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Probable G-protein coupled receptor 179 is a protein that in humans is encoded by the GPR179 gene. 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.
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Protein Aliases: G-protein coupled receptor 179; GPR158-like; GPR158-like 1; GPR158-like 1 receptor; Probable G-protein coupled receptor 158-like 1; Probable G-protein coupled receptor 179
Gene Aliases: 5330439C02Rik; CSNB1E; GPR158L; GPR158L1; GPR179; Nob5
UniProt ID: (Human) Q6PRD1, (Mouse) E9PY61
Entrez Gene ID: (Human) 440435, (Mouse) 217143
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