Entity Details
| Primary name |
TM260_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | Q9NX78 |
| EntryName | TM260_HUMAN |
| FullName | Transmembrane protein 260 |
| TaxID | 9606 |
| Evidence | evidence at protein level |
| Length | 707 |
| SequenceStatus | complete |
| DateCreated | 2003-10-24 |
| DateModified | 2021-06-02 |
Subcellular Location
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| Subcellular Location |
| Membrane |
Domains
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| Domain | Name | Category | Type |
| IPR021280 | Protein of unknown function DUF2723 | Family | Family |
Diseases
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| Disease ID | Source | Name | Description |
| 617478 | OMIM | Structural heart defects and renal anomalies syndrome (SHDRA) | An autosomal recessive syndrome characterized by central nervous system, cardiac, renal, and digit abnormalities. Clinical features include ventricular and atrial septal defects, truncus arteriosus, tetralogy of Fallot, partial anomalous pulmonary venous return, renal cysts, renal failure, and generalized edema. Some patients show partial agenesis of corpus callosum. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
0 interactions
| Interactor | Partner | Sources | Publications | Link |