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Query author contributions in Reactome

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Details on Person FGFR2c A315S [plasma membrane]

Class:IdEntityWithAccessionedSequence:2071931
_displayNameFGFR2c A315S [plasma membrane]
_timestamp2014-11-20 17:27:28
compartment[Compartment:876] plasma membrane
created[InstanceEdit:2071930] Rothfels, K, 2012-01-26
disease[Disease:2032940] bone development disease
[Disease:2071917] syndactyly
endCoordinate821
hasModifiedResidue[ReplacedResidue:2071923] L-alanine 315 replaced with L-serine
literatureReference[LiteratureReference:2071925] FGFs, their receptors, and human limb malformations: clinical and molecular correlations
[LiteratureReference:2029802] Biochemical analysis of pathogenic ligand-dependent FGFR2 mutations suggests distinct pathophysiological mechanisms for craniofacial and limb abnormalities
modified[InstanceEdit:3612887] Jupe, S, 2013-05-23
[InstanceEdit:5649552] Rothfels, Karen, 2014-11-20
nameFGFR2c A315S
FGFR2-1 A315S
referenceEntity[ReferenceIsoform:54816] UniProt:P21802-1 FGFR2 [Homo sapiens]
species[Species:48887] Homo sapiens
stableIdentifier[StableIdentifier:2297589] R-HSA-2071931.1
startCoordinate22
(hasComponent)[Complex:2071933] FGFR2c A315S mutant dimer [plasma membrane] [Homo sapiens]
(hasMember)[CandidateSet:2033375] FGFR2c mutants with enhanced ligand binding [plasma membrane] [Homo sapiens]
(updatedInstance)[_UpdateTracker:9881323] Update Tracker - [EntityWithAccessionedSequence:2071931] FGFR2c A315S [plasma membrane] - v45:[addName]
[_UpdateTracker:9891719] Update Tracker - [EntityWithAccessionedSequence:2071931] FGFR2c A315S [plasma membrane] - v52:[modifyName]
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No pathways have been reviewed or authored by FGFR2c A315S [plasma membrane] (2071931)
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