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- NCIT_C13727 IAO_0000115 "A translocation between chromosomes 12 and 21 involved in TEL-AML1 oncogene formation. The translocation produces a chimeric gene encoding a protein consisting of the N-terminal HLH domain of the TEL ETS-like transcription factor fused with a nearly complete AML1 protein. t(12;21) is the most frequent translocation causing ALL, accounting for 20% of ALL cases." @default.
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- NCIT_C13727 NCIT_P106 "Cell or Molecular Dysfunction" @default.
- NCIT_C13727 NCIT_P108 "t(12;21)(p13.2;q22.1)" @default.
- NCIT_C13727 NCIT_P207 "C1515717" @default.
- NCIT_C13727 NCIT_P322 "PCDC" @default.
- NCIT_C13727 NCIT_P366 "t_12_21_p13_q22" @default.
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- NCIT_C13727 referenceCount "5" @default.
- NCIT_C13727 hasExactSynonym "t(12;21)(p13.2;q22.1)" @default.
- NCIT_C13727 hasExactSynonym "t(12;21)(p13;q22)" @default.
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