RAS mutants

Stable Identifier
R-HSA-6802608
Type
Set [DefinedSet]
Species
Homo sapiens
Compartment
Locations in the PathwayBrowser
Literature References
PubMed ID Title Journal Year
16474405 Germline KRAS mutations cause Noonan syndrome

Schubbert, S, Zenker, M, Rowe, SL, Böll, S, Klein, C, Bollag, G, van der Burgt, I, Musante, L, Kalscheuer, V, Wehner, LE, Nguyen, H, West, B, Zhang, KY, Sistermans, E, Rauch, A, Niemeyer, CM, Shannon, K, Kratz, CP

Nat. Genet. 2006
21993244 RAS oncogenes: weaving a tumorigenic web

Pylayeva-Gupta, Y, Grabocka, E, Bar-Sagi, D

Nat. Rev. Cancer 2011
22589270 A comprehensive survey of Ras mutations in cancer

Prior, IA, Lewis, PD, Mattos, C

Cancer Res. 2012
Participants
Participant Of
Disease
Name Identifier Synonyms
Noonan syndrome 3490 Turner's phenotype, karyotype normal (disorder)
cancer 162 malignant tumor, malignant neoplasm, primary cancer