Amino acid replacement: W1439term.
G21575066A
W1587term | InR-PA; W1587term | InR-PB; W1587term | InR-PC; W1587term | InR-PD
W1439term
Mutation is in the cytoplasmic region.
G to A nucleotide change at the second or third position of the wild type Trp codon leads to a nonsense mutation. InR[31] and InR[304] have mutations at adjacent G residues; specific changes for each not reported. The mutation was annotated at the second base of the codon.
Selective removal of InRE19 function in eye progenitor cells generates flies with strongly reduced eye and head capsule while all other parts are wild-type. Mosaic eyes show photoreceptors that are reduced in size by more than half.
CNS defect and failure of germ band retraction, failure dorsal closure and defects in head structure.
InR31 is a non-enhancer of visible phenotype of upd1GMR.PB
InR31 is a non-suppressor of visible phenotype of upd1GMR.PB
InR31 is a non-enhancer of eye phenotype of upd1GMR.PB
InR31 is a non-suppressor of eye phenotype of upd1GMR.PB
Alleles of InR form an allelic series based on phenotypic strength: InR339 > InR31 > InR211 > InRE19 > InR353.
When in trans with Df(3R)e-D7 the lethal phenotype can be rescued by P{hs-inr}.