FLT3-ITD mutation

GPTKB entity

Statements (28)
Predicate Object
gptkbp:instanceOf genetic disorder
gptkbp:associatedWith gptkb:acute_myeloid_leukemia
myelodysplastic syndromes
gptkbp:cause increased cell proliferation
poor prognosis in AML
gptkbp:co-occursWith gptkb:NPM1_mutation
gptkb:DNMT3A_mutation
gptkbp:commonIn adult AML
pediatric AML
gptkbp:detects PCR
gptkbp:firstDescribed 1996
gptkbp:frequencyInAML about 20-30%
gptkbp:fullName FMS-like tyrosine kinase 3 internal tandem duplication mutation
https://www.w3.org/2000/01/rdf-schema#label FLT3-ITD mutation
gptkbp:impact overall survival in AML patients
relapse rate in AML
gptkbp:location juxtamembrane domain of FLT3 gene
gptkbp:mutationAssociatedWith internal tandem duplication
gptkbp:prognosticMarker yes
gptkbp:regulates gptkb:FLT3
gptkbp:result constitutive activation of FLT3 receptor
gptkbp:target FLT3 inhibitors
gptkbp:therapiesInclude gptkb:gilteritinib
gptkb:quizartinib
gptkb:crenolanib
gptkb:midostaurin
gptkbp:bfsParent gptkb:NPM1_mutation
gptkbp:bfsLayer 6