About: FGFR1OP2/FGFR1 Fusion Gene     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : owl:Class, within Data Space : linked.opendata.cz:8890 associated with source document(s)

AttributesValues
rdf:type
rdfs:label
  • FGFR1OP2/FGFR1 Fusion Gene
rdfs:subClassOf
Semantic_Type
  • Gene or Genome
Preferred_Name
  • FGFR1OP2/FGFR1 Fusion Gene
UMLS_CUI
  • C1851030
FULL_SYN
  • FGFR1OP2-FGFR1 Fusion GeneSYNCI
  • FGFR1OP2/FGFR1 Fusion GenePTNCI
  • FGFR1/FGFR1OP2 Fusion GeneSYNCI
DEFINITION
  • A fusion gene that results from a chromosomal insertion ins(12;8)(p11;p11p22) that fuses exon 4 of the FGFR1OP2 gene with exon 9 of the FGFR1 gene. This translocation is associated with 8p11 myeloproliferative disorder.NCI
DesignNote
  • Since the direction of FGFR1OP2 transcription is in the opposite orientation to the direction of FGFR1 transcription, an inversion must have taken place during the formation of the chimeric gene. (OMIM)
code
  • C99835
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