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

Preferred Label : t(7;12)(p21-22;q13-15);

NCIt synonyms : t(7;12)(p22;q13);

NCIt 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.;

NCI Metathesaurus CUI : CL358501;

Détails

Origin ID

C170892;

UMLS CUI

C5418864;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 12 [NCIt concept]
- Human Chromosome 7 [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Intravascular Myopericytoma [NCIt concept]
- Myopericytoma [NCIt concept]
- Myopericytomatosis [NCIt concept]
molecular_abnormality_involves_gene
- ACTB Gene [NCIt concept]
- ACTB/GLI1 Fusion Gene [NCIt concept]
- GLI1 Gene [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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