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t(1;19)(q23;p13.3)

MedGen UID:
271871
•Concept ID:
C1515739
•
Cell or Molecular Dysfunction
Synonyms: t(1;19) (q23;p13.3); PBX/E2A; t(1;19)(q23;p13.3); PBX/E2A

Definition

A chromosomal abnormality consisting of the translocation of 19p13.3 with 1q23, resulting in the fusion of the TCF3 (E2A) gene with the PBX1 gene. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVt(1;19)(q23;p13.3)

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