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Go!
Schema
>
CandidateSet
>
Entries
FGFR3 point mutants with enhanced kinase activity [plasma membrane]
Show undefined attributes
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compartment
[Compartment:876] plasma membrane
consumedByEvent
[Reaction:R-HSA-2033476] Dimerization of FGFR3 point mutants with enhanced kinase activity - Homo sapiens
[Reaction:R-HSA-2033476] Dimerization of FGFR3 point mutants with enhanced kinase activity - Homo sapiens
created
[InstanceEdit:2018769] Rothfels, K, 2011年11月24日
crossReference
[DatabaseIdentifier:11944971] Mondo:0005497
[DatabaseIdentifier:11944892] Mondo:0004992
dbId
2018770
disease
[Disease:1500689] cancer
[Disease:2032940] bone development disease
displayName
FGFR3 point mutants with enhanced kinase activity [plasma membrane]
hasCandidate
[EntityWithAccessionedSequence:R-HSA-1614390] FGFR3 A391E [plasma membrane] - Homo sapiens
hasMember
[EntityWithAccessionedSequence:R-HSA-1614398] FGFR3 G380R [plasma membrane] - Homo sapiens
[EntityWithAccessionedSequence:R-HSA-2018740] FGFR3 G382D [plasma membrane] - Homo sapiens
[EntityWithAccessionedSequence:R-HSA-1614400] FGFR3 K650E [plasma membrane] - Homo sapiens
[EntityWithAccessionedSequence:R-HSA-1614402] FGFR3 K650M [plasma membrane] - Homo sapiens
[EntityWithAccessionedSequence:R-HSA-1614406] FGFR3 K650N [plasma membrane] - Homo sapiens
[EntityWithAccessionedSequence:R-HSA-1614410] FGFR3 K650Q [plasma membrane] - Homo sapiens
[EntityWithAccessionedSequence:R-HSA-1614411] FGFR3 K650T [plasma membrane] - Homo sapiens
[EntityWithAccessionedSequence:R-HSA-2018743] FGFR3b G697C [plasma membrane] - Homo sapiens
inDisease
true
maxDepth
2
modified
[InstanceEdit:2065853] Rothfels, K, 2012年01月24日
name
FGFR3 point mutants with enhanced kinase activity
schemaClass
CandidateSet
species
[Species:48887] Homo sapiens
stId
R-HSA-2018770
Referrals
(input)
[Reaction:R-HSA-2033476] Dimerization of FGFR3 point mutants with enhanced kinase activity
(diseaseEntity)
[EntityFunctionalStatus:5654492] gain_of_function of FGFR3 point mutants with enhanced kinase activity [plasma membrane]
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