Entity Details
| Primary name |
GPR179 |
| Entity type |
gene |
| Source |
Source Link |
Details
| PrimaryID | 440435 |
| RefseqGene | NG_032655 |
| Symbol | GPR179 |
| Name | G protein-coupled receptor 179 |
| Chromosome | 17 |
| Location | 17q12 |
| TaxID | 9606 |
| Status | live |
| SourceGenome | genomic |
| SourceOrigin | natural |
| CreationDate | 2004-07-21 |
| ModificationDate | 2021-06-11 |
Diseases
Show/Hide Table
| Disease ID | Source | Name | Description |
| 614565 | OMIM | Night blindness, congenital stationary, 1E (CSNB1E) | An autosomal recessive, non-progressive retinal disorder characterized by impaired night vision, absence of the electroretinogram (ERG) b-wave, and variable degrees of involvement of other visual functions. Affected individuals have an ERG waveform that lacks the b-wave because of failure to transmit the photoreceptor signal through the retinal depolarizing bipolar cells. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
2 interactions