Entity Details

Primary name TET3
Entity type gene
Source Source Link

Details

PrimaryID200424
RefseqGene
SymbolTET3
Nametet methylcytosine dioxygenase 3
Chromosome2
Location2p13.1
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2002-04-30
ModificationDate2021-06-13

Ontological Relatives

UniProt IDsTET3_HUMAN

GO terms

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GOName
GO:0001939 female pronucleus
GO:0001940 male pronucleus
GO:0005634 nucleus
GO:0005694 chromosome
GO:0005737 cytoplasm
GO:0006211 5-methylcytosine catabolic process
GO:0006493 protein O-linked glycosylation
GO:0008270 zinc ion binding
GO:0008327 methyl-CpG binding
GO:0044727 DNA demethylation of male pronucleus
GO:0045944 positive regulation of transcription by RNA polymerase II
GO:0070579 methylcytosine dioxygenase activity
GO:0070989 oxidative demethylation
GO:0080111 DNA demethylation
GO:0080182 histone H3-K4 trimethylation

Diseases

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Disease IDSourceNameDescription
618798 OMIMBeck-Fahrner syndrome (BEFAHRS)A developmental disorder characterized by mild to severe intellectual disability, global developmental delay, hypotonia, autistic traits, movement disorders, growth abnormalities including overgrowth or poor growth, and facial dysmorphism. Both autosomal dominant and autosomal recessive inheritance has been reported. The disease is caused by variants affecting the gene represented in this entry.