
|Volkova and Zhimulev
|2001
PHP|Homozygotes do not show changes in developmental time.
}
REFDSR
{
RDID|FBrf0151235
|Moshkin et al.
|2002
PHP|A number of heterochromatic regions of polytene chromosomes show a
|reproducible banded structure in FBal0091620==SuURES mutants. The frequency
|of ectopic contacts between pericentric regions decreases in polytene
|chromosomes of FBal0091620==SuURES mutants.
PHM|heterochromatin
}
REFDSR
{
RDID|FBrf0158793
|Zhimulev et al.
|2003
PHP|The pattern of completion of replication in the polytene chromosomes
|of FBal0091620==SuURES third instar larvae differs from that of
| Oregon R third
|instar larvae. The FBal0091620==SuURES larvae have a much lower
| number of late-replicating
|regions than Oregon R larvae. The sets of late-replicating sites in
|FBal0091620==SuURES and Oregon R are very similar on the whole.
| However, in
|many cases, regions that show typical late replication in Oregon R
|are not labelled in FBal0091620==SuURES animals. These regions
| include 21D,
|... (see FBal0091620==SuURES report)
PHM|polytene chromosome
}
REFDSR
{
RDID|FBrf0167627
|Belyaeva et al.
|2003
PHP|Homozygotes show a reduced frequency of heterochromatization in the
|distal parts of the X chromosome of the
| FBab0006121==T(1;2)dorvar7 rearrangement
|compared to animals which are wild-type for FBgn0025355==SuUR.
|Homozygotes show a reduced frequency of heterochromatization in the
|distal parts of the X chromosome of the FBab0003093==Dp(1;1)pn2 rearrangement
|compared to animals which are wild-type for FBgn0025355==SuUR.
|XO FBal0091620==SuURES/+ males show a reduced frequency of heterochromatization
|... (see FBal0091620==SuURES report)
}
REF
{
REFM|FBrf0102893
|Belyaeva et al.
|1998
REFM|FBrf0104733
|Belyaeva et al.
|1998
REFM|FBrf0144771
|Semeshin et al.
|2001
REFM|FBrf0150705
|Volkova and Zhimulev
|2001
REFM|FBrf0151235
|Moshkin et al.
|2002
REFM|FBrf0158793
|Zhimulev et al.
|2003
REFM|FBrf0167627
|Belyaeva et al.
|2003
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015006 ICL 1 ? SYM 1 ?{}svr73L12 ASTR 1 - CLOC 1 1B5--7 REF 1 2 DT 1 6 Jan 2000 RESZ 400
ID|FBti0015006
SYM|?{}svr73L12
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0004648==svr
REFDSR
{
RDID|FBrf0084356
|Settle et al.
|1995
SYN|?{}svr73L12
ASAL|FBal0050589==svr73L12
CLOC|1B5--7
|Insertion site
LOCB|Proximity to gene: FBgn0004648==svr
}
REF
{
REFM|FBrf0084356
|Settle et al.
|1995
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014231 ICL 1 ? SYM 1 ?{}Sxlf2 ASTR 1 - CLOC 1 6F3--5 REF 1 3 DT 1 6 Jan 2000 RESZ 506
ID|FBti0014231
SYM|?{}Sxlf2
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003659==Sxl
REFDSR
{
RDID|FBrf0042036
|Maine et al.
|1985
SYN|?{}Sxlf2
ASAL|FBal0016681==Sxlf2
CLOC|6F3--5
|Insertion site
LOCB|Proximity to gene: FBgn0003659==Sxl
}
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
PHC|sterile | female
}
REF
{
REFM|FBrf0042036
|Maine et al.
|1985
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0016681==Sxlf2
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
PHP|Homozygous females are either inviable or very poorly viable,
|depending on genetic background. Escapers are invariably sterile but
|otherwise display no obvious sexual abnormalities. Homozygotes
|defective in dosage compensation as indicated by hyperincorporation of
|uridine by their polytene chromosomes. Allele fails to support
|oogenesis in germ-line clones induced by mitotic recombination.
}
REFDSR
{
RDID|FBrf0072617
|Bernstein and Cline
|1994
PHP|Sexual differentiation of external adult tissues in heteroallelic escaper
|females carrying FBal0016701==SxlfPRJ2 or
| FBal0016689==SxlfLS is normal. Sexual differentiation
|of homozygous escaper females is also normal, as is the differentiation
|of clones of homozygous FBal0016681==Sxlf2 tissue in a
| heterozygous background.
|Nonetheless escaper females have rudimentary gonads that are covered
|with testes sheath tissue.
| FBal0016701==SxlfPRJ2/FBal0016680==Sxlf1 shows wild type
|dosage compensation in FBal0014870==run25 phenotype assay.
}
REFDSR
{
RDID|FBrf0075013
|Hilfiker et al.
|1994
PHP|Some escaper adult females.
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0072617
|Bernstein and Cline
|1994
REFM|FBrf0075013
|Hilfiker et al.
|1994
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014987 ICL 1 ? SYM 1 ?{}Sxlfb ASTR 1 - CLOC 1 6F3--5 REF 1 2 DT 1 6 Jan 2000 RESZ 441
ID|FBti0014987
SYM|?{}Sxlfb
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003659==Sxl
REFDSR
{
RDID|FBrf0054147
|Granadino et al.
|1991
SYN|?{}Sxlfb
ASAL|FBal0049190==Sxlfb
CLOC|6F3--5
|Insertion site
LOCB|Proximity to gene: FBgn0003659==Sxl
PHC|lethal | recessive | female | partially
}
REF
{
REFM|FBrf0054147
|Granadino et al.
|1991
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0049190==Sxlfb
REFDSR
{
RDID|FBrf0054147
|Granadino et al.
|1991
PHP|Fully complements FBal0016689==SxlfLS. Homozygous females show a
| high degree
|of lethality; 70% die as embryos, 28% die as larvae. Those that survive
|are normal females. Homozygous clones also develop female structures.
|Homozygous germ cell clones give rise to functional eggs. FBal0016685==Sxlf7,M1/FBal0049190==Sxlfb
|flies lack gonads and occasionally have a male spot on the fifth and
|sixth tergites. Viability is greatly reduced in heterozygous combination
|with FBab0000599==Df(1)N71 or FBab0000974==Df(1)svr.
}
REF
{
REFM|FBrf0054147
|Granadino et al.
|1991
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014236 ICL 1 ? SYM 1 ?{}Sxlfc ASTR 1 - CLOC 1 6F3--5 REF 1 2 DT 1 6 Jan 2000 RESZ 441
ID|FBti0014236
SYM|?{}Sxlfc
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003659==Sxl
REFDSR
{
RDID|FBrf0054147
|Granadino et al.
|1991
SYN|?{}Sxlfc
ASAL|FBal0030317==Sxlfc
CLOC|6F3--5
|Insertion site
LOCB|Proximity to gene: FBgn0003659==Sxl
PHC|lethal | recessive | female | partially
}
REF
{
REFM|FBrf0054147
|Granadino et al.
|1991
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0030317==Sxlfc
REFDSR
{
RDID|FBrf0054147
|Granadino et al.
|1991
PHP|Fully complements FBal0016689==SxlfLS. Homozygous females show a
| high degree
|of lethality; 70% die as embryos, 28% die as larvae. Those that survive
|are normal females. Homozygous clones also develop female structures.
|Homozygous germ cell clones give rise to functional eggs. FBal0016685==Sxlf7,M1/FBal0030317==Sxlfc
|flies lack gonads and occasionally have a male spot on the fifth and
|sixth tergites. Viability is greatly reduced in heterozygous combination
|with FBab0000599==Df(1)N71 or FBab0000974==Df(1)svr.
}
REFDSR
{
RDID|FBrf0058121
|Granadino et al.
|1993
PHP|FBal0016685==Sxlf7,M1/FBal0030317==Sxlfc females do
| not develop ovaries, though germ
|cells of this genotype transplanted into wild-type hosts produce functional
|oocytes, suggesting that it is in the somatic cells of this genotype
|that the ovaries are affected.
PHM|ovary
}
REF
{
REFM|FBrf0054147
|Granadino et al.
|1991
REFM|FBrf0058121
|Granadino et al.
|1993
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014237 ICL 1 ? SYM 1 ?{}Sxlfhv1 ASTR 1 - CLOC 1 6F3--5 REF 1 3 DT 1 6 Jan 2000 RESZ 540
ID|FBti0014237
SYM|?{}Sxlfhv1
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003659==Sxl
REFDSR
{
RDID|FBrf0042036
|Maine et al.
|1985
SYN|?{}Sxlfhv1
ASAL|FBal0016688==Sxlfhv1
MU|spontaneous
CLOC|6F3--5
|Insertion site
LOCB|Proximity to gene: FBgn0003659==Sxl
}
REFDSR
{
RDID|FBrf0094158
|Bhadra et al.
|1997
PHC|(with Sxlf1) lethal | female
}
REF
{
REFM|FBrf0042036
|Maine et al.
|1985
REFM|FBrf0094158
|Bhadra et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0016688==Sxlfhv1
REFDSR
{
RDID|FBrf0057886
|Gorman et al.
|1993
PHP|Viability of FBal0016680==Sxlf1/FBal0016688==Sxlfhv1
| females reduced compared to wild type,
|but some individuals survive into larvae and a few survive to adult
|hood. The larvae are mosaic for Sxl function: Sxl protein is bound
|to X chromosomes in approximately half of the cells in the salivary
|glands, mle protein is bound to X chromosomes in those cells where
|Sxl is not. FBal0016680==Sxlf1/FBal0016688==Sxlfhv1
| females that are also homozygous for
|mutants at msl-1, msl-2 or msl-3 develop as intersexes of the mosaic
|... (see FBal0016688==Sxlfhv1 report)
}
REFDSR
{
RDID|FBrf0068422
|Bone et al.
|1994
PHP|Heterozygous FBal0016680==Sxlf1/FBal0016688==Sxlfhv1
| female larvae are mosaics of male
|and female cells.
}
REFDSR
{
RDID|FBrf0076498
|Palmer et al.
|1994
PHP|50% females heteroallelic for FBal0016680==Sxlf1 and
| FBal0016688==Sxlfhv1 survive to
|the third instar larval stage and are mosaic for FBgn0003659==Sxl expression.
}
REFDSR
{
RDID|FBrf0099764
|Lyman et al.
|1997
PHP|Females of the genotype
| FBal0016680==Sxlf1/FBal0016688==Sxlfhv1 fail to
| activate the
|FBgn0003659==Sxl locus in a subset of their cells and thus are mosaic for cells
|that follow either the male of female pathway for dosage compensation.
|In XX cells that have adopted the male fate FBgn0005616==msl-2 interacts in a
|full male-like pattern. Mosaics lacking FBgn0002774==mle or FBgn0002775==msl-3 show partial
|immunostaining patterns for FBgn0005616==msl-2. FBgn0005617==msl-1 and FBgn0005616==msl-2 precisely
|colocalize at the FBgn0002775==msl-3 and FBgn0002774==mle independent sites. FBgn0005616==msl-2 localization
|... (see FBal0016688==Sxlfhv1 report)
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|A subliminal allele, viable and fertile as homozygous
|females, but with greatly reduced viability in trans
|to nulls. Polytene chromosomes of FBal0016688==Sxlfhv1/FBal0016680==Sxlf1
|larvae that survive to third instar hyperincorporate
|uridine, revealing female dosage compensation upsets.
|Mutation of mle appears to partially masculinize this
|heteroallelic combination and may slightly increase
|... (see FBal0016688==Sxlfhv1 report)
}
REFDSR
{
RDID|FBrf0128400
|Bhadra et al.
|2000
PHP|A few percent of the
| FBal0016680==Sxlf1/FBal0016688==Sxlfhv1 female
| progeny survive to
|the third larval instar stage.
}
REFDSR
{
RDID|FBrf0151234
|Alekseyenko et al.
|2002
PHP|The salivary gland cells of
| FBal0016680==Sxlf1/FBal0016688==Sxlfhv1 females show somatic
|mosaicism; some cells are of "male" type (FBgn0003659==Sxl is not expressed),
|while others are of "female" type (FBgn0003659==Sxl is expressed). The frequency
|of weak spots in the intercalary heterochromatin regions of the X chromosomes
|is much lower in the "male" cells compared to in the "female" cells
|and bands of intercalary heterochromatin in the X chromosome look solid,
|dense and non-broken in the "male" cells, as occurs in normal males.
PHM|(with Sxlf1) intercalary heterochromatin & polytene chromosome | female
}
REF
{
REFM|FBrf0057886
|Gorman et al.
|1993
REFM|FBrf0068422
|Bone et al.
|1994
REFM|FBrf0076498
|Palmer et al.
|1994
REFM|FBrf0099764
|Lyman et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0128400
|Bhadra et al.
|2000
REFM|FBrf0151234
|Alekseyenko et al.
|2002
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0025481 ICL 1 ? SYM 1 ?{}SxlMf1b ASTR 1 - CLOC 1 6F3--5 REF 1 2 DT 1 7 Jul 2003 RESZ 592
ID|FBti0025481
SYM|?{}SxlMf1b
SYN|?{}Doc{}SxlMf1
DT|7 Jul 2003
|7 Jul 2003
ICL|?
ID2|FBti0015698
ASGN|FBgn0003659==Sxl
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
CC|One of two insertions associated with this allele; see FBti0025480==Doc{}SxlMf1a.
}
REFDSR
{
RDID|FBrf0122991
|Cline et al.
|1999
SYN|?{}SxlMf1b
ASAL|FBal0103943==SxlMf1
CLOC|6F3--5
|Insertion site
LOCB|Proximity to gene: FBgn0003659==Sxl
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0122991
|Cline et al.
|1999
}
ALESR
{
ASYM|FBal0103943==SxlMf1
REFDSR
{
RDID|FBrf0122991
|Cline et al.
|1999
PHP|Most FBal0103943==SxlMf1/Y males lack part or all of their terminalia.
|FBal0103943==SxlMf1/FBal0042765==Sxlunspecified
| females have low viability and
|fertility.
PHM|terminalia
}
REF
{
REFM|FBrf0122991
|Cline et al.
|1999
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0017441 ICL 1 ? SYM 1 ?{}tra2OTF ASTR 1 - CLOC 1 51B6 REF 1 2 DT 1 4 Jun 2001 RESZ 429
ID|FBti0017441
SYM|?{}tra2OTF
DT|4 Jun 2001
|4 Jun 2001
ICL|?
ASGN|FBgn0003742==tra2
ARGS|FBgn0003742
REFDSR
{
RDID|FBrf0047627
|Amrein et al.
|1988
SYN|?{}tra2OTF
ASAL|FBal0017023==tra2OTF
MU|spontaneous
CLOC|51B6
|Insertion site
LOCB|Proximity to gene: FBgn0003742==tra2
}
REF
{
REFM|FBrf0047627
|Amrein et al.
|1988
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0017023==tra2OTF
REFDSR
{
RDID|FBrf0037844
|Schupbach
|1982
PHP|Homozygous XX flies are intersex.
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Ovaries rudimentary (Fujihara, Kawabe and Oishi, 1978).
}
REF
{
REFM|FBrf0037844
|Schupbach
|1982
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014249 ICL 1 ? SYM 1 ?{}Ubxbxd-SR ASTR 1 - CLOC 1 89D6--9 REF 1 2 DT 1 6 Jan 2000 RESZ 404
ID|FBti0014249
SYM|?{}Ubxbxd-SR
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003944==Ubx
REFDSR
{
RDID|FBrf0040194
|Bender et al.
|1983
SYN|?{}Ubxbxd-SR
ASAL|FBal0017560==Ubxbxd-SR
CLOC|89D6--9
|Insertion site
LOCB|Proximity to gene: FBgn0003944==Ubx
}
REF
{
REFM|FBrf0040194
|Bender et al.
|1983
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0012725 ICL 1 ? SYM 1 ?{}UJB6 ASTR 1 - CLOC 1 55A1 REF 1 2 DT 1 30 Jun 1999 RESZ 526
ID|FBti0012725
SYM|?{}UJB6
SYN|?{}thr4
DT|30 Jun 1999
|25 Jun 1999
ICL|?
ASGN|FBgn0022742==anon-UJB6
ARGS|FBgn0003701
REFDSR
{
RDID|FBrf0065368
|D'Andrea et al.
|1993
CLOC|55A1
|Insertion site
LOCB|Proximity to gene: FBgn0022742==anon-UJB6
CC|Second insertion on FBal0016789==thr4 chromosome; see
| FBti0012877==P{}thr4. Identity of insertion unknown.
}
REF
{
REFM|FBrf0065368
|D'Andrea et al.
|1993
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0015007 ICL 1 ? SYM 1 ?{}vAmh ASTR 1 - CLOC 1 9F11 REF 1 2 DT 1 6 Jan 2000 RESZ 382
ID|FBti0015007
SYM|?{}vAmh
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003965==v
REFDSR
{
RDID|FBrf0056245
|Nivard et al.
|1992
SYN|?{}vAmh
ASAL|FBal0050730==vAmh
CLOC|9F11
|Insertion site
LOCB|Proximity to gene: FBgn0003965==v
}
REF
{
REFM|FBrf0056245
|Nivard et al.
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014741 ICL 1 ? SYM 1 ?{}vg12 ASTR 1 - CLOC 1 49E1 REF 1 5 DT 1 6 Jan 2000 RESZ 673
ID|FBti0014741
SYM|?{}vg12
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003975==vg
REFDSR
{
RDID|FBrf0047923
|Williams and Bell
|1988
PHC|lethal | recessive
}
REFDSR
{
RDID|FBrf0052606
|Williams et al.
|1990
SYN|?{}vg12
ASAL|FBal0017871==vg12
MU|&ggr; ray
CLOC|49E1
|Insertion site
LOCB|Proximity to gene: FBgn0003975==vg
}
REFDSR
{
RDID|FBrf0064705
|Silber et al.
|1993
PHC|lethal | recessive
}
REF
{
REFM|FBrf0047923
|Williams and Bell
|1988
REFM|FBrf0052606
|Williams et al.
|1990
REFM|FBrf0064705
|Silber et al.
|1993
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0017871==vg12
REFDSR
{
RDID|FBrf0054054
|Williams et al.
|1991
PHP|Heterozygotes with FBal0017976==vg83b27 have a less extreme
| reduction of wings
|and haltere structures.
}
REFDSR
{
RDID|FBrf0064705
|Silber et al.
|1993
PHP|Sensitive to aminopterin.
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|like FBal0017868==vg1; FBal0017871==vg12/Df inviable
}
REF
{
REFM|FBrf0054054
|Williams et al.
|1991
REFM|FBrf0064705
|Silber et al.
|1993
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014759 ICL 1 ? SYM 1 ?{}vgnp ASTR 1 - CLOC 1 49E1 REF 1 3 DT 1 6 Jan 2000 RESZ 445
ID|FBti0014759
SYM|?{}vgnp
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003975==vg
REFDSR
{
RDID|FBrf0052606
|Williams et al.
|1990
SYN|?{}vgnp
ASAL|FBal0017899==vgnp
MU|spontaneous
CLOC|49E1
|Insertion site
LOCB|Proximity to gene: FBgn0003975==vg
}
REF
{
REFM|FBrf0052606
|Williams et al.
|1990
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0017899==vgnp
REFDSR
{
RDID|FBrf0056344
|Bazin and Silber
|1992
PHP|Not suppressed by FBal0016572==Su(vg)B271,
| FBal0016573==Su(vg)E41 or FBal0016574==Su(vg)E61.
}
REFDSR
{
RDID|FBrf0064705
|Silber et al.
|1993
PHP|Homozygotes display high resistance to aminopterin.
}
REFDSR
{
RDID|FBrf0090702
|Morcillo et al.
|1996
PHP|FBal0002014==ctL32; FBal0035732==su(Hw)e2 flies
| heterozygous for FBal0017899==vgnp display a
|significant FBgn0004198==ct wing phenotype.
}
REFDSR
{
RDID|FBrf0099521
|Silber et al.
|1997
PHP|Wing length decreases with increasing temperature.
PHM|wing | conditional ts
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|terminal incisions in wings; overlaps wild type at 25oC, not at
| 19oC. Wing buds show scalloping.
|RK2.
}
REF
{
REFM|FBrf0056344
|Bazin and Silber
|1992
REFM|FBrf0064705
|Silber et al.
|1993
REFM|FBrf0090702
|Morcillo et al.
|1996
REFM|FBrf0099521
|Silber et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0025360 ICL 1 ? SYM 1 ?{}vgTPb ASTR 1 - CLOC 1 49E1 REF 1 3 DT 1 7 Jul 2003 RESZ 618
ID|FBti0025360
SYM|?{}vgTPb
SYN|412{}?{}vgTP
DT|7 Jul 2003
|7 Jul 2003
ICL|?
ID2|FBti0014754
ASGN|FBgn0003975==vg
REFDSR
{
RDID|FBrf0064705
|Silber et al.
|1993
SYN|?{}vgTPb
ASAL|FBal0035915==vgTP
CLOC|49E1
|Insertion site
LOCB|Proximity to gene: FBgn0003975==vg
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
CC|One of two insertions associated with this allele; see FBti0025359==412{}vgTPa.
}
REF
{
REFM|FBrf0064705
|Silber et al.
|1993
REFM|FBrf0099521
|Silber et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0035915==vgTP
REFDSR
{
RDID|FBrf0064705
|Silber et al.
|1993
PHP|Homozygotes display highly resistance to aminopterin.
}
REFDSR
{
RDID|FBrf0099521
|Silber et al.
|1997
PHP|Wing length increases with increasing temperature.
