oocyte ; it is expressed in the embryo (nucleus, cytoplasm and nucleus) and ovary (egg chamber, nurse cell, oocyte and ovary). It has been sequenced and its amino acid sequence is also available. It has been mapped by recombination to 1-15.9 and cytologically to 5F4. There are 14 recorded alleles: 3 in vitro constructs (none available from the public stock centers), 10 classical mutants (3 available from the public stock centers) and 1 wild-type. Mutations have been isolated which affect the embryonic head, the embryonic abdomen, the denticle belt and 5 other listed tissues and are maternal effect lethal. swa is discussed in 106 references (excluding sequence accessions), dated between 1975 and 2004. These include at least 7 studies of mutant phenotypes, 4 studies of wild-type function and 7 molecular studies. Among findings on swa mutants, mutations in swa affect cephalogenesis.
}
# EOR
GENR
{
SUMX| The D. melanogaster gene short wing, abbreviated as sw, is reported here. It has also been known in FlyBase as CG18000 and Cdic. It encodes a product with microtubule motor activity putatively involved in microtubule-based movement which is a component of the cytoplasmic dynein complex. It has been sequenced. It has been mapped by recombination to 1-64.0 and cytologically to 19C1. It interacts genetically with Gl. There are 38 recorded alleles: 8 in vitro constructs (none available from the public stock centers), 29 classical mutants (2 available from the public stock centers) and 1 wild-type. Mutations have been isolated which affect the wing and the wing vein and are female sterile. sw is discussed in 57 references (excluding sequence accessions), dated between 1935 and 2004. These include at least 2 studies of mutant phenotypes, 2 studies of natural polymorphisms and 7 molecular studies.
}
# EOR
GENR
{
SUMX| The D. melanogaster gene shortened veins, abbreviated as svs, is reported here. It has been mapped by recombination to 1-24.6. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. Mutations have been isolated which affect the wing, the wing vein, the wing vein L4 and 2 other listed tissues and are female sterile, male fertile, male reduced viable and visible. svs is discussed in 3 references, dated between 1959 and 1992. These include at least one study of mutant phenotypes.
}
# EOR
GENR
{
SUMX| The D. melanogaster gene silver, abbreviated as svr, is reported here. It has also been known in FlyBase as CG18503 and CpepE. It encodes a product with metallocarboxypeptidase D activity (EC:3.4.17.22) involved in cuticle biosynthesis (sensu Insecta). It has been sequenced and its amino acid sequence contains a zinc carboxypeptidases, carboxypeptidase A metalloprotease (M14) family. It has been mapped by recombination to 1-0.0 and cytologically to 1B5--7. It interacts genetically with a and pnr. There are 46 recorded alleles: 1 in vitro construct (not available from the public stock centers), 44 classical mutants (4 available from the public stock centers) and 1 wild-type. Hypomorphic mutations have been isolated which affect the wing and are recessive body color defective and viable. svr is discussed in 52 references (excluding sequence accessions), dated between 1923 and 2003. These include at least one study of mutant phenotypes and 4 molecular studies.
}
# EOR
GENR
{
SUMX| The D. melanogaster gene seven up, abbreviated as svp, is reported here. It has also been known in FlyBase as BcDNA:GH08189 and CG18158. It encodes a product with ligand-dependent nuclear receptor activity involved in ventral cord development which is a component of the nucleus; it is expressed in the embryo (Malpighian tubule and Malpighian tubule tip cell) and larva (morphogenetic furrow, photoreceptor cell R1 and photoreceptor cell R3 to 4). It has been sequenced and its amino acid sequence contains a ligand-binding domain of nuclear hormone receptor, a C4-type steroid receptor zinc finger, a steroid hormone receptor and a COUP transcription factor (2F nuclear receptor). It has been mapped by recombination to 3-54.2 and cytologically to 87B4--5. It interacts genetically with Egfr, Ras85D, rl, Sos, csw and 14 other listed genes. There are 46 recorded alleles: 14 in vitro constructs (none available from the public stock centers), 31 classical mutants (4 available from the public stock centers) and 1 wild-type. Amorphic mutations have been isolated which affect the photoreceptor cell R1, the photoreceptor cell R6, the embryonic posterior Malpighian tubule and 6 other listed tissues and are embryonic recessive lethal and recessive somatic clone tissue polarity. svp is discussed in 173 references (excluding sequence accessions), dated between 1981 and 2004. These include at least 22 studies of mutant phenotypes, one study of wild-type function and 7 molecular studies. Among findings on svp function, svp controls cell proliferation in the developing Malpighian tubules.
}
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GENR
{
SUMX| The D. melanogaster gene sva53 is reported here. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. Mutations have been isolated which are recessive maternal effect lethal. sva53 is discussed in one reference, dating from 1999.
}
# EOR
GENR
{
SUMX| The D. melanogaster gene shaven, abbreviated as sv, is reported here. It has also been known in FlyBase as Pax258 and spa. It encodes a product with transcription factor activity involved in cone cell fate commitment (sensu Drosophila) which is localized to the nucleus; it is expressed in the embryo (embryonic nervous system and peripheral nervous system), larva (antennal disc, cone cell, dorsal mesothoracic disc, eye disc and 4 other listed tissues) and prepupa and pupa (eye disc, mechanosensory chaetae and primary pigment cell). It has been sequenced. It has been mapped by recombination to 4-3.0 and cytologically to 102D4. It interacts genetically with lz, wg, H, P29, CycE and 4 other listed genes. There are 47 recorded alleles: 23 in vitro constructs (none available from the public stock centers), 23 classical mutants (7 available from the public stock centers) and 1 wild-type. Loss-of-function mutations have been isolated which affect the macrochaeta, the eye, the ommatidium and the lens and are recessive lethal. sv is discussed in 101 references (excluding sequence accessions), dated between 1925 and 2004. These include at least 7 studies of mutant phenotypes, 2 studies of wild-type function and 2 molecular studies. Among findings on sv mutants, flies carrying strong loss of function sv mutations specifically lack the shaft structures of the adult bristles. Among findings on sv function, sv is required for the proper specification and differentiation of cone and primary pigment cells in the eye.
}
# EOR
GENR
{
SUMX| The D. melanogaster gene schmalspur, abbreviated as sur, is reported here. It has been mapped by recombination to 3-2 and cytologically to 62A--B. It interacts genetically with pnt. There are 3 recorded alleles: 2 classical mutants (none available from the public stock centers) and 1 wild-type. Mutations have been isolated which affect the embryonic central nervous system, the commissure, the midline glial cell and 4 other listed tissues. sur is discussed in 3 references, all dating from 1999. These include at least 2 studies of mutant phenotypes.
