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RAF1 mutants [cytosol]
Stable Identifier
R-HSA-9656167
Type
Set [DefinedSet]
Species
Homo sapiens
Compartment
cytosol
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 RAF1 mutants (Homo sapiens)
Phosphorylation of RAF1 mutants (Homo sapiens)
p21 RAS:GTP:RAF1 mutant heterodimers [plasma membrane] (Homo sapiens)
RAF1 mutants [cytosol] (Homo sapiens)
RAF1 mutants show enhanced heterodimerization with BRAF (Homo sapiens)
RAF1 mutants [cytosol] (Homo sapiens)
p21 RAS:GTP:RAF1 mutant heterodimers [plasma membrane] (Homo sapiens)
RAF1 mutants [cytosol] (Homo sapiens)
Participants
members
p-S621 RAF1 CR2 mutants [cytosol]
(Homo sapiens)
p-S621 RAF1 CR3 mutants [cytosol]
(Homo sapiens)
Participates
as an input of
RAF1 mutants show enhanced heterodimerization with BRAF (Homo sapiens)
as a component of
p21 RAS:GTP:RAF1 mutant heterodimers [plasma membrane] (Homo sapiens)
Disease
Name
Identifier
Synonyms
Costello syndrome
DOID:0050469
Faciocutaneoskeletal Syndrome, FCS SYNDROME
LEOPARD syndrome
DOID:14291
Generalized lentiginosis, Multiple lentigines syndrome, Moynahan syndrome, Cardiocutaneous syndrome, Capute-Rimoin-Konigsmark-Esterly-Richardson syndrome, Lentiginosis profusa syndrome, Gorlin syndrome II, Progressive cardiomyopathic lentiginosis
cancer
DOID:162
malignant tumor, malignant neoplasm, primary cancer
Noonan syndrome
DOID:3490
Turner's phenotype, karyotype normal (disorder)
hypertrophic cardiomyopathy
DOID:11984
familial hypertrophic cardiomyopathy, hypertrophic obstructive cardiomyopathy
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