PHM|wing | conditional cs
}
REF
{
REFM|FBrf0064705
|Silber et al.
|1993
REFM|FBrf0099521
|Silber et al.
|1997
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014763 ICL 1 ? SYM 1 ?{}w132 ASTR 1 - CLOC 1 3C1 REF 1 2 DT 1 6 Jan 2000 RESZ 404
ID|FBti0014763
SYM|?{}w132
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003996==w
REFDSR
{
RDID|FBrf0048732
|Pastink et al.
|1988
SYN|?{}w132
ASAL|FBal0018168==w132
MU|ethyl nitrosourea
CLOC|3C1
|Insertion site
LOCB|Proximity to gene: FBgn0003996==w
}
REF
{
REFM|FBrf0048732
|Pastink et al.
|1988
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0018168==w132
REFDSR
{
RDID|FBrf0048732
|Pastink et al.
|1988
PHP|Eye color: pigmented.
PHM|pigment cell
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye color: pigmented.
}
REF
{
REFM|FBrf0048732
|Pastink et al.
|1988
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014784 ICL 1 ? SYM 1 ?{}waR79l27 ASTR 1 - CLOC 1 3C1 REF 1 2 DT 1 8 Jul 2003 RESZ 451
ID|FBti0014784
SYM|?{}waR79l27
SYN|?{}waR79l27
|copia{}wa
DT|8 Jul 2003
|6 Jan 2000
ICL|?
ASGN|FBgn0003996==w
REFDSR
{
RDID|FBrf0048200
|Mount et al.
|1988
SYN|?{}waR79l27
ASAL|FBal0018209==waR79l27
MU|spontaneous
CLOC|3C1
|Insertion site
LOCB|Proximity to gene: FBgn0003996==w
}
REF
{
REFM|FBrf0048200
|Mount et al.
|1988
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0018209==waR79l27
REFDSR
{
RDID|FBrf0043247
|Carbonare and Gehring
|1985
PHP|Eye pigment is restored to 80% of wild type levels.
PHM|pigment cell
}
REF
{
REFM|FBrf0043247
|Carbonare and Gehring
|1985
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014786 ICL 1 ? SYM 1 ?{}waR84e7 ASTR 1 - CLOC 1 3C1 REF 1 2 DT 1 6 Jan 2000 RESZ 394
ID|FBti0014786
SYM|?{}waR84e7
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003996==w
REFDSR
{
RDID|FBrf0043227
|Mount and Rubin
|1985
SYN|?{}waR84e7
ASAL|FBal0018210==waR84e7
CLOC|3C1
|Insertion site
LOCB|Proximity to gene: FBgn0003996==w
}
REF
{
REFM|FBrf0043227
|Mount and Rubin
|1985
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0018210==waR84e7
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
PHP|Increased pigmentation seen in this derivative of FBal0018195==wa
| is due to
|increased gene copy number rather than change in gene properties.
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014785 ICL 1 ? SYM 1 ?{}waR84e19 ASTR 1 - CLOC 1 3C1 REF 1 2 DT 1 8 Jul 2003 RESZ 451
ID|FBti0014785
SYM|?{}waR84e19
SYN|?{}waR84e19
|copia{}wa
DT|8 Jul 2003
|6 Jan 2000
ICL|?
ASGN|FBgn0003996==w
REFDSR
{
RDID|FBrf0048200
|Mount et al.
|1988
SYN|?{}waR84e19
ASAL|FBal0018211==waR84e19
MU|spontaneous
CLOC|3C1
|Insertion site
LOCB|Proximity to gene: FBgn0003996==w
}
REF
{
REFM|FBrf0048200
|Mount et al.
|1988
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014905 ICL 1 ? SYM 1 ?{}wM1 ASTR 1 - CLOC 1 3C1 REF 1 2 DT 1 6 Jan 2000 RESZ 380
ID|FBti0014905
SYM|?{}wM1
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003996==w
REFDSR
{
RDID|FBrf0083252
|Leblanc et al.
|1995
SYN|?{}wM1
ASAL|FBal0044451==wM1
CLOC|3C1
|Insertion site
LOCB|Proximity to gene: FBgn0003996==w
}
REF
{
REFM|FBrf0083252
|Leblanc et al.
|1995
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0044451==wM1
REFDSR
{
RDID|FBrf0083252
|Leblanc et al.
|1995
PHP|Eye color: wild-type.
}
REF
{
REFM|FBrf0083252
|Leblanc et al.
|1995
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015038 ICL 1 ? SYM 1 ?{}wMR17 ASTR 1 - CLOC 1 3C1 REF 1 2 DT 1 6 Jan 2000 RESZ 388
ID|FBti0015038
SYM|?{}wMR17
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003996==w
REFDSR
{
RDID|FBrf0050015
|Georgiev et al.
|1989
SYN|?{}wMR17
ASAL|FBal0055919==wMR17
CLOC|3C1
|Insertion site
LOCB|Proximity to gene: FBgn0003996==w
}
REF
{
REFM|FBrf0050015
|Georgiev et al.
|1989
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0015037 ICL 1 ? SYM 1 ?{}wMR19d ASTR 1 - CLOC 1 3C1 REF 1 2 DT 1 6 Jan 2000 RESZ 391
ID|FBti0015037
SYM|?{}wMR19d
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003996==w
REFDSR
{
RDID|FBrf0050015
|Georgiev et al.
|1989
SYN|?{}wMR19d
ASAL|FBal0055916==wMR19d
CLOC|3C1
|Insertion site
LOCB|Proximity to gene: FBgn0003996==w
}
REF
{
REFM|FBrf0050015
|Georgiev et al.
|1989
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0015218 ICL 1 ? SYM 1 ?{}wRSV-3 ASTR 1 - CLOC 1 3C1 REF 1 2 DT 1 6 Jan 2000 RESZ 397
ID|FBti0015218
SYM|?{}wRSV-3
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003996==w
REFDSR
{
RDID|FBrf0104490
|Nabirochkin et al.
|1998
SYN|?{}wRSV-3
ASAL|FBal0092448==wRSV-3
CLOC|3C1
|Insertion site
LOCB|Proximity to gene: FBgn0003996==w
}
REF
{
REFM|FBrf0104490
|Nabirochkin et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0015057 ICL 1 ? SYM 1 ?{}wstr ASTR 1 - CLOC 1 3C1 REF 1 2 DT 1 6 Jan 2000 RESZ 387
ID|FBti0015057
SYM|?{}wstr
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0003996==w
REFDSR
{
RDID|FBrf0090437
|Aslanukov et al.
|1996
SYN|?{}wstr
ASAL|FBal0059694==wstr
CLOC|3C1
|Insertion site
LOCB|Proximity to gene: FBgn0003996==w
}
REF
{
REFM|FBrf0090437
|Aslanukov et al.
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0059694==wstr
REFDSR
{
RDID|FBrf0090437
|Aslanukov et al.
|1996
PHP|Eye color: uniform light.
PHM|pigment cell
}
REF
{
REFM|FBrf0090437
|Aslanukov et al.
|1996
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015603 ICL 1 ? SYM 1 ?{}wapl2 ASTR 1 - CLOC 1 2D5 REF 1 6 DT 1 31 May 2000 RESZ 980
ID|FBti0015603
SYM|?{}wapl2
DT|31 May 2000
|31 May 2000
ICL|?
ASGN|FBgn0004655==wapl
REFDSR
{
RDID|FBrf0039985
|Kramers et al.
|1983
PHC|lethal | recessive
}
REFDSR
{
RDID|FBrf0042629
|Perrimon et al.
|1985
PHC|lethal | recessive
}
REFDSR
{
RDID|FBrf0049894
|Perrimon et al.
|1989
PHC|lethal | recessive
|lethal | recessive | germ-line clone | maternal effect
}
REFDSR
{
RDID|FBrf0055783
|Gandhi et al.
|1992
PHC|lethal | recessive
}
REFDSR
{
RDID|FBrf0127372
|Verni et al.
|2000
SYN|?{}wapl2
ASAL|FBal0018419==wapl2
MU|X ray
CLOC|2D5
|Insertion site
LOCB|Proximity to gene: FBgn0004655==wapl
PHC|lethal | embryonic | maternal effect | recessive | germ-line clone
}
REF
{
REFM|FBrf0039985
|Kramers et al.
|1983
REFM|FBrf0042629
|Perrimon et al.
|1985
REFM|FBrf0049894
|Perrimon et al.
|1989
REFM|FBrf0055783
|Gandhi et al.
|1992
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0127372
|Verni et al.
|2000
}
ALESR
{
ASYM|FBal0018419==wapl2
REFDSR
{
RDID|FBrf0042629
|Perrimon et al.
|1985
PHP|Lethality occurs during larval and pupal stages. Phenotype of homozygous
|germ line clones is maternal effect lethal.
}
REFDSR
{
RDID|FBrf0049894
|Perrimon et al.
|1989
PHM|pre-blastoderm | germ-line clone
}
REFDSR
{
RDID|FBrf0092503
|Cook et al.
|1997
PHP|Transmission rate of FBab0024065==Dp(1;f)J21A through females to progeny is 28%,
|FBgn0004655==wapl mutation has no effect on transmission.
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|L3 larval/pupal boundary lethal
|exhibit small disk
|phenotype; homozygous germ-line clones produce zygotes
|that arrest in preblastoderm stage.
}
REFDSR
{
RDID|FBrf0127372
|Verni et al.
|2000
PHP|Embryos derived from germline clones usually arrest prior to blastoderm
|formation but manage to form small patches of cuticle.
|Brain cells of mutant larvae show defects in heterochromatin organization.
|In metaphase figures, the sister chromatids of the major autosomes
|and of the X chromosome are aligned parallel to each other, instead
|of the wild-type X- and V- shaped arrangements. The Y and 4th chromosomes
|are resolved into two distinct sister chromatids, in contrast to wild
|... (see FBal0018419==wapl2 report)
PHM|pre-blastoderm | germ-line clone | maternal effect
|heterochromatin | maternal effect
|metaphase chromosome | maternal effect
}
REF
{
REFM|FBrf0042629
|Perrimon et al.
|1985
REFM|FBrf0049894
|Perrimon et al.
|1989
REFM|FBrf0092503
|Cook et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0127372
|Verni et al.
|2000
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0004730 ICL 1 ? SYM 1 ?{}wgl-16 ASTR 1 - CLOC 1 27F1 REF 1 9 DT 1 5 Feb 1999 RESZ 1368
ID|FBti0004730
SYM|?{}wgl-16
DT|5 Feb 1999
|29 Dec 1997
ICL|?
ASGN|FBgn0004009==wg
ABA|FBab0001921==Df(2L)wg-CX3
REFDSR
{
RDID|FBrf0066940
|van den Heuvel et al.
|1993
PHC|lethal | pupal | recessive
}
REFDSR
{
RDID|FBrf0078043
|Bejsovec and Wieschaus
|1995
PHC|lethal | pupal | recessive
}
REFDSR
{
RDID|FBrf0079914
|Buratovich and Bryant
|1995
PHC|lethal | pupal | recessive
}
REFDSR
{
RDID|FBrf0087628
|Neumann and Cohen
|1996
ASAL|FBal0018508==wgl-16
MU|X ray
CLOC|27F1
|Insertion site
LOCB|Proximity to gene: FBgn0004009==wg
PHC|lethal | pupal | recessive
}
REFDSR
{
RDID|FBrf0088886
|Royet and Finkelstein
|1996
PHC|lethal | pupal | recessive
}
REFDSR
{
RDID|FBrf0089604
|Brook and Cohen
|1996
PHC|lethal | pupal | recessive
}
REFDSR
{
RDID|FBrf0093385
|Buratovich et al.
|1997
PHC|lethal | pupal | recessive
}
REFDSR
{
RDID|FBrf0099199
|Emerald and Roy
|1997
PHC|lethal | recessive
}
REF
{
REFM|FBrf0066940
|van den Heuvel et al.
|1993
REFM|FBrf0078043
|Bejsovec and Wieschaus
|1995
REFM|FBrf0079914
|Buratovich and Bryant
|1995
REFM|FBrf0087628
|Neumann and Cohen
|1996
REFM|FBrf0088886
|Royet and Finkelstein
|1996
REFM|FBrf0089604
|Brook and Cohen
|1996
REFM|FBrf0093385
|Buratovich et al.
|1997
REFM|FBrf0099199
|Emerald and Roy
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0018508==wgl-16
REFDSR
{
RDID|FBrf0046100
|Baker
|1987
PHP|Adult homeotic transformation of wing to notum.
PHM|wing
}
REFDSR
{
RDID|FBrf0059333
|Couso et al.
|1993
PHP|The heteroallelic combination
| FBal0018504==wgl-12/FBal0018508==wgl-16 has been used
| as a
|temperature sensitive genotype to study the requirement for wg gene
|product in the development of the leg, wing and haltere imaginal discs:
|wg is required only during the second larval instar in the wing and
|haltere discs, whereas legs are affected by temperature shifts at all
|times up until 96 hours after egg laying (at 25oC).
}
REFDSR
{
RDID|FBrf0078043
|Bejsovec and Wieschaus
|1995
PHP|FBal0027936==wgCE7/FBal0018508==wgl-16
| transheterozygotes are pupal lethal. Lethality
|can be suppressed by FBal0046803==wgPE1.
}
REFDSR
{
RDID|FBrf0079914
|Buratovich and Bryant
|1995
PHP|Homozygotes display leg pattern element disruptions, these are also
|seen in the pupal lethal
| FBal0018508==wgl-16/FBal0044466==wgNZ combination.
}
REFDSR
{
RDID|FBrf0087628
|Neumann and Cohen
|1996
PHP|FBal0018508==wgl-16/FBal0015984==wgSp-1 individuals
| are lethal. Adult escapers lack
|one or both anterior dorsocentral bristles and more rarely also the
|posterior postalar bristle and the presutural bristle. They also exhibit
|loss of distal antennal segments and in rare cases exhibit antennal
|duplication. Individuals in combination with
| FBal0050823==wgSp-revP, FBal0018510==wgP
|and FBal0018509==wgl-17 are pupal lethal. Individuals are adult
| viable and
|exhibit the wing phenotype when in combination with
| FBal0018482==wg1. When
|... (see FBal0018508==wgl-16 report)
}
REFDSR
{
RDID|FBrf0088886
|Royet and Finkelstein
|1996
PHP|FBal0018508==wgl-16/FBal0018504==wgl-12 larvae grown
| at the restrictive temperature result
|in heads that lack both the lateral and mediolateral structures causing
|the ocelli to be directly adjacent to the compound eyes. Ocellar cuticle
|and the ocelli are larger than wild type.
}
REFDSR
{
RDID|FBrf0089305
|Baker
|1996.8.23
PHP|In trans to null alleles of FBgn0004009==wg, FBal0018508==wgl-16 gives pupal lethality,
|indicating FBal0018508==wgl-16 is not a null allele of FBgn0004009==wg.
}
REFDSR
{
RDID|FBrf0091028
|Chen and Baker
|1997
PHP|FBal0018508==wgl-16/FBal0018509==wgl-17 mutant clones
| cause a phenotype in the external
|male genitalia; a reduction in number of clasper teeth, two lateral
|plates are fused to one with reduced number of bristles and there is
|rudimentary penis apparatus. Internal male and female genitalia are
|completely deleted. External female genitalia is generally normal.
PHM|clasper
|lateral plate
|penis
|female reproductive system
|male reproductive system
}
REFDSR
{
RDID|FBrf0099199
|Emerald and Roy
|1997
PHP|25% of FBal0018508==wgl-16/FBal0018510==wgP flies have
| wings on the prothoracic segment,
|and the mesothoracic wings and metathoracic halteres are always absent.
|10% of FBal0018508==wgl-16/FBal0018510==wgP flies show
| a varying degree of transformation
|of the metathoracic legs to halteres, ranging from graded removal of
|the distal segments (tibia and tarsus), through distortion of the femur
|and graded removal of leg bristles, to transformation of the coxa and
|trochanter into the first and second segments of the haltere.
PHM|prothoracic segment | adult
|wing
|haltere
|metathoracic leg
|metathoracic tibia
|metathoracic metatarsus
|metathoracic femur
|metathoracic leg sensillum
|metathoracic coxa
|metathoracic trochanter
}
REFDSR
{
RDID|FBrf0101933
|Klein and Martinez Arias
|1998
PHP|FBal0018508==wgl-16/FBal0018509==wgl-17 is a strong
| hypomorphic combination that causes
|a wing to notum transformation in 92% of flies.
PHM|wing
|(with wgl-17) wing
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|pupal lethal
}
REFDSR
{
RDID|FBrf0108559
|Adachi-Yamada et al.
|1999
PHP|Dominantly enhances the appearance of an apoptotic cluster of cells
|in the primordial wing tip of the late third larval instar FBal0001122==biomb-1/Y
|wing disc.
}
REFDSR
{
RDID|FBrf0111481
|Sato et al.
|1999
PHP|Most FBal0018508==wgl-16/FBal0036007==wgen11 flies
| lack antennal structures.
PHM|antenna
}
REFDSR
{
RDID|FBrf0135727
|Keisman and Baker
|2001
PHP|FBal0018508==wgl-16/FBal0018509==wgl-17 genital discs
| are smaller than wild type.
PHM|(with wgl-17) genital disc
}
REFDSR
{
RDID|FBrf0135994
|Gieseler et al.
|2001
PHP|The FBal0018508==wgl-16/FBal0018509==wgl-17
| combination results in pharate adults with
|wing to notum transformations and loss of halteres. Loss of antennae
|and dorsalization of leg structures is also seen. Wing discs show
|replacement of the wing blade by a mirror duplication of the notum
|in these animals.
PHM|(with wgl-17) wing
|(with wgl-17) haltere
|(with wgl-17) mesothoracic tergum | ectopic
|(with wgl-17) dorsal mesothoracic disc
|(with wgl-17) antenna
|(with wgl-17) leg
}
REFDSR
{
RDID|FBrf0151271
|Cavodeassi et al.
|2002
PHP|FBal0018508==wgl-16/FBal0018509==wgl-17 wing discs
| raised at 18oC show a double notum
|phenotype.
PHM|(with wgl-17) dorsal mesothoracic disc
}
REFDSR
{
RDID|FBrf0155710
|Gorfinkiel et al.
|2003
PHP|FBal0018508==wgl-16/FBal0015984==wgSp-1 females have
| reduced vaginal plates and tergite
|eight and the vulva is mainly absent.
|FBal0018508==wgl-16/FBal0015984==wgSp-1 males lack the
| penis apparatus and most of the
|clasper, and the lateral plates are fused.
PHM|(with wgSp-1) female gonopod
|(with wgSp-1) abdominal tergite 8 | female
|(with wgSp-1) vulva
|(with wgSp-1) penis
|(with wgSp-1) clasper
|(with wgSp-1) lateral plate
}
REF
{
REFM|FBrf0046100
|Baker
|1987
REFM|FBrf0059333
|Couso et al.
|1993
REFM|FBrf0078043
|Bejsovec and Wieschaus
|1995
REFM|FBrf0079914
|Buratovich and Bryant
|1995
REFM|FBrf0087628
|Neumann and Cohen
|1996
REFM|FBrf0088886
|Royet and Finkelstein
|1996
REFM|FBrf0089305
|Baker
|1996.8.23
REFM|FBrf0091028
|Chen and Baker
|1997
REFM|FBrf0099199
|Emerald and Roy
|1997
REFM|FBrf0101933
|Klein and Martinez Arias
|1998
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0108559
|Adachi-Yamada et al.
|1999
REFM|FBrf0111481
|Sato et al.
|1999
REFM|FBrf0135727
|Keisman and Baker
|2001
REFM|FBrf0135994
|Gieseler et al.
|2001
REFM|FBrf0151271
|Cavodeassi et al.
|2002
REFM|FBrf0155710
|Gorfinkiel et al.
|2003
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0016827 ICL 1 ? SYM 1 ?{}y2D ASTR 1 - CLOC 1 1A5 REF 1 2 DT 1 20 Nov 2000 RESZ 376
ID|FBti0016827
SYM|?{}y2D
DT|20 Nov 2000
|20 Nov 2000
ICL|?
ASGN|FBgn0004034==y
REFDSR
{
RDID|FBrf0044248
|Chia et al.
|1986
SYN|?{}y2D
ASAL|FBal0117985==y2D
CLOC|1A5
|Insertion site
LOCB|Proximity to gene: FBgn0004034==y
}
REF
{
REFM|FBrf0044248
|Chia et al.
|1986
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014815 ICL 1 ? SYM 1 ?{}y2S ASTR 1 - CLOC 1 1A5 REF 1 2 DT 1 6 Jan 2000 RESZ 413
ID|FBti0014815
SYM|?{}y2S
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0004034==y
REFDSR
{
RDID|FBrf0050555
|Georgiev and Gerasimova
|1989
SYN|?{}y2S
ASAL|FBal0018615==y2S
MU|spontaneous
CLOC|1A5
|Insertion site
LOCB|Proximity to gene: FBgn0004034==y
}
REF
{
REFM|FBrf0050555
|Georgiev and Gerasimova
|1989
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0018615==y2S
REFDSR
{
RDID|FBrf0044248
|Chia et al.
|1986
PHP|Body color: type 2 allele - some areas of cuticle are wild type, others
|have mutant pigmentation.
PHM|adult cuticle
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Body color: body yellow, but darker than that of FBal0018612==y2;
| bristles lighter.
|Larval mouth part color: golden-brown; mouth-hooks light.
}
REFDSR
{
RDID|FBrf0106981
|Morris et al.
|1999
PHP|Similar to FBal0018622==y25.
}
REF
{
REFM|FBrf0044248
|Chia et al.
|1986
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0106981
|Morris et al.
|1999
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015216 ICL 1 ? SYM 1 ?{}y2Sa7-1 ASTR 1 - CLOC 1 1A5 REF 1 2 DT 1 6 Jan 2000 RESZ 400
ID|FBti0015216
SYM|?{}y2Sa7-1
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0004034==y
REFDSR
{
RDID|FBrf0104490
|Nabirochkin et al.
|1998
SYN|?{}y2Sa7-1
ASAL|FBal0092429==y2Sa7-1
CLOC|1A5
|Insertion site
LOCB|Proximity to gene: FBgn0004034==y
}
REF
{
REFM|FBrf0104490
|Nabirochkin et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0016781 ICL 1 ? SYM 1 ?{}y3d ASTR 1 - CLOC 1 1A5 REF 1 2 DT 1 20 Nov 2000 RESZ 391
ID|FBti0016781
SYM|?{}y3d
DT|20 Nov 2000
|20 Nov 2000
ICL|?
