Imprecise excision of the progenitor insertion, resulting in a 1.4kb deletion that deletes all of the coding exons and the 3' UTR.
No apparent defects in cleavage furrows are observed in cleavage furrows in embryos derived from Arf51FΔKG1 mutant mothers, although patches of nuclear loss (nuclear fall-ot) are observed in some embryos.
The patterning defects in retinas expressing Arf51FGD13822 under the control of Scer\GAL4GMR.PF is enhanced by heterozygosity for Arf51FΔKG1.
Arf51F[+]/Arf6ΔKG1 is an enhancer of ommatidium phenotype of Scer\GAL4GMR.PF, cindrRNAi.PC.PD.UAS
Arf6ΔKG1, Arf6GD13822, Dcr-2UAS.cDa, Scer\GAL4GMR.PF has retina phenotype
The ommatidial patterning errors resulting from the expression of cindrdsRNA.PC.PD.Scer\UAS via Scer\GAL4GMR.PF are strongly enhanced in Arf51FΔKG1 heterozygotes.