Nucleotide substitution: C1099T. Amino acid replacement: R244C.
C21555541T
C1099T
R244C | Egfr-PA; R293C | Egfr-PB
R244C
Homozygous adult viable.
Homozygotes and hemizygotes are viable. Adults exhibit milder eye defects than would be expected from the severity of the wing and haltere defects.
Mutation of Egfr that affects the gene function required for imaginal disc derivatives, a class IV lesion.
Class IV allele.