FGFR2b S373C mutant dimer

Stable Identifier
R-HSA-2029923
Type
Complex
Species
Homo sapiens
Compartment
Locations in the PathwayBrowser
Literature References
PubMed ID Title Journal Year
17525745 Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes

Pollock, PM, Gartside, MG, Dejeza, LC, Powell, MA, Mallon, MA, Davies, H, Mohammadi, M, Futreal, PA, Stratton, MR, Trent, JM, Goodfellow, PJ

Oncogene 2007
Participants
Participant Of
Disease
Name Identifier Synonyms
female reproductive endometrioid cancer 3001 endometrioid tumor (morphologic abnormality), endometrioid neoplasm