Excel File Text File *Disease is associated/modeled with this Gene or a homolog. More...
			Disease Term	Human Homologs	Mouse Homologs	Mouse Models	Homology Source
			congenital stationary night blindness 1A	NYX*	Nyx*	1 model	Alliance of Genome Resources
			congenital stationary night blindness 1B	GRM6*	Grm6*	2 models	Alliance of Genome Resources
			congenital stationary night blindness 1C	TRPM1*	Trpm1*	2 models	Alliance of Genome Resources
			congenital stationary night blindness 1D	SLC24A1*	Slc24a1*	1 model	Alliance of Genome Resources
			congenital stationary night blindness 1E	GPR179*	Gpr179*	1 model	Alliance of Genome Resources
			congenital stationary night blindness 1F	LRIT3*	Lrit3*	1 model	Alliance of Genome Resources
			congenital stationary night blindness 2A	CACNA1F*	Cacna1f*	12 models	Alliance of Genome Resources
			congenital stationary night blindness autosomal dominant 1	RHO*	Rho*	1 model	Alliance of Genome Resources
			congenital stationary night blindness autosomal dominant 2	PDE6B*	Pde6b*	14 models	Alliance of Genome Resources
			Oguchi disease-2	GRK1*	Grk1*	1 model	Alliance of Genome Resources
			congenital stationary night blindness	GUCY2D*	Gucy2e		Alliance of Genome Resources
			congenital stationary night blindness	TRPM1*	Trpm1		Alliance of Genome Resources
			congenital stationary night blindness	TRPV3*	Trpv3		Alliance of Genome Resources
			congenital stationary night blindness	CACNA1F*	Cacna1f		Alliance of Genome Resources
			congenital stationary night blindness 1G	GNAT1*	Gnat1		Alliance of Genome Resources
			congenital stationary night blindness 1H	GNB3*	Gnb3		Alliance of Genome Resources
			congenital stationary night blindness autosomal dominant 3	GNAT1*	Gnat1		Alliance of Genome Resources
			hereditary night blindness	SAG*	Sag		Alliance of Genome Resources
			Oguchi disease-1	SAG*	Sag		Alliance of Genome Resources

	Transgenes and other genome features developed in mice to model this disease.
	Disease Term	Transgenes and Other Genome Features	Mouse Models
	congenital stationary night blindness autosomal dominant 1	Tg(Rho*G90D*A337V)202Sie	1 model