Amino acid replacement: D?N.
Mutation is in amino acid 491 of the EcR-B1 open reading frame, in the ligand-binding domain.
Nucleotide substitution: G?A.
G6093817A
G?A
D462N | EcR-PA; D491N | EcR-PB; D282N | EcR-PC; D462N | EcR-PD; D462N | EcR-PE; D491N | EcR-PG
D491N
Heterozygotes are phenotypically wild type.
EcRD491N, Hsc70-4195/Hsc70-4[+] has visible | dominant phenotype
EcRD491N/EcR[+], Hsc70-4195 has visible | dominant phenotype
EcRD491N, Hsc70-4195/Hsc70-4[+] has wing phenotype
EcRD491N, Hsc70-4195/Hsc70-4[+] has leg phenotype
EcRD491N/EcR[+], Hsc70-4195 has wing phenotype
EcRD491N/EcR[+], Hsc70-4195 has leg phenotype
In transheterozygous combination with Hsc70-4195, wings are frequently blistered and legs are frequently malformed. This enhancement is completely suppressed by P{Hsc70-4.14}.