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

MedGen UID:
272953
•Concept ID:
C1515741
•
Cell or Molecular Dysfunction
Synonym: t(1;22)(p13;q13)

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. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVt(1;22)(p13.3;q13.1)

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