Entity Details
| Primary name |
S26A8_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | Q96RN1 |
| EntryName | S26A8_HUMAN |
| FullName | Testis anion transporter 1 |
| TaxID | 9606 |
| Evidence | evidence at protein level |
| Length | 970 |
| SequenceStatus | complete |
| DateCreated | 2008-02-26 |
| DateModified | 2021-06-02 |
Subcellular Location
Show/Hide Table
| Subcellular Location |
| Membrane |
Domains
Show/Hide Table
| Domain | Name | Category | Type |
| IPR001902 | SLC26A/SulP transporter | Family | Family |
| IPR002645 | STAS domain | Domain | Domain |
| IPR011547 | SLC26A/SulP transporter domain | Domain | Domain |
| IPR030303 | Solute carrier family 26 member 8 (testis anion transporter 1) | Family | Family |
| IPR036513 | STAS domain superfamily | Family | Homologous superfamily |
Diseases
Show/Hide Table
| Disease ID | Source | Name | Description |
| 606766 | OMIM | Spermatogenic failure 3 (SPGF3) | A disorder characterized by primary infertility, sperm morphologic abnormalities, and moderate to severe asthenozoospermia, condition in which the percentage of progressively motile sperm is abnormally low. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
3 interactions