ASGN|FBgn0004034==y
REFDSR
{
RDID|FBrf0044248
|Chia et al.
|1986
SYN|?{}y3d
ASAL|FBal0018616==y3d
MU|spontaneous
CLOC|1A5
|Insertion site
LOCB|Proximity to gene: FBgn0004034==y
}
REF
{
REFM|FBrf0044248
|Chia et al.
|1986
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0018616==y3d
REFDSR
{
RDID|FBrf0044248
|Chia et al.
|1986
PHP|Body color: type 2 allele - some areas of cuticle are wild type, others
|have mutant pigmentation.
PHM|adult cuticle
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Body color: body, bristles, yellow; wings gray.
|Larval mouth part color: yellow; hooks, light.
}
REF
{
REFM|FBrf0044248
|Chia et al.
|1986
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015260 ICL 1 ? SYM 1 ?{}y76-1 ASTR 1 - CLOC 1 1A5 REF 1 2 DT 1 6 Jan 2000 RESZ 384
ID|FBti0015260
SYM|?{}y76-1
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0004034==y
REFDSR
{
RDID|FBrf0106981
|Morris et al.
|1999
SYN|?{}y76-1
ASAL|FBal0095126==y76-1
CLOC|1A5
|Insertion site
LOCB|Proximity to gene: FBgn0004034==y
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0106981
|Morris et al.
|1999
}
ALESR
{
ASYM|FBal0095126==y76-1
REFDSR
{
RDID|FBrf0106981
|Morris et al.
|1999
PHP|Pigmentation is abnormal.
}
REF
{
REFM|FBrf0106981
|Morris et al.
|1999
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0025397 ICL 1 ? SYM 1 ?{}y2374b ASTR 1 - CLOC 1 1A5 REF 1 2 DT 1 7 Jul 2003 RESZ 628
ID|FBti0025397
SYM|?{}y2374b
SYN|H{}?{}H{}y2374
DT|7 Jul 2003
|7 Jul 2003
ICL|?
ID2|FBti0015159
ASGN|FBgn0004034==y
REFDSR
{
RDID|FBrf0101815
|Chen et al.
|1998
SYN|?{}y2374b
ASAL|FBal0086263==y2374
CLOC|1A5
|Insertion site
LOCB|Proximity to gene: FBgn0004034==y
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
CC|One of 3 insertions associated with this allele; see
| FBti0025396==H{}y2374a and FBti0025398==H{}y2374c.
}
REF
{
REFM|FBrf0101815
|Chen et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0086263==y2374
REFDSR
{
RDID|FBrf0101815
|Chen et al.
|1998
PHP|Body color: body & wing yellow.
PHM|adult cuticle
}
REFDSR
{
RDID|FBrf0106981
|Morris et al.
|1999
PHP|Similar to FBal0095127==y2364.
}
REF
{
REFM|FBrf0101815
|Chen et al.
|1998
REFM|FBrf0106981
|Morris et al.
|1999
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014818 ICL 1 ? SYM 1 ?{}yc4 ASTR 1 - CLOC 1 1A5 REF 1 2 DT 1 6 Jan 2000 RESZ 391
ID|FBti0014818
SYM|?{}yc4
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0004034==y
REFDSR
{
RDID|FBrf0051634
|Geyer et al.
|1990
SYN|?{}yc4
ASAL|FBal0018663==yc4
MU|spontaneous
CLOC|1A5
|Insertion site
LOCB|Proximity to gene: FBgn0004034==y
}
REF
{
REFM|FBrf0051634
|Geyer et al.
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0018663==yc4
REFDSR
{
RDID|FBrf0051634
|Geyer et al.
|1990
PHP|Body color: tan.
|Larval cuticle color: reduced pigmentation.
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Body color: yellow; hairs & bristles brown with yellow tips, but darker
|than in FBal0018607==y1; wing veins, wing hairs, yellow.
}
REF
{
REFM|FBrf0051634
|Geyer et al.
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014825 ICL 1 P SYM 1 ?{}yhd3 ASTR 1 - CLOC 1 1A5 REF 1 2 DT 1 9 Jun 2000 RESZ 434
ID|FBti0014825
SYM|?{}yhd3
SYN|P{}yhd3
DT|9 Jun 2000
|6 Jan 2000
ICL|P
ASGN|FBgn0004034==y
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|P{}yhd3
ASAL|FBal0018678==yhd3
MU|PM hybrid dysgenesis
CLOC|1A5
|Insertion site
LOCB|Proximity to gene: FBgn0004034==y
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0018678==yhd3
REFDSR
{
RDID|FBrf0044248
|Chia et al.
|1986
PHP|Body color: type 1 mutant - total loss of pigmentation from all cuticle
|structures.
PHM|adult cuticle
}
REFDSR
{
RDID|FBrf0048812
|Howes et al.
|1988
PHP|Body color: abolishes pigment in all larval and adult cuticular structures.
|Type 1 allele.
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Body color: yellow; hairs & bristles brown with yellow tips; wing
|veins, wing hairs, yellow.
PHM|adult cuticle
|wing vein
|macrochaeta
|wing hair
}
REF
{
REFM|FBrf0044248
|Chia et al.
|1986
REFM|FBrf0048812
|Howes et al.
|1988
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0015111 ICL 1 ? SYM 1 ?{}yhd8#49 ASTR 1 - CLOC 1 1A5 REF 1 2 DT 1 6 Jan 2000 RESZ 402
ID|FBti0015111
SYM|?{}yhd8#49
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0004034==y
REFDSR
{
RDID|FBrf0057308
|Norris and Woodruff
|1992
SYN|?{}yhd8#49
ASAL|FBal0063667==yhd8#49
CLOC|1A5
|Insertion site
LOCB|Proximity to gene: FBgn0004034==y
}
REF
{
REFM|FBrf0057308
|Norris and Woodruff
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0015008 ICL 1 ? SYM 1 ?{}ySa7 ASTR 1 - CLOC 1 1A5 REF 1 2 DT 1 6 Jan 2000 RESZ 401
ID|FBti0015008
SYM|?{}ySa7
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0004034==y
REFDSR
{
RDID|FBrf0050555
|Georgiev and Gerasimova
|1989
SYN|?{}ySa7
ASAL|FBal0050837==ySa7
CLOC|1A5
|Insertion site
LOCB|Proximity to gene: FBgn0004034==y
}
REF
{
REFM|FBrf0050555
|Georgiev and Gerasimova
|1989
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0050837==ySa7
REFDSR
{
RDID|FBrf0050555
|Georgiev and Gerasimova
|1989
PHP|Body color: bristles, hairs, wild-type.
}
REF
{
REFM|FBrf0050555
|Georgiev and Gerasimova
|1989
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014832 ICL 1 ? SYM 1 ?{}ytd ASTR 1 - CLOC 1 1A5 REF 1 2 DT 1 6 Jan 2000 RESZ 413
ID|FBti0014832
SYM|?{}ytd
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|FBgn0004034==y
REFDSR
{
RDID|FBrf0050555
|Georgiev and Gerasimova
|1989
SYN|?{}ytd
ASAL|FBal0018729==ytd
MU|spontaneous
CLOC|1A5
|Insertion site
LOCB|Proximity to gene: FBgn0004034==y
}
REF
{
REFM|FBrf0050555
|Georgiev and Gerasimova
|1989
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0018729==ytd
REFDSR
{
RDID|FBrf0044248
|Chia et al.
|1986
PHP|Body color: type 2 allele - some areas of cuticle are wild type, others
|have mutant pigmentation.
PHM|adult cuticle
}
REFDSR
{
RDID|FBrf0050555
|Georgiev and Gerasimova
|1989
PHP|Body color: bristles, hairs, wild-type.
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Body color: body rich tan, antennae light yellow, bristles black.
|Larval mouth part color: golden brown.
PHM|adult cuticle
|antenna
|cephalopharyngeal skeleton
}
REF
{
REFM|FBrf0044248
|Chia et al.
|1986
REFM|FBrf0050555
|Georgiev and Gerasimova
|1989
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0018951 ICL 1 accord SYM 1 accord{}818 ASTR 1 - CLOC 1 49D5-49D6 REF 1 2 DT 1 21 Aug 2003 RESZ 357
ID|FBti0018951
SYM|accord{}818
SYN|TE18951
ASTP|FBtp0017053==accord
DT|21 Aug 2003
|21 Aug 2003
ICL|accord
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|accord{}818
CLOC|49D5-49D6
LOCB|genomic location inferred from flanking sequence
DBAF|AE003820.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0027409 ICL 1 accord SYM 1 accord{}Cyp6g1DDT-R ASTR 1 - CLOC 1 48E7 REF 1 2 DT 1 22 Aug 2003 RESZ 470
ID|FBti0027409
SYM|accord{}Cyp6g1DDT-R
ASTP|FBtp0017053==accord
DT|22 Aug 2003
|22 Aug 2003
ICL|accord
ASGN|FBgn0025454==Cyp6g1
REFDSR
{
RDID|FBrf0152338
|Daborn et al.
|2002
SYN|accord{}Cyp6g1DDT-R
ASAL|FBal0014805==Cyp6g1DDT-R
CLOC|48E7
|Insertion site
LOCB|Proximity to gene: FBgn0025454==Cyp6g1
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0152338
|Daborn et al.
|2002
}
ALESR
{
ASYM|FBal0014805==Cyp6g1DDT-R
REFDSR
{
RDID|FBrf0011830
|Ogita
|1958
PHP|Sensitive to phenylthiourea.
}
REFDSR
{
RDID|FBrf0063398
|Davring and Sunner
|1971
PHP|Sensitive to phenylthiocarbamide.
}
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
PHP|FBgn0025454==Cyp6g1 is a major dominant gene responsible for the phenotype of
|a line selected for resistance to DDT. Median lethal dose of DDT for
|FBgn0025454==Cyp6g1 lines is about 4000 mug/cc of medium; that for sensitive
|lines is 50-100 mug/cc. Also resistant to BHC (benzene hexachloride)
|and organophosphorus insecticides such as parathion and malathion.
|Median lethal dose of parathion is 2 ppm for resistant line and 0.08
|ppm for sensitive. Shows maternal effect in that progeny of FBgn0025454==Cyp6g1/+
|... (see FBal0014805==Cyp6g1DDT-R report)
}
REFDSR
{
RDID|FBrf0145128
|Daborn et al.
|2001
PHP|FBal0014805==Cyp6g1DDT-R animals show increased resistance to DDT
| and imidacloprid
|relative to Canton-S animals.
}
REFDSR
{
RDID|FBrf0160720
|Le Goff et al.
|2003
PHP|FBal0014805==Cyp6g1DDT-R adults show increased resistance to DDT
| compared to
|Canton-S flies.
|FBal0014805==Cyp6g1DDT-R larvae show increased resistance to
| imidacloprid and
|to malathion compared to Canton-S larvae.
}
REF
{
REFM|FBrf0011830
|Ogita
|1958
REFM|FBrf0063398
|Davring and Sunner
|1971
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0145128
|Daborn et al.
|2001
REFM|FBrf0160720
|Le Goff et al.
|2003
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0018952 ICL 1 aurora-ele SYM 1 aurora{}589 ASTR 1 - CLOC 1 41E3-41E3 REF 1 2 DT 1 21 Aug 2003 RESZ 369
ID|FBti0018952
SYM|aurora{}589
SYN|TE18952
ASTP|FBtp0011411==aurora-element
DT|21 Aug 2003
|21 Aug 2003
ICL|aurora-ele
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|aurora{}589
CLOC|41E3-41E3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003788.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0018953 ICL 1 aurora-ele SYM 1 aurora{}649 ASTR 1 - CLOC 1 41F3-41F3 REF 1 3 DT 1 21 Aug 2003 RESZ 468
ID|FBti0018953
SYM|aurora{}649
SYN|CG10394
|TE18953
ASTP|FBtp0011411==aurora-element
DT|21 Aug 2003
|21 Aug 2003
ICL|aurora-ele
REFDSR
{
RDID|FBrf0104946
|FlyBase
|1996-
SYN|CG10394
}
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|aurora{}649
CLOC|41F3-41F3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003787.4
}
REF
{
REFM|FBrf0104946
|FlyBase
|1996-
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020269 ICL 1 aurora-ele SYM 1 aurora{}1158 ASTR 1 - CLOC 1 80E2-80E2 REF 1 3 DT 1 21 Aug 2003 RESZ 470
ID|FBti0020269
SYM|aurora{}1158
SYN|CG12616
|TE20269
ASTP|FBtp0011411==aurora-element
DT|21 Aug 2003
|21 Aug 2003
ICL|aurora-ele
REFDSR
{
RDID|FBrf0104946
|FlyBase
|1996-
SYN|CG12616
}
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|aurora{}1158
CLOC|80E2-80E2
LOCB|genomic location inferred from flanking sequence
DBAF|AE002656.3
}
REF
{
REFM|FBrf0104946
|FlyBase
|1996-
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019530 ICL 1 baggins SYM 1 baggins{}11 ASTR 1 - CLOC 1 1E1-1E1 REF 1 2 DT 1 21 Aug 2003 RESZ 357
ID|FBti0019530
SYM|baggins{}11
SYN|TE19530
ASTP|FBtp0017054==baggins
DT|21 Aug 2003
|21 Aug 2003
ICL|baggins
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|baggins{}11
CLOC|1E1-1E1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003419.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019221 ICL 1 baggins SYM 1 baggins{}485 ASTR 1 - CLOC 1 39C1-39C1 REF 1 3 DT 1 21 Aug 2003 RESZ 458
ID|FBti0019221
SYM|baggins{}485
SYN|CG8672
|TE19221
ASTP|FBtp0017054==baggins
DT|21 Aug 2003
|21 Aug 2003
ICL|baggins
REFDSR
{
RDID|FBrf0104946
|FlyBase
|1996-
SYN|CG8672
}
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|baggins{}485
CLOC|39C1-39C1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003669.4
}
REF
{
REFM|FBrf0104946
|FlyBase
|1996-
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019255 ICL 1 baggins SYM 1 baggins{}554 ASTR 1 - CLOC 1 40F7-40F7 REF 1 2 DT 1 21 Aug 2003 RESZ 361
ID|FBti0019255
SYM|baggins{}554
SYN|TE19255
ASTP|FBtp0017054==baggins
DT|21 Aug 2003
|21 Aug 2003
ICL|baggins
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|baggins{}554
CLOC|40F7-40F7
LOCB|genomic location inferred from flanking sequence
DBAF|AE002603.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0018954 ICL 1 baggins SYM 1 baggins{}618 ASTR 1 - CLOC 1 41E6-41E6 REF 1 2 DT 1 21 Aug 2003 RESZ 361
ID|FBti0018954
SYM|baggins{}618
SYN|TE18954
ASTP|FBtp0017054==baggins
DT|21 Aug 2003
|21 Aug 2003
ICL|baggins
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|baggins{}618
CLOC|41E6-41E6
LOCB|genomic location inferred from flanking sequence
DBAF|AE003787.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0018955 ICL 1 baggins SYM 1 baggins{}630 ASTR 1 - CLOC 1 41F1-41F1 REF 1 3 DT 1 21 Aug 2003 RESZ 458
ID|FBti0018955
SYM|baggins{}630
SYN|CG3392
|TE18955
ASTP|FBtp0017054==baggins
DT|21 Aug 2003
|21 Aug 2003
ICL|baggins
REFDSR
{
RDID|FBrf0104946
|FlyBase
|1996-
SYN|CG3392
}
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|baggins{}630
CLOC|41F1-41F1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003787.4
}
REF
{
REFM|FBrf0104946
|FlyBase
|1996-
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0018956 ICL 1 baggins SYM 1 baggins{}662 ASTR 1 - CLOC 1 41F3-41F3 REF 1 2 DT 1 21 Aug 2003 RESZ 361
ID|FBti0018956
SYM|baggins{}662
SYN|TE18956
ASTP|FBtp0017054==baggins
DT|21 Aug 2003
|21 Aug 2003
ICL|baggins
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|baggins{}662
CLOC|41F3-41F3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003786.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0018957 ICL 1 baggins SYM 1 baggins{}668 ASTR 1 - CLOC 1 41F4-41F4 REF 1 2 DT 1 21 Aug 2003 RESZ 361
ID|FBti0018957
SYM|baggins{}668
SYN|TE18957
ASTP|FBtp0017054==baggins
DT|21 Aug 2003
|21 Aug 2003
ICL|baggins
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|baggins{}668
CLOC|41F4-41F4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003786.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019924 ICL 1 baggins SYM 1 baggins{}682 ASTR 1 - CLOC 1 41F6-41F6 REF 1 2 DT 1 21 Aug 2003 RESZ 361
ID|FBti0019924
SYM|baggins{}682
SYN|TE19924
ASTP|FBtp0017054==baggins
DT|21 Aug 2003
|21 Aug 2003
ICL|baggins
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|baggins{}682
CLOC|41F6-41F6
LOCB|genomic location inferred from flanking sequence
DBAF|AE003786.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019925 ICL 1 baggins SYM 1 baggins{}683 ASTR 1 - CLOC 1 41F6-41F6 REF 1 2 DT 1 21 Aug 2003 RESZ 361
ID|FBti0019925
SYM|baggins{}683
SYN|TE19925
ASTP|FBtp0017054==baggins
DT|21 Aug 2003
|21 Aug 2003
ICL|baggins
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|baggins{}683
CLOC|41F6-41F6
LOCB|genomic location inferred from flanking sequence
DBAF|AE003786.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019926 ICL 1 baggins SYM 1 baggins{}684 ASTR 1 - CLOC 1 41F6-41F6 REF 1 2 DT 1 21 Aug 2003 RESZ 361
ID|FBti0019926
SYM|baggins{}684
SYN|TE19926
ASTP|FBtp0017054==baggins
DT|21 Aug 2003
|21 Aug 2003
ICL|baggins
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|baggins{}684
CLOC|41F6-41F6
LOCB|genomic location inferred from flanking sequence
DBAF|AE003786.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019927 ICL 1 baggins SYM 1 baggins{}685 ASTR 1 - CLOC 1 41F6-41F6 REF 1 2 DT 1 21 Aug 2003 RESZ 361
ID|FBti0019927
SYM|baggins{}685
SYN|TE19927
ASTP|FBtp0017054==baggins
DT|21 Aug 2003
|21 Aug 2003
ICL|baggins
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|baggins{}685
CLOC|41F6-41F6
LOCB|genomic location inferred from flanking sequence
DBAF|AE003786.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019928 ICL 1 baggins SYM 1 baggins{}686 ASTR 1 - CLOC 1 41F6-41F6 REF 1 2 DT 1 21 Aug 2003 RESZ 361
ID|FBti0019928
SYM|baggins{}686
SYN|TE19928
ASTP|FBtp0017054==baggins
DT|21 Aug 2003
|21 Aug 2003
ICL|baggins
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|baggins{}686
CLOC|41F6-41F6
LOCB|genomic location inferred from flanking sequence
DBAF|AE003786.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019929 ICL 1 baggins SYM 1 baggins{}687 ASTR 1 - CLOC 1 41F6-41F6 REF 1 2 DT 1 21 Aug 2003 RESZ 361
ID|FBti0019929
SYM|baggins{}687
SYN|TE19929
ASTP|FBtp0017054==baggins
DT|21 Aug 2003
|21 Aug 2003
ICL|baggins
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|baggins{}687
CLOC|41F6-41F6
LOCB|genomic location inferred from flanking sequence
DBAF|AE003786.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020395 ICL 1 baggins SYM 1 baggins{}1471 ASTR 1 - CLOC 1 102A1-102A1 REF 1 2 DT 1 21 Aug 2003 RESZ 365
ID|FBti0020395
SYM|baggins{}1471
SYN|TE20395
ASTP|FBtp0017054==baggins
DT|21 Aug 2003
|21 Aug 2003
ICL|baggins
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|baggins{}1471
CLOC|102A1-102A1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003845.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019099 ICL 1 Bari1 SYM 1 Bari1{}282 ASTR 1 - CLOC 1 21D2-21D2 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019099
SYM|Bari1{}282
SYN|TE19099
ASTP|FBtp0011412==Bari1
DT|21 Aug 2003
|21 Aug 2003
ICL|Bari1
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Bari1{}282
CLOC|21D2-21D2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003588.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0018880 ICL 1 Bari1 SYM 1 Bari1{}855 ASTR 1 - CLOC 1 55F8-55F8 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0018880
SYM|Bari1{}855
SYN|TE18880
ASTP|FBtp0011412==Bari1
