Amino acid replacement: L49R. Amino acid replacement: G589E. Mutation near the amino terminus, and at the C-terminal end of putative transmembrane spanning α-helix 5.
Point mutation.
Point mutation in the structural portion of w.
Drosopterin (red pigment) levels are 29% of wild-type levels, xanthommatin levels (brown pigments) are 64% of wild-type levels.
Increase in wild type eye pigment in the presence of Mowgamma.
Phenotype is not affected by Doa mutations.
Eye colour: reddish brown.
Eye colour: deep ruby, later sepia-like. Eye colour: like wcf when heterozygous with w1. Eye colour: like wcf when heterozygous with wa. Eye colour: like wcf when heterozygous with wbl. Eye colour: like wcf when heterozygous with wco. Eye colour: like wcf when heterozygous with wcol. Eye colour: like wcf when heterozygous with wsat. Malpighian tubule colour: bright yellow.
wcf has abnormal eye color phenotype, suppressible by ox[+]/ox1
wcf has abnormal eye color | recessive phenotype, suppressible by Rga[+]/Rga03834
wcf has abnormal eye color | recessive phenotype, suppressible by Low1
wcf has pigment cell phenotype, suppressible by RpLP001544
wcf has pigment cell phenotype, suppressible by Rga[+]/Rga03834
wcf has pigment cell phenotype, suppressible by Low1
sgl05007, wcf has pigment cell phenotype
Nicoletti, 1960.
Located near wBwx and just distal to wa.