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 | 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 | GUCY2D* | Gucy2e | 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 | ||||
Oguchi disease-1 | SAG* | Sag | Alliance of Genome Resources |
Transgenes and other genome features developed in mice to model this disease.
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Disease Term | Transgenes and Other Genome Features | Mouse Models | |
congenital stationary night blindness autosomal dominant 1 | Tg(Rho*G90D*A337V)202Sie | 1 model |