FlyBase curator comment: Interactions with Dg[086] and/or Dg[323] were detected in a Dg[086]/+ or Dg[323]/+ background which exhibits no obvious changes in muscle morphology. Nonetheless, these interactions have been captured as 'modifier' ('exacerbates') annotations here to best capture the experimental finding and the authors' intention.
SP2353MB00605/+ mutant flies exhibit temperature-induced mobility defects.
SP2353MB00605 homozygous mutant third instar larvae do not show any significant defects in axon migration in the brain compared to controls.
SP2353MB00605/SP2353[+] is a non-enhancer of indirect flight muscle cell phenotype of DysRNAi.NH2.UAS, Scer\GAL4Act.PU
SP2353MB00605/SP2353[+] is a non-enhancer of indirect flight muscle cell phenotype of DgRNAi.UAS, Scer\GAL4Act.PU
Dg[+]/DgO86, SP2353MB00605 has indirect flight muscle cell phenotype
Dg[+]/Dg323, SP2353MB00605 has indirect flight muscle cell phenotype
SP2353 Dys double heterozygous flies (SP2353MB00605/Df(3R)Exel6184) do not exhibit indirect flight muscle degeneration.
SP2353MB00605 DgO86 double heterozygous flies exhibit indirect flight muscle degeneration.
One copy of SP2353MB00605 does not enhance the indirect flight muscle degeneration seen when DysdsRNA.NH2.Scer\UAS is expressed under the control of Scer\GAL4Act.PU.
One copy of SP2353MB00605 does not enhance the indirect flight muscle degeneration seen when DgdsRNA.Scer\UAS is expressed under the control of Scer\GAL4tub.PU.
SP2353MB00605 Dg323 double heterozygous flies exhibit indirect flight muscle degeneration.
Combination of either DgO86 or Df(3R)Exel6184 in heterozygous state with a single copy of SP2353MB00605 does not significantly affect the frequency of lamina plexus defects in the third instar larvae.