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FGFR2c S372C mutant dimer [plasma membrane]
Stable Identifier
R-HSA-2029928
Type
Complex
Species
Homo sapiens
Compartment
plasma membrane
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Diseases of signal transduction by growth factor receptors and second messengers (Homo sapiens)
Signaling by FGFR in disease (Homo sapiens)
Signaling by FGFR2 in disease (Homo sapiens)
FGFR2 mutant receptor activation (Homo sapiens)
Activated point mutants of FGFR2 (Homo sapiens)
Autocatalytic phosphorylation of FGFR2 ligand-independent mutants (Homo sapiens)
FGFR2 ligand-independent mutant dimers [plasma membrane] (Homo sapiens)
FGFR2c S372C mutant dimer [plasma membrane] (Homo sapiens)
Dimerization of FGFR2 ligand-independent mutants (Homo sapiens)
FGFR2 ligand-independent mutant dimers [plasma membrane] (Homo sapiens)
FGFR2c S372C mutant dimer [plasma membrane] (Homo sapiens)
Point mutants of FGFR2 bind and are inactivated by tyrosine kinase inhibitors (Homo sapiens)
FGFR2 point mutant dimers [plasma membrane] (Homo sapiens)
FGFR2 ligand-independent mutant dimers [plasma membrane] (Homo sapiens)
FGFR2c S372C mutant dimer [plasma membrane] (Homo sapiens)
FGFR2 point mutant dimers:TKIs [plasma membrane] (Homo sapiens)
FGFR2 point mutant dimers [plasma membrane] (Homo sapiens)
FGFR2 ligand-independent mutant dimers [plasma membrane] (Homo sapiens)
FGFR2c S372C mutant dimer [plasma membrane] (Homo sapiens)
Participants
components
x 2
FGFR2c S372C [plasma membrane]
(Homo sapiens)
Participates
as a candidate of
FGFR2 ligand-independent mutant dimers [plasma membrane] (Homo sapiens)
Disease
Name
Identifier
Synonyms
Beare-Stevenson cutis gyrata syndrome
DOID:0050660
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