Enables retinal binding activity and spectrin binding activity. Involved in red, far-red light phototransduction and rhodopsin mediated signaling pathway. Located in photoreceptor outer segment membrane and rough endoplasmic reticulum membrane. Human ortholog(s) of this gene implicated in congenital stationary night blindness autosomal dominant 1; fundus albipunctatus; night blindness; retinitis pigmentosa; and retinitis pigmentosa 4. Orthologous to human RHO (rhodopsin); PARTICIPATES IN altered visual phototransduction pathway; retinitis pigmentosa pathway; retinoid cycle metabolic pathway; INTERACTS WITH 3,7-dihydropurine-6-thione; ammonium chloride; bisphenol A.
astragaloside A inhibits the reaction [[Iron-Dextran Complex results in increased abundance of Iron] which results in decreased expression of RHO mRNA]
[Iron-Dextran Complex results in increased abundance of Iron] which results in decreased expression of RHO mRNA and astragaloside A inhibits the reaction [[Iron-Dextran Complex results in increased abundance of Iron] which results in decreased expression of RHO mRNA]
[Iron-Dextran Complex results in increased abundance of Iron] which results in decreased expression of RHO mRNA and astragaloside A inhibits the reaction [[Iron-Dextran Complex results in increased abundance of Iron] which results in decreased expression of RHO mRNA]
[Iron-Dextran Complex results in increased abundance of Iron] which results in decreased expression of RHO mRNA and astragaloside A inhibits the reaction [[Iron-Dextran Complex results in increased abundance of Iron] which results in decreased expression of RHO mRNA]
[lead acetate results in increased abundance of Lead] which results in decreased expression of RHO mRNA and [lead acetate results in increased abundance of Lead] which results in decreased expression of RHO protein
[lead acetate results in increased abundance of Lead] which results in decreased expression of RHO mRNA and [lead acetate results in increased abundance of Lead] which results in decreased expression of RHO protein
Aberrant retinal tight junction and adherens junction protein expression in an animal model of autosomal dominant Retinitis pigmentosa: the Rho(-/-) mouse.
Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho(-/-) mice.