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t(7;12)(p21-22;q13-15)

MedGen UID:
1731074
•Concept ID:
C5418864
•
Cell or Molecular Dysfunction
Synonym: t(7;12)(p22;q13)

Definition

A cytogenetic abnormality that refers to the translocation of the short arm (p21-22) of chromosome 7 and the long arm (q13-15) of chromosome 12. It results in the formation of ACTB/GLI1 fusion gene. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVt(7;12)(p21-22;q13-15)

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