Entity Details
| Primary name |
GP179_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | Q6PRD1 |
| EntryName | GP179_HUMAN |
| FullName | Probable G-protein coupled receptor 179 |
| TaxID | 9606 |
| Evidence | evidence at transcript level |
| Length | 2367 |
| SequenceStatus | complete |
| DateCreated | 2006-01-10 |
| DateModified | 2021-06-02 |
Subcellular Location
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| Subcellular Location |
| Cell membrane |
Domains
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| Domain | Name | Category | Type |
| IPR017978 | GPCR family 3, C-terminal | Domain | Domain |
| IPR032964 | Probable G-protein coupled receptor 179 | Family | Family |
| IPR043458 | G-protein coupled receptor 158/179 | Family | Family |
Diseases
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| 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
0 interactions
| Interactor | Partner | Sources | Publications | Link |