DT|21 Aug 2003
|21 Aug 2003
ICL|Bari1
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Bari1{}855
CLOC|55F8-55F8
LOCB|genomic location inferred from flanking sequence
DBAF|AE003798.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019400 ICL 1 Bari1 SYM 1 Bari1{}1386 ASTR 1 - CLOC 1 91F3-91F3 REF 1 2 DT 1 21 Aug 2003 RESZ 355
ID|FBti0019400
SYM|Bari1{}1386
SYN|TE19400
ASTP|FBtp0011412==Bari1
DT|21 Aug 2003
|21 Aug 2003
ICL|Bari1
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Bari1{}1386
CLOC|91F3-91F3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003725.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019419 ICL 1 Bari1 SYM 1 Bari1{}1409 ASTR 1 - CLOC 1 95A2-95A2 REF 1 2 DT 1 21 Aug 2003 RESZ 355
ID|FBti0019419
SYM|Bari1{}1409
SYN|TE19419
ASTP|FBtp0011412==Bari1
DT|21 Aug 2003
|21 Aug 2003
ICL|Bari1
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Bari1{}1409
CLOC|95A2-95A2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003744.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019499 ICL 1 Bari1 SYM 1 Bari1{}1534 ASTR 1 - CLOC 1 102F1-102F1 REF 1 2 DT 1 21 Aug 2003 RESZ 357
ID|FBti0019499
SYM|Bari1{}1534
SYN|TE19499
ASTP|FBtp0011412==Bari1
DT|21 Aug 2003
|21 Aug 2003
ICL|Bari1
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Bari1{}1534
CLOC|102F1-102F1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003847.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019843 ICL 1 Bari2 SYM 1 Bari2{}506 ASTR 1 - CLOC 1 39E2-39E2 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019843
SYM|Bari2{}506
SYN|TE19843
ASTP|FBtp0017031==Bari2
DT|21 Aug 2003
|21 Aug 2003
ICL|Bari2
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Bari2{}506
CLOC|39E2-39E2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003781.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019878 ICL 1 Bari2 SYM 1 Bari2{}574 ASTR 1 - CLOC 1 40F7-40F7 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019878
SYM|Bari2{}574
SYN|TE19878
ASTP|FBtp0017031==Bari2
DT|21 Aug 2003
|21 Aug 2003
ICL|Bari2
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Bari2{}574
CLOC|40F7-40F7
LOCB|genomic location inferred from flanking sequence
DBAF|AE002603.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020303 ICL 1 Bari2 SYM 1 Bari2{}1203 ASTR 1 - CLOC 1 82C3-82C3 REF 1 2 DT 1 21 Aug 2003 RESZ 355
ID|FBti0020303
SYM|Bari2{}1203
SYN|TE20303
ASTP|FBtp0017031==Bari2
DT|21 Aug 2003
|21 Aug 2003
ICL|Bari2
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Bari2{}1203
CLOC|82C3-82C3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003605.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020436 ICL 1 Bari2 SYM 1 Bari2{}1537 ASTR 1 - CLOC 1 102F3-102F3 REF 1 2 DT 1 21 Aug 2003 RESZ 357
ID|FBti0020436
SYM|Bari2{}1537
SYN|TE20436
ASTP|FBtp0017031==Bari2
DT|21 Aug 2003
|21 Aug 2003
ICL|Bari2
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Bari2{}1537
CLOC|102F3-102F3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003847.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019690 ICL 1 blood SYM 1 blood{}218 ASTR 1 - CLOC 1 20A2-20A3 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019690
SYM|blood{}218
SYN|TE19690
ASTP|FBtp0011415==blood
DT|21 Aug 2003
|21 Aug 2003
ICL|blood
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|blood{}218
CLOC|20A2-20A3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003122.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019096 ICL 1 blood SYM 1 blood{}280 ASTR 1 - CLOC 1 21C2-21C2 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019096
SYM|blood{}280
SYN|TE19096
ASTP|FBtp0011415==blood
DT|21 Aug 2003
|21 Aug 2003
ICL|blood
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|blood{}280
CLOC|21C2-21C2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003589.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019102 ICL 1 blood SYM 1 blood{}285 ASTR 1 - CLOC 1 21F3-21F3 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019102
SYM|blood{}285
SYN|TE19102
ASTP|FBtp0011415==blood
DT|21 Aug 2003
|21 Aug 2003
ICL|blood
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|blood{}285
CLOC|21F3-21F3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003587.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019106 ICL 1 blood SYM 1 blood{}289 ASTR 1 - CLOC 1 22A7-22A7 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019106
SYM|blood{}289
SYN|TE19106
ASTP|FBtp0011415==blood
DT|21 Aug 2003
|21 Aug 2003
ICL|blood
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|blood{}289
CLOC|22A7-22A7
LOCB|genomic location inferred from flanking sequence
DBAF|AE003585.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019145 ICL 1 blood SYM 1 blood{}335 ASTR 1 - CLOC 1 31A3-31A3 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019145
SYM|blood{}335
SYN|TE19145
ASTP|FBtp0011415==blood
DT|21 Aug 2003
|21 Aug 2003
ICL|blood
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|blood{}335
CLOC|31A3-31A3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003627.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019152 ICL 1 blood SYM 1 blood{}344 ASTR 1 - CLOC 1 33A1-33A1 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019152
SYM|blood{}344
SYN|TE19152
ASTP|FBtp0011415==blood
DT|21 Aug 2003
|21 Aug 2003
ICL|blood
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|blood{}344
CLOC|33A1-33A1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003633.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019163 ICL 1 blood SYM 1 blood{}356 ASTR 1 - CLOC 1 34A2-34A2 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019163
SYM|blood{}356
SYN|TE19163
ASTP|FBtp0011415==blood
DT|21 Aug 2003
|21 Aug 2003
ICL|blood
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|blood{}356
CLOC|34A2-34A2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003638.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019179 ICL 1 blood SYM 1 blood{}375 ASTR 1 - CLOC 1 35D2-35D2 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019179
SYM|blood{}375
SYN|TE19179
ASTP|FBtp0011415==blood
DT|21 Aug 2003
|21 Aug 2003
ICL|blood
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|blood{}375
CLOC|35D2-35D2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003647.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019773 ICL 1 blood SYM 1 blood{}409 ASTR 1 - CLOC 1 37D2-37D2 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019773
SYM|blood{}409
SYN|TE19773
ASTP|FBtp0011415==blood
DT|21 Aug 2003
|21 Aug 2003
ICL|blood
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|blood{}409
CLOC|37D2-37D2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003662.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019210 ICL 1 blood SYM 1 blood{}468 ASTR 1 - CLOC 1 38C5-38C5 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019210
SYM|blood{}468
SYN|TE19210
ASTP|FBtp0011415==blood
DT|21 Aug 2003
|21 Aug 2003
ICL|blood
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|blood{}468
CLOC|38C5-38C5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003666.5
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019214 ICL 1 blood SYM 1 blood{}472 ASTR 1 - CLOC 1 38C10-38D1 REF 1 2 DT 1 21 Aug 2003 RESZ 354
ID|FBti0019214
SYM|blood{}472
SYN|TE19214
ASTP|FBtp0011415==blood
DT|21 Aug 2003
|21 Aug 2003
ICL|blood
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|blood{}472
CLOC|38C10-38D1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003667.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019224 ICL 1 blood SYM 1 blood{}488 ASTR 1 - CLOC 1 39D3-39D3 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019224
SYM|blood{}488
SYN|TE19224
ASTP|FBtp0011415==blood
DT|21 Aug 2003
|21 Aug 2003
ICL|blood
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|blood{}488
CLOC|39D3-39D3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003670.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0018965 ICL 1 blood SYM 1 blood{}852 ASTR 1 - CLOC 1 55C13-55C13 REF 1 2 DT 1 21 Aug 2003 RESZ 355
ID|FBti0018965
SYM|blood{}852
SYN|TE18965
ASTP|FBtp0011415==blood
DT|21 Aug 2003
|21 Aug 2003
ICL|blood
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|blood{}852
CLOC|55C13-55C13
LOCB|genomic location inferred from flanking sequence
DBAF|AE003799.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0018966 ICL 1 blood SYM 1 blood{}856 ASTR 1 - CLOC 1 56E6-56F1 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0018966
SYM|blood{}856
SYN|TE18966
ASTP|FBtp0011415==blood
DT|21 Aug 2003
|21 Aug 2003
ICL|blood
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|blood{}856
CLOC|56E6-56F1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003794.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020070 ICL 1 blood SYM 1 blood{}959 ASTR 1 - CLOC 1 66D3-66D4 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020070
SYM|blood{}959
SYN|TE20070
ASTP|FBtp0011415==blood
DT|21 Aug 2003
|21 Aug 2003
ICL|blood
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|blood{}959
CLOC|66D3-66D4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003555.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020203 ICL 1 blood SYM 1 blood{}1092 ASTR 1 - CLOC 1 79F1-79F1 REF 1 2 DT 1 21 Aug 2003 RESZ 355
ID|FBti0020203
SYM|blood{}1092
SYN|TE20203
ASTP|FBtp0011415==blood
DT|21 Aug 2003
|21 Aug 2003
ICL|blood
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|blood{}1092
CLOC|79F1-79F1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003598.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020205 ICL 1 blood SYM 1 blood{}1094 ASTR 1 - CLOC 1 79F2-79F3 REF 1 2 DT 1 21 Aug 2003 RESZ 355
ID|FBti0020205
SYM|blood{}1094
SYN|TE20205
ASTP|FBtp0011415==blood
DT|21 Aug 2003
|21 Aug 2003
ICL|blood
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|blood{}1094
CLOC|79F2-79F3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003598.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019384 ICL 1 blood SYM 1 blood{}1369 ASTR 1 - CLOC 1 88F9-89A1 REF 1 2 DT 1 21 Aug 2003 RESZ 355
ID|FBti0019384
SYM|blood{}1369
SYN|TE19384
ASTP|FBtp0011415==blood
DT|21 Aug 2003
|21 Aug 2003
ICL|blood
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|blood{}1369
CLOC|88F9-89A1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003709.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019391 ICL 1 blood SYM 1 blood{}1376 ASTR 1 - CLOC 1 90B5-90B5 REF 1 2 DT 1 21 Aug 2003 RESZ 355
ID|FBti0019391
SYM|blood{}1376
SYN|TE19391
ASTP|FBtp0011415==blood
DT|21 Aug 2003
|21 Aug 2003
ICL|blood
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|blood{}1376
CLOC|90B5-90B5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003718.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019403 ICL 1 blood SYM 1 blood{}1389 ASTR 1 - CLOC 1 92B1-92B1 REF 1 2 DT 1 21 Aug 2003 RESZ 355
ID|FBti0019403
SYM|blood{}1389
SYN|TE19403
ASTP|FBtp0011415==blood
DT|21 Aug 2003
|21 Aug 2003
ICL|blood
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|blood{}1389
CLOC|92B1-92B1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003727.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019465 ICL 1 blood SYM 1 blood{}1462 ASTR 1 - CLOC 1 100A2-100A2 REF 1 2 DT 1 21 Aug 2003 RESZ 357
ID|FBti0019465
SYM|blood{}1462
SYN|TE19465
ASTP|FBtp0011415==blood
DT|21 Aug 2003
|21 Aug 2003
ICL|blood
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|blood{}1462
CLOC|100A2-100A2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003775.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019471 ICL 1 blood SYM 1 blood{}1470 ASTR 1 - CLOC 1 100D1-100D1 REF 1 2 DT 1 21 Aug 2003 RESZ 357
ID|FBti0019471
SYM|blood{}1470
SYN|TE19471
ASTP|FBtp0011415==blood
DT|21 Aug 2003
|21 Aug 2003
ICL|blood
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|blood{}1470
CLOC|100D1-100D1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003780.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014091 ICL 1 blood SYM 1 blood{}Brd1 ASTR 1 - CLOC 1 71A4 REF 1 3 DT 1 6 Jan 2000 RESZ 643
ID|FBti0014091
SYM|blood{}Brd1
ASTP|FBtp0011415==blood
DT|6 Jan 2000
|6 Jan 2000
ICL|blood
ASGN|FBgn0000216==Brd
ARGS|FBgn0000216
REFDSR
{
RDID|FBrf0088401
|Leviten and Posakony
|1996
ASAL|FBal0001282==BrdP1
MU|P-element activity
}
REFDSR
{
RDID|FBrf0099359
|Leviten et al.
|1997
SYN|blood{}Brd1
ASAL|FBal0001270==Brd1
MU|spontaneous
CLOC|71A4
|Insertion site
LOCB|Proximity to gene: FBgn0000216==Brd
}
REF
{
REFM|FBrf0088401
|Leviten and Posakony
|1996
REFM|FBrf0099359
|Leviten et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0001282==BrdP1
REFDSR
{
RDID|FBrf0088401
|Leviten and Posakony
|1996
PHP|Partially suppressed bristle multiplication phenotype.
PHM|macrochaeta
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Weaker phenotype than that of FBal0001270==Brd1.
}
REF
{
REFM|FBrf0088401
|Leviten and Posakony
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
ALESR
{
ASYM|FBal0001270==Brd1
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
PHP|FBal0001270==Brd1 homozygotes survive and exhibit more severe
| phenotypes than
|heterozygotes. FBal0001270==Brd1/+ = FBal0001270==Brd1
| hemizygous with FBgn0000216==Brd-. FBal0001270==Brd1
|strongly affects macrochaetae and other imaginal-disc sensilla (i.e.,
|trichoid, campaniform, basiconic), but only mildly increases
|microchaete density. In addition to sensillum multiplication, FBal0001270==Brd1
|homozygotes also exhibit bristle loss, with anterior orbitals absent
|(>90%) and a less frequent loss of ocellar macrochaetae (<5%).The
|... (see FBal0001270==Brd1 report)
PHM|macrochaeta
|microchaeta
|sensillum trichodeum
|sensillum campaniformium
|sensillum basiconicum
}
REFDSR
{
RDID|FBrf0088401
|Leviten and Posakony
|1996
PHP|Bristle multiplication phenotype, ectopic bristles are complete sensory
|organs. Anterior orbital, ocellar and posterior supra-alar bristle
|loss due to defects in the cell fate specification in the bristle lineage.
PHM|macrochaeta | ectopic
|macrochaeta
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0088401
|Leviten and Posakony
|1996
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0013355 ICL 1 blood SYM 1 blood{}GpdhAKy33 ASTR 1 - CLOC 1 Inserts in Gpdh REF 1 2 DT 1 4 Feb 2000 RESZ 425
ID|FBti0013355
SYM|blood{}GpdhAKy33
ASTP|FBtp0011415==blood
DT|4 Feb 2000
|3 Nov 1999
ICL|blood
ASGN|FBgn0001128==Gpdh
ARGS|FBgn0001128
REFDSR
{
RDID|FBrf0086147
|Wilanowski et al.
|1995
ASAL|FBal0048805==GpdhAKy33
CLOC|Gpdh
|Insertion site
LOCB|in situ
PHC|viable
|fertile
}
REF
{
REFM|FBrf0086147
|Wilanowski et al.
|1995
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0048805==GpdhAKy33
REFDSR
{
RDID|FBrf0052093
|Gibson et al.
|1990
PHP|FBal0048805==GpdhAKy33/FBab0001468==Df(2L)GpdhA flies have
| reduced FBgn0001128==Gpdh enzyme activity
|compared to wild-type.
}
REF
{
REFM|FBrf0052093
|Gibson et al.
|1990
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014791 ICL 1 blood SYM 1 blood{}wbl ASTR 1 - CLOC 1 3C1 REF 1 8 DT 1 6 Jan 2000 RESZ 681
ID|FBti0014791
SYM|blood{}wbl
ASTP|FBtp0011415==blood
DT|6 Jan 2000
|6 Jan 2000
ICL|blood
ASGN|FBgn0003996==w
REFDSR
{
RDID|FBrf0084258
|Peng and Mount
|1995
SYN|blood{}wbl
ASAL|FBal0018218==wbl
MU|spontaneous
CLOC|3C1
|Insertion site
LOCB|Proximity to gene: FBgn0003996==w
}
REF
{
REFM|FBrf0084258
|Peng and Mount
|1995
REFM|FBrf0084324
|Roseman et al.
|1995
REFM|FBrf0086910
|Bhadra and Birchler
|1996
REFM|FBrf0094158
|Bhadra et al.
|1997
REFM|FBrf0094159
|Bhadra et al.
|1997
REFM|FBrf0098391
|Costas et al.
|1997
REFM|FBrf0100562
|Frolov et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0018218==wbl
REFDSR
{
RDID|FBrf0006364
|Ephrussi and Herold
|1945
PHP|Temperature sensitivity greatest 40-48 hr after pupation.
}
REFDSR
{
RDID|FBrf0056147
|Birchler
|1992
PHP|Homozygous males are darker than homozygous females. Triple X metafemale
|individuals homozygous for FBal0018218==wbl have pigment levels
| near the normal
|intensity of FBal0018218==wbl homozygous XX females.
}
REFDSR
{
RDID|FBrf0084258
|Peng and Mount
|1995
PHM|pigment cell
}
REFDSR
{
RDID|FBrf0100562
|Frolov et al.
|1998
PHM|pigment cell
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye color: yellowish-ruby, later FBgn0003351==se-like; female lighter than male;
|at 19oC as dark as FBal0013871==pn1; at 30oC,
| as light as FBal0018215==wbf or FBal0018254==wi.
|Testis color: colorless.
|Malpighian tubule color: pale yellow at 25oC.
PHM|pigment cell
|testis pigment cell
|Malpighian tubule
}
REFDSR
{
RDID|FBrf0105774
|Benevolenskaya et al.
|1998
PHM|pigment cell
}
REF
{
REFM|FBrf0006364
|Ephrussi and Herold
|1945
REFM|FBrf0056147
|Birchler
|1992
REFM|FBrf0084258
|Peng and Mount
|1995
REFM|FBrf0100562
|Frolov et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0105774
|Benevolenskaya et al.
