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Rabbit Anti-GPR179 antibody
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]
Function:
Orphan receptor.
Subcellular Location:
Cell membrane.
Similarity:
Belongs to the G-protein coupled receptor 3 family.
SWISS:
Q6PRD1
Gene ID:
88435
Database links:
Entrez Gene: 88435 Human
SwissProt: Q6PRD1 Human
Unigene: 462915 Human
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