Amino acid replacement: ?635term.
G8532822A
W635term | foi-PA; W635term | foi-PB; W635term | foi-PC; W635term | foi-PD
?635term
G to A nucleotide change at the second or third position of the Trp codon leads to a nonsense mutation. (exact site of mutation unspecified). Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
A foi16.33/+ background enhances the visual system degeneration seen in Scer\GAL4GMR.PF, Ppt1Scer\UAS.cKa flies.
In mutant embryos with severe gonad coalescence defects, the gonadal mesoderm cells fail to coalesce and, instead, extend into the neighbouring mesoderm. In mutant embryos with moderate gonad coalescence defects, the gonadal mesoderm partially coalesces with the germ cells, but the gonad does not attain the compact, spherical appearance seen in the wild type, resulting in misshapen gonads.
foi[+]/foi16.33 is an enhancer of abnormal neuroanatomy phenotype of Ppt1UAS.cKa, Scer\GAL4GMR.PF
foi[+]/foi16.33 is an enhancer of eye phenotype of Ppt1UAS.cKa, Scer\GAL4GMR.PF