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SHOC2 M173I:MRAS:PP1 [plasma membrane]
Stable Identifier
R-HSA-9660490
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)
Oncogenic MAPK signaling (Homo sapiens)
Signaling by MRAS-complex mutants (Homo sapiens)
SHOC2 M1731 mutant abolishes MRAS complex function (Homo sapiens)
SHOC2 M173I disrupts the SHOC2:MRAS:PP1 complex (Homo sapiens)
SHOC2 M173I:MRAS:PP1 [plasma membrane] (Homo sapiens)
Participants
components
PPP1CB, PPP1CB [cytosol]
(Homo sapiens)
S-GCC MRAS:GTP [plasma membrane]
(Homo sapiens)
SHOC2 M173I [cytosol]
(Homo sapiens)
Disease
Name
Identifier
Synonyms
Noonan syndrome
DOID:3490
Turner's phenotype, karyotype normal (disorder)
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