We performed RT-qPCR analyses on the following eleven genes: Rhodopsin (phototransduction, RP and Congenital stationary night blindness (CSNB)), Gnat1 (phototransduction, CSNB), S-opsin, M-opsin (phototransduction, color blindness), Pde6g (phototransduction, RP), Slc24a1 (phototransduction, CSNB), Rdh12 (visual cycle, LCA and RP), Rpgrip1 (ciliary function, LCA and CORD), Nrl (transcription regulation, RP), Cabp4 (synaptic function, CSNB, LCA), and Fscn2 (Cytoskeleton regulation, RP and macular dystrophy). This evidence concerns the gene FSCN2 and Leber congenital amaurosis.