Table 2. Disease genes: human congenital stationary night blindness.

Genes~	Inheritance*	Phenotype	Studies
GNAT1, PDE6B, RHO	Dominant	Night blindness	(138-140)
CABP4, CACNA2D4	Recessive	Incomplete night blindness	(141,142)
GRM6, TRPM1	Recessive	Night blindness	(137,143-145)
SAG, GRK1	Recessive	Oguchi disease	(146,147)
CACNA1F	X-Linked	Incomplete night blindness (CSNB2)	(148,149)
NYX	X-Linked	Night blindness (CSNB1)	(150)

^~, adapted from source https://sph.uth.edu/Retnet/; *, dominant, autosomal dominant; recessive, autosomal recessive.