CNTRL/FGFR1 Fusion Gene

**Semantic type:** Gene or Genome

**Definition:** A fusion gene that results from a chromosomal translocation t(8;9)(p12;q33) which fuses exon 15 of the CNTRL gene with exon 8 of the FGFR1 gene. This translocation is associated with 8p11 myeloproliferative syndrome.

**Synonyms:** - CEP1-FGFR1 Fusion Gene - CEP1/FGFR1 Fusion Gene - CEP110-FGFR1 Fusion Gene - CEP110/FGFR1 Fusion Gene - CNTRL-FGFR1 Fusion Gene - CNTRL::FGFR1 Fusion Gene