Entity Details

Primary name TCF20_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9UGU0
EntryNameTCF20_HUMAN
FullNameTranscription factor 20
TaxID9606
Evidenceevidence at protein level
Length1960
SequenceStatuscomplete
DateCreated2002-08-02
DateModified2021-06-02

Ontological Relatives

GenesTCF20

GO terms

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GOName
GO:0003677 DNA binding
GO:0003723 RNA binding
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0006357 regulation of transcription by RNA polymerase II
GO:0016604 nuclear body
GO:0045944 positive regulation of transcription by RNA polymerase II
GO:0046872 metal ion binding

Subcellular Location

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Subcellular Location
Nucleus

Domains

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DomainNameCategoryType
IPR001965 Zinc finger, PHD-typeDomainDomain
IPR013083 Zinc finger, RING/FYVE/PHD-typeFamilyHomologous superfamily
IPR034732 Extended PHD (ePHD) domainDomainDomain
IPR041972 Transcription factor 20, ePHD domainDomainDomain

Diseases

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Disease IDSourceNameDescription
618430 OMIMDevelopmental delay with variable intellectual impairment and behavioral abnormalities (DDVIBA)An autosomal dominant disorder characterized by impaired intellectual development with speech difficulties, dysmorphic features, and behavioral abnormalities including autism spectrum disorder, attention deficit and hyperactivity. Additional variable features may include hypotonia, somatic overgrowth, macrocephaly, mild distal skeletal anomalies, sleep disturbances, movement disorders, and gastrointestinal issues, such as constipation. The disease is caused by variants affecting the gene represented in this entry.