Enables retinal binding activity and spectrin binding activity. Involved in G protein-coupled opsin signaling pathway and red, far-red light phototransduction. 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.