Amino acid replacement: ?319term.
C22453307T
Q319term | wap-PA; Q319term | wap-PB; Q319term | wap-PC; Q319term | wap-PD
?319term
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
lethal (with Dp(1;3)DC382)
lethal (with Dp(1;3)DC383)
lethal (with Dp(1;3)DC384)
lethal (with Dp(1;3)DC386)
lethal (with Dp(1;3)DC387)
lethal (with Dp(1;3)DC388)
lethal (with Dp(1;3)DC390)
lethal (with Dp(1;3)DC562)
viable (with Df(1)DCB1-35c), with Dp(1;3)DC389
viable (with Df(1)Exel6255), with Dp(1;3)DC389
viable (with Dp(1;3)DC389)
visible (with Df(1)Exel6255)
crossvein | increased number (with wap9)
wap2/wap9 mutant flies are characterised by three phenotypes: 1) In ~10% of adult flies there are supernumerary crossveins located between the second and third longitudinal wing veins 2) the tergal depressor of the trochanter (TDT) (a prominent tubular jump muscle in the thorax) is missing 3) mutants show semi-lethality.
wap2 mutants initiate founder cell specification and myoblast fusion of the tergal depressor of the trochanter (TDT) jump muscle, but this is not sustained and the nascent jump muscles don't continue development.
wap2/Df(1)BSC708 mutant flies are viable and have normal vein vein patterning and an intact tergal depressor of the trochanter (TDT) jump muscle.
wap2/Df(1)LB6 mutant flies are viable and have normal vein vein patterning and an intact tergal depressor of the trochanter (TDT) jump muscle.
wap2/Df(1)R8A mutant flies are viable and have normal vein vein patterning and an intact tergal depressor of the trochanter (TDT) jump muscle.
wap2/Df(1)Exel6255 mutant flies are semi-lethal and exhibit an additional crossvein between the second and third longitudinal vein. The jump muscle is absent in almost all flies. In cases where the muscle is present, it exhibits highly abnormal morphology and a >60% reduction in the number of fibres compared to wild type.
Lethality occurs during pupal or adult stages. Homozygous germline clones display no maternal effect. Embryos derived from heterozygous mothers exhibit no CNS or PNS defects.
Most flies die just before eclosion, those which do hatch usually have their wings slightly set apart, a somewhat darker than normal thorax and one or more extra crossveins. Hemizygous females have the same phenotype as hemizygous males and homozygous females. Approximately 50% of the expected number of wap2/Df(1)su(f)5 females survive at 24-25oC, whereas only about 1% hatch at 29-30oC. The mutant phenotype is more extreme at the higher temperature.
no maternal effect in homozygous germ-line clones
Lifschytz.
Maternal germline clonal analysis demonstrates there is no maternal effect.