Gene Symbol | GPR179 |
Entrez Gene ID | 440435 |
Full Name | G protein-coupled receptor 179 |
Synonyms | CSNB1E,GPR158L,GPR158L1 |
General protein information |
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Gene Type | protein-coding |
Organism | Homo sapiens(human) |
Genome | |
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. [provided by RefSeq, Apr 2012]. |
Disorder MIM: | |
Disorder Html: | Night blindness, congenital stationary (complete), 1E, autosomal recessive, 614565 (3) |