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t(1;22)(q23;q12)

MedGen UID:: 1739959
•Concept ID:: C5420795
•: Cell or Molecular Dysfunction

Definition

A chromosomal translocation involving the PBX1 gene at 1q23 and the EWSR1 gene at 22q12. [from NCI]

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVt(1;22)(q23;q12)

Molecular Abnormality
- Cytogenetic Abnormality
  - Chromosome 1 Abnormality
    - t(1;22)(q23;q12)

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t(1;22)(q23;q12)
t(1;22)(q23;q12)

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CDKN2C Gene Deletion
CDKN2C Gene Deletion

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Loss of Chromosome 1
Loss of Chromosome 1

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