Entity Details
| Primary name |
CGNL1_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | Q0VF96 |
| EntryName | CGNL1_HUMAN |
| FullName | Cingulin-like protein 1 |
| TaxID | 9606 |
| Evidence | evidence at protein level |
| Length | 1302 |
| SequenceStatus | complete |
| DateCreated | 2007-12-04 |
| DateModified | 2021-06-02 |
Subcellular Location
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| Subcellular Location |
| Cell junction |
Domains
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| Domain | Name | Category | Type |
| IPR002928 | Myosin tail | Domain | Domain |
Diseases
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| Disease ID | Source | Name | Description |
| 139300 | OMIM | Aromatase excess syndrome (AEXS) | An autosomal dominant disorder characterized by increased extraglandular aromatization of steroids that presents with heterosexual precocity in males and isosexual precocity in females. The gene represented in this entry is involved in disease pathogenesis. A chromosomal aberration inv(15)(q21.2;q21.3) has been found in patients with aromatase excess syndrome. The inversion moves the promoter of the CGNL1 gene into a 5-prime position in relation to the aromatase coding region. |
Interactions
6 interactions