GPR179

Last updated
GPR179
Identifiers
Aliases GPR179 , CSNB1E, GPR158L, GPR158L1, G protein-coupled receptor 179
External IDs OMIM: 614515 MGI: 2443409 HomoloGene: 34917 GeneCards: GPR179
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001004334

NM_001081220
NM_175453

RefSeq (protein)

NP_001004334

NP_001074689

Location (UCSC) Chr 17: 38.32 – 38.34 Mb Chr 11: 97.22 – 97.24 Mb
PubMed search [3] [4]
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. [5]

Contents

Clinical relevance

Mutations in this gene have been associated to cases of congenital stationary Night Blindness. [6]

Related Research Articles

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GPR20 Protein-coding gene in the species Homo sapiens

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GPR124 Protein-coding gene in the species Homo sapiens

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GPR171

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GPR135

Probable G-protein coupled receptor 135 is a protein that in humans is encoded by the GPR135 gene.

GPR157

Probable G-protein coupled receptor 157 is a protein that in humans is encoded by the GPR157 gene.

GPR101 Protein-coding gene in the species Homo sapiens

Probable G-protein coupled receptor 101 is a protein that in humans is encoded by the GPR101 gene.

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Probable G-protein coupled receptor 62 is a protein that in humans is encoded by the GPR62 gene.

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GPR139

Probable G-protein coupled receptor 139 is a protein that in humans is encoded by the GPR139 gene.

TAAR9 Protein-coding gene in the species Homo sapiens

Trace amine-associated receptor 9 is a protein that in humans is encoded by the TAAR9 gene.

References

  1. 1 2 3 ENSG00000277399 GRCh38: Ensembl release 89: ENSG00000276469, ENSG00000277399 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000070337 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. "Entrez Gene: GPR179 G protein-coupled receptor 179".
  6. 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.

Further reading