ZMYM2/FGFR1 Fusion Gene

Preferred Label : ZMYM2/FGFR1 Fusion Gene;

NCIt synonyms : ZNF198-FGFR1 Fusion Gene; FIM-FGFR1 Fusion Gene; ZMYM2-FGFR1 Fusion Gene; ZNF198/FGFR1 Fusion Gene; FIM/FGFR1 Fusion Gene; ZMYM2::FGFR1 Fusion Gene;

NCIt definition : A fusion gene that results from a chromosomal translocation t(8;13)(p11;q12) which fuses exon 17 of the ZMYM2 gene to exon 9 of the FGFR1 gene. This rearrangement is associated with 8p11 myeloproliferative syndrome.;

NCIt note : The ZMYM2/FGFR1 fusion gene is the most common chromosomal rearrangement found in patients with 8p11 myeloproliferative syndrome.;

Details

Origin ID

C99519;

UMLS CUI

C1865737;

Automatic exact mappings (from CISMeF team)
- Fibroblast growth factor receptor 1 [OMIM gene]
- Zinc finger, mym-type 2 [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
- ZMYM2/FGFR1 Fusion Protein [NCIt concept]
related_to_genetic_biomarker
- FGFR1 Gene [NCIt concept]
- ZMYM2 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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