Mutation in the transmembrane anchor domain.
Amino acid replacement: S219F.
C878115T
S219F | ninaA-PA
S219F
Site of nucleic acid substitution inferred by FlyBase based on reported amino acid change
visible | recessive
Deep pseudopupil score of 2.
This particular substitution was isolated independently twice. Strong ninaA phenotype, even though this amino acid replacement does not significantly alter the hydrophobic character of the region.
This particular substitution was isolated independently twice. Strong ninaA phenotype, even though this amino acid replacement does not significantly alter the hydrophobic character of the region.