FGFR1/FGFR1OP Fusion Gene

**Semantic type:** Gene or Genome

**Definition:** A fusion gene that results from a chromosomal translocation t(6;8)(q27;p11) that fuses intron 8 of the FGFR1 gene with intron 6, 7 or 8 of the FGFR1OP gene. This translocation is associated with 8p11 myeloproliferative disorder.

**Synonyms:** - FGFR1-FGFR1OP Fusion Gene - FGFR1-FOP Fusion Gene - FGFR1/FOP Fusion Gene - FGFR1::CEP43 Fusion Gene - FGFR1::FGFR1OP Fusion Gene