Amino acid replacement: G666R.
G12100362A
G666R | Ced-12-PA
G666R
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change. Could alternatively be a G to C nucleotide change; unspecified.
Homozygous embryos have minor defects in myoblast fusion: a small number of myoblasts remain unfused and muscles are occasionally missing.
Ced-128C6/Df(2L)HO55 embryos exhibit modest myoblast fusion defects: the overall muscle pattern is unperturbed, but some unfused myoblasts are present just under the muscle layer.
Germline clone embryos maternally mutant for Ced-128C6 and zygotically heterozygous for Df(2L)Prl (that removes Ced-12) exhibit a greater number of missing muscles and unfused myoblasts compared to zygotic Ced-128C6 trans-heterozygotes.