CBFA2T2

Protein found in humans From Wikipedia, the free encyclopedia

Protein CBFA2T2 is a protein that in humans is encoded by the CBFA2T2 gene.[5][6]

AliasesCBFA2T2, EHT, MTGR1, ZMYND3, p85, CBFA2/RUNX1 translocation partner 2, CBFA2/RUNX1 partner transcriptional co-repressor 2
End33,650,036 bp[1]
Quick facts Identifiers, Aliases ...
CBFA2T2
Identifiers
AliasesCBFA2T2, EHT, MTGR1, ZMYND3, p85, CBFA2/RUNX1 translocation partner 2, CBFA2/RUNX1 partner transcriptional co-repressor 2
External IDsOMIM: 603672; MGI: 1333833; HomoloGene: 3733; GeneCards: CBFA2T2; OMA:CBFA2T2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001032999
NM_001039709
NM_005093
NM_175864

NM_001285446
NM_009823
NM_172860

RefSeq (protein)

NP_001028171
NP_001034798
NP_005084

NP_001272375
NP_033953
NP_766448

Location (UCSC)Chr 20: 33.49 – 33.65 MbChr 2: 154.28 – 154.38 Mb
PubMed search[3][4]
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Function

In acute myeloid leukemia, especially in the M2 subtype, the t(8;21)(q22;q22) translocation is one of the most frequent karyotypic abnormalities. The translocation produces a chimeric gene made up of the 5′-region of the RUNX1 (AML1) gene fused to the 3'-region of the CBFA2T1 (MTG8) gene. The chimeric protein is thought to associate with the nuclear corepressor/histone deacetylase complex to block hematopoietic differentiation. The protein encoded by this gene binds to the AML1-MTG8 complex and may be important in promoting leukemogenesis. Several transcript variants are thought to exist for this gene, but the full-length natures of only three have been described.[6]

Interactions

CBFA2T2 has been shown to interact with RUNX1T1.[7][8][9]

References

Further reading

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