Entity Details

Primary name ZBTB20
Entity type gene
Source Source Link

Details

PrimaryID26137
RefseqGeneNG_052992
SymbolZBTB20
Namezinc finger and BTB domain containing 20
Chromosome3
Location3q13.31
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2000-10-20
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsZBT20_HUMAN

GO terms

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GOName
GO:0000976 transcription cis-regulatory region binding
GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding
GO:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0005737 cytoplasm
GO:0006357 regulation of transcription by RNA polymerase II
GO:0016604 nuclear body
GO:0045821 positive regulation of glycolytic process
GO:0046872 metal ion binding
GO:0046889 positive regulation of lipid biosynthetic process
GO:0055088 lipid homeostasis
GO:0071333 cellular response to glucose stimulus
GO:1990837 sequence-specific double-stranded DNA binding

Diseases

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Disease IDSourceNameDescription
259050 OMIMPrimrose syndrome (PRIMS)A disease characterized by macrocephaly, intellectual disability, disturbed behavior, dysmorphic facial features, ectopic calcifications, large calcified ear auricles, and progressive muscle wasting. The disease is caused by variants affecting the gene represented in this entry.