Amino acid replacement: T58M.
C1861039T
T58M | Rap1-PA; T58M | Rap1-PB; T58M | Rap1-PC
T58M
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
Homozygotes exhibit rough eyes, some facets are missing R7 cells and numbers of outer R cells.
Roughened external eye morphology, internally most facets are missing R7 and some are missing outer cells.
Rap1E127 has eye photoreceptor cell phenotype, enhanceable by fafBX3
Rap1E127 has eye photoreceptor cell phenotype, enhanceable by fafFO8
Mutation is not a simple hypermorph or hypomorph. The protein does provide some wild type activity and also antagonises the wild-type function in some manner.