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Query author contributions in Reactome

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Details on Person FGFR1c P252R [plasma membrane]

Class:IdEntityWithAccessionedSequence:2011838
_displayNameFGFR1c P252R [plasma membrane]
_timestamp2014-11-20 17:26:17
compartment[Compartment:876] plasma membrane
created[InstanceEdit:2011839] Rothfels, K, 2011-11-22
disease[Disease:2011836] Pfeiffer syndrome
[Disease:2032940] bone development disease
endCoordinate822
hasModifiedResidue[ReplacedResidue:2011837] L-proline 252 replaced with L-arginine
literatureReference[LiteratureReference:2023308] A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome
[LiteratureReference:2011820] Proline to arginine mutations in FGF receptors 1 and 3 result in Pfeiffer and Muenke craniosynostosis syndromes through enhancement of FGF binding affinity
modified[InstanceEdit:2011845] Rothfels, K, 2011-11-22
[InstanceEdit:2054068] Rothfels, K, 2012-01-12
[InstanceEdit:2066023] Rothfels, K, 2012-01-25
[InstanceEdit:3450990] Jupe, S, 2013-05-16
[InstanceEdit:5649529] Rothfels, Karen, 2014-11-20
nameFGFR1c P252R
FGFR1-1 P252R
referenceEntity[ReferenceIsoform:54814] UniProt:P11362-1 FGFR1 [Homo sapiens]
species[Species:48887] Homo sapiens
stableIdentifier[StableIdentifier:2296258] R-HSA-2011838.1
startCoordinate22
(hasComponent)[Complex:2011923] FGFR1c P252R mutant dimer [plasma membrane] [Homo sapiens]
(hasMember)[DefinedSet:2012029] FGFR1c P252X mutants [plasma membrane] [Homo sapiens]
(updatedInstance)[_UpdateTracker:9882123] Update Tracker - [EntityWithAccessionedSequence:2011838] FGFR1c P252R [plasma membrane] - v45:[addName]
[_UpdateTracker:9891820] Update Tracker - [EntityWithAccessionedSequence:2011838] FGFR1c P252R [plasma membrane] - v52:[modifyName]
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No pathways have been reviewed or authored by FGFR1c P252R [plasma membrane] (2011838)
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