extracellular domain mutants of KIT [plasma membrane]

Stable Identifier
Set [CandidateSet]
Homo sapiens
Locations in the PathwayBrowser
Literature References
PubMed ID Title Journal Year
19865100 Pediatric mastocytosis is a clonal disease associated with D816V and other activating c-KIT mutations

Nasca, L, Lortholary, O, Sobol, H, Catteau, B, Barete, S, Stalder, JF, Grandpeix-Guyodo, C, Launay, JM, Lorette, G, Plantin, P, Georgin-Lavialle, S, Cohen-Akenine, A, Bordigoni, P, Palmérini, F, Arock, M, Dubreuil, P, Sans, B, Feger, F, Bodemer, C, Hermine, O, Yang, Y, de Prost, Y, Leventhal, PS, Skowron, F, Thomas, L, Moussy, A, Hadj-Rabia, S

J. Invest. Dermatol. 2010
16081693 Extracellular KIT receptor mutants, commonly found in core binding factor AML, are constitutively active and respond to imatinib mesylate

Besmer, P, Fiedler, W, Cammenga, J, Stocking, C, Horn, S, Bergholz, U, Sommer, G

Blood 2005
Name Identifier Synonyms
cancer DOID:162 malignant tumor, malignant neoplasm, primary cancer
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