t(12;22)(q13.12;q12)

Preferred Label : t(12;22)(q13.12;q12);

NCIt definition : A chromosomal translocation involving the ATF1 gene at 12q13.12 and the EWSR1 gene at 22q12.;

NCI Metathesaurus CUI : CL1411988;

Details

Origin ID

C174478;

UMLS CUI

C5420796;

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 12 [NCIt concept]
- Human Chromosome 22 [NCIt concept]
is_abnormality_of_gene
- EWSR1/ATF1 Fusion Gene [NCIt concept]
- EWSR1/ATF1 Fusion Gene Type 1 [NCIt concept]
- EWSR1/ATF1 Fusion Gene Type 2 [NCIt concept]
molecular_abnormality_involves_gene
- ATF1 Gene [NCIt concept]
- EWSR1 Gene [NCIt concept]
- EWSR1/ATF1 Fusion Gene [NCIt concept]
- FET Family Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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