GPR179

GPR179
Identifiers
Aliases	GPR179, CSNB1E, GPR158L, GPR158L1, G protein-coupled receptor 179
External IDs	MGI: 2443409 HomoloGene: 34917 GeneCards: GPR179
Gene ontology
Molecular function	• G-protein coupled receptor activity; • signal transducer activity;
Cellular component	• integral component of membrane; • plasma membrane; • membrane;
Biological process	• G-protein coupled receptor signaling pathway; • signal transduction; • visual perception; • response to stimulus;
	Sources:Amigo / QuickGO
Orthologs
	440435
	217143
	n/a
	ENSMUSG00000070337
	Q6PRD1
	n/a
	NM_001004334
	NM_001081220; NM_175453
	NP_001004334
	n/a
	Wikidata
View/Edit Human	View/Edit Mouse

Probable G-protein coupled receptor 179 is a protein that in humans is encoded by the GPR179 gene.^[3]

Clinical relevance[edit]

Mutations in this gene have been associated to cases of congenital stationary Night Blindness.^[4]

^ "Human PubMed Reference:".
^ "Mouse PubMed Reference:".
^ "Entrez Gene: GPR179 G protein-coupled receptor 179".
^ Audo I, Bujakowska K, Orhan E, Poloschek CM, Defoort-Dhellemmes S, Drumare I, Kohl S, Luu TD, Lecompte O, Zrenner E, Lancelot ME, Antonio A, Germain A, Michiels C, Audier C, Letexier M, Saraiva JP, Leroy BP, Munier FL, Mohand-Saïd S, Lorenz B, Friedburg C, Preising M, Kellner U, Renner AB, Moskova-Doumanova V, Berger W, Wissinger B, Hamel CP, Schorderet DF, De Baere E, Sharon D, Banin E, Jacobson SG, Bonneau D, Zanlonghi X, Le Meur G, Casteels I, Koenekoop R, Long VW, Meire F, Prescott K, de Ravel T, Simmons I, Nguyen H, Dollfus H, Poch O, Léveillard T, Nguyen-Ba-Charvet K, Sahel JA, Bhattacharya SS, Zeitz C (Feb 10, 2012). "Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness.". American Journal of Human Genetics. 90 (2): 321–30. doi:10.1016/j.ajhg.2011.12.007. PMC 3276675. PMID 22325361.