Gene: GPR179
Alternate names for this Gene: CSNB1E|GPR158L|GPR158L1
Gene Summary: 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.
Gene is located in Chromosome: 17
Location in Chromosome : 17q12
Description of this Gene: G protein-coupled receptor 179
Type of Gene: protein-coding