| Gene Symbol | GPR179 |
| Entrez Gene ID | 440435 |
| Full Name | G protein-coupled receptor 179 |
| Synonyms | CSNB1E,GPR158L,GPR158L1 |
| General protein information |
|
| 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) |








































User Manual