About: RUNX1/MECOM Fusion Gene     Goto   Sponge   NotDistinct   Permalink

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AttributesValues
rdf:type
rdfs:label
  • RUNX1/MECOM Fusion Gene
rdfs:subClassOf
GenBank_Accession_Number
  • S69002
Semantic_Type
  • Gene or Genome
Preferred_Name
  • RUNX1/MECOM Fusion Gene
UMLS_CUI
  • C1838720
FULL_SYN
  • RUNX1-MECOM Fusion GeneSYNCI
  • RUNX1/MECOM Fusion GenePTNCI
  • AML/MDS1/EVI1 Fusion GeneSYNCI
  • AML1-MDS1-EVI1 Fusion GeneSYNCI
  • AML1/MDS1/EVI1 Fusion GeneSYNCI
  • AME Fusion GeneSYNCI
  • AML-EAP Fusion GeneSYNCI
  • AML/EAP Fusion GeneSYNCI
  • AML1/MDS1 Fusion GeneSYNCI
  • MDS1/AML1 Fusion GeneSYNCI
  • AML1-EVI-1 Fusion GeneSYNCI
DEFINITION
  • A fusion gene (~5.9 kb) that results from a chromosomal translocation t(3;21)(q26;q22) which fuses the first 5 exons of the RUNX1 gene to most of the MECOM gene. This rearrangement is associated with acute myelogenous leukemia, chronic myelogenous leukemia and myelodysplasic syndrome.NCI
code
  • C99295
is someValuesFrom of
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