Entity Details
| Primary name |
S26A5_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | P58743 |
| EntryName | S26A5_HUMAN |
| FullName | Prestin |
| TaxID | 9606 |
| Evidence | evidence at protein level |
| Length | 744 |
| SequenceStatus | complete |
| DateCreated | 2002-03-27 |
| DateModified | 2021-06-02 |
GO terms
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| GO | Name |
| GO:0005887 | integral component of plasma membrane |
| GO:0007605 | sensory perception of sound |
| GO:0008271 | secondary active sulfate transmembrane transporter activity |
| GO:0008360 | regulation of cell shape |
| GO:0015106 | bicarbonate transmembrane transporter activity |
| GO:0015108 | chloride transmembrane transporter activity |
| GO:0015116 | sulfate transmembrane transporter activity |
| GO:0015301 | anion:anion antiporter activity |
| GO:0019531 | oxalate transmembrane transporter activity |
Subcellular Location
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| Subcellular Location |
| Cell membrane |
Domains
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| Domain | Name | Category | Type |
| IPR001902 | SLC26A/SulP transporter | Family | Family |
| IPR002645 | STAS domain | Domain | Domain |
| IPR011547 | SLC26A/SulP transporter domain | Domain | Domain |
| IPR018045 | Sulphate anion transporter, conserved site | Site | Conserved site |
| IPR030282 | Prestin | Family | Family |
| IPR036513 | STAS domain superfamily | Family | Homologous superfamily |
Diseases
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| Disease ID | Source | Name | Description |
| 613865 | OMIM | Deafness, autosomal recessive, 61 (DFNB61) | A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
1 interaction