Amino acid replacement: V419D. Mutation in region of protein that is involved in substrate binding.
T6469152A
V419D | mmy-PA; V382D | mmy-PB; V382D | mmy-PD
V419D
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
mmyGA74 mutants have a CNS phenotype that is characteristic of defects in midline signalling. The commissural pathways appear diffuse and there is a reduction in the thickness of longitudinal tracts. The Fas2-positive fascicles are not as well defined as in wild type, and Fas2-positive axons are observed extending towards the midline.