Reactome | p-8Y-FGFR2 S267P [plasma membrane]

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p-8Y-FGFR2 S267P [plasma membrane] Show undefined attributes

compartment	[Compartment:876] plasma membrane
componentOf	[Complex:R-HSA-2033319] Activated FGFR2 S267C mutant [plasma membrane] - Homo sapiens [Complex:R-HSA-2033319] Activated FGFR2 S267C mutant [plasma membrane] - Homo sapiens
created	[InstanceEdit:2029880] Rothfels, K, 2012-01-05
crossReference	[DatabaseIdentifier:12021291] Mondo:0007405
dbId	2029879
disease	[Disease:1500689] cancer [Disease:1500687] stomach cancer [Disease:1625203] Crouzon syndrome
displayName	p-8Y-FGFR2 S267P [plasma membrane]
endCoordinate	821
hasModifiedResidue	[ModifiedResidue:2029853] O4'-phospho-L-tyrosine at unknown position [ModifiedResidue:2029853] O4'-phospho-L-tyrosine at unknown position [ModifiedResidue:2029853] O4'-phospho-L-tyrosine at unknown position [ModifiedResidue:2029853] O4'-phospho-L-tyrosine at unknown position [ModifiedResidue:2029853] O4'-phospho-L-tyrosine at unknown position [ModifiedResidue:2029853] O4'-phospho-L-tyrosine at unknown position [ModifiedResidue:2029853] O4'-phospho-L-tyrosine at unknown position [ModifiedResidue:2029853] O4'-phospho-L-tyrosine at unknown position [ReplacedResidue:1637922] L-serine 267 replaced with L-proline
inDisease	true
maxDepth	1
modified	[InstanceEdit:5649612] Rothfels, Karen, 2014-11-20
name	p-8Y-FGFR2 S267P
referenceEntity	[ReferenceGeneProduct:uniprot:P21802] UniProt:P21802 FGFR2
referenceType	ReferenceGeneProduct
schemaClass	EntityWithAccessionedSequence
species	[Species:48887] Homo sapiens
stId	R-HSA-2029879
startCoordinate	22
summation	[Summation:2029878] This represents FGFR2 S267C of either the IIIb or IIIC isofo...
updateTrackers	[UpdateTracker:9890850] Update Tracker - [EntityWithAccessionedSequence:2029879] p-8Y-FGFR2 S267P [plasma membrane] - v52:[modifyName]

Referrals

(updatedInstance)	[UpdateTracker:9890850] Update Tracker - [EntityWithAccessionedSequence:2029879] p-8Y-FGFR2 S267P [plasma membrane] - v52:[modifyName]
(hasComponent)	[Complex:R-HSA-2033319] Activated FGFR2 S267C mutant [plasma membrane]

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