Entity Details

Primary name ZNF142
Entity type gene
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Details

PrimaryID7701
RefseqGeneNG_033099
SymbolZNF142
Namezinc finger protein 142
Chromosome2
Location2q35
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1998-08-19
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsZN142_HUMAN

GO terms

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GOName
GO:0000977 RNA polymerase II transcription regulatory region sequence-specific DNA binding
GO:0000981 DNA-binding transcription factor activity, RNA polymerase II-specific
GO:0005634 nucleus
GO:0006357 regulation of transcription by RNA polymerase II
GO:0046872 metal ion binding

Diseases

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Disease IDSourceNameDescription
618425 OMIMNeurodevelopmental disorder with impaired speech and hyperkinetic movements (NEDISHM)An autosomal recessive disorder characterized by global developmental delay, impaired intellectual development, delayed walking, poor or absent speech, and a hyperkinetic movement disorder with dystonia, tremor, ataxia, or chorea. Some patients develop seizures. The disease is caused by variants affecting the gene represented in this entry.