|1998
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0019604 ICL 1 BS SYM 1 BS{}85 ASTR 1 - CLOC 1 7E4-7E4 REF 1 2 DT 1 21 Aug 2003 RESZ 337
ID|FBti0019604
SYM|BS{}85
SYN|TE19604
ASTP|FBtp0011416==BS
DT|21 Aug 2003
|21 Aug 2003
ICL|BS
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|BS{}85
CLOC|7E4-7E4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003443.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019079 ICL 1 BS SYM 1 BS{}155 ASTR 1 - CLOC 1 17A2-17A2 REF 1 2 DT 1 21 Aug 2003 RESZ 341
ID|FBti0019079
SYM|BS{}155
SYN|TE19079
ASTP|FBtp0011416==BS
DT|21 Aug 2003
|21 Aug 2003
ICL|BS
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|BS{}155
CLOC|17A2-17A2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003508.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019133 ICL 1 BS SYM 1 BS{}321 ASTR 1 - CLOC 1 28B2-28B2 REF 1 2 DT 1 21 Aug 2003 RESZ 341
ID|FBti0019133
SYM|BS{}321
SYN|TE19133
ASTP|FBtp0011416==BS
DT|21 Aug 2003
|21 Aug 2003
ICL|BS
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|BS{}321
CLOC|28B2-28B2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003618.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019158 ICL 1 BS SYM 1 BS{}351 ASTR 1 - CLOC 1 33F5-33F5 REF 1 2 DT 1 21 Aug 2003 RESZ 341
ID|FBti0019158
SYM|BS{}351
SYN|TE19158
ASTP|FBtp0011416==BS
DT|21 Aug 2003
|21 Aug 2003
ICL|BS
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|BS{}351
CLOC|33F5-33F5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003637.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019165 ICL 1 BS SYM 1 BS{}358 ASTR 1 - CLOC 1 34B1-34B1 REF 1 2 DT 1 21 Aug 2003 RESZ 341
ID|FBti0019165
SYM|BS{}358
SYN|TE19165
ASTP|FBtp0011416==BS
DT|21 Aug 2003
|21 Aug 2003
ICL|BS
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|BS{}358
CLOC|34B1-34B1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003639.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019784 ICL 1 BS SYM 1 BS{}426 ASTR 1 - CLOC 1 38C1-38C1 REF 1 2 DT 1 21 Aug 2003 RESZ 341
ID|FBti0019784
SYM|BS{}426
SYN|TE19784
ASTP|FBtp0011416==BS
DT|21 Aug 2003
|21 Aug 2003
ICL|BS
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|BS{}426
CLOC|38C1-38C1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003665.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019223 ICL 1 BS SYM 1 BS{}487 ASTR 1 - CLOC 1 39D2-39D2 REF 1 2 DT 1 21 Aug 2003 RESZ 341
ID|FBti0019223
SYM|BS{}487
SYN|TE19223
ASTP|FBtp0011416==BS
DT|21 Aug 2003
|21 Aug 2003
ICL|BS
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|BS{}487
CLOC|39D2-39D2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003670.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019834 ICL 1 BS SYM 1 BS{}497 ASTR 1 - CLOC 1 39D5-39E1 REF 1 2 DT 1 21 Aug 2003 RESZ 341
ID|FBti0019834
SYM|BS{}497
SYN|TE19834
ASTP|FBtp0011416==BS
DT|21 Aug 2003
|21 Aug 2003
ICL|BS
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|BS{}497
CLOC|39D5-39E1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003670.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0018875 ICL 1 BS SYM 1 BS{}707 ASTR 1 - CLOC 1 42A9-42A9 REF 1 2 DT 1 21 Aug 2003 RESZ 341
ID|FBti0018875
SYM|BS{}707
SYN|TE18875
ASTP|FBtp0011416==BS
DT|21 Aug 2003
|21 Aug 2003
ICL|BS
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|BS{}707
CLOC|42A9-42A9
LOCB|genomic location inferred from flanking sequence
DBAF|AE003784.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019957 ICL 1 BS SYM 1 BS{}729 ASTR 1 - CLOC 1 42A18-42A18 REF 1 2 DT 1 21 Aug 2003 RESZ 343
ID|FBti0019957
SYM|BS{}729
SYN|TE19957
ASTP|FBtp0011416==BS
DT|21 Aug 2003
|21 Aug 2003
ICL|BS
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|BS{}729
CLOC|42A18-42A18
LOCB|genomic location inferred from flanking sequence
DBAF|AE003789.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0018876 ICL 1 BS SYM 1 BS{}759 ASTR 1 - CLOC 1 42D1-42D1 REF 1 2 DT 1 21 Aug 2003 RESZ 341
ID|FBti0018876
SYM|BS{}759
SYN|TE18876
ASTP|FBtp0011416==BS
DT|21 Aug 2003
|21 Aug 2003
ICL|BS
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|BS{}759
CLOC|42D1-42D1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003790.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0018877 ICL 1 BS SYM 1 BS{}794 ASTR 1 - CLOC 1 46C6-46C6 REF 1 2 DT 1 21 Aug 2003 RESZ 341
ID|FBti0018877
SYM|BS{}794
SYN|TE18877
ASTP|FBtp0011416==BS
DT|21 Aug 2003
|21 Aug 2003
ICL|BS
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|BS{}794
CLOC|46C6-46C6
LOCB|genomic location inferred from flanking sequence
DBAF|AE003831.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0018878 ICL 1 BS SYM 1 BS{}809 ASTR 1 - CLOC 1 47D7-47D7 REF 1 2 DT 1 21 Aug 2003 RESZ 341
ID|FBti0018878
SYM|BS{}809
SYN|TE18878
ASTP|FBtp0011416==BS
DT|21 Aug 2003
|21 Aug 2003
ICL|BS
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|BS{}809
CLOC|47D7-47D7
LOCB|genomic location inferred from flanking sequence
DBAF|AE003826.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0018879 ICL 1 BS SYM 1 BS{}871 ASTR 1 - CLOC 1 58E2-58E2 REF 1 2 DT 1 21 Aug 2003 RESZ 341
ID|FBti0018879
SYM|BS{}871
SYN|TE18879
ASTP|FBtp0011416==BS
DT|21 Aug 2003
|21 Aug 2003
ICL|BS
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|BS{}871
CLOC|58E2-58E2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003457.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020044 ICL 1 BS SYM 1 BS{}933 ASTR 1 - CLOC 1 64F5-64F5 REF 1 2 DT 1 21 Aug 2003 RESZ 341
ID|FBti0020044
SYM|BS{}933
SYN|TE20044
ASTP|FBtp0011416==BS
DT|21 Aug 2003
|21 Aug 2003
ICL|BS
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|BS{}933
CLOC|64F5-64F5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003564.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020056 ICL 1 BS SYM 1 BS{}945 ASTR 1 - CLOC 1 65E1-65E1 REF 1 2 DT 1 21 Aug 2003 RESZ 341
ID|FBti0020056
SYM|BS{}945
SYN|TE20056
ASTP|FBtp0011416==BS
DT|21 Aug 2003
|21 Aug 2003
ICL|BS
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|BS{}945
CLOC|65E1-65E1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003560.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020057 ICL 1 BS SYM 1 BS{}946 ASTR 1 - CLOC 1 65E7-65E7 REF 1 2 DT 1 21 Aug 2003 RESZ 341
ID|FBti0020057
SYM|BS{}946
SYN|TE20057
ASTP|FBtp0011416==BS
DT|21 Aug 2003
|21 Aug 2003
ICL|BS
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|BS{}946
CLOC|65E7-65E7
LOCB|genomic location inferred from flanking sequence
DBAF|AE003560.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020125 ICL 1 BS SYM 1 BS{}1014 ASTR 1 - CLOC 1 73A4-73A4 REF 1 2 DT 1 21 Aug 2003 RESZ 343
ID|FBti0020125
SYM|BS{}1014
SYN|TE20125
ASTP|FBtp0011416==BS
DT|21 Aug 2003
|21 Aug 2003
ICL|BS
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|BS{}1014
CLOC|73A4-73A4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003527.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020128 ICL 1 BS SYM 1 BS{}1017 ASTR 1 - CLOC 1 73C2-73C2 REF 1 2 DT 1 21 Aug 2003 RESZ 343
ID|FBti0020128
SYM|BS{}1017
SYN|TE20128
ASTP|FBtp0011416==BS
DT|21 Aug 2003
|21 Aug 2003
ICL|BS
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|BS{}1017
CLOC|73C2-73C2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003526.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020149 ICL 1 BS SYM 1 BS{}1038 ASTR 1 - CLOC 1 75D1-75D1 REF 1 2 DT 1 21 Aug 2003 RESZ 343
ID|FBti0020149
SYM|BS{}1038
SYN|TE20149
ASTP|FBtp0011416==BS
DT|21 Aug 2003
|21 Aug 2003
ICL|BS
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|BS{}1038
CLOC|75D1-75D1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003520.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020157 ICL 1 BS SYM 1 BS{}1046 ASTR 1 - CLOC 1 75F8-75F8 REF 1 2 DT 1 21 Aug 2003 RESZ 343
ID|FBti0020157
SYM|BS{}1046
SYN|TE20157
ASTP|FBtp0011416==BS
DT|21 Aug 2003
|21 Aug 2003
ICL|BS
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|BS{}1046
CLOC|75F8-75F8
LOCB|genomic location inferred from flanking sequence
DBAF|AE003518.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019312 ICL 1 BS SYM 1 BS{}1230 ASTR 1 - CLOC 1 83D4-83D4 REF 1 2 DT 1 21 Aug 2003 RESZ 343
ID|FBti0019312
SYM|BS{}1230
SYN|TE19312
ASTP|FBtp0011416==BS
DT|21 Aug 2003
|21 Aug 2003
ICL|BS
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|BS{}1230
CLOC|83D4-83D4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003600.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019315 ICL 1 BS SYM 1 BS{}1233 ASTR 1 - CLOC 1 83E1-83E1 REF 1 2 DT 1 21 Aug 2003 RESZ 343
ID|FBti0019315
SYM|BS{}1233
SYN|TE19315
ASTP|FBtp0011416==BS
DT|21 Aug 2003
|21 Aug 2003
ICL|BS
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|BS{}1233
CLOC|83E1-83E1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003600.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019332 ICL 1 BS SYM 1 BS{}1260 ASTR 1 - CLOC 1 84E10-84E10 REF 1 2 DT 1 21 Aug 2003 RESZ 345
ID|FBti0019332
SYM|BS{}1260
SYN|TE19332
ASTP|FBtp0011416==BS
DT|21 Aug 2003
|21 Aug 2003
ICL|BS
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|BS{}1260
CLOC|84E10-84E10
LOCB|genomic location inferred from flanking sequence
DBAF|AE003677.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019358 ICL 1 BS SYM 1 BS{}1292 ASTR 1 - CLOC 1 86F9-86F10 REF 1 2 DT 1 21 Aug 2003 RESZ 344
ID|FBti0019358
SYM|BS{}1292
SYN|TE19358
ASTP|FBtp0011416==BS
DT|21 Aug 2003
|21 Aug 2003
ICL|BS
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|BS{}1292
CLOC|86F9-86F10
LOCB|genomic location inferred from flanking sequence
DBAF|AE003693.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019378 ICL 1 BS SYM 1 BS{}1363 ASTR 1 - CLOC 1 88E1-88E1 REF 1 2 DT 1 21 Aug 2003 RESZ 343
ID|FBti0019378
SYM|BS{}1363
SYN|TE19378
ASTP|FBtp0011416==BS
DT|21 Aug 2003
|21 Aug 2003
ICL|BS
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|BS{}1363
CLOC|88E1-88E1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003707.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019388 ICL 1 BS SYM 1 BS{}1373 ASTR 1 - CLOC 1 90A1-90A1 REF 1 2 DT 1 21 Aug 2003 RESZ 343
ID|FBti0019388
SYM|BS{}1373
SYN|TE19388
ASTP|FBtp0011416==BS
DT|21 Aug 2003
|21 Aug 2003
ICL|BS
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|BS{}1373
CLOC|90A1-90A1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003717.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019410 ICL 1 BS SYM 1 BS{}1396 ASTR 1 - CLOC 1 92E14-92E14 REF 1 2 DT 1 21 Aug 2003 RESZ 345
ID|FBti0019410
SYM|BS{}1396
SYN|TE19410
ASTP|FBtp0011416==BS
DT|21 Aug 2003
|21 Aug 2003
ICL|BS
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|BS{}1396
CLOC|92E14-92E14
LOCB|genomic location inferred from flanking sequence
DBAF|AE003730.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019426 ICL 1 BS SYM 1 BS{}1416 ASTR 1 - CLOC 1 96A3-96A3 REF 1 2 DT 1 21 Aug 2003 RESZ 343
ID|FBti0019426
SYM|BS{}1416
SYN|TE19426
ASTP|FBtp0011416==BS
DT|21 Aug 2003
|21 Aug 2003
ICL|BS
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|BS{}1416
CLOC|96A3-96A3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003748.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019593 ICL 1 Burdock SYM 1 Burdock{}74 ASTR 1 - CLOC 1 6C1-6C1 REF 1 2 DT 1 21 Aug 2003 RESZ 357
ID|FBti0019593
SYM|Burdock{}74
SYN|TE19593
ASTP|FBtp0011417==Burdock
DT|21 Aug 2003
|21 Aug 2003
ICL|Burdock
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Burdock{}74
CLOC|6C1-6C1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003438.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019626 ICL 1 Burdock SYM 1 Burdock{}107 ASTR 1 - CLOC 1 10C4-10C4 REF 1 2 DT 1 21 Aug 2003 RESZ 361
ID|FBti0019626
SYM|Burdock{}107
SYN|TE19626
ASTP|FBtp0011417==Burdock
DT|21 Aug 2003
|21 Aug 2003
ICL|Burdock
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Burdock{}107
CLOC|10C4-10C4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003486.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019119 ICL 1 Burdock SYM 1 Burdock{}304 ASTR 1 - CLOC 1 24D7-24D7 REF 1 2 DT 1 21 Aug 2003 RESZ 361
ID|FBti0019119
SYM|Burdock{}304
SYN|TE19119
ASTP|FBtp0011417==Burdock
DT|21 Aug 2003
|21 Aug 2003
ICL|Burdock
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Burdock{}304
CLOC|24D7-24D7
LOCB|genomic location inferred from flanking sequence
DBAF|AE003577.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019128 ICL 1 Burdock SYM 1 Burdock{}313 ASTR 1 - CLOC 1 26C3-26C4 REF 1 2 DT 1 21 Aug 2003 RESZ 361
ID|FBti0019128
SYM|Burdock{}313
SYN|TE19128
ASTP|FBtp0011417==Burdock
DT|21 Aug 2003
|21 Aug 2003
ICL|Burdock
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Burdock{}313
CLOC|26C3-26C4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003613.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019132 ICL 1 Burdock SYM 1 Burdock{}320 ASTR 1 - CLOC 1 28A6-28A6 REF 1 2 DT 1 21 Aug 2003 RESZ 361
ID|FBti0019132
SYM|Burdock{}320
SYN|TE19132
ASTP|FBtp0011417==Burdock
DT|21 Aug 2003
|21 Aug 2003
ICL|Burdock
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Burdock{}320
CLOC|28A6-28A6
LOCB|genomic location inferred from flanking sequence
DBAF|AE003617.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019236 ICL 1 Burdock SYM 1 Burdock{}514 ASTR 1 - CLOC 1 39F1-39F1 REF 1 2 DT 1 21 Aug 2003 RESZ 361
ID|FBti0019236
SYM|Burdock{}514
SYN|TE19236
ASTP|FBtp0011417==Burdock
DT|21 Aug 2003
|21 Aug 2003
ICL|Burdock
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Burdock{}514
CLOC|39F1-39F1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003781.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0018881 ICL 1 Burdock SYM 1 Burdock{}664 ASTR 1 - CLOC 1 41F3-41F3 REF 1 2 DT 1 21 Aug 2003 RESZ 361
ID|FBti0018881
SYM|Burdock{}664
SYN|TE18881
ASTP|FBtp0011417==Burdock
DT|21 Aug 2003
|21 Aug 2003
ICL|Burdock
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Burdock{}664
CLOC|41F3-41F3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003786.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0018882 ICL 1 Burdock SYM 1 Burdock{}770 ASTR 1 - CLOC 1 43E18-43E18 REF 1 2 DT 1 21 Aug 2003 RESZ 363
ID|FBti0018882
SYM|Burdock{}770
SYN|TE18882
ASTP|FBtp0011417==Burdock
DT|21 Aug 2003
|21 Aug 2003
ICL|Burdock
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Burdock{}770
CLOC|43E18-43E18
LOCB|genomic location inferred from flanking sequence
DBAF|AE003839.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0018883 ICL 1 Burdock SYM 1 Burdock{}783 ASTR 1 - CLOC 1 45A13-45B1 REF 1 2 DT 1 21 Aug 2003 RESZ 362
ID|FBti0018883
SYM|Burdock{}783
SYN|TE18883
ASTP|FBtp0011417==Burdock
DT|21 Aug 2003
|21 Aug 2003
ICL|Burdock
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Burdock{}783
CLOC|45A13-45B1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003834.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0018884 ICL 1 Burdock SYM 1 Burdock{}836 ASTR 1 - CLOC 1 52E1-52E1 REF 1 2 DT 1 21 Aug 2003 RESZ 361
ID|FBti0018884
SYM|Burdock{}836
SYN|TE18884
ASTP|FBtp0011417==Burdock
DT|21 Aug 2003
|21 Aug 2003
ICL|Burdock
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Burdock{}836
CLOC|52E1-52E1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003808.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019283 ICL 1 Burdock SYM 1 Burdock{}1187 ASTR 1 - CLOC 1 82A1-82A3 REF 1 2 DT 1 21 Aug 2003 RESZ 363
ID|FBti0019283
SYM|Burdock{}1187
SYN|TE19283
ASTP|FBtp0011417==Burdock
DT|21 Aug 2003
|21 Aug 2003
ICL|Burdock
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Burdock{}1187
CLOC|82A1-82A3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003606.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019305 ICL 1 Burdock SYM 1 Burdock{}1221 ASTR 1 - CLOC 1 83A3-83A3 REF 1 2 DT 1 21 Aug 2003 RESZ 363
ID|FBti0019305
SYM|Burdock{}1221
SYN|TE19305
ASTP|FBtp0011417==Burdock
DT|21 Aug 2003
|21 Aug 2003
ICL|Burdock
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Burdock{}1221
CLOC|83A3-83A3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003602.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019408 ICL 1 Burdock SYM 1 Burdock{}1394 ASTR 1 - CLOC 1 92E1-92E1 REF 1 2 DT 1 21 Aug 2003 RESZ 363
ID|FBti0019408
SYM|Burdock{}1394
SYN|TE19408
ASTP|FBtp0011417==Burdock
DT|21 Aug 2003
|21 Aug 2003
ICL|Burdock
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Burdock{}1394
CLOC|92E1-92E1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003729.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0015137 ICL 1 Burdock SYM 1 Burdock{}ctMR21K1 ASTR 1 - CLOC 1 7B4--5 REF 1 2 DT 1 6 Jan 2000 RESZ 467
ID|FBti0015137
SYM|Burdock{}ctMR21K1
ASTP|FBtp0011417==Burdock
DT|6 Jan 2000
|6 Jan 2000
ICL|Burdock
ASGN|FBgn0004198==ct
REFDSR
{
RDID|FBrf0098327
|Ponomarenko et al.
|1997
SYN|Burdock{}ctMR21K1
ASAL|FBal0064922==ctMR21K1
CLOC|7B4--5
|Insertion site
LOCB|Proximity to gene: FBgn0004198==ct
}
REF
{
REFM|FBrf0098327
|Ponomarenko et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014346 ICL 1 Burdock SYM 1 Burdock{}ctMRl1 ASTR 1 - CLOC 1 7B4--5 REF 1 3 DT 1 4 Apr 2003 RESZ 566
ID|FBti0014346
SYM|Burdock{}ctMRl1
ASTP|FBtp0011417==Burdock
DT|4 Apr 2003
|6 Jan 2000
ICL|Burdock
ASGN|FBgn0004198==ct
REFDSR
{
RDID|FBrf0050561
|Tchurikov et al.
|1989
SYN|Burdock{}ctMRl1
ASAL|FBal0002058==ctMRl1
CLOC|7B4--5
|Insertion site
LOCB|Proximity to gene: FBgn0004198==ct
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHC|lethal | recessive
}
REF
{
REFM|FBrf0050561
|Tchurikov et al.
|1989
REFM|FBrf0098741
|Tchurikov et al.
|1988
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014350 ICL 1 Burdock SYM 1 Burdock{}ctMRl8 ASTR 1 - CLOC 1 7B4--5 REF 1 3 DT 1 4 Apr 2003 RESZ 566
ID|FBti0014350
SYM|Burdock{}ctMRl8
ASTP|FBtp0011417==Burdock
DT|4 Apr 2003
|6 Jan 2000
ICL|Burdock
ASGN|FBgn0004198==ct
REFDSR
{
RDID|FBrf0050561
|Tchurikov et al.
|1989
SYN|Burdock{}ctMRl8
ASAL|FBal0002059==ctMRl8
CLOC|7B4--5
|Insertion site
LOCB|Proximity to gene: FBgn0004198==ct
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHC|lethal | recessive
}
REF
{
REFM|FBrf0050561
|Tchurikov et al.
|1989
REFM|FBrf0098741
|Tchurikov et al.
|1988
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014348 ICL 1 Burdock SYM 1 Burdock{}ctMRl37 ASTR 1 - CLOC 1 7B4--5 REF 1 3 DT 1 4 Apr 2003 RESZ 624
ID|FBti0014348
SYM|Burdock{}ctMRl37
ASTP|FBtp0011417==Burdock
DT|4 Apr 2003
|6 Jan 2000
ICL|Burdock
ASGN|FBgn0004198==ct
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|Burdock{}ctMRl37
CLOC|7B4--5
|Insertion site
LOCB|Proximity to gene: FBgn0004198==ct
}
REFDSR
{
RDID|FBrf0098741
|Tchurikov et al.
|1988
ASAL|FBal0002060==ctMRl37
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHC|lethal | recessive
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0098741
|Tchurikov et al.
|1988
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014349 ICL 1 Burdock SYM 1 Burdock{}ctMRl377 ASTR 1 - CLOC 1 7B4--5 REF 1 2 DT 1 6 Jan 2000 RESZ 463
ID|FBti0014349
SYM|Burdock{}ctMRl377
ASTP|FBtp0011417==Burdock
DT|6 Jan 2000
|6 Jan 2000
ICL|Burdock
ASGN|FBgn0004198==ct
REFDSR
{
RDID|FBrf0050561
|Tchurikov et al.
|1989
SYN|Burdock{}ctMRl377
ASAL|FBal0030986==ctMRl377
CLOC|7B4--5
|Insertion site
LOCB|Proximity to gene: FBgn0004198==ct
}
REF
{
REFM|FBrf0050561
|Tchurikov et al.
|1989
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014351 ICL 1 Burdock SYM 1 Burdock{}ctMRlA1 ASTR 1 - CLOC 1 7B4--5 REF 1 3 DT 1 4 Apr 2003 RESZ 569
ID|FBti0014351
SYM|Burdock{}ctMRlA1
ASTP|FBtp0011417==Burdock
DT|4 Apr 2003
|6 Jan 2000
ICL|Burdock
ASGN|FBgn0004198==ct
REFDSR
{
RDID|FBrf0050561
|Tchurikov et al.
|1989
SYN|Burdock{}ctMRlA1
ASAL|FBal0002061==ctMRlA1
CLOC|7B4--5
|Insertion site
LOCB|Proximity to gene: FBgn0004198==ct
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHC|lethal | recessive
}
REF
{
REFM|FBrf0050561
|Tchurikov et al.
|1989
REFM|FBrf0098741
|Tchurikov et al.
|1988
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014352 ICL 1 Burdock SYM 1 Burdock{}ctMRlA12 ASTR 1 - CLOC 1 7B4--5 REF 1 3 DT 1 4 Apr 2003 RESZ 572
ID|FBti0014352
SYM|Burdock{}ctMRlA12
ASTP|FBtp0011417==Burdock
DT|4 Apr 2003
|6 Jan 2000
ICL|Burdock
ASGN|FBgn0004198==ct
REFDSR
{
RDID|FBrf0050561
|Tchurikov et al.
|1989
SYN|Burdock{}ctMRlA12
ASAL|FBal0002062==ctMRlA12
CLOC|7B4--5
|Insertion site
LOCB|Proximity to gene: FBgn0004198==ct
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHC|lethal | recessive
}
REF
{
REFM|FBrf0050561
|Tchurikov et al.
|1989
REFM|FBrf0098741
|Tchurikov et al.
|1988
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014353 ICL 1 Burdock SYM 1 Burdock{}ctMRlB1 ASTR 1 - CLOC 1 7B4--5 REF 1 3 DT 1 4 Apr 2003 RESZ 569
ID|FBti0014353
SYM|Burdock{}ctMRlB1
ASTP|FBtp0011417==Burdock
DT|4 Apr 2003
|6 Jan 2000
ICL|Burdock
ASGN|FBgn0004198==ct
REFDSR
{
RDID|FBrf0050561
|Tchurikov et al.
|1989
SYN|Burdock{}ctMRlB1
ASAL|FBal0002063==ctMRlB1
CLOC|7B4--5
|Insertion site
LOCB|Proximity to gene: FBgn0004198==ct
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHC|lethal | recessive
}
REF
{
REFM|FBrf0050561
|Tchurikov et al.
|1989
REFM|FBrf0098741
|Tchurikov et al.
|1988
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014354 ICL 1 Burdock SYM 1 Burdock{}ctMRlE1 ASTR 1 - CLOC 1 7B4--5 REF 1 3 DT 1 4 Apr 2003 RESZ 569
ID|FBti0014354
SYM|Burdock{}ctMRlE1
ASTP|FBtp0011417==Burdock
DT|4 Apr 2003
|6 Jan 2000
ICL|Burdock
ASGN|FBgn0004198==ct
REFDSR
{
RDID|FBrf0050561
|Tchurikov et al.
|1989
SYN|Burdock{}ctMRlE1
ASAL|FBal0002064==ctMRlE1
CLOC|7B4--5
|Insertion site
LOCB|Proximity to gene: FBgn0004198==ct
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHC|lethal | recessive
}
REF
{
REFM|FBrf0050561
|Tchurikov et al.
|1989
REFM|FBrf0098741
|Tchurikov et al.
|1988
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0025336 ICL 1 Burdock SYM 1 Burdock{}ctMRlK1a ASTR 1 - CLOC 1 7B4--5 REF 1 3 DT 1 7 Jul 2003 RESZ 759
ID|FBti0025336
SYM|Burdock{}ctMRlK1a
SYN|Burdock{}Hercules{}ctMRlK1
ASTP|FBtp0011417==Burdock
DT|7 Jul 2003
|7 Jul 2003
ICL|Burdock
ID2|FBti0014355
ASGN|FBgn0004198==ct
REFDSR
{
RDID|FBrf0050561
|Tchurikov et al.
|1989
SYN|Burdock{}ctMRlK1a
ASAL|FBal0002065==ctMRlK1
MU|hobo activity
CLOC|7B4--5
|Insertion site
LOCB|Proximity to gene: FBgn0004198==ct
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHC|lethal | recessive
CC|One of two insertions associated with this allele; see FBti0025337==Hercules{}ctMRlK1b.
