Nucleotide substitution: G931A. Amino acid replacement: E188K.
G21555373A
G931A
E188K | Egfr-PA; E237K | Egfr-PB
E188K
In trans to Egfrt1, Egfrtop-EA and Egfrtop-EB show unusually severe bristle defects.
Homozygous embryos show no defects, hemizygotes are pupal lethal. Adults preferentially produce bristle defects. Embryos produced from heteroallelic combination with Egfrt1 have a severe ventralised phenotype, reduction in size of their dorsal appendage.
Mutation of Egfr that affects the gene function required for imaginal disc derivatives, a class IV lesion.
Class IV allele.