Entity Details
Primary name |
ZN711_HUMAN |
Entity type |
UniProt |
Source |
Source Link |
Details
Accession | Q9Y462 |
EntryName | ZN711_HUMAN |
FullName | Zinc finger protein 711 |
TaxID | 9606 |
Evidence | evidence at protein level |
Length | 761 |
SequenceStatus | complete |
DateCreated | 2002-09-19 |
DateModified | 2021-06-02 |
Subcellular Location
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Subcellular Location |
Nucleus |
Domains
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Domain | Name | Category | Type |
IPR006794 | Transcriptional activator, Zfx / Zfy domain | Domain | Domain |
IPR013087 | Zinc finger C2H2-type | Domain | Domain |
IPR036236 | Zinc finger C2H2 superfamily | Family | Homologous superfamily |
Diseases
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Disease ID | Source | Name | Description |
300803 | OMIM | Mental retardation, X-linked 97 (MRX97) | A disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
4 interactions