Entity Details

Primary name ZNF711
Entity type gene
Source Source Link

Details

PrimaryID7552
RefseqGeneNG_012535
SymbolZNF711
Namezinc finger protein 711
ChromosomeX
LocationXq21.1
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1989-09-07
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsZN711_HUMAN

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

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.