Entity Details
| Primary name |
ZBT11_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | O95625 |
| EntryName | ZBT11_HUMAN |
| FullName | Zinc finger and BTB domain-containing protein 11 |
| TaxID | 9606 |
| Evidence | evidence at protein level |
| Length | 1053 |
| SequenceStatus | complete |
| DateCreated | 2004-08-16 |
| DateModified | 2021-06-02 |
Subcellular Location
Show/Hide Table
| Subcellular Location |
| Nucleus |
Domains
Show/Hide Table
| Domain | Name | Category | Type |
| IPR000210 | BTB/POZ domain | Domain | Domain |
| IPR011333 | SKP1/BTB/POZ domain superfamily | Family | Homologous superfamily |
| IPR013087 | Zinc finger C2H2-type | Domain | Domain |
| IPR036236 | Zinc finger C2H2 superfamily | Family | Homologous superfamily |
| IPR041588 | Integrase zinc-binding domain | Domain | Domain |
Diseases
Show/Hide Table
| Disease ID | Source | Name | Description |
| 618383 | OMIM | Intellectual developmental disorder, autosomal recessive 69 (MRT69) | A form of mental retardation, a disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. Intellectual deficiency is the only primary symptom of non-syndromic mental retardation, while syndromic mental retardation presents with associated physical, neurological and/or psychiatric manifestations. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
2 interactions