Amino acid replacement: G89D.
G877627A
G89D | ninaA-PA
G89D
Site of nucleic acid substitution inferred by FlyBase based on reported amino acid change
abnormal neurophysiology
visible | recessive
Mutant photoreceptors do not undergo a prolonged depolarising afterpotential (DPA). Double mutants with Arr23 can trigger and support strong PDAs.
Deep pseudopupil score of 1. ninaE product, Rh1, is probably immature in this allele, as indicated by its glycosylated state.
Ondek.