Entity Details
| Primary name |
PRCD_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | Q00LT1 |
| EntryName | PRCD_HUMAN |
| FullName | Photoreceptor disk component PRCD |
| TaxID | 9606 |
| Evidence | evidence at protein level |
| Length | 54 |
| SequenceStatus | complete |
| DateCreated | 2007-03-20 |
| DateModified | 2021-06-02 |
Subcellular Location
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| Subcellular Location |
| Cell projection |
| Endoplasmic reticulum |
| Golgi apparatus |
| Membrane |
Domains
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| Domain | Name | Category | Type |
| IPR027937 | Photoreceptor disk component PRCD | Family | Family |
Diseases
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| Disease ID | Source | Name | Description |
| 610599 | OMIM | Retinitis pigmentosa 36 (RP36) | A retinal dystrophy belonging to the group of pigmentary retinopathies. Retinitis pigmentosa is characterized by retinal pigment deposits visible on fundus examination and primary loss of rod photoreceptor cells followed by secondary loss of cone photoreceptors. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
0 interactions
| Interactor | Partner | Sources | Publications | Link |