ZMYM2-FGFR1 fusion mutant dimer

Stable Identifier
R-HSA-1604545
Type
Complex
Species
Homo sapiens
Compartment
Synonyms
ZMYM2(1-913)-FGFR1(429-822) fusion dimer, t(8;13) ZMYM2-FGFR1 fusion dimer, ZNF198-FGFR1 fusion dimer, ZNF198(1-913)-FGFR1(429-822) fusion dimer, t(8;13) ZNF198-FGFR1 fusion dimer
Locations in the PathwayBrowser
Literature References
PubMed ID Title Journal Year
9716603 Consistent fusion of ZNF198 to the fibroblast growth factor receptor-1 in the t(8;13)(p11;q12) myeloproliferative syndrome

Reiter, A, Sohal, J, Kulkarni, S, Chase, A, Macdonald, DH, Aguiar, RC, Gonçalves, C, Hernandez, JM, Jennings, BA, Goldman, JM, Cross, NC

Blood 1998
9425908 FGFR1 is fused with a novel zinc-finger gene, ZNF198, in the t(8;13) leukaemia/lymphoma syndrome

Xiao, S, Nalabolu, SR, Aster, JC, Ma, J, Abruzzo, L, Jaffe, ES, Stone, R, Weissman, SM, Hudson, TJ, Fletcher, JA

Nat Genet 1998
9576949 Fibroblast growth factor receptor 1 is fused to FIM in stem-cell myeloproliferative disorder with t(8;13)

Popovici, C, Adelaide, J, Ollendorff, V, Chaffanet, M, Guasch, G, Jacrot, M, Leroux, D, Birnbaum, D, Pébusque, MJ

Proc Natl Acad Sci U S A 1998
Participants
Participant Of
Disease
Name Identifier Synonyms
precursor lymphoblastic lymphoma/leukemia 5600
subacute leukemia 3264
myelodysplastic myeloproliferative cancer 4972 Myeloproliferative/Myelodysplastic syndromes, unclassifiable myelodysplastic myeloproliferative disease, Unclassifiable Myeloproliferative/Myelodysplastic syndrome, Myelodysplastic/myeloproliferative disease (morphologic abnormality)