GPR179

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GPR179
Identifiers
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
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
View/Edit HumanView/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

  1. ^ a b c ENSG00000277399 GRCh38: Ensembl release 89: ENSG00000276469, ENSG00000277399Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000070337Ensembl, 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. PMID 22325361
    .

Further reading

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