Source: UNIPROT ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1050
Gene Symbol: CEBPA
CEBPA 		1.000 GeneticVariation disease UNIPROT CEBPA mutation is apparently the primary event in the development of AML in this family. 15575056 2004
Entrez Id: 1050
Gene Symbol: CEBPA
CEBPA 		1.000 GeneticVariation disease UNIPROT CEBPA mutation status was not demonstrated to be of prognostic importance in this patient group, although this may reflect the selection and size of the AML population studied. 12661007 2003
Entrez Id: 1050
Gene Symbol: CEBPA
CEBPA 		1.000 GeneticVariation disease UNIPROT Ours is the first report of CEBPA mutations in human neoplasia, and such mutations are likely to induce the differentiation block found in AML. 11242107 2001
Entrez Id: 2322
Gene Symbol: FLT3
FLT3 		1.000 GeneticVariation disease UNIPROT
Entrez Id: 3717
Gene Symbol: JAK2
JAK2 		0.800 GeneticVariation disease UNIPROT This is the first report on the JAK2 gene mutation in AML, and the data indicated that the JAK2 gene mutation may not only contribute to the development of chronic myeloid disorders, but also to some AMLs. 16247455 2006
Entrez Id: 5781
Gene Symbol: PTPN11
PTPN11 		0.800 GeneticVariation disease UNIPROT
Entrez Id: 26040
Gene Symbol: SETBP1
SETBP1 		0.590 GeneticVariation disease UNIPROT Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression. 23889083 2013
Entrez Id: 26040
Gene Symbol: SETBP1
SETBP1 		0.590 GeneticVariation disease UNIPROT SETBP1 mutation analysis in 944 patients with MDS and AML. 23648668 2013
Entrez Id: 54790
Gene Symbol: TET2
TET2 		0.500 GeneticVariation disease UNIPROT
Entrez Id: 11122
Gene Symbol: PTPRT
PTPRT 		0.400 GeneticVariation disease UNIPROT
Entrez Id: 29072
Gene Symbol: SETD2
SETD2 		0.350 GeneticVariation disease UNIPROT Identification of functional cooperative mutations of SETD2 in human acute leukemia. 24509477 2014
Entrez Id: 29072
Gene Symbol: SETD2
SETD2 		0.350 GeneticVariation disease UNIPROT Solution structure of the Set2-Rpb1 interacting domain of human Set2 and its interaction with the hyperphosphorylated C-terminal domain of Rpb1. 16314571 2005
Entrez Id: 1880
Gene Symbol: GPR183
GPR183 		0.300 GeneticVariation disease UNIPROT
Entrez Id: 339970
Gene Symbol: GCOM2
GCOM2 		0.300 GeneticVariation disease UNIPROT