| RUNX1T1 | |||||||||||||||||||||||||||||||
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| Identifiers | |||||||||||||||||||||||||||||||
| Aliases | RUNX1T1, AML1T1, CBFA2T1, CDR, ETO, MTG8, ZMYND2, AML1-MTG8, t(8;21)(q22;q22), RUNX1 translocation partner 1, RUNX1 partner transcriptional co-repressor 1 | ||||||||||||||||||||||||||||||
| External IDs | OMIM:133435;MGI:104793;HomoloGene:3801;GeneCards:RUNX1T1;OMA:RUNX1T1 - orthologs | ||||||||||||||||||||||||||||||
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| Wikidata | |||||||||||||||||||||||||||||||
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Protein CBFA2T1 is aprotein that in humans is encoded by theRUNX1T1gene.[5][6][7]
The protein encoded by this gene is a putative zinc finger transcription factor and oncoprotein. Inacute myeloid leukemia, especially in theM2 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 the5′-region of theRUNX1 gene fused to the 3′-region of this gene. The chimeric protein is thought to associate with the nuclear corepressor/histone deacetylase complex to block hematopoietic differentiation. Several transcript variants encoding multiple isoforms have been found for this gene.[7]
RUNX1T1 has been shown tointeract with: