Entity Details

Primary name GLIS3
Entity type gene
Source Source Link

Details

PrimaryID169792
RefseqGeneNG_011782
SymbolGLIS3
NameGLIS family zinc finger 3
Chromosome9
Location9p24.2
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2002-01-27
ModificationDate2021-06-15

Ontological Relatives

UniProt IDsGLIS3_HUMAN

GO terms

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GOName
GO:0000122 negative regulation of transcription by RNA polymerase II
GO:0000978 RNA polymerase II cis-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:0006366 transcription by RNA polymerase II
GO:0045944 positive regulation of transcription by RNA polymerase II
GO:0046872 metal ion binding

Diseases

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Disease IDSourceNameDescription
610199 OMIMDiabetes mellitus, neonatal, with congenital hypothyroidism (NDH)A syndrome of neonatal diabetes syndrome associated with congenital hypothyroidism, congenital glaucoma, hepatic fibrosis and polycystic kidneys. The disease is caused by variants affecting the gene represented in this entry.

Interactions

17 interactions