Gene

tet2

ID
ZDB-GENE-090312-98
Name
tet methylcytosine dioxygenase 2
Symbol
tet2 Nomenclature History
Previous Names
  • tet2l (1)
  • im:7136741
  • si:ch211-216c6.1
Type
protein_coding_gene
Location
Chr: 1 Mapping Details/Browsers
Description
Enables 5-methylcytosine dioxygenase activity and broad specificity oxidative DNA demethylase activity. Involved in regulation of gene expression. Acts upstream of or within cell surface receptor signaling pathway; endothelial to hematopoietic transition; and hemopoiesis. Predicted to be located in chromosome. Predicted to be active in nucleus. Is expressed in several structures, including cardiovascular system; eye; hematopoietic system; liver; and pleuroperitoneal region. Used to study myelodysplastic syndrome. Human ortholog(s) of this gene implicated in gastrointestinal system cancer (multiple); hematologic cancer (multiple); lung non-small cell carcinoma; and primary immunodeficiency disease. Orthologous to human TET2 (tet methylcytosine dioxygenase 2).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
13 figures from 11 publications
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
Wild Type Expression Summary
Phenotype
All Phenotype Data
13 figures from 3 publications
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Allele Type Localization Consequence Mutagen Supplier
au59Allele with one deletionExon 1Frameshift, Premature StopTALEN
hsi12Allele with one deletionExon 2UnknownCRISPR
ihb2019Allele with one insertionExon 2UnknownTALEN
ki117Allele with one deletionUnknownUnknownnot specified
mk17Allele with one deletionExon 8Frameshift, Premature StopTALEN
sa8671Allele with one point mutationUnknownPremature StopENU
sa11184Allele with one point mutationUnknownPremature StopENU
sa13278Allele with one point mutationUnknownPremature StopENU
sa14623Allele with one point mutationUnknownPremature StopENU
sa32686Allele with one point mutationUnknownPremature StopENU
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Sequence Targeting Reagents
Human Disease
Associated With tet2 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
myelodysplastic syndrome Alliance Myelodysplastic syndrome, somatic 614286
Immunodeficiency 75 619126
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Associated With tet2 Via Experimental Models
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Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Domain IPR024779 2OGFeDO JBP1/TET, oxygenase domain
Domain IPR046942 Methylcytosine dioxygenase TET1-3, oxygenase domain
Family IPR040175 Methylcytosine dioxygenase TET1/2/3
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Domain Details Per Protein
Protein Additional Resources Length 2OGFeDO JBP1/TET, oxygenase domain Methylcytosine dioxygenase TET1/2/3 Methylcytosine dioxygenase TET1-3, oxygenase domain
UniProtKB:E7F958 InterPro 1715
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Transcripts
Genome Browsers
Genome Build: GRCz11Chromosome: 1
Type Name Annotation Method Has Havana Data Length (nt) Analysis
mRNA tet2-201 (1) Ensembl 8,807 nt
mRNA tet2-202 (1) Ensembl 5,887 nt
mRNA tet2-203 (1) Ensembl 6,319 nt
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Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
No data available
Marker Relationships
Relationship Marker Type Marker Accession Numbers Citations
Contained inBACCH211-216C6ZFIN Curated Data
EncodesESTIMAGE:7136741Thisse et al., 2004
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Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Species Symbol Chromosome Accession # Evidence
HumanTET24
Phylogenetic tree (1)
Conserved genome location (synteny) (2)
Amino acid sequence comparison (3)
MouseTet23
Phylogenetic tree (1)
Amino acid sequence comparison (2)
Conserved genome location (synteny) (2)
Citations
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