}
# EOR
GENR
{
SUMX| The D. melanogaster gene suppressor activated, abbreviated as supact, is reported here. It has been mapped by recombination to 1-0.0. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. Mutations have been isolated which affect the female eye and the female macrochaeta. supact is discussed in 2 references, dated between 1970 and 1992.
}
# EOR
GENR
{
SUMX| The D. melanogaster gene superwith, abbreviated as sup, is reported here. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. Mutations have been isolated which affect the trident and are body color defective. sup is discussed in 2 references, dated between 1923 and 1992.
}
# EOR
GENR
{
SUMX| The D. melanogaster gene stunted, abbreviated as sun, is reported here. It has also been known in FlyBase as BcDNA:RE19513, BcDNA:RH48911, CG9032 and l(1)13Fe. It encodes a product with hydrogen-exporting ATPase activity, phosphorylative mechanism (EC:3.6.3.6) involved in proton transport which is a component of the proton-transporting ATP synthase complex, catalytic core F(1) (sensu Eukarya). It has been sequenced. It has been mapped cytologically to 13F12. There are 4 recorded alleles: 1 in vitro construct (not available from the public stock centers), 2 classical mutants (none available from the public stock centers) and 1 wild-type. Mutations have been isolated which are recessive lethal. sun is discussed in 8 references (excluding sequence accessions), dated between 1990 and 2003. These include at least 3 studies of mutant phenotypes and one molecular study. Among findings on sun mutants, the maternal effect of the sun mutation leads to abnormalities that are most apparent in the cortical embryonic divisions.
}
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GENR
{
SUMX| The D. melanogaster repetitive element suffix element, abbreviated as suffix, is reported here. It has been sequenced. There is one recorded allele, which is wild-type. suffix is discussed in 12 references (excluding sequence accessions), dated between 1984 and 2003. These include at least one molecular study.
}
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GENR
{
SUMX| The D. melanogaster gene subito, abbreviated as sub, is reported here. It has also been known in FlyBase as CG12298, Dub and mei-1794. It encodes a product with motor activity involved in meiotic spindle assembly which is a component of the plus-end kinesin complex. It has been sequenced. It has been mapped by recombination to 2-86 and cytologically to 54E7. It interacts genetically with ncd and nod. There are 15 recorded alleles: 14 classical mutants (1 available from the public stock centers) and 1 wild-type. Loss-of-function mutations have been isolated which affect the (with subDub) eye, the (with subDub) wing, the (with subDub) wing margin and the spindle and are recessive female sterile, (with subDub) female sterile, (with subDub) visible, recessive meiotic, maternal effect recessive lethal and maternal effect recessive mitotic. sub is discussed in 30 references (excluding sequence accessions), dated between 1989 and 2004. These include at least 6 studies of mutant phenotypes, 2 studies of wild-type function and 2 molecular studies. Among findings on sub mutants, mutations in sub show a strict maternal effect phenotype with defects in fertilization or early embryonic development. Among findings on sub function, sub is required for bipolar spindle formation.
}
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GENR
{
SUMX| The D. melanogaster gene suppressor of white-spotted, abbreviated as su(wsp), is reported here. It has been mapped by recombination to 1-0.16 and cytologically to 2B17. It interacts genetically with w. There are 3 recorded alleles: 2 classical mutants (1 available from the public stock centers) and 1 wild-type. su(wsp) is discussed in 6 references, dated between 1985 and 1998. These include at least 4 studies of mutant phenotypes.
}
# EOR
GENR
{
SUMX| The D. melanogaster gene suppressor of white-honey, abbreviated as su(wh), is reported here. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. su(wh) is discussed in 2 references, dated between 1972 and 1992.
}
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GENR
{
SUMX| The D. melanogaster/D. melanogaster fusion gene su(wa)::tra is reported here. There are two recorded alleles, both in vitro constructs, neither available from the public stock centers. su(wa)::tra is discussed in one reference, dating from 1991.
}
# EOR
GENR
{
SUMX| The D. melanogaster gene suppressor of white-apricot, abbreviated as su(wa), is reported here. It encodes a product with pre-mRNA splicing factor activity involved in nuclear mRNA splicing, via spliceosome which is a component of the spliceosome complex. It has been sequenced and its amino acid sequence contains a SWAP / SURP. It has been mapped by recombination to 1-0.1 and cytologically to 1E1. It interacts genetically with w. There are 45 recorded alleles: 22 in vitro constructs (none available from the public stock centers), 22 classical mutants (2 available from the public stock centers) and 1 wild-type. Mutations have been isolated which affect the conditional ts pigment cell and are conditional ts visible. su(wa) is discussed in 67 references (excluding sequence accessions), dated between 1954 and 2003. These include at least 6 studies of mutant phenotypes, one study of wild-type function and 12 molecular studies.
}
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GENR
{
SUMX| The D. melanogaster gene suppressor of vestigial, abbreviated as su(vg), is reported here. It has been mapped by recombination to 3-98. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. su(vg) is discussed in 2 references, dated between 1970 and 1992.
}
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GENR
{
SUMX| The D. melanogaster gene suppressor of veinlet, abbreviated as su(ve), is reported here. It has been mapped by recombination to 3-. There are 2 recorded alleles: 1 classical mutant (available from the public stock centers) and 1 wild-type. su(ve) is discussed in 2 references, dated between 1992 and 2000.
}
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GENR
{
SUMX| The D. melanogaster gene suppressor of tumor-brown, abbreviated as su(tu-bw), is reported here. There are 2 recorded alleles: 1 classical mutant (available from the public stock centers) and 1 wild-type. su(tu-bw) is discussed in 6 references, dated between 1952 and 1992.
}
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GENR
{
SUMX| The D. melanogaster gene suppressor of tan, abbreviated as su(t), is reported here. It has been mapped by recombination to 3-26. There are 2 recorded alleles: 1 classical mutant (available from the public stock centers) and 1 wild-type. su(t) is discussed in 2 references, dated between 1992 and 1997.
}
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GENR
{
SUMX| The D. melanogaster gene suppressor of scute, abbreviated as su(sc), is reported here. It has been mapped by recombination to 1-50.0 and cytologically to 13E. It interacts genetically with ac and sc. There are 6 recorded alleles: 5 classical mutants (none available from the public stock centers) and 1 wild-type. Mutations have been isolated which affect the male wing and are male sterile. su(sc) is discussed in 2 references, dated between 1990 and 1992. These include at least 2 studies of mutant phenotypes.
