The K88N mutation is associated with Leber congenital amaurosis in humans, though expression of Hsap\CRXK88N.Scer\UAS.T:Zzzz\FLAG is not stated to specifically model this retinopathy in D. melanogaster.
Scer\GAL4oc.1.6/Hsap\CRXK88N.UAS.Tag:FLAG is a non-suppressor of rhabdomere phenotype of ocuvi
Scer\GAL4oc.1.6/Hsap\CRXK88N.UAS.Tag:FLAG is a non-suppressor of ommatidium phenotype of ocuvi
Expression of Hsap\CRXK88N.Scer\UAS.T:Zzzz\FLAG under the control of Scer\GAL4oc.1.6 does not rescue rhabdomere or ommatidial morphology in ocuvi flies.