Entity Details

Primary name GZF1
Entity type gene
Source Source Link

Details

PrimaryID64412
RefseqGene
SymbolGZF1
NameGDNF inducible zinc finger protein 1
Chromosome20
Location20p11.21
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2001-05-30
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsGZF1_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:0001227 DNA-binding transcription repressor activity, RNA polymerase II-specific
GO:0001658 branching involved in ureteric bud morphogenesis
GO:0005654 nucleoplasm
GO:0005730 nucleolus
GO:0005737 cytoplasm
GO:0006355 regulation of transcription, DNA-templated
GO:0043565 sequence-specific DNA binding
GO:0045892 negative regulation of transcription, DNA-templated
GO:0046872 metal ion binding

Diseases

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Disease IDSourceNameDescription
617662 OMIMJoint laxity, short stature, and myopia (JLSM)An autosomal recessive disease characterized by generalized joint laxity, joint dislocation, pectus carinatum, short stature, and severe myopia with retinal detachment. The disease is caused by variants affecting the gene represented in this entry.

Interactions

19 interactions