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Search ...
Go!
Schema
>
EntityWithAccessionedSequence
>
Entries
p-8Y-FGFR2b S373C [plasma membrane]
Show undefined attributes
Go to Details
compartment
[Compartment:876] plasma membrane
componentOf
[Complex:R-HSA-2029906] Activated FGFR2b S373C mutant [plasma membrane] - Homo sapiens
[Complex:R-HSA-2029906] Activated FGFR2b S373C mutant [plasma membrane] - Homo sapiens
created
[InstanceEdit:2029868] Rothfels, K, 2012-01-05
crossReference
[DatabaseIdentifier:12020811] Mondo:0002480
dbId
2029869
disease
[Disease:1614674] female reproductive endometrioid cancer
displayName
p-8Y-FGFR2b S373C [plasma membrane]
endCoordinate
822
hasModifiedResidue
[ModifiedResidue:190945] O4'-phospho-L-tyrosine at 467
[ModifiedResidue:190951] O4'-phospho-L-tyrosine at 587
[ModifiedResidue:190950] O4'-phospho-L-tyrosine at 589
[ModifiedResidue:190947] O4'-phospho-L-tyrosine at 657
[ModifiedResidue:190409] O4'-phospho-L-tyrosine at 658
[ModifiedResidue:190948] O4'-phospho-L-tyrosine at 734
[ModifiedResidue:190949] O4'-phospho-L-tyrosine at 770
[ModifiedResidue:1307909] O4'-phospho-L-tyrosine at 780
[ReplacedResidue:1637926] L-serine 373 replaced with L-cysteine
inDisease
true
literatureReference
[LiteratureReference:1637882] Drug-sensitive FGFR2 mutations in endometrial carcinoma
[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
[LiteratureReference:1637876] Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome
maxDepth
1
modified
[InstanceEdit:5649616] Rothfels, Karen, 2014-11-20
name
p-8Y-FGFR2b S373C
p-8Y-FGFR2-3 S373C
referenceEntity
[ReferenceIsoform:uniprot:P21802-3] UniProt:P21802-3 FGFR2
referenceType
ReferenceIsoform
schemaClass
EntityWithAccessionedSequence
species
[Species:48887] Homo sapiens
stId
R-HSA-2029869
startCoordinate
22
summation
[Summation:1637914] also Apert
updateTrackers
[UpdateTracker:9891037] Update Tracker - [EntityWithAccessionedSequence:2029869] p-8Y-FGFR2b S373C [plasma membrane] - v52:[modifyName]
[UpdateTracker:9885865] Update Tracker - [EntityWithAccessionedSequence:2029869] p-8Y-FGFR2b S373C [plasma membrane] - v45:[modifyName]
Referrals
(updatedInstance)
[UpdateTracker:9891037] Update Tracker - [EntityWithAccessionedSequence:2029869] p-8Y-FGFR2b S373C [plasma membrane] - v52:[modifyName]
[UpdateTracker:9885865] Update Tracker - [EntityWithAccessionedSequence:2029869] p-8Y-FGFR2b S373C [plasma membrane] - v45:[modifyName]
(hasComponent)
[Complex:R-HSA-2029906] Activated FGFR2b S373C mutant [plasma membrane]
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