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MRAS mutants [plasma membrane]
Stable Identifier
R-HSA-9660500
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)
Oncogenic MAPK signaling (Homo sapiens)
Signaling by MRAS-complex mutants (Homo sapiens)
Gain-of-function MRAS complexes activate RAF signaling (Homo sapiens)
Mutant MRAS:SHOC2:PPP1CC complexes dephosphorylate inactive RAFs (Homo sapiens)
mutant MRAS:SHOC2:PP1 complexes [plasma membrane] (Homo sapiens)
S-GCC MRAS mutants:GTP:SHOC2:PP1 [plasma membrane] (Homo sapiens)
MRAS mutants:GTP [plasma membrane] (Homo sapiens)
MRAS mutants [plasma membrane] (Homo sapiens)
Participants
members
S-GGC MRAS G23V [plasma membrane]
(Homo sapiens)
S-GGC MRAS T68I [plasma membrane]
(Homo sapiens)
S-GGC MRAS G23R [plasma membrane]
(Homo sapiens)
candidates
S-GGC MRAS G23D [plasma membrane]
(Homo sapiens)
Participates
as a component of
MRAS mutants:GTP [plasma membrane] (Homo sapiens)
Disease
Name
Identifier
Synonyms
esophageal carcinoma
DOID:1107
carcinoma OF ESOPHAGUS, carcinoma of oesophagus, cancer of esophagus, cancer of oesophagus, carcinoma of esophagus (disorder), carcinoma of esophagus (disorder)
Noonan syndrome
DOID:3490
Turner's phenotype, karyotype normal (disorder)
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