ZBTB16/RARA Fusion Gene

Preferred Label : ZBTB16/RARA Fusion Gene;

NCIt synonyms : PLZF/RARA Fusion Gene; PLZF-RARalpha Fusion Gene; PLZF-RARA Fusion Gene; ZBTB16-RARA Fusion Gene; PLZF-RAR-alpha Fusion Gene; ZBTB16::RARA Fusion Gene;

NCIt definition : A fusion gene that results from a chromosomal translocation t(11;17)(q23;q21) which fuses the 5' portion of the ZBTB16 gene to exon 4 of the RARA gene. This rearrangement is associated with acute promyelocytic leukemia.;

Details

Origin ID

C99371;

UMLS CUI

C1867727;

Automatic exact mappings (from CISMeF team)
- Retinoic acid receptor, alpha [OMIM gene]
- Zinc finger- and btb domain-containing protein 16 [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
- ZBTB16/RARA Fusion Protein [NCIt concept]
gene_has_abnormality
- t(11;17)(q23;q21) [NCIt concept]
gene_involved_in_molecular_abnormality
- ZBTB16-RARA Fusion Protein Expression [NCIt concept]
- t(11;17)(q23;q21) [NCIt concept]
gene_involved_in_pathogenesis_of_disease
- Acute Promyelocytic Leukemia with t(11;17)(q23;q21); ZBTB16-RARA [NCIt concept]
gene_mapped_to_disease
- Acute Promyelocytic Leukemia with t(11;17)(q23;q21); ZBTB16-RARA [NCIt concept]
related_to_genetic_biomarker
- RARA Gene [NCIt concept]
- ZBTB16 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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