}
# EOR
GENR
{
SUMX| The D. melanogaster gene suppressor of sable, abbreviated as su(s), is reported here. It encodes a product with transcriptional repressor activity which is localized to the nucleus; it is expressed in the larva (nucleus). It has been sequenced and its amino acid sequence is also available. It has been mapped by recombination to 1-0+ and cytologically to 1B13. It interacts genetically with v, s, sp, y and pr. There are 148 recorded alleles: 7 in vitro constructs (none available from the public stock centers), 140 classical mutants (5 available from the public stock centers) and 1 wild-type. Hypomorphic mutations have been isolated which are good viable. su(s) is discussed in 89 references (excluding sequence accessions), dated between 1919 and 2003. These include at least 17 studies of mutant phenotypes and 11 molecular studies.
}
# EOR
GENR
{
SUMX| The D. melanogaster gene su(rdgB)82 is reported here. It has been mapped by recombination to 2-82. It interacts genetically with rdgB. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. su(rdgB)82 is discussed in one reference, dating from 1999.
}
# EOR
GENR
{
SUMX| The D. melanogaster gene su(rdgB)69 is reported here. It has been mapped by recombination to 3-101 and cytologically to 100B5--C4. It interacts genetically with rdgB. There are 5 recorded alleles: 4 classical mutants (none available from the public stock centers) and 1 wild-type. su(rdgB)69 is discussed in 3 references, dated between 1999 and 2002. These include at least 2 studies of mutant phenotypes.
}
# EOR
GENR
{
SUMX| The D. melanogaster gene suppressor of rudimentary, abbreviated as su(r), is reported here. It encodes a product with dihydrouracil dehydrogenase (NAD+) activity (EC:1.3.1.1). It has been mapped by recombination to 1-27.7. It interacts genetically with r. There are 12 recorded alleles: 11 classical mutants (1 available from the public stock centers) and 1 wild-type. su(r) is discussed in 7 references, dated between 1972 and 1992. These include at least one study of mutant phenotypes.
}
# EOR
GENR
{
SUMX| The D. melanogaster gene suppressor of purple, abbreviated as su(pr), is reported here. It has been mapped by recombination to 3-95.5. There are 5 recorded alleles: 4 classical mutants (3 available from the public stock centers) and 1 wild-type. su(pr) is discussed in 7 references, dated between 1929 and 1997.
}
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GENR
{
SUMX| The D. melanogaster gene suppressor of purpleoid, abbreviated as su(pd), is reported here. There are 2 recorded alleles: 1 classical mutant (available from the public stock centers) and 1 wild-type. su(pd) is discussed in one reference, dating from 1968.
}
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GENR
{
SUMX| The D. melanogaster gene suppressor of msm1, abbreviated as su(msm1), is reported here. It interacts genetically with ms(3)HO5A. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. su(msm1) is discussed in 2 references, dated between 1980 and 1992. These include at least one study of mutant phenotypes.
}
# EOR
GENR
{
SUMX| The D. melanogaster gene suppressor of mushroom body miniature, abbreviated as su(mbm), is reported here. It interacts genetically with mbm. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. su(mbm) is discussed in one reference, dating from 1996.
}
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GENR
{
SUMX| The D. melanogaster gene suppressor of lozenge-34, abbreviated as su(lz34), is reported here. It interacts genetically with lz. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. Mutations have been isolated which affect the female accessory gland, the spermathecum and the eye and are good female fertile. su(lz34) is discussed in 5 references, dated between 1960 and 2003. These include at least one study of mutant phenotypes.
}
# EOR
GENR
{
SUMX| The D. melanogaster gene suppressor of lozenge, abbreviated as su(lz), is reported here. There are 2 recorded alleles: 1 classical mutant (available from the public stock centers) and 1 wild-type. su(lz) is discussed in one reference, dating from 1983.
}
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GENR
{
SUMX| The D. melanogaster gene suppressor of facet-strawberry, abbreviated as su(faswb), is reported here. It has been mapped by recombination to 1-1.96 and cytologically to 3C5--6+. It interacts genetically with N. There are 2 recorded alleles: 1 classical mutant (available from the public stock centers) and 1 wild-type. su(faswb) is discussed in 4 references, dated between 1963 and 1992. These include at least one study of mutant phenotypes.
}
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GENR
{
SUMX| The D. melanogaster gene suppressor of forked, abbreviated as su(f), is reported here. It has also been known in FlyBase as l(1)G0393. It encodes a product with putative poly(A) binding involved in mRNA cleavage which is a component of the mRNA cleavage and polyadenylation specificity factor complex. It has been sequenced and its amino acid sequence is also available. It has been mapped by recombination to 1-65.9 and cytologically to 20E. It interacts genetically with lz, f, w, dy, Dfd and 4 other listed genes. There are 48 recorded alleles: 7 in vitro constructs (none available from the public stock centers), 39 classical mutants (5 available from the public stock centers) and 2 wild-type. Hypomorphic mutations have been isolated which affect the macrochaeta, the microchaeta, the dorsal anterior adult thorax and the wing and are recessive conditional ts lethal, recessive visible, recessive male mating defective, recessive male hypoactive and body color defective. su(f) is discussed in 182 references (excluding sequence accessions), dated between 1937 and 2004. These include at least 18 studies of mutant phenotypes, 4 studies of wild-type function, 7 studies of natural polymorphisms and 11 molecular studies. Among findings on su(f) mutants, su(f) mutations are found with several levels of reduced expression and some if not all mutant alleles are sensitive to temperature. Among findings on su(f) function, su(f) is required during cell division for progression through metaphase.
}
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GENR
{
SUMX| The D. melanogaster gene suppressor of deltex, abbreviated as su(dx), is reported here. It has been mapped by recombination to 1-5. There are 2 recorded alleles: 1 classical mutant (available from the public stock centers) and 1 wild-type. su(dx) is discussed in 2 references, dated between 1992 and 2002.
}
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GENR
{
SUMX| The D. melanogaster gene suppressor of dumpyoblique-vortex, abbreviated as su(dpov), is reported here. It has been mapped by recombination to 1-53.2. It interacts genetically with dp. There are 4 recorded alleles: 3 classical mutants (none available from the public stock centers) and 1 wild-type. Mutations have been isolated which are viable and fertile. su(dpov) is discussed in 4 references, dated between 1986 and 1992. These include at least one study of mutant phenotypes.
}
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GENR
{
SUMX| The D. melanogaster gene suppressor of black, abbreviated as su(b), is reported here. It has been mapped by recombination to 1-0.0. It interacts genetically with b. There are 13 recorded alleles: 12 classical mutants (1 available from the public stock centers) and 1 wild-type. Mutations have been isolated which are reduced fertile. su(b) is discussed in 10 references, dated between 1928 and 1997. These include at least one study of mutant phenotypes.
