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Go!
Schema
>
EntityWithAccessionedSequence
>
Entries
p-8Y-FGFR2c Y375C [plasma membrane]
Show undefined attributes
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compartment
[Compartment:876] plasma membrane
componentOf
[Complex:R-HSA-2029915] Activated FGFR2c Y375C mutant [plasma membrane] - Homo sapiens
created
[InstanceEdit:2029859] Rothfels, K, 2012-01-05
dbId
2029861
disease
[Disease:2029860] Beare-Stevenson cutis gyrata syndrome
displayName
p-8Y-FGFR2c Y375C [plasma membrane]
endCoordinate
821
hasModifiedResidue
[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
[ReplacedResidue:2029822] L-tyrosine 375 replaced with L-cysteine
inDisease
true
modified
[InstanceEdit:5649626] Rothfels, Karen, 2014-11-20
name
p-8Y-FGFR2c Y375C
p-8Y-FGFR2-1 Y375C
referenceEntity
[ReferenceIsoform:54816] UniProt:P21802-1 FGFR2
referenceType
ReferenceIsoform
schemaClass
EntityWithAccessionedSequence
species
[Species:48887] Homo sapiens
stId
R-HSA-2029861
startCoordinate
22
Referrals
(hasComponent)
[Complex:R-HSA-2029915] Activated FGFR2c Y375C mutant [plasma membrane]
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