Reactome: A Curated Pathway Database
THIS SITE IS USED FOR CURATION AND TESTING
IT IS NOT STABLE, IS LINKED TO AN INCOMPLETE DATA SET, AND IS NOT MONITORED FOR PERFORMANCE. WE STRONGLY RECOMMEND THE USE OF OUR PUBLIC SITE

Query author contributions in Reactome

Reactome depends on collaboration between our curation team and outside experts to assemble and peer-review its pathway modules. The integration of ORCID within Reactome enables us to meet a key challenge with authoring, curating and reviewing biological information by incentivizing and crediting the external experts that contribute their expertise and time to the Reactome curation process. More information is available at ORCID and Reactome.

If you have an ORCID ID that is not listed on this page, please forward this information to us and we will update your Reactome pathway records.

Name Email address

Details on Person p-8Y-FGFR2c P253R [plasma membrane]

Class:IdEntityWithAccessionedSequence:2011880
_displayNamep-8Y-FGFR2c P253R [plasma membrane]
_timestamp2014-11-20 17:34:56
compartment[Compartment:876] plasma membrane
created[InstanceEdit:2011881] Rothfels, K, 2011-11-22
disease[Disease:1614674] female reproductive endometrioid cancer
[Disease:2011822] acrocephalosyndactylia
endCoordinate821
hasModifiedResidue[ReplacedResidue:1637915] L-proline 253 replaced with L-arginine
[ModifiedResidue:1307864] O4'-phospho-L-tyrosine at 466
[ModifiedResidue:1307872] O4'-phospho-L-tyrosine at 586
[ModifiedResidue:1307873] O4'-phospho-L-tyrosine at 588
[ModifiedResidue:1307882] O4'-phospho-L-tyrosine at 656
[ModifiedResidue:1307883] O4'-phospho-L-tyrosine at 657
[ModifiedResidue:1307889] O4'-phospho-L-tyrosine at 733
[ModifiedResidue:1307900] O4'-phospho-L-tyrosine at 769
[ModifiedResidue:1307907] O4'-phospho-L-tyrosine at 779
literatureReference[LiteratureReference:1637882] Drug-sensitive FGFR2 mutations in endometrial carcinoma
[LiteratureReference:1637876] Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon 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:2029887] Rothfels, K, 2012-01-05
[InstanceEdit:2071964] Rothfels, K, 2012-01-26
[InstanceEdit:3612887] Jupe, S, 2013-05-23
[InstanceEdit:3622479] Rothfels, K, 2013-05-24
[InstanceEdit:5649622] Rothfels, Karen, 2014-11-20
namep-8Y-FGFR2c P253R
p-8Y-FGFR2-1 P253R
referenceEntity[ReferenceIsoform:54816] UniProt:P21802-1 FGFR2 [Homo sapiens]
species[Species:48887] Homo sapiens
stableIdentifier[StableIdentifier:2295864] R-HSA-2011880.1
startCoordinate22
summation[Summation:1637914] also Apert
(hasComponent)[Complex:2011967] p-8Y-FGFR2c P253R dimer [plasma membrane] [Homo sapiens]
(updatedInstance)[_UpdateTracker:9883298] Update Tracker - [EntityWithAccessionedSequence:2011880] p-8Y-FGFR2c P253R [plasma membrane] - v45:[addName]
[_UpdateTracker:9891581] Update Tracker - [EntityWithAccessionedSequence:2011880] p-8Y-FGFR2c P253R [plasma membrane] - v52:[modifyName]
[Change default viewing format]
No pathways have been reviewed or authored by p-8Y-FGFR2c P253R [plasma membrane] (2011880)