}
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GENR
{
SUMX| The D. melanogaster gene su(Ubxbx-1) is reported here. It has also been known in FlyBase as anon-85AB. It has been mapped cytologically to 85A3--B1. It interacts genetically with Ubx. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. su(Ubxbx-1) is discussed in one reference, dating from 1992.
}
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GENR
{
SUMX| The D. melanogaster gene su(RpII215)S3 is reported here. It has also been known in FlyBase as anon-S3/S13. It interacts genetically with RpII215. There are 5 recorded alleles: 4 classical mutants (none available from the public stock centers) and 1 wild-type. su(RpII215)S3 is discussed in 2 references, dated between 1990 and 1998. These include at least 2 studies of mutant phenotypes.
}
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GENR
{
SUMX| The D. melanogaster gene su(RpII140Z36)S9 is reported here. It interacts genetically with RpII140. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. su(RpII140Z36)S9 is discussed in one reference, dating from 1998.
}
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GENR
{
SUMX| The D. melanogaster gene su(RpII140Z36)S8 is reported here. It interacts genetically with RpII140. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. su(RpII140Z36)S8 is discussed in one reference, dating from 1998.
}
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GENR
{
SUMX| The D. melanogaster gene su(RpII140Z36)S7 is reported here. It interacts genetically with RpII140. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. su(RpII140Z36)S7 is discussed in one reference, dating from 1998.
}
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GENR
{
SUMX| The D. melanogaster gene su(RpII140Z36)S6 is reported here. It interacts genetically with RpII140. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. su(RpII140Z36)S6 is discussed in one reference, dating from 1998.
}
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GENR
{
SUMX| The D. melanogaster gene su(RpII140Z36)S5 is reported here. It interacts genetically with RpII140. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. su(RpII140Z36)S5 is discussed in one reference, dating from 1998.
}
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GENR
{
SUMX| The D. melanogaster gene su(RpII140Z36)S4 is reported here. It interacts genetically with RpII140. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. su(RpII140Z36)S4 is discussed in one reference, dating from 1998.
}
# EOR
GENR
{
SUMX| The D. melanogaster gene su(RpII140Z36)S3 is reported here. It interacts genetically with RpII140. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. su(RpII140Z36)S3 is discussed in one reference, dating from 1998.
}
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GENR
{
SUMX| The D. melanogaster gene su(RpII140Z36)S20 is reported here. It interacts genetically with RpII140. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. su(RpII140Z36)S20 is discussed in one reference, dating from 1998.
}
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GENR
{
SUMX| The D. melanogaster gene su(RpII140Z36)S2 is reported here. It interacts genetically with RpII140. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. su(RpII140Z36)S2 is discussed in one reference, dating from 1998.
}
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GENR
{
SUMX| The D. melanogaster gene su(RpII140Z36)S19 is reported here. It interacts genetically with RpII140. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. su(RpII140Z36)S19 is discussed in one reference, dating from 1998.
}
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GENR
{
SUMX| The D. melanogaster gene su(RpII140Z36)S18 is reported here. It interacts genetically with RpII140. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. su(RpII140Z36)S18 is discussed in one reference, dating from 1998.
}
# EOR
GENR
{
SUMX| The D. melanogaster gene su(RpII140Z36)S17 is reported here. It interacts genetically with RpII140. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. su(RpII140Z36)S17 is discussed in one reference, dating from 1998.
}
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GENR
{
SUMX| The D. melanogaster gene su(RpII140Z36)S16 is reported here. It interacts genetically with RpII140. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. su(RpII140Z36)S16 is discussed in one reference, dating from 1998.
}
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GENR
{
SUMX| The D. melanogaster gene su(RpII140Z36)S15 is reported here. It interacts genetically with RpII140. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. su(RpII140Z36)S15 is discussed in one reference, dating from 1998.
}
# EOR
GENR
{
SUMX| The D. melanogaster gene su(RpII140Z36)S14 is reported here. It interacts genetically with RpII140. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. su(RpII140Z36)S14 is discussed in one reference, dating from 1998.
}
# EOR
GENR
{
SUMX| The D. melanogaster gene su(RpII140Z36)S13 is reported here. It interacts genetically with RpII140. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. su(RpII140Z36)S13 is discussed in one reference, dating from 1998.
}
# EOR
GENR
{
SUMX| The D. melanogaster gene su(RpII140Z36)S12 is reported here. It interacts genetically with RpII140. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. su(RpII140Z36)S12 is discussed in one reference, dating from 1998.
}
# EOR
GENR
{
SUMX| The D. melanogaster gene su(RpII140Z36)S11 is reported here. It interacts genetically with RpII140. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. su(RpII140Z36)S11 is discussed in one reference, dating from 1998.
}
# EOR
GENR
{
SUMX| The D. melanogaster gene su(RpII140Z36)S10 is reported here. It interacts genetically with RpII140. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. su(RpII140Z36)S10 is discussed in one reference, dating from 1998.
}
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GENR
{
SUMX| The D. melanogaster gene su(RpII140Z36)S1 is reported here. It interacts genetically with RpII140. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. su(RpII140Z36)S1 is discussed in one reference, dating from 1998.
}
# EOR
GENR
{
SUMX| The D. melanogaster gene e(Pc)84DE is reported here. It has also been known in FlyBase as su(Pc)84DE. It has been mapped cytologically to 84D--E. It interacts genetically with ph-p. There are 2 recorded alleles: 1 classical mutant (available from the public stock centers) and 1 wild-type. e(Pc)84DE is discussed in 2 references, dated between 1993 and 2000. These include at least one study of mutant phenotypes.
}
# EOR
GENR
{
SUMX| The D. melanogaster gene su(N) is reported here. It has been mapped by recombination to 1-28. It interacts genetically with N. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. su(N) is discussed in one reference, dating from 1940.
}
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GENR
{
SUMX| The D. melanogaster gene suppressor of Hairy wing, abbreviated as su(Hw), is reported here. It encodes a product with transcription regulator activity involved in negative regulation of transcription which is localized to the nucleus and the polytene chromosome; it is expressed in the ovary (ovary). It has been sequenced and its amino acid sequence contains a zinc finger, C2H2 type. It has been mapped by recombination to 3-54.8 and cytologically to 88B3. It interacts genetically with y, ct, Ubx, abd-A, sc and 15 other listed genes. There are 49 recorded alleles: 26 in vitro constructs (none available from the public stock centers), 22 classical mutants (4 available from the public stock centers) and 1 wild-type. Amorphic mutations have been isolated which affect the egg chamber and are recessive female sterile and viable. su(Hw) is discussed in 207 references (excluding sequence accessions), dated between 1929 and 2004. These include at least 35 studies of mutant phenotypes, one study of wild-type function and 7 molecular studies. Among findings on su(Hw) function, the su(Hw) chromatin insulator protein alters double-strand break repair frequencies in the Drosophila germ line.