}
REF
{
REFM|FBrf0050561
|Tchurikov et al.
|1989
REFM|FBrf0098741
|Tchurikov et al.
|1988
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014356 ICL 1 Burdock SYM 1 Burdock{}ctMRlL2 ASTR 1 - CLOC 1 7B4--5 REF 1 3 DT 1 4 Apr 2003 RESZ 569
ID|FBti0014356
SYM|Burdock{}ctMRlL2
ASTP|FBtp0011417==Burdock
DT|4 Apr 2003
|6 Jan 2000
ICL|Burdock
ASGN|FBgn0004198==ct
REFDSR
{
RDID|FBrf0050561
|Tchurikov et al.
|1989
SYN|Burdock{}ctMRlL2
ASAL|FBal0002066==ctMRlL2
CLOC|7B4--5
|Insertion site
LOCB|Proximity to gene: FBgn0004198==ct
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHC|lethal | recessive
}
REF
{
REFM|FBrf0050561
|Tchurikov et al.
|1989
REFM|FBrf0098741
|Tchurikov et al.
|1988
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014357 ICL 1 Burdock SYM 1 Burdock{}ctMRlL46 ASTR 1 - CLOC 1 7B4--5 REF 1 3 DT 1 4 Apr 2003 RESZ 572
ID|FBti0014357
SYM|Burdock{}ctMRlL46
ASTP|FBtp0011417==Burdock
DT|4 Apr 2003
|6 Jan 2000
ICL|Burdock
ASGN|FBgn0004198==ct
REFDSR
{
RDID|FBrf0050561
|Tchurikov et al.
|1989
SYN|Burdock{}ctMRlL46
ASAL|FBal0002067==ctMRlL46
CLOC|7B4--5
|Insertion site
LOCB|Proximity to gene: FBgn0004198==ct
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHC|lethal | recessive
}
REF
{
REFM|FBrf0050561
|Tchurikov et al.
|1989
REFM|FBrf0098741
|Tchurikov et al.
|1988
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0025338 ICL 1 Burdock SYM 1 Burdock{}ctMRlLD1a ASTR 1 - CLOC 1 7B4--5 REF 1 3 DT 1 7 Jul 2003 RESZ 764
ID|FBti0025338
SYM|Burdock{}ctMRlLD1a
SYN|Burdock{}Hercules{}ctMRlLD1
ASTP|FBtp0011417==Burdock
DT|7 Jul 2003
|7 Jul 2003
ICL|Burdock
ID2|FBti0014358
ASGN|FBgn0004198==ct
REFDSR
{
RDID|FBrf0050561
|Tchurikov et al.
|1989
SYN|Burdock{}ctMRlLD1a
ASAL|FBal0002068==ctMRlLD1
MU|hobo activity
CLOC|7B4--5
|Insertion site
LOCB|Proximity to gene: FBgn0004198==ct
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHC|lethal | recessive
CC|One of two insertions associated with this allele; see FBti0025339==Hercules{}ctMRlLD1b.
}
REF
{
REFM|FBrf0050561
|Tchurikov et al.
|1989
REFM|FBrf0098741
|Tchurikov et al.
|1988
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014359 ICL 1 Burdock SYM 1 Burdock{}ctMRlLM1 ASTR 1 - CLOC 1 7B4--5 REF 1 3 DT 1 4 Apr 2003 RESZ 504
ID|FBti0014359
SYM|Burdock{}ctMRlLM1
ASTP|FBtp0011417==Burdock
DT|4 Apr 2003
|6 Jan 2000
ICL|Burdock
ASGN|FBgn0004198==ct
REFDSR
{
RDID|FBrf0050561
|Tchurikov et al.
|1989
SYN|Burdock{}ctMRlLM1
ASAL|FBal0002069==ctMRlLM1
CLOC|7B4--5
|Insertion site
LOCB|Proximity to gene: FBgn0004198==ct
}
REF
{
REFM|FBrf0050561
|Tchurikov et al.
|1989
REFM|FBrf0098741
|Tchurikov et al.
|1988
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014616 ICL 1 Calypso SYM 1 Calypso{}ry301 ASTR 1 - CLOC 1 87D9 REF 1 2 DT 1 6 Jan 2000 RESZ 454
ID|FBti0014616
SYM|Calypso{}ry301
ASTP|FBtp0011418==Calypso
DT|6 Jan 2000
|6 Jan 2000
ICL|Calypso
ASGN|FBgn0003308==ry
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|Calypso{}ry301
ASAL|FBal0014995==ry301
CLOC|87D9
|Insertion site
LOCB|Proximity to gene: FBgn0003308==ry
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0014995==ry301
REFDSR
{
RDID|FBrf0057531
|Hilliker et al.
|1992
PHP|Homozygotes are hypersensitive to paraquat. FBal0014995==ry301
| FBal0015933==Sodn1 double
|homozygotes die during late metamorphosis and during the process of
|eclosion.
}
REF
{
REFM|FBrf0057531
|Hilliker et al.
|1992
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0018885 ICL 1 Circe SYM 1 Circe{}737 ASTR 1 - CLOC 1 42A19-42B1 REF 1 2 DT 1 21 Aug 2003 RESZ 354
ID|FBti0018885
SYM|Circe{}737
SYN|TE18885
ASTP|FBtp0012709==Circe
DT|21 Aug 2003
|21 Aug 2003
ICL|Circe
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Circe{}737
CLOC|42A19-42B1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003789.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0018886 ICL 1 Circe SYM 1 Circe{}753 ASTR 1 - CLOC 1 42B2-42B2 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0018886
SYM|Circe{}753
SYN|TE18886
ASTP|FBtp0012709==Circe
DT|21 Aug 2003
|21 Aug 2003
ICL|Circe
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Circe{}753
CLOC|42B2-42B2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003789.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0013043 ICL 1 copia SYM 1 copia{3'LTR}wa59k1 ASTR 1 - CLOC 1 3C1 REF 1 11 DT 1 14 Sep 1999 RESZ 871
ID|FBti0013043
SYM|copia{3'LTR}wa59k1
SYN|copia{3'LTR}wa59k1
ASTP|FBtp0002767==copia{3'LTR}
DT|14 Sep 1999
|14 Sep 1999
ICL|copia
ASGN|FBgn0003996==w
REFDSR
{
RDID|FBrf0043247
|Carbonare and Gehring
|1985
SYN|copia{3'LTR}wa59k1
ASAL|FBal0018348==wa59k1
MU|X ray
CLOC|3C1
|Insertion site
LOCB|Proximity to gene: FBgn0003996==w
}
REF
{
REFM|FBrf0043247
|Carbonare and Gehring
|1985
REFM|FBrf0048200
|Mount et al.
|1988
REFM|FBrf0049880
|Birchler and Hiebert
|1989
REFM|FBrf0054158
|Rabinow et al.
|1991
REFM|FBrf0054964
|Kurkulos et al.
|1991
REFM|FBrf0058584
|Rabinow et al.
|1993
REFM|FBrf0076540
|Csink et al.
|1994
REFM|FBrf0086910
|Bhadra and Birchler
|1996
REFM|FBrf0094158
|Bhadra et al.
|1997
REFM|FBrf0094159
|Bhadra et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0018348==wa59k1
REFDSR
{
RDID|FBrf0043247
|Carbonare and Gehring
|1985
PHP|Eye pigment is restored to 80% of wild type levels.
PHM|pigment cell
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye color: darker than FBal0018195==wa, with more brown pigment.
PHM|pigment cell
}
REF
{
REFM|FBrf0043247
|Carbonare and Gehring
|1985
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0026992 ICL 1 copia{P SYM 1 copia{P{lacW}}Rep116-11-36 ASTR 1 - CLOC 1 - REF 1 2 DT 1 8 Jul 2003 RESZ 439
ID|FBti0026992
SYM|copia{P{lacW}}Rep116-11-36
SYN|16-11-36
|16-11
ASTP|FBtp0000204==P{lacW}
DT|8 Jul 2003
|8 Jul 2003
ICL|copia{P
PRG|FBti0026991==P{lacW}P228
ASGN|FBgn0024732==Rep1
REFDSR
{
RDID|FBrf0152010
|Mukae et al.
|2002
SYN|16-11-36
|16-11
ASAL|FBal0141564==Rep116-11-36
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0152010
|Mukae et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014805 ICL 1 roo SYM 1 copia{roo{}}wric ASTR 1 - CLOC 1 3C1 REF 1 7 DT 1 1 Mar 2004 RESZ 790
ID|FBti0014805
SYM|copia{roo{}}wric
SYN|roo{}wric
DT|1 Mar 2004
|6 Jan 2000
ICL|roo
ASGN|FBgn0003996==w
REFDSR
{
RDID|FBrf0073744
|Lim and Simmons
|1994
SYN|roo{}wric
ASAL|FBal0018294==wric
MU|spontaneous
CLOC|3C1
|Insertion site
LOCB|Proximity to gene: FBgn0003996==w
}
REFDSR
{
RDID|FBrf0152010
|Mukae et al.
|2002
CC|Nested insertion of FBgn0000155==roo element into FBgn0000349==copia element.
}
REF
{
REFM|FBrf0073744
|Lim and Simmons
|1994
REFM|FBrf0076540
|Csink et al.
|1994
REFM|FBrf0086910
|Bhadra and Birchler
|1996
REFM|FBrf0094158
|Bhadra et al.
|1997
REFM|FBrf0094159
|Bhadra et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0152010
|Mukae et al.
|2002
}
ALESR
{
ASYM|FBal0018294==wric
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye color: like FBal0018195==wa.
PHM|pigment cell
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0019568 ICL 1 copia SYM 1 copia{}49 ASTR 1 - CLOC 1 4B4-4B5 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019568
SYM|copia{}49
SYN|TE19568
ASTP|FBtp0011420==copia
DT|21 Aug 2003
|21 Aug 2003
ICL|copia
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|copia{}49
CLOC|4B4-4B5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003430.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019586 ICL 1 copia SYM 1 copia{}67 ASTR 1 - CLOC 1 5C8-5C9 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019586
SYM|copia{}67
SYN|TE19586
ASTP|FBtp0011420==copia
DT|21 Aug 2003
|21 Aug 2003
ICL|copia
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|copia{}67
CLOC|5C8-5C9
LOCB|genomic location inferred from flanking sequence
DBAF|AE003436.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019050 ICL 1 copia SYM 1 copia{}122 ASTR 1 - CLOC 1 12D2-12D2 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019050
SYM|copia{}122
SYN|TE19050
ASTP|FBtp0011420==copia
DT|21 Aug 2003
|21 Aug 2003
ICL|copia
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|copia{}122
CLOC|12D2-12D2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003494.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019059 ICL 1 copia SYM 1 copia{}131 ASTR 1 - CLOC 1 12F4-12F4 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019059
SYM|copia{}131
SYN|TE19059
ASTP|FBtp0011420==copia
DT|21 Aug 2003
|21 Aug 2003
ICL|copia
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|copia{}131
CLOC|12F4-12F4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003497.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019110 ICL 1 copia SYM 1 copia{}293 ASTR 1 - CLOC 1 22E1-22E1 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019110
SYM|copia{}293
SYN|TE19110
ASTP|FBtp0011420==copia
DT|21 Aug 2003
|21 Aug 2003
ICL|copia
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|copia{}293
CLOC|22E1-22E1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003583.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019113 ICL 1 copia SYM 1 copia{}298 ASTR 1 - CLOC 1 23D1-23D1 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019113
SYM|copia{}298
SYN|TE19113
ASTP|FBtp0011420==copia
DT|21 Aug 2003
|21 Aug 2003
ICL|copia
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|copia{}298
CLOC|23D1-23D1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003581.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019117 ICL 1 copia SYM 1 copia{}302 ASTR 1 - CLOC 1 24A4-24A4 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019117
SYM|copia{}302
SYN|TE19117
ASTP|FBtp0011420==copia
DT|21 Aug 2003
|21 Aug 2003
ICL|copia
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|copia{}302
CLOC|24A4-24A4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003579.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019136 ICL 1 copia SYM 1 copia{}324 ASTR 1 - CLOC 1 28D6-28D7 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019136
SYM|copia{}324
SYN|TE19136
ASTP|FBtp0011420==copia
DT|21 Aug 2003
|21 Aug 2003
ICL|copia
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|copia{}324
CLOC|28D6-28D7
LOCB|genomic location inferred from flanking sequence
DBAF|AE003619.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019151 ICL 1 copia SYM 1 copia{}342 ASTR 1 - CLOC 1 32F3-32F3 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019151
SYM|copia{}342
SYN|TE19151
ASTP|FBtp0011420==copia
DT|21 Aug 2003
|21 Aug 2003
ICL|copia
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|copia{}342
CLOC|32F3-32F3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003633.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019176 ICL 1 copia SYM 1 copia{}372 ASTR 1 - CLOC 1 35B6-35B6 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019176
SYM|copia{}372
SYN|TE19176
ASTP|FBtp0011420==copia
DT|21 Aug 2003
|21 Aug 2003
ICL|copia
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|copia{}372
CLOC|35B6-35B6
LOCB|genomic location inferred from flanking sequence
DBAF|AE003645.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019183 ICL 1 copia SYM 1 copia{}387 ASTR 1 - CLOC 1 35E4-35E4 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019183
SYM|copia{}387
SYN|TE19183
ASTP|FBtp0011420==copia
DT|21 Aug 2003
|21 Aug 2003
ICL|copia
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|copia{}387
CLOC|35E4-35E4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003650.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019193 ICL 1 copia SYM 1 copia{}399 ASTR 1 - CLOC 1 36D1-36D2 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019193
SYM|copia{}399
SYN|TE19193
ASTP|FBtp0011420==copia
DT|21 Aug 2003
|21 Aug 2003
ICL|copia
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|copia{}399
CLOC|36D1-36D2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003656.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019792 ICL 1 copia SYM 1 copia{}434 ASTR 1 - CLOC 1 38C2-38C2 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019792
SYM|copia{}434
SYN|TE19792
ASTP|FBtp0011420==copia
DT|21 Aug 2003
|21 Aug 2003
ICL|copia
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|copia{}434
CLOC|38C2-38C2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003665.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019794 ICL 1 copia SYM 1 copia{}436 ASTR 1 - CLOC 1 38C2-38C2 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019794
SYM|copia{}436
SYN|TE19794
ASTP|FBtp0011420==copia
DT|21 Aug 2003
|21 Aug 2003
ICL|copia
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|copia{}436
CLOC|38C2-38C2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003666.5
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019796 ICL 1 copia SYM 1 copia{}438 ASTR 1 - CLOC 1 38C2-38C2 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019796
SYM|copia{}438
SYN|TE19796
ASTP|FBtp0011420==copia
DT|21 Aug 2003
|21 Aug 2003
ICL|copia
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|copia{}438
CLOC|38C2-38C2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003666.5
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019822 ICL 1 copia SYM 1 copia{}466 ASTR 1 - CLOC 1 38C3-38C3 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019822
SYM|copia{}466
SYN|TE19822
ASTP|FBtp0011420==copia
DT|21 Aug 2003
|21 Aug 2003
ICL|copia
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|copia{}466
CLOC|38C3-38C3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003666.5
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019250 ICL 1 copia SYM 1 copia{}539 ASTR 1 - CLOC 1 40F3-40F3 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0019250
SYM|copia{}539
SYN|TE19250
ASTP|FBtp0011420==copia
DT|21 Aug 2003
|21 Aug 2003
ICL|copia
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|copia{}539
CLOC|40F3-40F3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003783.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0018967 ICL 1 copia SYM 1 copia{}631 ASTR 1 - CLOC 1 41F1-41F1 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0018967
SYM|copia{}631
SYN|TE18967
ASTP|FBtp0011420==copia
DT|21 Aug 2003
|21 Aug 2003
ICL|copia
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|copia{}631
CLOC|41F1-41F1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003787.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0018968 ICL 1 copia SYM 1 copia{}837 ASTR 1 - CLOC 1 53C7-53C7 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0018968
SYM|copia{}837
SYN|TE18968
ASTP|FBtp0011420==copia
DT|21 Aug 2003
|21 Aug 2003
ICL|copia
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|copia{}837
CLOC|53C7-53C7
LOCB|genomic location inferred from flanking sequence
DBAF|AE003806.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0018969 ICL 1 copia SYM 1 copia{}840 ASTR 1 - CLOC 1 54B1-54B1 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0018969
SYM|copia{}840
SYN|TE18969
ASTP|FBtp0011420==copia
DT|21 Aug 2003
|21 Aug 2003
ICL|copia
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|copia{}840
CLOC|54B1-54B1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003804.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0018970 ICL 1 copia SYM 1 copia{}860 ASTR 1 - CLOC 1 56F5-56F5 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0018970
SYM|copia{}860
SYN|TE18970
ASTP|FBtp0011420==copia
DT|21 Aug 2003
|21 Aug 2003
ICL|copia
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|copia{}860
CLOC|56F5-56F5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003794.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020021 ICL 1 copia SYM 1 copia{}910 ASTR 1 - CLOC 1 62C3-62C4 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020021
SYM|copia{}910
SYN|TE20021
ASTP|FBtp0011420==copia
DT|21 Aug 2003
|21 Aug 2003
ICL|copia
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|copia{}910
CLOC|62C3-62C4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003473.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020031 ICL 1 copia SYM 1 copia{}920 ASTR 1 - CLOC 1 63E4-63E4 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020031
SYM|copia{}920
SYN|TE20031
ASTP|FBtp0011420==copia
DT|21 Aug 2003
|21 Aug 2003
ICL|copia
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|copia{}920
CLOC|63E4-63E4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003478.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020099 ICL 1 copia SYM 1 copia{}988 ASTR 1 - CLOC 1 69F2-69F2 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020099
SYM|copia{}988
SYN|TE20099
ASTP|FBtp0011420==copia
DT|21 Aug 2003
|21 Aug 2003
ICL|copia
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|copia{}988
CLOC|69F2-69F2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003539.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020108 ICL 1 copia SYM 1 copia{}997 ASTR 1 - CLOC 1 70E1-70E1 REF 1 2 DT 1 21 Aug 2003 RESZ 353
ID|FBti0020108
SYM|copia{}997
SYN|TE20108
ASTP|FBtp0011420==copia
DT|21 Aug 2003
|21 Aug 2003
ICL|copia
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|copia{}997
CLOC|70E1-70E1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003534.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0020127 ICL 1 copia SYM 1 copia{}1016 ASTR 1 - CLOC 1 73B6-73B7 REF 1 2 DT 1 21 Aug 2003 RESZ 355
ID|FBti0020127
SYM|copia{}1016
SYN|TE20127
ASTP|FBtp0011420==copia
DT|21 Aug 2003
|21 Aug 2003
ICL|copia
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|copia{}1016
CLOC|73B6-73B7
LOCB|genomic location inferred from flanking sequence
DBAF|AE003526.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019364 ICL 1 copia SYM 1 copia{}1349 ASTR 1 - CLOC 1 87D4-87D4 REF 1 2 DT 1 21 Aug 2003 RESZ 355
ID|FBti0019364
SYM|copia{}1349
SYN|TE19364
ASTP|FBtp0011420==copia
DT|21 Aug 2003
|21 Aug 2003
ICL|copia
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|copia{}1349
CLOC|87D4-87D4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003698.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019405 ICL 1 copia SYM 1 copia{}1391 ASTR 1 - CLOC 1 92D1-92D1 REF 1 2 DT 1 21 Aug 2003 RESZ 355
ID|FBti0019405
SYM|copia{}1391
SYN|TE19405
ASTP|FBtp0011420==copia
DT|21 Aug 2003
|21 Aug 2003
ICL|copia
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|copia{}1391
CLOC|92D1-92D1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003729.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019468 ICL 1 copia SYM 1 copia{}1466 ASTR 1 - CLOC 1 100B5-100B5 REF 1 2 DT 1 21 Aug 2003 RESZ 357
ID|FBti0019468
SYM|copia{}1466
SYN|TE19468
ASTP|FBtp0011420==copia
DT|21 Aug 2003
|21 Aug 2003
ICL|copia
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|copia{}1466
CLOC|100B5-100B5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003777.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019469 ICL 1 copia SYM 1 copia{}1467 ASTR 1 - CLOC 1 100B6-100B6 REF 1 2 DT 1 21 Aug 2003 RESZ 357
ID|FBti0019469
SYM|copia{}1467
SYN|TE19469
ASTP|FBtp0011420==copia
DT|21 Aug 2003
|21 Aug 2003
ICL|copia
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|copia{}1467
CLOC|100B6-100B6
LOCB|genomic location inferred from flanking sequence
DBAF|AE003778.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014084 ICL 1 copia SYM 1 copia{}AdhRI-42 ASTR 1 - CLOC 1 35B3 REF 1 4 DT 1 6 Jan 2000 RESZ 568
ID|FBti0014084
SYM|copia{}AdhRI-42
ASTP|FBtp0011420==copia
DT|6 Jan 2000
|6 Jan 2000
ICL|copia
ASGN|FBgn0000055==Adh
REFDSR
{
RDID|FBrf0049930
|Strand and McDonald
|1989
SYN|copia{}AdhRI-42
ASAL|FBal0000376==AdhRI-42
MU|natural population
CLOC|35B3
|Insertion site
LOCB|Proximity to gene: FBgn0000055==Adh
}
REF
{
REFM|FBrf0049930
|Strand and McDonald
|1989
REFM|FBrf0081965
|Dunn and Laurie
|1995
REFM|FBrf0093378
|Brogna and Ashburner
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014098 ICL 1 copia SYM 1 copia{}Bx46 ASTR 1 - CLOC 1 17C3--4 REF 1 2 DT 1 6 Jan 2000 RESZ 440
ID|FBti0014098
SYM|copia{}Bx46
ASTP|FBtp0011420==copia
DT|6 Jan 2000
|6 Jan 2000
ICL|copia
ASGN|FBgn0000242==Bx
REFDSR
{
RDID|FBrf0058584
|Rabinow et al.
|1993
SYN|copia{}Bx46
ASAL|FBal0001437==Bx46
CLOC|17C3--4
|Insertion site
LOCB|Proximity to gene: FBgn0000242==Bx
}
REF
{
REFM|FBrf0058584
|Rabinow et al.
|1993
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0001437==Bx46
REFDSR
{
RDID|FBrf0058584
|Rabinow et al.
|1993
PHP|Loss of posterior wing margins.
