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t(1;16)(p34;p11)

MedGen UID:: 1725255
•Concept ID:: C5420793
•: Cell or Molecular Dysfunction

Definition

A chromosomal translocation involving the KLF17 gene at 1p34 and the FUS gene at 16p11. [from NCI]

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVt(1;16)(p34;p11)

Molecular Abnormality
- Cytogenetic Abnormality
  - Chromosome 1 Abnormality
    - t(1;16)(p34;p11)

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