Entity Details

Primary name ZN711_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9Y462
EntryNameZN711_HUMAN
FullNameZinc finger protein 711
TaxID9606
Evidenceevidence at protein level
Length761
SequenceStatuscomplete
DateCreated2002-09-19
DateModified2021-06-02

Ontological Relatives

GenesZNF711

GO terms

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GOName
GO:0005634 nucleus
GO:0010468 regulation of gene expression
GO:0043565 sequence-specific DNA binding
GO:0045893 positive regulation of transcription, DNA-templated
GO:0046872 metal ion binding

Subcellular Location

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Subcellular Location
Nucleus

Domains

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DomainNameCategoryType
IPR006794 Transcriptional activator, Zfx / Zfy domainDomainDomain
IPR013087 Zinc finger C2H2-typeDomainDomain
IPR036236 Zinc finger C2H2 superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
300803 OMIMMental 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