GPR179
GPR179 | |||
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Identifiers | |||
Gene ontology | |||
Molecular function | |||
Cellular component | |||
Biological process | |||
Sources:Amigo / QuickGO |
Ensembl | |||||||||
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UniProt | |||||||||
RefSeq (mRNA) | |||||||||
RefSeq (protein) | |||||||||
Location (UCSC) | Chr 17: 38.32 – 38.34 Mb | Chr 11: 97.22 – 97.24 Mb | |||||||
PubMed search | [3] | [4] |
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]
Clinical relevance
Mutations in this gene have been associated to cases of congenital stationary
Night Blindness.[6]
References
- ^ a b c ENSG00000277399 GRCh38: Ensembl release 89: ENSG00000276469, ENSG00000277399 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000070337 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Entrez Gene: GPR179 G protein-coupled receptor 179".
- PMID 22325361.
Further reading
- Bjarnadóttir TK, Fredriksson R, Schiöth HB (2006). "The gene repertoire and the common evolutionary history of glutamate, pheromone (V2R), taste(1) and other related G protein-coupled receptors". Gene. 362: 70–84. PMID 16229975.