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FGFR2c mutants with enhanced ligand binding [plasma membrane]
Stable Identifier
R-HSA-2033375
Type
Set [CandidateSet]
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)
FGFR2c mutants bind an expanded range of ligands (Homo sapiens)
FGFR2c mutants with enhanced ligand binding [plasma membrane] (Homo sapiens)
Participants
members
FGFR2c S252W [plasma membrane]
(Homo sapiens)
FGFR2c P253R [plasma membrane]
(Homo sapiens)
FGFR2c A315S [plasma membrane]
(Homo sapiens)
candidates
FGFR2c A314D [plasma membrane]
(Homo sapiens)
FGFR2c A315T [plasma membrane]
(Homo sapiens)
FGFR2c A314S [plasma membrane]
(Homo sapiens)
Participates
as an input of
FGFR2c mutants bind an expanded range of ligands (Homo sapiens)
Disease
Name
Identifier
Synonyms
female reproductive endometrioid cancer
DOID:3001
endometrioid tumor (morphologic abnormality), endometrioid neoplasm
ovarian cancer
DOID:2394
ovarian neoplasm, malignant tumour of ovary, neoplasm of ovary (disorder), ovary neoplasm, primary malignant neoplasm of ovary and other uterine adnexa (disorder), ovarian cancer, tumor of the Ovary, ovary cancer, malignant Ovarian tumor, primary ovarian cancer, malignant tumor of ovary (disorder)
cancer
DOID:162
malignant tumor, malignant neoplasm, primary cancer
bone development disease
DOID:0080006
acrocephalosyndactylia
DOID:12960
Apert syndrome
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