GMR regulatory sequences drive expression of a constitutively active form of InR (carries the amino acid replacement A1325D). The mutation mimics the human V938D protein variant of Longo et al., 1992 (PMID:1618747).
Eyes are slightly larger than wild type.
InRA1325D.GMR has abnormal size phenotype, enhanceable by Ptp61F[+]/Ptp61F4-10
InRA1325D.GMR has abnormal size phenotype, enhanceable by Ptp61FRNAi.UAS.WIZ/Scer\GAL4GMR.PU
InRA1325D.GMR has abnormal size phenotype, enhanceable by Ptp61FGD3571/Scer\GAL4GMR.PU
InRA1325D.GMR has abnormal size phenotype, suppressible by Ptp61FUAS.cBa/Scer\GAL4GMR.PU
InRA1325D.GMR has eye phenotype, enhanceable by Ptp61F[+]/Ptp61F4-10
InRA1325D.GMR has eye phenotype, enhanceable by Ptp61FRNAi.UAS.WIZ/Scer\GAL4GMR.PU
InRA1325D.GMR has eye phenotype, enhanceable by Ptp61FGD3571/Scer\GAL4GMR.PU
InRA1325D.GMR has eye phenotype, suppressible by Ptp61FUAS.cBa/Scer\GAL4GMR.PU