GPR179

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Probable G-protein coupled receptor 179 is a protein that in humans is encoded by the GPR179 gene.[5]

AliasesGPR179, CSNB1E, GPR158L, GPR158L1, G protein-coupled receptor 179
End38,343,956 bp[1]
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GPR179
Identifiers
AliasesGPR179, CSNB1E, GPR158L, GPR158L1, G protein-coupled receptor 179
External IDsOMIM: 614515; MGI: 2443409; HomoloGene: 34917; GeneCards: GPR179; OMA:GPR179 - orthologs
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 MbChr 11: 97.22 – 97.24 Mb
PubMed search[3][4]
Wikidata
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Clinical relevance

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

References

Further reading

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