}
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GENR
{
SUMX| The D. melanogaster gene suppressor of Curly, abbreviated as su(Cy), is reported here. There are 3 recorded alleles: 2 classical mutants (none available from the public stock centers) and 1 wild-type. su(Cy) is discussed in 3 references, dated between 1965 and 1992.
}
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GENR
{
SUMX| The D. melanogaster gene suppressor of Contrabithorax, abbreviated as su(Cbx), is reported here. It has been mapped cytologically to 7F1--8C6. There are 2 recorded alleles: 1 classical mutant (available from the public stock centers) and 1 wild-type. su(Cbx) is discussed in 3 references, dated between 1955 and 1992.
}
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GENR
{
SUMX| The D. melanogaster gene suppressor of Bar on 4, abbreviated as su(B)4, is reported here. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. su(B)4 is discussed in 2 references, dated between 1942 and 1992.
}
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GENR
{
SUMX| The D. melanogaster gene suppressor of Bar on 2, abbreviated as su(B)2, is reported here. It has been mapped cytologically to 21--60. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. su(B)2 is discussed in one reference, dating from 1992.
}
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GENR
{
SUMX| The D. melanogaster gene suppressor of Bar, abbreviated as su(B), is reported here. It has been mapped by recombination to 2-94. It interacts genetically with B. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. Mutations have been isolated which affect the ommatidium. su(B) is discussed in 6 references, dated between 1937 and 1992. These include at least one study of mutant phenotypes.
}
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GENR
{
SUMX| The D. melanogaster gene sprouty, abbreviated as sty, is reported here. It encodes a product with putative receptor binding involved in torso signaling pathway which is localized to the plasma membrane; it is expressed in the embryo (embryonic/larval dorsal vessel, embryonic/larval tracheal system, midline glial cell, neuron and oenocyte). It has been sequenced. It has been mapped cytologically to 63D2--3. It interacts genetically with argos, Egfr, W, sev, S and 17 other listed genes. There are 28 recorded alleles: 9 in vitro constructs (none available from the public stock centers), 18 classical mutants (2 available from the public stock centers) and 1 wild-type. Amorphic mutations have been isolated which affect the somatic clone cell non-autonomous ganglionic branch 2, the somatic clone cell non-autonomous dorsal branch 1, the lateral trunk anterior branch and 13 other listed tissues and are pupal recessive lethal, recessive visible and recessive neuroanatomy defective. sty is discussed in 86 references (excluding sequence accessions), dated between 1994 and 2004. These include at least 12 studies of mutant phenotypes, 3 studies of wild-type function and 3 molecular studies. Among findings on sty mutants, in sty mutants twice the wild type number of terminal branches form. Among findings on sty function, sty acts as an antagonist of EGF as well as FGF signalling pathways.
}
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GENR
{
SUMX| The D. melanogaster gene streakex, abbreviated as stx, is reported here. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. Mutations have been isolated which affect the thorax and are semi-lethal and body color defective. stx is discussed in 2 references, dated between 1935 and 1992.
}
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GENR
{
SUMX| The D. melanogaster gene stonewall, abbreviated as stwl, is reported here. It encodes a product with RNA polymerase II transcription factor activity involved in oocyte cell fate determination (sensu Insecta) which is localized to the nucleus; it is expressed in the ovary (female germline stem cell, germarium region 1 to 3, nurse cell and oocyte). It has been sequenced and its amino acid sequence is also available. It has been mapped cytologically to 70D6--7. There are 19 recorded alleles: 2 in vitro constructs (none available from the public stock centers), 16 classical mutants (2 available from the public stock centers) and 1 wild-type. Mutations have been isolated which affect the ovary and are recessive female sterile and male fertile. stwl is discussed in 28 references (excluding sequence accessions), dated between 1989 and 2003. These include at least one study of mutant phenotypes and 3 molecular studies.
}
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GENR
{
SUMX| The D. melanogaster gene straw, abbreviated as stw, is reported here. It has been mapped by recombination to 2-55.1 and cytologically to h46--41A3. There are 11 recorded alleles: 10 classical mutants (4 available from the public stock centers) and 1 wild-type. Mutations have been isolated which affect the wing and are recessive visible and body color defective. stw is discussed in 28 references, dated between 1925 and 2001. These include at least one study of mutant phenotypes.
}
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GENR
{
SUMX| The D. melanogaster gene stumps is reported here. It has also been known in FlyBase as CG18485, CG31317, anon-ESTCL47, anon-estC, dof, hbr and l(3)S083710. It encodes a product involved in gastrulation which is a component of the cytoplasm; it is expressed in the embryo (anterior midgut primordium, embryonic glial cell, embryonic/larval heart, embryonic/larval tracheal system and 6 other listed tissues). It has been sequenced and its amino acid sequence is also available. It has been mapped cytologically to 88C8--9. It interacts genetically with Ras85D, bnl, tor, btl and htl. There are 9 recorded alleles: 3 in vitro constructs (none available from the public stock centers), 5 classical mutants (1 available from the public stock centers) and 1 wild-type. Amorphic mutations have been isolated which affect the egg, the embryonic/larval tracheal system, the embryonic mesoderm and 9 other listed tissues and are embryonic recessive lethal and female sterile. stumps is discussed in 68 references (excluding sequence accessions), dated between 1996 and 2004. These include at least 4 studies of mutant phenotypes, 4 studies of wild-type function and 3 molecular studies. Among findings on stumps mutants, mutations in stumps are associated with defects in the migration and later specification of mesodermal and tracheal cells. Among findings on stumps function, stumps function promotes FGF-directed cell migrations, either by potentiating the FGF signalling process or by coupling the signal to the cellular machinery required for directed cell movement.
}
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GENR
{
SUMX| The D. melanogaster gene small tumoroid, abbreviated as stu, is reported here. It has been mapped by recombination to 1-20.4. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. Mutations have been isolated which affect the melanotic mass and are male poor viable, male fertile, visible and melanotic 'tumor'. stu is discussed in 2 references, dated between 1959 and 1992.
