rs777934036
This variant is located in the SAG gene.
▶ClinVar annotation
Retinitis pigmentosa; Oguchi disease; not provided; Retinitis pigmentosa 47;Oguchi disease-1; Inborn genetic diseases
View on ClinVar →About SAG
Members of arrestin/beta-arrestin protein family are thought to participate in agonist-mediated desensitization of G-protein-coupled receptors and cause specific dampening of cellular responses to stimuli such as hormones, neurotransmitters, or sensory signals. S-arrestin, also known as S-antigen, is a major soluble photoreceptor protein that is involved in desensitization of the photoactivated transduction cascade. It is expressed in the retina and the pineal gland and inhibits coupling of rhodopsin to transducin in vitro. Additionally, S-arrestin is highly antigenic, and is capable of inducing experimental autoimmune uveoretinitis. Mutations in this gene have been associated with Oguchi disease, a rare autosomal recessive form of night blindness. [provided by RefSeq, Jul 2008]
View all SAG variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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