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Go!
Schema
>
Complex
>
Entries
Activated FGFR2 K660N mutant [plasma membrane]
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compartment
[Compartment:876] plasma membrane
created
[InstanceEdit:2033313] Rothfels, K, 2012年01月09日
crossReference
[DatabaseIdentifier:11945425] Mondo:0007405
[DatabaseIdentifier:11944971] Mondo:0005497
[DatabaseIdentifier:11944956] Mondo:0002480
[DatabaseIdentifier:11944892] Mondo:0004992
dbId
2033312
disease
[Disease:1500689] cancer
[Disease:1625203] Crouzon syndrome
[Disease:2032940] bone development disease
[Disease:1614674] female reproductive endometrioid cancer
displayName
Activated FGFR2 K660N mutant [plasma membrane]
hasComponent
2 ×
[EntityWithAccessionedSequence:R-HSA-2033301] p-8Y-FGFR2 K660N [plasma membrane]
inDisease
true
isChimeric
false
maxDepth
2
memberOf
[CandidateSet:R-HSA-2033348] Activated FGFR2 mutants with enhanced kinase activity [plasma membrane] - Homo sapiens
name
Activated FGFR2 K660N mutant
schemaClass
Complex
species
[Species:48887] Homo sapiens
stId
R-HSA-2033312
Referrals
(hasMember)
[CandidateSet:R-HSA-2033348] Activated FGFR2 mutants with enhanced kinase activity [plasma membrane]
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