Entity Details
| Primary name |
C1QT5_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | Q9BXJ0 |
| EntryName | C1QT5_HUMAN |
| FullName | Complement C1q tumor necrosis factor-related protein 5 |
| TaxID | 9606 |
| Evidence | evidence at protein level |
| Length | 243 |
| SequenceStatus | complete |
| DateCreated | 2002-04-16 |
| DateModified | 2021-06-02 |
Subcellular Location
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| Subcellular Location |
| Secreted |
Domains
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| Domain | Name | Category | Type |
| IPR001073 | C1q domain | Domain | Domain |
| IPR008160 | Collagen triple helix repeat | Repeat | Repeat |
| IPR008983 | Tumour necrosis factor-like domain superfamily | Family | Homologous superfamily |
Diseases
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| Disease ID | Source | Name | Description |
| 605670 | OMIM | Late-onset retinal degeneration (LORD) | Autosomal dominant disorder characterized by onset in the fifth to sixth decade with night blindness and punctate yellow-white deposits in the retinal fundus, progressing to severe central and peripheral degeneration, with choroidal neovascularization and chorioretinal atrophy. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
6 interactions