Amino acid replacement: R312Q.
G8067180A
R312Q | mys-PA; R312Q | mys-PB; R312Q | mys-PC; R312Q | mys-PD
R312Q
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
Mutants show normal location of photoreceptor nuclei in the retina.
Moderate allele.
The phenotype of mild displacement of photoreceptor nuclei that is seen in the retina of mosaic animals in which the eyes are homozygous for Bsgk13638 is enhanced if the animals are also hemizygous for mysb45.
The severity of the displacement of photoreceptor nuclei phenotype that is seen in the retina of mosaic animals in which the eyes are homozygous for Bsgδ265 is enhanced if the animals are also hemizygous for mysb45.
mewM6 mysb45 double heterozygotes show displacement of photoreceptor nuclei in the retina in 3% of cases.
Selected as: a mutation that permits the survival of an F1 male.