Entity Details
| Primary name |
SLUR1_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | P55000 |
| EntryName | SLUR1_HUMAN |
| FullName | Secreted Ly-6/uPAR-related protein 1 |
| TaxID | 9606 |
| Evidence | evidence at protein level |
| Length | 103 |
| SequenceStatus | complete |
| DateCreated | 1996-10-01 |
| DateModified | 2021-06-02 |
Subcellular Location
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| Subcellular Location |
| Secreted |
Domains
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| Domain | Name | Category | Type |
| IPR016054 | Ly-6 antigen/uPA receptor-like | Domain | Domain |
| IPR027103 | Secreted Ly-6/uPAR-related protein 1 | Family | Family |
Diseases
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| Disease ID | Source | Name | Description |
| 248300 | OMIM | Mal de Meleda (MDM) | A rare autosomal recessive skin disorder, characterized by diffuse transgressive palmoplantar keratoderma with keratotic lesions extending onto the dorsa of the hands and the feet (transgrediens). Patients may have hyperhidrosis. Other features include perioral erythema, lichenoid plaques on the knees and the elbows, and nail abnormalities. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
2 interactions