Missense mutation (R31C) and a 36bp deletion that removes amino acid residues 67-78.
A 36bp deletion that removes amino acid residues 67-78. One of two lesions in mutant.
C7244478T
R31C | mei-P22-PA
R31C
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change. One of two lesions in mutant.
mei-P22CA1215 is a suppressor of dorsal appendage | maternal effect phenotype of spn-BBU
mei-P22CA1215 is a suppressor of karyosome phenotype of spn-BBU
The ventralisation phenotype seen in eggs laid by spn-BBU females is suppressed if the females are also mutant for mei-P22CA1215.
The failure of karyosome condensation which is seen in spn-BBU oocytes is suppressed by mei-P22CA1215.