NUMA1/RARA Fusion Gene

Preferred Label : NUMA1/RARA Fusion Gene;

NCIt synonyms : NUMA-RARA Fusion Gene; NUMA1-RARA Fusion Gene; NuMA/RARA Fusion Gene; RARA/NUMA1 Fusion Gene; NUMA1::RARA Fusion Gene;

NCIt definition : A fusion gene that results from a chromosomal translocation t(11;17)(q13;q21) which fuses the 5' half of the NUMA gene to the most of the RARA gene. This rearrangement may be associated with acute promyelocytic leukemia.;

Détails

Origin ID

C99359;

UMLS CUI

C1834115;

Automatic exact mappings (from CISMeF team)
- Nuclear mitotic apparatus protein 1 [OMIM gene]
- Retinoic acid receptor, alpha [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
gene_encodes_gene_product
- NUMA1/RARA Fusion Protein [NCIt concept]
gene_has_abnormality
- t(11;17)(q13;q21) [NCIt concept]
gene_involved_in_molecular_abnormality
- NUMA1-RARA Fusion Protein Expression [NCIt concept]
- t(11;17)(q13;q21) [NCIt concept]
gene_involved_in_pathogenesis_of_disease
- Acute Promyelocytic Leukemia with t(11;17)(q13;q21); NUMA1-RARA [NCIt concept]
gene_mapped_to_disease
- Acute Promyelocytic Leukemia with t(11;17)(q13;q21); NUMA1-RARA [NCIt concept]
related_to_genetic_biomarker
- NUMA1 Gene [NCIt concept]
- RARA Gene [NCIt concept]

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

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