RAF1 mutants [cytosol]

Stable Identifier
R-HSA-9656167
Type
Set [DefinedSet]
Species
Homo sapiens
Compartment
Locations in the PathwayBrowser
Participants
Participant Of
Disease
Name Identifier Synonyms
LEOPARD syndrome 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
Costello syndrome 0050469 Faciocutaneoskeletal Syndrome, FCS SYNDROME
cancer 162 malignant tumor, malignant neoplasm, primary cancer
Noonan syndrome 3490 Turner's phenotype, karyotype normal (disorder)
hypertrophic cardiomyopathy 11984 familial hypertrophic cardiomyopathy, hypertrophic obstructive cardiomyopathy
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