Amino acid replacement: D564N.
The D564N missense mutation hits a conserved residue in the fourth ankyrin repeat.
G19039662A
D564N | mib2-PA; D564N | mib2-PB; D564N | mib2-PC
D564N
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
flightless (with mib2S1259)
flightless (with mib2S1456)
mib2S2616 homozygous late stage 16 embryos display severe loss and detachment of somatic muscles, as compared to controls; mib2S2616 homozygous and mib2S0768/mib21 transheterozygous late stage 16 embryos present a bloated midgut phenotype, and an irregular arrangement of longitudinal visceral muscle fibers, as compared to controls.
mib2S1456/mib2S2616 and mib2S1259/mib2S2616 transheterozygotes present a fully (or nearly fully) penetrant flightless phenotype, as compared to controls.