t(1;22)(p13.3;q13.1)

Preferred Label : t(1;22)(p13.3;q13.1);

NCIt synonyms : t(1;22)(p13;q13); t 1 22 p13 q13;

NCIt definition : A cytogenetic abnormality that refers to the translocation of the short arm (p13.3) of chromosome 1 and the long arm (q13.1) of chromosome 22. It is associated with RBM15/MRTFA (MKL1) fusions and acute megakaryocytic leukemia.;

Details

Origin ID

C36417;

UMLS CUI

C1515741;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 1 [NCIt concept]
- Human Chromosome 22 [NCIt concept]
molecular_abnormality_involves_gene
- MRTFA Gene [NCIt concept]
- RBM15 Gene [NCIt concept]
- RBM15/MKL1 Fusion Gene [NCIt concept]

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