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t(8;9)(p22;p24.1)

MedGen UID:
1390377
•Concept ID:
C4331810
•
Cell or Molecular Dysfunction

Definition

A cytogenetic abnormality that refers to the translocation of 8p22 and 9p24.1. This translocation results in the fusion of the PCM1 gene and the JAK2 gene. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVt(8;9)(p22;p24.1)

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