Entity Details
| Primary name |
GIPC3_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | Q8TF64 |
| EntryName | GIPC3_HUMAN |
| FullName | PDZ domain-containing protein GIPC3 |
| TaxID | 9606 |
| Evidence | evidence at protein level |
| Length | 312 |
| SequenceStatus | complete |
| DateCreated | 2006-07-25 |
| DateModified | 2021-06-02 |
Subcellular Location
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Domains
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| Domain | Name | Category | Type |
| IPR001478 | PDZ domain | Domain | Domain |
| IPR017379 | PDZ domain-containing protein GIPC1/2/3 | Family | Family |
| IPR036034 | PDZ superfamily | Family | Homologous superfamily |
Diseases
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| Disease ID | Source | Name | Description |
| 601869 | OMIM | Deafness, autosomal recessive, 15 (DFNB15) | A form of non-syndromic sensorineural hearing loss with prelingual onset. 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
3 interactions