PHM|wing
}
REF
{
REFM|FBrf0058584
|Rabinow et al.
|1993
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014391 ICL 1 copia SYM 1 copia{}ctlS1 ASTR 1 - CLOC 1 7B4--5 REF 1 4 DT 1 6 Jan 2000 RESZ 706
ID|FBti0014391
SYM|copia{}ctlS1
ASTP|FBtp0011420==copia
DT|6 Jan 2000
|6 Jan 2000
ICL|copia
ASGN|FBgn0004198==ct
REFDSR
{
RDID|FBrf0051828
|Blochlinger et al.
|1990
PHC|lethal
}
REFDSR
{
RDID|FBrf0054133
|Liu et al.
|1991
PHC|lethal
}
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|copia{}ctlS1
ASAL|FBal0002040==ctlS1
CLOC|7B4--5
|Insertion site
LOCB|Proximity to gene: FBgn0004198==ct
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHC|lethal
}
REF
{
REFM|FBrf0051828
|Blochlinger et al.
|1990
REFM|FBrf0054133
|Liu et al.
|1991
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0002040==ctlS1
REFDSR
{
RDID|FBrf0054133
|Liu et al.
|1991
PHP|Homozygous embryos lack Malpighian tubules and the gut wall is 3--4
|fold thicker than wild type at the junction of the posterior and anterior
|midgut.
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|a member of cut Lethal II group, maps
|proximal to FBal0001952==ctC145 (Jack, 1985). Not suppressed by
|FBal0016319==su(Hw)2 (Schalet). FBal0002040==ctlS1/+
| males, frequently show
|thoracic protuberances (Schalet).
}
REF
{
REFM|FBrf0054133
|Liu et al.
|1991
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014394 ICL 1 copia SYM 1 copia{}ctns ASTR 1 - CLOC 1 7B4--5 REF 1 2 DT 1 6 Jan 2000 RESZ 451
ID|FBti0014394
SYM|copia{}ctns
ASTP|FBtp0011420==copia
DT|6 Jan 2000
|6 Jan 2000
ICL|copia
ASGN|FBgn0004198==ct
REFDSR
{
RDID|FBrf0051869
|Rabinow and Birchler
|1990
SYN|copia{}ctns
ASAL|FBal0002095==ctns
CLOC|7B4--5
|Insertion site
LOCB|Proximity to gene: FBgn0004198==ct
}
REF
{
REFM|FBrf0051869
|Rabinow and Birchler
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0002095==ctns
REFDSR
{
RDID|FBrf0033190
|Johnson and Judd
|1979
PHP|Notched wings.
PHM|wing
}
REFDSR
{
RDID|FBrf0053813
|Jack et al.
|1991
PHP|Adult wing margin has gaps at the tip.
PHM|wing
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|weak allele
}
REF
{
REFM|FBrf0033190
|Johnson and Judd
|1979
REFM|FBrf0053813
|Jack et al.
|1991
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014463 ICL 1 copia SYM 1 copia{}fs(1)h17 ASTR 1 - CLOC 1 7D3--5 REF 1 4 DT 1 6 Jan 2000 RESZ 692
ID|FBti0014463
SYM|copia{}fs(1)h17
ASTP|FBtp0011420==copia
DT|6 Jan 2000
|6 Jan 2000
ICL|copia
ASGN|FBgn0004656==fs(1)h
REFDSR
{
RDID|FBrf0044139
|Digan et al.
|1986
PHC|lethal | larval | male
}
REFDSR
{
RDID|FBrf0045066
|Schalet
|1986
PHC|lethal | recessive
}
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|copia{}fs(1)h17
ASAL|FBal0004294==fs(1)h17
MU|spontaneous
CLOC|7D3--5
|Insertion site
LOCB|Proximity to gene: FBgn0004656==fs(1)h
}
REF
{
REFM|FBrf0044139
|Digan et al.
|1986
REFM|FBrf0045066
|Schalet
|1986
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0004294==fs(1)h17
REFDSR
{
RDID|FBrf0044139
|Digan et al.
|1986
PHP|Males carrying FBal0004294==fs(1)h17 die during larval stages.
}
REF
{
REFM|FBrf0044139
|Digan et al.
|1986
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014861 ICL 1 copia SYM 1 copia{}ovoD1R1 ASTR 1 - CLOC 1 4E2 REF 1 2 DT 1 6 Jan 2000 RESZ 441
ID|FBti0014861
SYM|copia{}ovoD1R1
ASTP|FBtp0011420==copia
DT|6 Jan 2000
|6 Jan 2000
ICL|copia
ASGN|FBgn0003028==ovo
REFDSR
{
RDID|FBrf0076503
|Song et al.
|1994
SYN|copia{}ovoD1R1
ASAL|FBal0039716==ovoD1R1
CLOC|4E2
|Insertion site
LOCB|Proximity to gene: FBgn0003028==ovo
}
REF
{
REFM|FBrf0076503
|Song et al.
|1994
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014868 ICL 1 copia SYM 1 copia{}ovoD1R2 ASTR 1 - CLOC 1 4E2 REF 1 2 DT 1 6 Jan 2000 RESZ 441
ID|FBti0014868
SYM|copia{}ovoD1R2
ASTP|FBtp0011420==copia
DT|6 Jan 2000
|6 Jan 2000
ICL|copia
ASGN|FBgn0003028==ovo
REFDSR
{
RDID|FBrf0076503
|Song et al.
|1994
SYN|copia{}ovoD1R2
ASAL|FBal0039723==ovoD1R2
CLOC|4E2
|Insertion site
LOCB|Proximity to gene: FBgn0003028==ovo
}
REF
{
REFM|FBrf0076503
|Song et al.
|1994
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014869 ICL 1 copia SYM 1 copia{}ovoD1R3 ASTR 1 - CLOC 1 4E2 REF 1 2 DT 1 6 Jan 2000 RESZ 441
ID|FBti0014869
SYM|copia{}ovoD1R3
ASTP|FBtp0011420==copia
DT|6 Jan 2000
|6 Jan 2000
ICL|copia
ASGN|FBgn0003028==ovo
REFDSR
{
RDID|FBrf0076503
|Song et al.
|1994
SYN|copia{}ovoD1R3
ASAL|FBal0039724==ovoD1R3
CLOC|4E2
|Insertion site
LOCB|Proximity to gene: FBgn0003028==ovo
}
REF
{
REFM|FBrf0076503
|Song et al.
|1994
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014871 ICL 1 copia SYM 1 copia{}ovoD1R6 ASTR 1 - CLOC 1 4E2 REF 1 2 DT 1 6 Jan 2000 RESZ 441
ID|FBti0014871
SYM|copia{}ovoD1R6
ASTP|FBtp0011420==copia
DT|6 Jan 2000
|6 Jan 2000
ICL|copia
ASGN|FBgn0003028==ovo
REFDSR
{
RDID|FBrf0076503
|Song et al.
|1994
SYN|copia{}ovoD1R6
ASAL|FBal0039726==ovoD1R6
CLOC|4E2
|Insertion site
LOCB|Proximity to gene: FBgn0003028==ovo
}
REF
{
REFM|FBrf0076503
|Song et al.
|1994
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014862 ICL 1 copia SYM 1 copia{}ovoD1R10 ASTR 1 - CLOC 1 4E2 REF 1 2 DT 1 6 Jan 2000 RESZ 444
ID|FBti0014862
SYM|copia{}ovoD1R10
ASTP|FBtp0011420==copia
DT|6 Jan 2000
|6 Jan 2000
ICL|copia
ASGN|FBgn0003028==ovo
REFDSR
{
RDID|FBrf0076503
|Song et al.
|1994
SYN|copia{}ovoD1R10
ASAL|FBal0039717==ovoD1R10
CLOC|4E2
|Insertion site
LOCB|Proximity to gene: FBgn0003028==ovo
}
REF
{
REFM|FBrf0076503
|Song et al.
|1994
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014864 ICL 1 copia SYM 1 copia{}ovoD1R12 ASTR 1 - CLOC 1 4E2 REF 1 2 DT 1 6 Jan 2000 RESZ 444
ID|FBti0014864
SYM|copia{}ovoD1R12
ASTP|FBtp0011420==copia
DT|6 Jan 2000
|6 Jan 2000
ICL|copia
ASGN|FBgn0003028==ovo
REFDSR
{
RDID|FBrf0076503
|Song et al.
|1994
SYN|copia{}ovoD1R12
ASAL|FBal0039719==ovoD1R12
CLOC|4E2
|Insertion site
LOCB|Proximity to gene: FBgn0003028==ovo
}
REF
{
REFM|FBrf0076503
|Song et al.
|1994
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014865 ICL 1 copia SYM 1 copia{}ovoD1R13 ASTR 1 - CLOC 1 4E2 REF 1 2 DT 1 6 Jan 2000 RESZ 444
ID|FBti0014865
SYM|copia{}ovoD1R13
ASTP|FBtp0011420==copia
DT|6 Jan 2000
|6 Jan 2000
ICL|copia
ASGN|FBgn0003028==ovo
REFDSR
{
RDID|FBrf0076503
|Song et al.
|1994
SYN|copia{}ovoD1R13
ASAL|FBal0039720==ovoD1R13
CLOC|4E2
|Insertion site
LOCB|Proximity to gene: FBgn0003028==ovo
}
REF
{
REFM|FBrf0076503
|Song et al.
|1994
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0002484 ICL 1 copia SYM 1 copia{}ovoD1rSHD90 ASTR 1 - CLOC 1 4E2 REF 1 2 DT 1 4 Feb 2000 RESZ 467
ID|FBti0002484
SYM|copia{}ovoD1rSHD90
ASTP|FBtp0011420==copia
DT|4 Feb 2000
|21 Mar 1997
ICL|copia
ASGN|FBgn0003028==ovo
REFDSR
{
RDID|FBrf0049605
|Mevel-Ninio et al.
|1989
ASAL|FBal0032368==ovoD1rSHD90
CLOC|4E2
|Insertion site
LOCB|Proximity to gene: FBgn0003028==ovo
PHC|female sterile | recessive
}
REF
{
REFM|FBrf0049605
|Mevel-Ninio et al.
|1989
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0032368==ovoD1rSHD90
REFDSR
{
RDID|FBrf0049605
|Mevel-Ninio et al.
|1989
PHP|Hemizygotes have one functioning ovary.
}
REF
{
REFM|FBrf0049605
|Mevel-Ninio et al.
|1989
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0002485 ICL 1 copia SYM 1 copia{}ovoD1rSHD91 ASTR 1 - CLOC 1 4E2 REF 1 2 DT 1 4 Feb 2000 RESZ 467
ID|FBti0002485
SYM|copia{}ovoD1rSHD91
ASTP|FBtp0011420==copia
DT|4 Feb 2000
|21 Mar 1997
ICL|copia
ASGN|FBgn0003028==ovo
REFDSR
{
RDID|FBrf0049605
|Mevel-Ninio et al.
|1989
ASAL|FBal0032369==ovoD1rSHD91
CLOC|4E2
|Insertion site
LOCB|Proximity to gene: FBgn0003028==ovo
PHC|female sterile | recessive
}
REF
{
REFM|FBrf0049605
|Mevel-Ninio et al.
|1989
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0032369==ovoD1rSHD91
REFDSR
{
RDID|FBrf0049605
|Mevel-Ninio et al.
|1989
PHP|Hemizygotes have one functioning ovary.
}
REF
{
REFM|FBrf0049605
|Mevel-Ninio et al.
|1989
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0002486 ICL 1 copia SYM 1 copia{}ovoD1rSHD93 ASTR 1 - CLOC 1 4E2 REF 1 2 DT 1 4 Feb 2000 RESZ 467
ID|FBti0002486
SYM|copia{}ovoD1rSHD93
ASTP|FBtp0011420==copia
DT|4 Feb 2000
|21 Mar 1997
ICL|copia
ASGN|FBgn0003028==ovo
REFDSR
{
RDID|FBrf0049605
|Mevel-Ninio et al.
|1989
ASAL|FBal0032370==ovoD1rSHD93
CLOC|4E2
|Insertion site
LOCB|Proximity to gene: FBgn0003028==ovo
PHC|female sterile | recessive
}
REF
{
REFM|FBrf0049605
|Mevel-Ninio et al.
|1989
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0032370==ovoD1rSHD93
REFDSR
{
RDID|FBrf0049605
|Mevel-Ninio et al.
|1989
PHP|Hemizygotes have one functioning ovary.
}
REF
{
REFM|FBrf0049605
|Mevel-Ninio et al.
|1989
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014566 ICL 1 copia SYM 1 copia{}ovoD1rv44 ASTR 1 - CLOC 1 4E2 REF 1 2 DT 1 6 Jan 2000 RESZ 459
ID|FBti0014566
SYM|copia{}ovoD1rv44
ASTP|FBtp0011420==copia
DT|6 Jan 2000
|6 Jan 2000
ICL|copia
ASGN|FBgn0003028==ovo
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|copia{}ovoD1rv44
ASAL|FBal0013421==ovoD1rv44
CLOC|4E2
|Insertion site
LOCB|Proximity to gene: FBgn0003028==ovo
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0013421==ovoD1rv44
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
PHP|Phenotypic category: svb-.
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0002487 ICL 1 copia SYM 1 copia{}ovoD3rv56 ASTR 1 - CLOC 1 4E2 REF 1 2 DT 1 4 Feb 2000 RESZ 463
ID|FBti0002487
SYM|copia{}ovoD3rv56
ASTP|FBtp0011420==copia
DT|4 Feb 2000
|21 Mar 1997
ICL|copia
ASGN|FBgn0003028==ovo
REFDSR
{
RDID|FBrf0049605
|Mevel-Ninio et al.
|1989
ASAL|FBal0013433==ovoD3rv56
CLOC|4E2
|Insertion site
LOCB|Proximity to gene: FBgn0003028==ovo
PHC|female sterile | recessive
}
REF
{
REFM|FBrf0049605
|Mevel-Ninio et al.
|1989
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0013433==ovoD3rv56
REFDSR
{
RDID|FBrf0049605
|Mevel-Ninio et al.
|1989
PHP|Hemizygotes exhibit extreme atrophy of the ovaries.
PHM|ovary
}
REF
{
REFM|FBrf0049605
|Mevel-Ninio et al.
|1989
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014614 ICL 1 copia SYM 1 copia{}ry2101 ASTR 1 - CLOC 1 87D9 REF 1 2 DT 1 6 Jan 2000 RESZ 473
ID|FBti0014614
SYM|copia{}ry2101
ASTP|FBtp0011420==copia
DT|6 Jan 2000
|6 Jan 2000
ICL|copia
ASGN|FBgn0003308==ry
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|copia{}ry2101
ASAL|FBal0015054==ry2101
MU|PM hybrid dysgenesis
CLOC|87D9
|Insertion site
LOCB|Proximity to gene: FBgn0003308==ry
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0002416 ICL 1 copia SYM 1 copia{}scHw-Ua ASTR 1 - CLOC 1 1A8 REF 1 4 DT 1 4 Feb 2000 RESZ 506
ID|FBti0002416
SYM|copia{}scHw-Ua
ASTP|FBtp0011420==copia
DT|4 Feb 2000
|21 Mar 1997
ICL|copia
ASGN|FBgn0004170==sc
REFDSR
{
RDID|FBrf0043905
|Campuzano et al.
|1986
ASAL|FBal0015253==scHw-Ua
CLOC|1A8
|Insertion site
LOCB|Proximity to gene: FBgn0004170==sc
}
REF
{
REFM|FBrf0043905
|Campuzano et al.
|1986
REFM|FBrf0051869
|Rabinow and Birchler
|1990
REFM|FBrf0058584
|Rabinow et al.
|1993
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0015253==scHw-Ua
REFDSR
{
RDID|FBrf0043905
|Campuzano et al.
|1986
PHP|Differentiation of extra chaetes on the cuticle.
}
REFDSR
{
RDID|FBrf0045360
|Garcia Alonso and Garcia-Bellido
|1986
PHP|Weak FBal0000167==acHw-1 phenotype in heterozygous females.
| Phenotype only slightly
|enhanced by suppressing the pre-existing FBal0015189==sc1 allele with
|FBal0016319==su(Hw)2.
}
REFDSR
{
RDID|FBrf0051869
|Rabinow and Birchler
|1990
PHP|See a partial suppression of the sc phenotype. Mutations in su(f),
|E(wa) and mw had no effect on the phenotype.
}
REFDSR
{
RDID|FBrf0058584
|Rabinow et al.
|1993
PHP|FBgn0000480==Doa mutants cause suppression of FBal0015253==scHw-Ua and
| result in loss of
|scutellar bristles.
}
REF
{
REFM|FBrf0043905
|Campuzano et al.
|1986
REFM|FBrf0045360
|Garcia Alonso and Garcia-Bellido
|1986
REFM|FBrf0051869
|Rabinow and Birchler
|1990
REFM|FBrf0058584
|Rabinow et al.
|1993
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0012680 ICL 1 copia SYM 1 copia{}toc-BDGP ASTR 1 - CLOC 1 23D1--3 REF 1 2 DT 1 4 Feb 2000 RESZ 397
ID|FBti0012680
SYM|copia{}toc-BDGP
SYN|copia{}BDGP1
ASTP|FBtp0011420==copia
DT|4 Feb 2000
|25 Jun 1999
ICL|copia
ASGN|FBgn0015600==toc
ARGS|FBgn0015600
REFDSR
{
RDID|FBrf0104946
|FlyBase
|1996-
CLOC|23D1--3
|Insertion site
LOCB|Proximity to gene: FBgn0015600==toc
}
REF
{
REFM|FBrf0104946
|FlyBase
|1996-
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014765 ICL 1 copia SYM 1 copia{}w60 ASTR 1 - CLOC 1 3C1 REF 1 2 DT 1 6 Jan 2000 RESZ 452
ID|FBti0014765
SYM|copia{}w60
ASTP|FBtp0011420==copia
DT|6 Jan 2000
|6 Jan 2000
ICL|copia
ASGN|FBgn0003996==w
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|copia{}w60
ASAL|FBal0018109==w60
MU|spontaneous
CLOC|3C1
|Insertion site
LOCB|Proximity to gene: FBgn0003996==w
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0018109==w60
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye color: white.
PHM|pigment cell
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014780 ICL 1 copia SYM 1 copia{}wa59k13 ASTR 1 - CLOC 1 3C1 REF 1 2 DT 1 6 Jan 2000 RESZ 464
ID|FBti0014780
SYM|copia{}wa59k13
ASTP|FBtp0011420==copia
DT|6 Jan 2000
|6 Jan 2000
ICL|copia
ASGN|FBgn0003996==w
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|copia{}wa59k13
ASAL|FBal0018199==wa59k13
MU|spontaneous
CLOC|3C1
|Insertion site
LOCB|Proximity to gene: FBgn0003996==w
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0018199==wa59k13
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye color: darker than FBal0018195==wa, with more brown pigment.
PHM|pigment cell
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0002388 ICL 1 copia SYM 1 copia{}wa ASTR 1 - CLOC 1 3C1 REF 1 30 DT 1 4 Feb 2000 RESZ 2032
ID|FBti0002388
SYM|copia{}wa
ASTP|FBtp0011420==copia
DT|4 Feb 2000
|21 Mar 1997
ICL|copia
ASGN|FBgn0003996==w
REFDSR
{
RDID|FBrf0037612
|Zachar and Bingham
|1982
ASAL|FBal0018195==wa
MU|spontaneous
CLOC|3C1
|Insertion site
LOCB|Proximity to gene: FBgn0003996==w
PHC|viable
}
REFDSR
{
RDID|FBrf0043227
|Mount and Rubin
|1985
ASAL|FBal0018210==waR84e7
}
REFDSR
{
RDID|FBrf0048200
|Mount et al.
|1988
ASAL|FBal0018209==waR79l27
MU|spontaneous
ASAL|FBal0018211==waR84e19
MU|spontaneous
}
REFDSR
{
RDID|FBrf0049635
|Rabinow and Birchler
|1989
ASAL|FBal0018205==waM
MU|spontaneous
ASAL|FBal0018212==waR84h
MU|spontaneous
}
REF
{
REFM|FBrf0037612
|Zachar and Bingham
|1982
REFM|FBrf0040134
|Goldberg et al.
|1983
REFM|FBrf0040771
|Gehring et al.
|1984
REFM|FBrf0042646
|Zachar et al.
|1985
REFM|FBrf0043227
|Mount and Rubin
|1985
REFM|FBrf0043247
|Carbonare and Gehring
|1985
REFM|FBrf0048200
|Mount et al.
|1988
REFM|FBrf0049635
|Rabinow and Birchler
|1989
REFM|FBrf0050555
|Georgiev and Gerasimova
|1989
REFM|FBrf0051376
|Engels et al.
|1990
REFM|FBrf0051917
|Peng and Mount
|1990
REFM|FBrf0051943
|Harden and Ashburner
|1990
REFM|FBrf0052719
|Brierley and Flavell
|1990
REFM|FBrf0054145
|Lovering et al.
|1991
REFM|FBrf0054158
|Rabinow et al.
|1991
REFM|FBrf0054964
|Kurkulos et al.
|1991
REFM|FBrf0056147
|Birchler
|1992
REFM|FBrf0056235
|Hiebert and Birchler
|1992
REFM|FBrf0058549
|Sabl and Birchler
|1993
REFM|FBrf0058584
|Rabinow et al.
|1993
REFM|FBrf0063381
|Collins et al.
|1983
REFM|FBrf0073744
|Lim and Simmons
|1994
REFM|FBrf0083249
|Lankenau
|1995
REFM|FBrf0084258
|Peng and Mount
|1995
REFM|FBrf0084324
|Roseman et al.
|1995
REFM|FBrf0086910
|Bhadra and Birchler
|1996
REFM|FBrf0087538
|Larsson et al.
|1996
REFM|FBrf0094158
|Bhadra et al.
|1997
REFM|FBrf0094159
|Bhadra et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0018209==waR79l27
REFDSR
{
RDID|FBrf0043247
|Carbonare and Gehring
|1985
PHP|Eye pigment is restored to 80% of wild type levels.
