Amino acid replacement: P669L.
C19132205T
P669L | botv-PA
P669L
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
botv510, Scer\GAL4GMR.PF is an enhancer of visible | adult stage phenotype of Hsap\INSC96Y.UAS, Scer\GAL4GMR.PF
botv510/botv[+] is a non-enhancer of abnormal neuroanatomy | embryonic stage phenotype of Scer\GAL4P52, Sema1aUAS.cYa, Sema1ak13702
botv510/botv[+] is a non-suppressor of abnormal neuroanatomy | embryonic stage phenotype of Scer\GAL4P52, Sema1aUAS.cYa, Sema1ak13702
botv510, Scer\GAL4GMR.PF is an enhancer of eye phenotype of Hsap\INSC96Y.UAS, Scer\GAL4GMR.PF
botv510/botv[+] is a non-enhancer of larval posterior commissure | embryonic stage phenotype of Scer\GAL4P52, Sema1aUAS.cYa, Sema1ak13702
botv510/botv[+] is a non-suppressor of larval posterior commissure | embryonic stage phenotype of Scer\GAL4P52, Sema1aUAS.cYa, Sema1ak13702
botv510, ttv524 has wing disc | somatic clone phenotype
botv510, ttv524 has cytoneme | larval stage phenotype
The commissural axon phenotype (failure to cross the midline) seen in embryos expressing Sema-1aScer\UAS.cYa under the control of Scer\GAL4P52 in a Sema-1ak13702 null background is not affected if the embryos are also heterozygous for botv510.
One copy of botv510 enhances the eye phenotype seen when Hsap\INSC96Y.Scer\UAS is expressed under the control of Scer\GAL4GMR.PF.