The P{lacW} insertion is 800bp downstream of the putative ATG start codon.
When heterozygous females are crossed to wild-type males, 22.7% of the heterozygous progeny have abdominal segmentation defects, while 9.5% of the +/+ offspring have defects.
No retinal phenotypes are seen in skdL7062 mutant flies.
The average number of crystal cells per embryo is reduced (to 9.9) in homozygous stage 13-14 embryos compared to wild type (36 +/- 2.2 cells on average). Mutant stage 14 embryos show cell cycle defects in the head region.
skdL7062 has visible | maternal effect | dominant phenotype, non-enhanceable by MED311/MED31[+]
skdL7062 has adult abdomen | maternal effect phenotype, non-enhanceable by MED311/MED31[+]
skdL7062/skd[+] is an enhancer of adult epidermis | maternal effect phenotype of MED311
skdL7062/skd[+] is an enhancer of retina phenotype of Hsap\HTT128Q.1-336.UAS, Scer\GAL4GMR.PU
skdL7062/skd[+] is an enhancer of retina phenotype of Hsap\ATXN182Q.UAS, Scer\GAL4GMR.PU
skdL7062 is an enhancer of eye phenotype of Hsap\ATXN182Q.UAS, Scer\GAL4GMR.PF
skdL7062 is an enhancer of retina phenotype of Hsap\ATXN182Q.UAS, Scer\GAL4GMR.PF
skdL7062/skd[+] is a suppressor of wing margin phenotype of Bx1
When MED311/MED311 females are crossed to skdL7062/+ males, 54.7% of the MED311/skdL7062 adult progeny have abdominal defects, indicating that zygotic skdL7062 enhances the MED311 phenotype.
No increase in abdominal segmentation defects is seen in the adult progeny of MED311/skdL7062 females compared to the defects of the progeny of skdL7062/+ females, indicating that MED311 is not an enhancer of skdL7062 when maternally supplied.
One copy of skdL7062 enhances the retinal phenotype seen when Hsap\HTT128Q.1-336.Scer\UAS is expressed under the control of Scer\GAL4GMR.PU.
One copy of skdL7062 enhances the retinal phenotype seen when Hsap\ATXN182Q.Scer\UAS is expressed under the control of Scer\GAL4GMR.PU.
Complements: l(3)L5541L5541. Complements: fngrG554.