PHM|pigment cell
}
REF
{
REFM|FBrf0043247
|Carbonare and Gehring
|1985
}
}
# EO ALESR
ALESR
{
ASYM|FBal0018210==waR84e7
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
PHP|Increased pigmentation seen in this derivative of FBal0018195==wa
| is due to
|increased gene copy number rather than change in gene properties.
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
}
}
# EO ALESR
ALESR
{
ASYM|FBal0018212==waR84h
REFDSR
{
RDID|FBrf0094159
|Bhadra et al.
|1997
PHM|pigment cell
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye color: mottled, with FBal0012670==mw1.
}
REF
{
REFM|FBrf0094159
|Bhadra et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
ALESR
{
ASYM|FBal0018195==wa
REFDSR
{
RDID|FBrf0002371
|Muller
|1932
PHP|The amount of pigment
|formed by FBal0018195==wa is a function of gene dose: FBal0018195==wa/-
|female < FBal0018195==wa/Y male = FBal0018195==wa/FBal0018195==wa
|female <
| FBal0018195==wa/FBal0018195==wa/FBal0018195==wa
| female < FBal0018195==wa/FBal0018195==wa male.
}
REFDSR
{
RDID|FBrf0003530
|Beadle and Ephrussi
|1936
PHP|A FBal0018195==wa optic disk transplanted into a
|wild-type host shows autonomous eye color development.
}
REFDSR
{
RDID|FBrf0022720
|Gelbart
|1971
PHM|pigment cell
}
REFDSR
{
RDID|FBrf0037612
|Zachar and Bingham
|1982
PHP|Eye color: orange-brown.
PHM|pigment cell
}
REFDSR
{
RDID|FBrf0040490
|Levis et al.
|1984
PHP|Eye color: slightly darker than FBal0018195==wa in the triple
| mutant FBgn0003638==su(wa)
|FBal0018195==wa FBal0016266==su(f)1.
}
REFDSR
{
RDID|FBrf0047022
|Pastink et al.
|1987
PHP|Eye color: FBal0018302==wsp1/FBal0018195==wa flies
| have brown eyes at eclosion, which
|become somewhat darker with age.
PHM|pigment cell
}
REFDSR
{
RDID|FBrf0049635
|Rabinow and Birchler
|1989
PHP|Enhanced by duplications of FBgn0000480==Doa+.
PHM|pigment cell
|ocellus
|testis
|Malpighian tubule
}
REFDSR
{
RDID|FBrf0049829
|Birchler et al.
|1989
PHM|pigment cell
}
REFDSR
{
RDID|FBrf0049880
|Birchler and Hiebert
|1989
PHP|Strong response to E(wa).
}
REFDSR
{
RDID|FBrf0051376
|Engels et al.
|1990
PHP|Eye color: orange.
PHM|pigment cell | adult
}
REFDSR
{
RDID|FBrf0055430
|Montell et al.
|1992
PHP|Eye color: orange.
PHM|pigment cell
}
REFDSR
{
RDID|FBrf0056147
|Birchler
|1992
PHP|Homozygous males are darker than homozygous females. Triple X metafemale
|individuals homozygous for FBal0018195==wa exhibit dosage
| compensation of pigment
|levels.
}
REFDSR
{
RDID|FBrf0056235
|Hiebert and Birchler
|1992
PHP|Eye color: yellow-orange.
|FBal0018195==wa is slightly dosage overcompensated in males conferring
|slightly more eye pigment.
}
REFDSR
{
RDID|FBrf0073338
|Hiebert and Birchler
|1994
PHP|FBal0012337==mle4 has very little effect on the dosage
| compensation of FBal0018195==wa:
|homozygous males have slightly darker eyes than their heterozygous
|brothers.
}
REFDSR
{
RDID|FBrf0080045
|Georgiev
|1994
PHP|Modified by FBgn0004050==z mutations.
}
REFDSR
{
RDID|FBrf0080335
|Qian and Pirrotta
|1995
PHP|Shows slight hyper dosage compensation.
}
REFDSR
{
RDID|FBrf0084258
|Peng and Mount
|1995
PHM|pigment cell
}
REFDSR
{
RDID|FBrf0100562
|Frolov et al.
|1998
PHM|pigment cell
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye color: white in FBal0018195==wa FBal0018224==wch.
|Eye color: white in FBal0018215==wbf FBal0018195==wa.
|Eye color: like FBal0018195==wa in FBal0018220==wBwx FBal0018195==wa.
|Eye color: yellowish with orange tone in males; lighter and somewhat
|yellower in females.
|Eye color: mottled, with FBal0012670==mw1.
|Eye color: nearly white with FBal0014434==rb1.
|Eye color: nearly white with FBal0004957==g1.
|Malpighian tubule color: colorless.
|Eye color: mottled, with FBal0012670==mw1.
PHM|pigment cell
|Malpighian tubule
}
REFDSR
{
RDID|FBrf0105774
|Benevolenskaya et al.
|1998
PHM|pigment cell
}
REFDSR
{
RDID|FBrf0128132
|Benevolenskaya et al.
|2000
PHM|pigment cell
}
REF
{
REFM|FBrf0002371
|Muller
|1932
REFM|FBrf0003530
|Beadle and Ephrussi
|1936
REFM|FBrf0022720
|Gelbart
|1971
REFM|FBrf0037612
|Zachar and Bingham
|1982
REFM|FBrf0040490
|Levis et al.
|1984
REFM|FBrf0047022
|Pastink et al.
|1987
REFM|FBrf0049635
|Rabinow and Birchler
|1989
REFM|FBrf0049829
|Birchler et al.
|1989
REFM|FBrf0049880
|Birchler and Hiebert
|1989
REFM|FBrf0051376
|Engels et al.
|1990
REFM|FBrf0055430
|Montell et al.
|1992
REFM|FBrf0056147
|Birchler
|1992
REFM|FBrf0056235
|Hiebert and Birchler
|1992
REFM|FBrf0073338
|Hiebert and Birchler
|1994
REFM|FBrf0080045
|Georgiev
|1994
REFM|FBrf0080335
|Qian and Pirrotta
|1995
REFM|FBrf0084258
|Peng and Mount
|1995
REFM|FBrf0100562
|Frolov et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0105774
|Benevolenskaya et al.
|1998
REFM|FBrf0128132
|Benevolenskaya et al.
|2000
}
}
# EO ALESR
ALESR
{
ASYM|FBal0018205==waM
REFDSR
{
RDID|FBrf0012636
|Green
|1959
PHP|Intermediate between FBal0018195==wa and wild-type in phenotype.
}
REFDSR
{
RDID|FBrf0043247
|Carbonare and Gehring
|1985
PHP|Eye pigmentation is restored to 80% of wild type levels.
PHM|pigment cell
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye color: darker than FBal0018195==wa, with more brown pigment.
|Eye color: mottled, with FBal0012670==mw1.
PHM|pigment cell
}
REF
{
REFM|FBrf0012636
|Green
|1959
REFM|FBrf0043247
|Carbonare and Gehring
|1985
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014782 ICL 1 copia SYM 1 copia{}waLTR1 ASTR 1 - CLOC 1 3C1 REF 1 2 DT 1 6 Jan 2000 RESZ 446
ID|FBti0014782
SYM|copia{}waLTR1
ASTP|FBtp0011420==copia
DT|6 Jan 2000
|6 Jan 2000
ICL|copia
ASGN|FBgn0003996==w
REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|copia{}waLTR1
ASAL|FBal0018204==waLTR1
CLOC|3C1
|Insertion site
LOCB|Proximity to gene: FBgn0003996==w
}
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EOR
TIR
{
RETE|ID 1 FBti0014800 ICL 1 copia SYM 1 copia{}whd81b6 ASTR 1 - CLOC 1 3C1 REF 1 2 DT 1 6 Jan 2000 RESZ 455
ID|FBti0014800
SYM|copia{}whd81b6
ASTP|FBtp0011420==copia
DT|6 Jan 2000
|6 Jan 2000
ICL|copia
ASGN|FBgn0003996==w
REFDSR
{
RDID|FBrf0051869
|Rabinow and Birchler
|1990
SYN|copia{}whd81b6
ASAL|FBal0018249==whd81b6
CLOC|3C1
|Insertion site
LOCB|Proximity to gene: FBgn0003996==w
}
REF
{
REFM|FBrf0051869
|Rabinow and Birchler
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0018249==whd81b6
REFDSR
{
RDID|FBrf0051869
|Rabinow and Birchler
|1990
PHP|Eye color: bleach white.
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye color: white.
PHM|pigment cell
}
REF
{
REFM|FBrf0051869
|Rabinow and Birchler
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0002409 ICL 1 copia SYM 1 copia{}whd81b11 ASTR 1 - CLOC 1 3C1 REF 1 4 DT 1 4 Feb 2000 RESZ 500
ID|FBti0002409
SYM|copia{}whd81b11
ASTP|FBtp0011420==copia
DT|4 Feb 2000
|21 Mar 1997
ICL|copia
ASGN|FBgn0003996==w
REFDSR
{
RDID|FBrf0042646
|Zachar et al.
|1985
ASAL|FBal0018251==whd81b11
CLOC|3C1
|Insertion site
LOCB|Proximity to gene: FBgn0003996==w
}
REF
{
REFM|FBrf0042646
|Zachar et al.
|1985
REFM|FBrf0051869
|Rabinow and Birchler
|1990
REFM|FBrf0063381
|Collins et al.
|1983
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0018251==whd81b11
REFDSR
{
RDID|FBrf0051869
|Rabinow and Birchler
|1990
PHP|Eye color: bleach white.
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye color: white.
PHM|pigment cell
}
REF
{
REFM|FBrf0051869
|Rabinow and Birchler
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014799 ICL 1 copia SYM 1 copia{}whd81b25 ASTR 1 - CLOC 1 3C1 REF 1 2 DT 1 6 Jan 2000 RESZ 458
ID|FBti0014799
SYM|copia{}whd81b25
ASTP|FBtp0011420==copia
DT|6 Jan 2000
|6 Jan 2000
ICL|copia
ASGN|FBgn0003996==w
REFDSR
{
RDID|FBrf0051869
|Rabinow and Birchler
|1990
SYN|copia{}whd81b25
ASAL|FBal0018252==whd81b25
CLOC|3C1
|Insertion site
LOCB|Proximity to gene: FBgn0003996==w
}
REF
{
REFM|FBrf0051869
|Rabinow and Birchler
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0018252==whd81b25
REFDSR
{
RDID|FBrf0051869
|Rabinow and Birchler
|1990
PHP|Eye color: bleach white.
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye color: white.
PHM|pigment cell
}
REF
{
REFM|FBrf0051869
|Rabinow and Birchler
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0014794 ICL 1 coral SYM 1 coral{}wco ASTR 1 - CLOC 1 3C1 REF 1 7 DT 1 6 Jan 2000 RESZ 639
ID|FBti0014794
SYM|coral{}wco
ASTP|FBtp0011421==coral
DT|6 Jan 2000
|6 Jan 2000
ICL|coral
ASGN|FBgn0003996==w
REFDSR
{
RDID|FBrf0068460
|Csink et al.
|1994
SYN|coral{}wco
ASAL|FBal0018225==wco
MU|spontaneous
CLOC|3C1
|Insertion site
LOCB|Proximity to gene: FBgn0003996==w
}
REF
{
REFM|FBrf0068460
|Csink et al.
|1994
REFM|FBrf0074960
|Birchler et al.
|1994
REFM|FBrf0076540
|Csink et al.
|1994
REFM|FBrf0086910
|Bhadra and Birchler
|1996
REFM|FBrf0094158
|Bhadra et al.
|1997
REFM|FBrf0100562
|Frolov et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}
ALESR
{
ASYM|FBal0018225==wco
REFDSR
{
RDID|FBrf0100562
|Frolov et al.
|1998
PHM|pigment cell
}
REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye color: deep ruby in male, darkening to FBgn0001087==g-like; lighter in female.
|Malpighian tubule color: pale yellow.
PHM|pigment cell
|Malpighian tubule
}
REF
{
REFM|FBrf0100562
|Frolov et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}
}
# EO ALESR
}
# EOR
TIR
{
RETE|ID 1 FBti0019700 ICL 1 Cr1a SYM 1 Cr1a{}228 ASTR 1 - CLOC 1 20A5-20A5 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019700
SYM|Cr1a{}228
SYN|TE19700
ASTP|FBtp0017032==Cr1a
DT|21 Aug 2003
|21 Aug 2003
ICL|Cr1a
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Cr1a{}228
CLOC|20A5-20A5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003122.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019203 ICL 1 Cr1a SYM 1 Cr1a{}412 ASTR 1 - CLOC 1 37E5-37E5 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019203
SYM|Cr1a{}412
SYN|TE19203
ASTP|FBtp0017032==Cr1a
DT|21 Aug 2003
|21 Aug 2003
ICL|Cr1a
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Cr1a{}412
CLOC|37E5-37E5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003663.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019215 ICL 1 Cr1a SYM 1 Cr1a{}474 ASTR 1 - CLOC 1 38D1-38D1 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019215
SYM|Cr1a{}474
SYN|TE19215
ASTP|FBtp0017032==Cr1a
DT|21 Aug 2003
|21 Aug 2003
ICL|Cr1a
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Cr1a{}474
CLOC|38D1-38D1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003667.3
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019222 ICL 1 Cr1a SYM 1 Cr1a{}486 ASTR 1 - CLOC 1 39C1-39C1 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019222
SYM|Cr1a{}486
SYN|TE19222
ASTP|FBtp0017032==Cr1a
DT|21 Aug 2003
|21 Aug 2003
ICL|Cr1a
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Cr1a{}486
CLOC|39C1-39C1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003669.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019247 ICL 1 Cr1a SYM 1 Cr1a{}534 ASTR 1 - CLOC 1 40F1-40F2 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019247
SYM|Cr1a{}534
SYN|TE19247
ASTP|FBtp0017032==Cr1a
DT|21 Aug 2003
|21 Aug 2003
ICL|Cr1a
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Cr1a{}534
CLOC|40F1-40F2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003783.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019263 ICL 1 Cr1a SYM 1 Cr1a{}575 ASTR 1 - CLOC 1 40F7-40F7 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019263
SYM|Cr1a{}575
SYN|TE19263
ASTP|FBtp0017032==Cr1a
DT|21 Aug 2003
|21 Aug 2003
ICL|Cr1a
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Cr1a{}575
CLOC|40F7-40F7
LOCB|genomic location inferred from flanking sequence
DBAF|AE002603.2
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0018887 ICL 1 Cr1a SYM 1 Cr1a{}584 ASTR 1 - CLOC 1 41E3-41E3 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0018887
SYM|Cr1a{}584
SYN|TE18887
ASTP|FBtp0017032==Cr1a
DT|21 Aug 2003
|21 Aug 2003
ICL|Cr1a
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Cr1a{}584
CLOC|41E3-41E3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003788.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0018888 ICL 1 Cr1a SYM 1 Cr1a{}592 ASTR 1 - CLOC 1 41E4-41E4 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0018888
SYM|Cr1a{}592
SYN|TE18888
ASTP|FBtp0017032==Cr1a
DT|21 Aug 2003
|21 Aug 2003
ICL|Cr1a
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Cr1a{}592
CLOC|41E4-41E4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003788.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019886 ICL 1 Cr1a SYM 1 Cr1a{}595 ASTR 1 - CLOC 1 41E4-41E4 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019886
SYM|Cr1a{}595
SYN|TE19886
ASTP|FBtp0017032==Cr1a
DT|21 Aug 2003
|21 Aug 2003
ICL|Cr1a
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Cr1a{}595
CLOC|41E4-41E4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003788.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0018889 ICL 1 Cr1a SYM 1 Cr1a{}607 ASTR 1 - CLOC 1 41E5-41E5 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0018889
SYM|Cr1a{}607
SYN|TE18889
ASTP|FBtp0017032==Cr1a
DT|21 Aug 2003
|21 Aug 2003
ICL|Cr1a
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Cr1a{}607
CLOC|41E5-41E5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003788.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0018890 ICL 1 Cr1a SYM 1 Cr1a{}620 ASTR 1 - CLOC 1 41E6-41E6 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0018890
SYM|Cr1a{}620
SYN|TE18890
ASTP|FBtp0017032==Cr1a
DT|21 Aug 2003
|21 Aug 2003
ICL|Cr1a
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Cr1a{}620
CLOC|41E6-41E6
LOCB|genomic location inferred from flanking sequence
DBAF|AE003787.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0018891 ICL 1 Cr1a SYM 1 Cr1a{}637 ASTR 1 - CLOC 1 41F2-41F2 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0018891
SYM|Cr1a{}637
SYN|TE18891
ASTP|FBtp0017032==Cr1a
DT|21 Aug 2003
|21 Aug 2003
ICL|Cr1a
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Cr1a{}637
CLOC|41F2-41F2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003787.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0018892 ICL 1 Cr1a SYM 1 Cr1a{}638 ASTR 1 - CLOC 1 41F2-41F2 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0018892
SYM|Cr1a{}638
SYN|TE18892
ASTP|FBtp0017032==Cr1a
DT|21 Aug 2003
|21 Aug 2003
ICL|Cr1a
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Cr1a{}638
CLOC|41F2-41F2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003787.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0018893 ICL 1 Cr1a SYM 1 Cr1a{}667 ASTR 1 - CLOC 1 41F3-41F3 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0018893
SYM|Cr1a{}667
SYN|TE18893
ASTP|FBtp0017032==Cr1a
DT|21 Aug 2003
|21 Aug 2003
ICL|Cr1a
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Cr1a{}667
CLOC|41F3-41F3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003786.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0018894 ICL 1 Cr1a SYM 1 Cr1a{}675 ASTR 1 - CLOC 1 41F5-41F5 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0018894
SYM|Cr1a{}675
SYN|TE18894
ASTP|FBtp0017032==Cr1a
DT|21 Aug 2003
|21 Aug 2003
ICL|Cr1a
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Cr1a{}675
CLOC|41F5-41F5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003786.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019921 ICL 1 Cr1a SYM 1 Cr1a{}679 ASTR 1 - CLOC 1 41F5-41F5 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019921
SYM|Cr1a{}679
SYN|TE19921
ASTP|FBtp0017032==Cr1a
DT|21 Aug 2003
|21 Aug 2003
ICL|Cr1a
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Cr1a{}679
CLOC|41F5-41F5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003786.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019923 ICL 1 Cr1a SYM 1 Cr1a{}681 ASTR 1 - CLOC 1 41F5-41F5 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019923
SYM|Cr1a{}681
SYN|TE19923
ASTP|FBtp0017032==Cr1a
DT|21 Aug 2003
|21 Aug 2003
ICL|Cr1a
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Cr1a{}681
CLOC|41F5-41F5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003786.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0018896 ICL 1 Cr1a SYM 1 Cr1a{}688 ASTR 1 - CLOC 1 41F6-41F6 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0018896
SYM|Cr1a{}688
SYN|TE18896
ASTP|FBtp0017032==Cr1a
DT|21 Aug 2003
|21 Aug 2003
ICL|Cr1a
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Cr1a{}688
CLOC|41F6-41F6
LOCB|genomic location inferred from flanking sequence
DBAF|AE003786.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0018897 ICL 1 Cr1a SYM 1 Cr1a{}693 ASTR 1 - CLOC 1 41F6-41F6 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0018897
SYM|Cr1a{}693
SYN|TE18897
ASTP|FBtp0017032==Cr1a
DT|21 Aug 2003
|21 Aug 2003
ICL|Cr1a
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Cr1a{}693
CLOC|41F6-41F6
LOCB|genomic location inferred from flanking sequence
DBAF|AE003786.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019934 ICL 1 Cr1a SYM 1 Cr1a{}697 ASTR 1 - CLOC 1 41F6-41F6 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019934
SYM|Cr1a{}697
SYN|TE19934
ASTP|FBtp0017032==Cr1a
DT|21 Aug 2003
|21 Aug 2003
ICL|Cr1a
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Cr1a{}697
CLOC|41F6-41F6
LOCB|genomic location inferred from flanking sequence
DBAF|AE003786.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019936 ICL 1 Cr1a SYM 1 Cr1a{}699 ASTR 1 - CLOC 1 41F6-41F6 REF 1 2 DT 1 21 Aug 2003 RESZ 349
ID|FBti0019936
SYM|Cr1a{}699
SYN|TE19936
ASTP|FBtp0017032==Cr1a
DT|21 Aug 2003
|21 Aug 2003
ICL|Cr1a
REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|Cr1a{}699
CLOC|41F6-41F6
LOCB|genomic location inferred from flanking sequence
DBAF|AE003786.4
}
REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
}
}
# EOR
TIR
{
RETE|ID 1 FBti0019938 ICL 1 Cr1a SYM 1 Cr1a{}701 ASTR 1 - CLOC 1 4