Amino acid replacement: E336K.
G21054324A
E336K | shg-PA
E336K
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
An average of 0.4 PGCs are left outside of the midgut in shgA9-49 mutants, with 25% of the embryos showing PGC adhesion defects. This phenotype is dependent on the maternal genotype, as a paternal wild-type copy does not alleviate the phenotype.
shgA9-49 is a non-suppressor of abnormal cell migration | embryonic stage phenotype of Df(2R)wun-GL, wun2EP2650ex34, wun49
shgA9-49 is a non-suppressor of germline cell | embryonic stage phenotype of Df(2R)wun-GL, wun2EP2650ex34, wun49
Loss of maternal shgA9-49 is unable to rescue the germ cell migration defects seen in embryos derived from females carrying wun49 wun2EP2650ex34 germline clones crossed to Df(2R)wun-GL males. Germ cell dispersal can be seen at stage 10.