}
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GENR
{
SUMX| The D. melanogaster gene spotty, abbreviated as stt, is reported here. It has been mapped by recombination to 1-34.3. There are 3 recorded alleles: 2 classical mutants (none available from the public stock centers) and 1 wild-type. Mutations have been isolated which affect the wing, the adult abdomen, the microchaeta and the eye and are male reduced viable, male sterile, visible and body color defective. stt is discussed in 2 references, dated between 1959 and 1992.
}
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GENR
{
SUMX| The D. melanogaster gene streaked sterni, abbreviated as sts, is reported here. It has been mapped by recombination to 1-60.3. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. Mutations have been isolated which affect the abdominal sternite and are recessive visible, poor viable, poor fertile and body color defective. sts is discussed in 2 references, dated between 1959 and 1992.
}
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GENR
{
SUMX| The D. melanogaster gene starburst, abbreviated as strb, is reported here. It interacts genetically with f. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. Mutations have been isolated which affect the wing hair. strb is discussed in 3 references, dated between 1996 and 2002. These include at least 2 studies of mutant phenotypes.
}
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GENR
{
SUMX| The D. melanogaster gene stripes, abbreviated as str, is reported here. It has been mapped cytologically to 82A. There is one recorded allele, which is wild-type. str is discussed in one reference, dating from 1995.
}
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GENR
{
SUMX| The D. melanogaster gene silver tips, abbreviated as stp, is reported here. It has been mapped by recombination to 1-46.1. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. Mutations have been isolated which affect the macrochaeta and the microchaeta and are visible, male sterile and male reduced viable. stp is discussed in 2 references, dated between 1959 and 1992.
}
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GENR
{
SUMX| The D. melanogaster gene strung out, abbreviated as stout, is reported here. It has also been known in FlyBase as l(1)6Ee. It has been mapped by recombination to 1-18.9 and cytologically to 6E4--6. It interacts genetically with Dfd. There are 21 recorded alleles: 20 classical mutants (3 available from the public stock centers) and 1 wild-type. Hypomorphic mutations have been isolated which affect the hypostomal sclerite, the latticed process and the mouth hooks and are embryonic recessive lethal. stout is discussed in 8 references, dated between 1983 and 2000. These include at least one study of mutant phenotypes.
}
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GENR
{
SUMX| The D. melanogaster gene stopped, abbreviated as stop, is reported here. It encodes a product involved in oogenesis (sensu Insecta). It has been mapped by recombination to 2-76. There are 3 recorded alleles: 2 classical mutants (1 available from the public stock centers) and 1 wild-type. Mutations have been isolated which are female sterile. stop is discussed in 2 references, dated between 1991 and 1992. These include at least one study of mutant phenotypes.
}
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GENR
{
SUMX| The D. melanogaster gene stocky, abbreviated as sto, is reported here. It has been mapped by recombination to 1-29.8. There are 4 recorded alleles: 3 classical mutants (none available from the public stock centers) and 1 wild-type. Mutations have been isolated which affect the adult abdomen, the wing, the eye and the macrochaeta and are recessive visible, recessive male sterile and male reduced viable. sto is discussed in 2 references, dated between 1958 and 1992.
}
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GENR
{
SUMX| The D. melanogaster gene stoned B, abbreviated as stnB, is reported here. It has also been known in FlyBase as stn. It encodes a product with protein binding involved in synaptic vesicle endocytosis which is a component of the plasma membrane; it is expressed in the adult (adult abdomen, adult head and adult thorax). It has been sequenced. It has been mapped cytologically to 20A4--5. It interacts genetically with shi and syt. There are 9 recorded alleles: 2 in vitro constructs (none available from the public stock centers), 6 classical mutants (none available from the public stock centers) and 1 wild-type. Loss-of-function mutations have been isolated which affect the nerve terminal, the synaptic vesicle and the multivesicular body and are recessive lethal, recessive behavioral, embryonic recessive uncoordinated and neurophysiology defective. stnB is discussed in 38 references (excluding sequence accessions), dated between 1985 and 2003. These include at least 4 studies of mutant phenotypes, 2 studies of wild-type function and 3 molecular studies.
}
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GENR
{
SUMX| The D. melanogaster gene stoned A, abbreviated as stnA, is reported here. It has also been known in FlyBase as stn. It encodes a product with protein binding involved in synaptic vesicle endocytosis which is a component of the synaptic vesicle; it is expressed in the adult (adult abdomen, adult head and adult thorax). It has been sequenced and its amino acid sequence is also available. It has been mapped by recombination to 1-66.3 and cytologically to 20A4--5. It interacts genetically with shi, Su(stn), dnc and syt. There are 22 recorded alleles: 2 in vitro constructs (none available from the public stock centers), 19 classical mutants (1 available from the public stock centers) and 1 wild-type. Hypomorphic mutations have been isolated which affect the nerve terminal, the synaptic vesicle and the multivesicular body and are recessive lethal, recessive behavioral, embryonic recessive uncoordinated and neurophysiology defective. stnA is discussed in 64 references (excluding sequence accessions), dated between 1968 and 2004. These include at least 10 studies of mutant phenotypes, 3 studies of wild-type function and 4 molecular studies. Among findings on stnA function, stnA functions either in the nervous system or in both the nervous system and the musculature, but is not required for gross neural development.
}
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GENR
{
SUMX| The D. melanogaster gene stambha C, abbreviated as stmC, is reported here. It has been mapped by recombination to 2-59.4. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. Mutations have been isolated which are recessive conditional ts paralytic. stmC is discussed in 3 references, dated between 1985 and 1992.
}
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GENR
{
SUMX| The D. melanogaster gene stambha B, abbreviated as stmB, is reported here. It has been mapped by recombination to 2-97.6. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. Mutations have been isolated which are recessive conditional ts paralytic. stmB is discussed in 3 references, dated between 1985 and 1992.
}
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GENR
{
SUMX| The D. melanogaster gene stambha A, abbreviated as stmA, is reported here. It has been mapped by recombination to 2-56.8 and cytologically to 42A8--19. There are 14 recorded alleles: 13 classical mutants (none available from the public stock centers) and 1 wild-type. Mutations have been isolated which affect the anterior dorsal cuticle, the embryonic cephalopharyngeal skeleton, the embryonic denticle belt and 10 other listed tissues and are embryonic recessive lethal, dominant paralytic, (with stmAPEL1) lethal, (with stmAPEL3 to 4) lethal, (with stmAPEL6) lethal, (with stmAPEL8) lethal and (with stmAPEL11) lethal. stmA is discussed in 6 references, dated between 1985 and 2001. These include at least one study of mutant phenotypes. Among findings on stmA mutants, mutation of stmA causing paralysis also confers veratridine resistance, the two effects are genetically inseparable.
