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.
Fkbp1400734/+ mutant flies do not exhibit temperature-induced mobility defects.
Fkbp1300734 mutants display ISNb bypass at a similar rate to wild-type embryos.
Fkbp14[+]/Fkbp1400734 is a non-enhancer of indirect flight muscle cell phenotype of DysRNAi.NH2.UAS, Scer\GAL4Act.PU
Fkbp14[+]/Fkbp1400734 is a non-enhancer of indirect flight muscle cell phenotype of DgRNAi.UAS, Scer\GAL4Act.PU
Fkbp1400734 is a non-enhancer of anterior fascicle & axon | ectopic phenotype of Larbypass
Dg[+]/DgO86, Fkbp1400734 has indirect flight muscle cell phenotype
Dg[+]/Dg323, Fkbp1400734 has indirect flight muscle cell phenotype
Fkbp14 Dys double heterozygous flies (Fkbp1400734/Df(3R)Exel6184) do not exhibit indirect flight muscle degeneration.
Fkbp1400734 DgO86 double heterozygous flies exhibit indirect flight muscle degeneration.
One copy of Fkbp1400734 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 Fkbp1400734 does not enhance the indirect flight muscle degeneration seen when DgdsRNA.Scer\UAS is expressed under the control of Scer\GAL4tub.PU.
Fkbp1400734 Dg323 double heterozygous flies exhibit indirect flight muscle degeneration.
The Fkbp1300734 mutation does not increase the frequency of the Larbypass ISNb bypass phenotype.
A. Spradling.
Reversion analysis proved that the P{PZ} is responsible for the lethal phenotype.
Complements: MESK201467. Complements: l(2)0360503605. Complements: MESK208827. Complements: MESK208882. Complements: Sdc10608. Complements: l(2)k10317k10317.