Entity Details
| Primary name |
DCA17_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | Q5H9S7 |
| EntryName | DCA17_HUMAN |
| FullName | DDB1- and CUL4-associated factor 17 |
| TaxID | 9606 |
| Evidence | evidence at protein level |
| Length | 520 |
| SequenceStatus | complete |
| DateCreated | 2007-09-11 |
| DateModified | 2021-06-02 |
Subcellular Location
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| Subcellular Location |
| Membrane |
| Nucleus |
Domains
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| Domain | Name | Category | Type |
| IPR031620 | DDB1- and CUL4-associated factor 17 | Family | Family |
Diseases
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| Disease ID | Source | Name | Description |
| 241080 | OMIM | Woodhouse-Sakati syndrome (WDSKS) | A rare autosomal recessive disorder characterized by hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
3 interactions