t(2;16)(q35;p11)

Preferred Label : t(2;16)(q35;p11);

NCIt definition : A chromosomal translocation involving the FEV gene at 2q35 and the FUS gene at 16p11.;

NCI Metathesaurus CUI : CL1412005;

PubMed : 17620387;

Details

Origin ID

C174465;

UMLS CUI

C5420789;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
concept_is_in_subset
- EWS Authorized Value Terminology [NCIt concept]
- EWS Molecular Analysis Table [NCIt concept]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 16 [NCIt concept]
- Human Chromosome 2 [NCIt concept]
is_abnormality_of_gene
- FUS/FEV Fusion Gene [NCIt concept]
molecular_abnormality_involves_gene
- ETS Family Gene [NCIt concept]
- FET Family Gene [NCIt concept]
- FEV Gene [NCIt concept]
- FUS Gene [NCIt concept]
- FUS/FEV Fusion Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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