Analogous mutation in human PINK1 implicated in Parkinson disease 6; mutation carried on in vitro construct; site of nucleotide substitution in fly gene and specific disease association inferred by FlyBase curator.
Expression of Pink1G426D.Scer\UAS under the control of Scer\GAL4GMR.PF at 18[o]C does not produce a visible eye phenotype.
HtrA2UAS.cYa, Pink1G426D.UAS, Scer\GAL4GMR.PF has visible | heat sensitive phenotype
HtrA2UAS.cYa, Pink1G426D.UAS, Scer\GAL4GMR.PF has eye | heat sensitive phenotype
Co-expression of HtrA2Scer\UAS.cYa and Pink1G426D.Scer\UAS under the control of Scer\GAL4GMR.PF at 18[o]C results in a small, rough eye phenotype.