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FGFR3 (4;14) translocation mutants [plasma membrane]
Stable Identifier
R-HSA-2038374
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 FGFR3 in disease (Homo sapiens)
FGFR3 mutant receptor activation (Homo sapiens)
t(4;14) translocations of FGFR3 (Homo sapiens)
Dimerization of FGFR3 t(4;14) translocation mutants (Homo sapiens)
FGFR3 (4;14) translocation mutants [plasma membrane] (Homo sapiens)
Participants
members
FGFR3 R248C [plasma membrane]
(Homo sapiens)
FGFR3 Y373C [plasma membrane]
(Homo sapiens)
FGFR3 G380R [plasma membrane]
(Homo sapiens)
FGFR3 G382D [plasma membrane]
(Homo sapiens)
FGFR3 K650E [plasma membrane]
(Homo sapiens)
FGFR3 805fs*141 [plasma membrane]
(Homo sapiens)
candidates
FGFR3 [plasma membrane]
(Homo sapiens)
Participates
as an input of
Dimerization of FGFR3 t(4;14) translocation mutants (Homo sapiens)
Disease
Name
Identifier
Synonyms
multiple myeloma
DOID:9538
cancer
DOID:162
malignant tumor, malignant neoplasm, primary cancer
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