Reactome Pathway Database

Schema > EntityWithAccessionedSequence > Entries

FLT3 V579A [plasma membrane] Show undefined attributes

compartment

[Compartment:876] plasma membrane

componentOf

created [InstanceEdit:9691063] Rothfels, Karen, 2020年06月08日

crossReference

dbId 9691051

disease

displayName FLT3 V579A [plasma membrane]

endCoordinate 993

hasModifiedResidue

[ReplacedResidue:9691043] L-valine 579 replaced with L-alanine

inDisease true

literatureReference

[LiteratureReference:9691015] Point mutations in the juxtamembrane domain of FLT3 define a new class of activating mutations in AML
[LiteratureReference:9691008] Novel FLT3 point mutations within exon 14 found in patients with acute myeloid leukaemia

maxDepth 1

memberOf

[CandidateSet:R-HSA-9691152] juxtamembrane domain mutants of FLT3 [plasma membrane] - Homo sapiens

name

FLT3 V579A
STK-1

referenceEntity [ReferenceGeneProduct:uniprot:P36888] UniProt:P36888 FLT3

referenceType ReferenceGeneProduct

schemaClass EntityWithAccessionedSequence

species [Species:48887] Homo sapiens

stId R-HSA-9691051

startCoordinate 27

Referrals

(hasMember)

[CandidateSet:R-HSA-9691152] juxtamembrane domain mutants of FLT3 [plasma membrane]

(hasComponent)

[Complex:R-HSA-9691121] FLT3 V579A dimer [plasma membrane]

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