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GPR179, G protein-coupled receptor 179

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GPR179, G protein-coupled receptor 179

  • This gene encodes a member of the glutamate receptor subfamily of G protein-coupled receptors. The encoded protein has an EGF-like calcium binding domain and a seven transmembrane domain in the N-terminal region of the protein. Mutations in this gene are associated with congenital stationary night blindness type 1E. [provided by RefSeq, Apr 2012]

  • Gene Synonyms (CSNB1E, GPR158L, GPR158L1, probable G-protein coupled receptor 179, GPR158-like 1, probable G-protein coupled receptor 158-like 1,)
  • NCBI Gene ID: 440435
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q6PRD1
    UNIPROT ID#>>A0A087X0K8
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

G protein-coupled receptor 179 interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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