Gene
TET2
tet methylcytosine dioxygenase 2
- HGNC 25941↗(opens in a new tab)
- Ensembl gene ENSG00000168769↗(opens in a new tab)
- NCBI Gene 54790↗(opens in a new tab)
Summary
- Cytogenetic location
- 4q24
- Coordinates
- Chromosome 4: 105,146,876–105,279,803 (GRCh38)
- Exons
- 11 exons across 132.9 kb
- Protein
- 2,002 amino acids
- Also known as
- FLJ20032
- Previous symbols
- KIAA1546
- MANE Select transcript
- ENST00000380013.9NM_001127208.3
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Other Inborn Errors of Immunity
- Immunodeficiency Disease
One of 170 genes linked to it
Disease in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral.
- 2 GenCC submitters rate it definitive or strong
What knowing changes
HSCT for SCID and severe PIDs; immunoglobulin replacement (IVIG/SCIG) for antibody deficiencies; leniolisib (Joenja, FDA 2023) for APDS; gene therapy for ADA-SCID; abatacept for CTLA4/LRBA deficiency; prophylactic antibiotics; G-CSF for CGD
How TET2 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
- Stretches short reads find hard
Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.
Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).
Nearby genes from Ensembl release 116, on GRCh38.
Exons make up 9.6 kb of the gene's 132.9 kb; 6,009 of those bases code for the protein.
How a genome test reads TET2
8
positions in TET2 where ClinVar classes a change as pathogenic or likely pathogenic
None of them falls in a region short reads find hard.
A whole genome covers all 132.9 kb of TET2, introns included, not only the 9.6 kb of exons.
Genes linked to the same conditions
- ADAadenosine deaminaseShares 1 condition
- AICDAactivation induced cytidine deaminaseShares 1 condition
- AK2adenylate kinase 2Shares 1 condition
- ARPC1Bactin related protein 2/3 complex subunit 1BShares 1 condition
- ARPC5actin related protein 2/3 complex subunit 5Shares 1 condition
- ATMATM serine/threonine kinaseShares 1 condition
- ATP6AP1ATPase H+ transporting accessory protein 1Shares 1 condition
- B2Mbeta-2-microglobulinShares 1 condition
- BACH2BACH transcriptional regulator 2Shares 1 condition
- BCL10BCL10 immune signaling adaptorShares 1 condition
- BCL11BBCL11 transcription factor BShares 1 condition
- BLNKB cell linkerShares 1 condition
Traits linked to TET2
The Human Phenotype Ontology lists these as features of the rare conditions TET2 can cause. Each trait's page lists the other genes linked to it.
Abnormality of blood and blood-forming tissues
- Cancer of lymphatic system
- Decreased class-switched memory B cell proportion
- Abnormal mast cell morphology
- Abnormal shape of platelets
- Anemia of inadequate production
- Blood clot in artery
- Blood clot in vein
- Blood tumor
Show 53 more traits
- Bone marrow disease
- Increased megakaryocyte count
- Increased number of platelets in blood
- Megakaryocyte nucleus hyperlobulation
- Myelodysplasia
- Myeloid leukemia
- Platelet abnormalities
- Prolonged bleeding time
- Refractory anemia with ringed sideroblasts
- Abnormal megakaryocyte morphology
- Abnormality of blood and blood-forming tissues
- Bleeding tendency
- Bone marrow hypercellularity
- Elevated white blood count
- Erythroid hyperplasia
- Erythroid hypoplasia
- High blood eosinophil count
- Increased CD25+ mast cell proportion
- Low number of red blood cells or hemoglobin
- Low platelet count
- Macrocytic anemia
- Megaloblastic erythroid hyperplasia
- Myeloproliferative disorder
- Normochromic anemia
- Normocytic anemia
- Single lineage myelodysplasia
- Abnormal blood clot
- Abnormal number of granulocyte precursors
- Acute blood cancer
- Acute myeloid leukemia
- Blood cancer
- Blood clot in liver vein
- Blood spots
- Bone marrow failure
- Bruising susceptibility
- Chronic myelomonocytic leukemia
- Dysplastic granulopoesis
- Ecchymosis
- Extramedullary hematopoiesis
- Gastrointestinal bleeding
- Granulocytic hyperplasia
- Hypochromic anemia
- Hyposegmentation of neutrophil nuclei
- Increased blood neutrophil counts
- Increased total basophil count
- Low blood cell count
- Low blood neutrophil count
- Myelofibrosis
- Petechiae
- Poikilocytosis
- Chronic lymphatic leukemia
- Decreased total granulocyte count
- Multiple myeloma
Abnormality of the digestive system
- Abdominal cramps
- Abdominal pain
- Anorexia
- Diarrhea
- Enlarged liver
- Malabsorption
- Accumulation of fluid in the abdomen
- Decreased liver function
Show 2 more traits
External links
Gene records
Transcript
Protein
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
- GenCC and ClinGen, released 2026-10-16: which conditions the gene is linked to, and how strongly.
- The ACMG secondary findings list, SF v3.2.
- ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). TET2 gene: tet methylcytosine dioxygenase 2. Retrieved 17 October 2026, from https://dantelabs.com/genes/tet2
Dante Labs. TET2 gene: tet methylcytosine dioxygenase 2 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/tet2
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