}
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GENR
{
SUMX| The D. melanogaster gene stalled, abbreviated as stld, is reported here. It encodes a product involved in grooming behavior. It has been mapped cytologically to 67C. There are 3 recorded alleles: 2 classical mutants (none available from the public stock centers) and 1 wild-type. Mutations have been isolated which are recessive behavioral. stld is discussed in 2 references, dated between 1993 and 1997.
}
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GENR
{
SUMX| The D. melanogaster gene stall, abbreviated as stl, is reported here. It has also been known in FlyBase as fs(2)A16. It encodes a product involved in stalk formation. It has been mapped by recombination to 2-102 and cytologically to 60B8--C5. It interacts genetically with da. There are 6 recorded alleles: 5 classical mutants (1 available from the public stock centers) and 1 wild-type. Mutations have been isolated which affect the basal stalk and are female sterile. stl is discussed in 14 references, dated between 1973 and 2004. These include at least 2 studies of mutant phenotypes.
}
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GENR
{
SUMX| The D. melanogaster gene sticking, abbreviated as stk, is reported here. It has been mapped cytologically to 84C1--2. There are 6 recorded alleles: 5 classical mutants (1 available from the public stock centers) and 1 wild-type. Mutations have been isolated which are lethal. stk is discussed in 6 references, dated between 1980 and 1992.
}
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GENR
{
SUMX| The D. melanogaster gene stand still, abbreviated as stil, is reported here. It encodes a product with molecular_function unknown involved in development which is localized to the nucleus; it is expressed in the adult (male germline stem cell, primary spermatocyte cyst, spermatocyte, spermatogonium and 2 other listed tissues), embryo (nucleus), larva (male germline stem cell, nucleus, ovary, primary spermatocyte cyst and 3 other listed tissues) and ovary (germarium and nurse cell). It has been sequenced. It has been mapped by recombination to 2-63 and cytologically to 49B5. There are 11 recorded alleles: 3 in vitro constructs (none available from the public stock centers), 7 classical mutants (1 available from the public stock centers) and 1 wild-type. Loss-of-function mutations have been isolated which affect the ovary, the egg chamber, the dorsal appendage and 2 other listed tissues and are recessive female sterile. stil is discussed in 20 references (excluding sequence accessions), dated between 1991 and 2003. These include at least 6 studies of mutant phenotypes, one study of wild-type function and 6 molecular studies. Among findings on stil mutants, surviving germ cells in stil mutants exhibit a primary spermatocyte morphology suggesting that stil is a germline sex determination gene. Among findings on stil function, stil has a role in specifying or maintaining a cytoskeletal component that is required in the germ line during oogenesis, and possibly during germ line sex determination.
}
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GENR
{
SUMX| The D. melanogaster gene sticky ch2, abbreviated as stich2, is reported here. It has also been known in FlyBase as sticky-chordotonals. It encodes a product involved in peripheral nervous system development. There are 2 recorded alleles: 1 classical mutant (available from the public stock centers) and 1 wild-type. Mutations have been isolated which affect the chordotonal organ and are recessive lethal. stich2 is discussed in 4 references, dated between 1994 and 2001. These include at least 2 studies of mutant phenotypes and one molecular study.
}
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GENR
{
SUMX| The D. melanogaster gene sticky ch1, abbreviated as stich1, is reported here. It has also been known in FlyBase as sticky-chordotonals. It encodes a product involved in peripheral nervous system development. It has been sequenced. It has been mapped cytologically to 86A. There are 4 recorded alleles: 3 classical mutants (1 available from the public stock centers) and 1 wild-type. Mutations have been isolated which affect the chordotonal organ and are recessive lethal. stich1 is discussed in 15 references (excluding sequence accessions), dated between 1994 and 2003. These include at least 2 studies of mutant phenotypes and one molecular study.
}
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GENR
{
SUMX| The D. melanogaster gene sticky, abbreviated as sti, is reported here. It has been mapped by recombination to 3-36.8 and cytologically to 69C3--70F4. There are 4 recorded alleles: 3 classical mutants (2 available from the public stock centers) and 1 wild-type. Hypomorphic mutations have been isolated which affect the imaginal disc and are larval recessive lethal and mitotic. sti is discussed in 10 references, dated between 1974 and 1998. These include at least one study of mutant phenotypes.
}
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GENR
{
SUMX| The D. melanogaster gene small thin, abbreviated as sth, is reported here. It has been mapped by recombination to 1-3.7. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. Mutations have been isolated which affect the macrochaeta, the adult abdomen, the eye and the wing and are female sterile, male fertile, viable and visible. sth is discussed in 2 references, dated between 1959 and 1992.
}
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GENR
{
SUMX| The D. melanogaster gene string, abbreviated as stg, is reported here. It has also been known in FlyBase as EP1213. It encodes a product with protein tyrosine/serine/threonine phosphatase activity (EC:3.1.3.-) involved in G2/M transition of mitotic cell cycle which is a component of the nucleus; it is expressed in the adult (testis), embryo (Malpighian tubule), larva (eye-antennal disc and optic lobe) and ovary (nurse cell and oocyte). It has been sequenced and its amino acid sequence is also available. It has been mapped by recombination to 3-99 and cytologically to 99A5. It interacts genetically with rux, N, noose, Myb, CycE and 13 other listed genes. There are 106 recorded alleles: 19 in vitro constructs (1 available from the public stock centers), 86 classical mutants (3 available from the public stock centers) and 1 wild-type. Amorphic mutations have been isolated which affect the multidendritic neuron, the external sensory organ, the chordotonal organ and 13 other listed tissues and are embryonic recessive lethal, female fertile, recessive mitotic and somatic clone increased cell size. stg is discussed in 339 references (excluding sequence accessions), dated between 1982 and 2004. These include at least 23 studies of mutant phenotypes, 10 studies of wild-type function, one study of natural polymorphisms and 16 molecular studies. Among findings on stg mutants, stg mutants display a strong reduction in the number of denticle rows. Among findings on stg function, stg is required for completion of daughter centriole assembly in embryos.
}
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GENR
{
SUMX| The D. melanogaster gene stormfront, abbreviated as stf, is reported here. It has been mapped by recombination to 1-35.0 and cytologically to 10A7--11. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. Mutations have been isolated which affect the denticle belt, the head involution stage and the contracted germ band stage and are embryonic recessive lethal. stf is discussed in 2 references, dated between 1988 and 1992. These include at least one study of mutant phenotypes.
}
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GENR
{
SUMX| The D. melanogaster gene stem cell tumor, abbreviated as stet, is reported here. It has also been known in FlyBase as CG12083, CG12504, rho-2 and rhomboid-2. It encodes a product with serine-type peptidase activity involved in epidermal growth factor receptor signaling pathway which is a component of the integral to membrane. It has been sequenced. It has been mapped cytologically to 62A5--6. It interacts genetically with grk, S and rho. There are 23 recorded alleles: 6 in vitro constructs (none available from the public stock centers), 16 classical mutants (none available from the public stock centers) and 1 wild-type. Mutations have been isolated which are viable and male sterile. stet is discussed in 19 references (excluding sequence accessions), dated between 1996 and 2003. These include at least 4 studies of mutant phenotypes and one molecular study. Among findings on stet mutants, somatic support cells fail to surround germ cells properly and germ cells accumulate at early stages of differentiation in stet mutants.
}
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GENR
{
SUMX| The D. melanogaster gene staroid, abbreviated as std, is reported here. It has been mapped by recombination to 2-56.5. It interacts genetically with rho. There are 2 recorded alleles: 1 classical mutant (available from the public stock centers) and 1 wild-type. Mutations have been isolated which affect the eye, the conditional macrochaeta, the conditional wing and 2 other listed tissues and are conditional female semi-sterile, conditional male sterile, reduced conditional viable and conditional small body. std is discussed in 5 references, dated between 1936 and 1995. These include at least one study of mutant phenotypes.
}
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GENR
{
SUMX| The D. melanogaster gene steamer duck, abbreviated as stck, is reported here. It has also been known in FlyBase as pin85A and steamer-duck. It encodes a product with putative structural constituent of cytoskeleton putatively involved in cell motility which is expressed in the embryo (mesoderm, muscle attachment site and visceral mesoderm). It has been sequenced. It has been mapped cytologically to 84F15. It interacts genetically with mys. There are 5 recorded alleles: 1 in vitro construct (not available from the public stock centers), 3 classical mutants (1 available from the public stock centers) and 1 wild-type. Loss-of-function mutations have been isolated which affect the somatic clone wing, the embryonic/larval somatic muscle, the larva and the (with Df(3R)097) embryonic somatic muscle and are larval recessive lethal and somatic clone visible. stck is discussed in 23 references (excluding sequence accessions), dated between 1997 and 2004. These include at least 2 studies of mutant phenotypes and 2 molecular studies.
}
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GENR
{
SUMX| The D. melanogaster gene shuttle craft, abbreviated as stc, is reported here. It encodes a product with single-stranded DNA binding involved in neurogenesis which is localized to the nuclear; it is expressed in the embryo (embryonic central nervous system and larval brain) and ovary (ovary). It has been sequenced and its amino acid sequence contains a 2Fe-2S Ferredoxin, a zinc finger NF-X1 type and a R3H domain. It has been mapped cytologically to 35C2. There are 11 recorded alleles: 10 classical mutants (1 available from the public stock centers) and 1 wild-type. Loss-of-function mutations have been isolated which affect the embryonic maternal effect anterior fascicle, the embryonic maternal effect abdominal posterior fascicle, the central nervous system and 4 other listed tissues and are embryonic recessive lethal. stc is discussed in 57 references (excluding sequence accessions), dated between 1982 and 2004. These include at least one study of mutant phenotypes, one study of wild-type function and 10 molecular studies. Among findings on stc function, a maternally derived source of stc protein is required during embryogenesis but not oogenesis.
}
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GENR
{
SUMX| The D. melanogaster gene short bristle, abbreviated as stb, is reported here. It has been mapped by recombination to 1-14.6. There are 2 recorded alleles: 1 classical mutant (not available from the public stock centers) and 1 wild-type. Mutations have been isolated which affect the macrochaeta and are recessive visible, viable and fertile. stb is discussed in 2 references, dated between 1958 and 1992.
}
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GENR
{
SUMX| The D. melanogaster gene staufen, abbreviated as stau, is reported here. It encodes a product with double-stranded RNA binding involved in pole plasm assembly which is localized to the plasma membrane; it is expressed in the embryo (central nervous system, embryonic nervous system and pole plasm), ovary (female germline stem cell, nurse cell and oocyte) and embryo). It has been sequenced and its amino acid sequence contains a double-stranded RNA binding (DsRBD) domain. It has been mapped by recombination to 2-83.5 and cytologically to 55B5--7. It interacts genetically with nos, neb and osk. There are 24 recorded alleles: 9 in vitro constructs (none available from the public stock centers), 14 classical mutants (2 available from the public stock centers) and 1 wild-type. Loss-of-function mutations have been isolated which affect the embryonic head, the embryonic abdomen and the pole cell and are maternal effect male sterile, maternal effect female sterile, maternal effect recessive lethal and conditional ts (with stau3) memory defective. stau is discussed in 301 references (excluding sequence accessions), dated between 1982 and 2004. These include at least 20 studies of mutant phenotypes, 5 studies of wild-type function and 14 molecular studies. Among findings on stau function, stau has a role in long-term memory.
}
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GENR
{
SUMX| The D. melanogaster gene starry night, abbreviated as stan, is reported here. It has also been known in FlyBase as fmi and starry-night. It encodes a product with receptor signaling protein activity involved in frizzled signaling pathway which is localized to the plasma membrane; it is expressed in the prepupa and pupa (wing). It has been sequenced. It has been mapped by recombination to 2-62 and cytologically to 47B6--7. It interacts genetically with Vang, fz, fy, in, pk and 2 other listed genes. There are 21 recorded alleles: 4 in vitro constructs (none available from the public stock centers), 16 classical mutants (2 available from the public stock centers) and 1 wild-type. Loss-of-function mutations have been isolated which affect the somatic clone cell autonomous ommatidium, the wing, the thorax and the leg and are somatic clone tissue polarity. stan is discussed in 108 references (excluding sequence accessions), dated between 1998 and 2004. These include at least 5 studies of mutant phenotypes, 10 studies of wild-type function and 3 molecular studies. Among findings on stan mutants, mutations in stan alter the polarity of cuticular structures in all regions of the adult body, affecting epidermal hairs, sensory bristles and ommatidia. Among findings on stan function, stan has a function in dendritic development.
}
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GENR
{
SUMX| The D. melanogaster gene stubarista, abbreviated as sta, is reported here. It has also been known in FlyBase as l(1)G0130 and l(1)G0448. It encodes a product with structural constituent of ribosome involved in protein biosynthesis which is localized to the ribosome. It has been sequenced and