Source: INFERRED ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
0.780 CausalMutation disease CLINVAR In conclusion, mutations in NRAS from individuals with Noonan syndrome activated N-Ras signaling and induced developmental defects in zebrafish embryos, indicating that activating mutations in NRAS cause Noonan syndrome. 21263000 2011
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
0.780 CausalMutation disease CLINVAR A restricted spectrum of NRAS mutations causes Noonan syndrome. 19966803 2010
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
0.780 CausalMutation disease CLINVAR RAS oncogene suppression induces apoptosis followed by more differentiated and less myelosuppressive disease upon relapse of acute myeloid leukemia. 18952898 2009
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
0.780 CausalMutation disease CLINVAR Correlation of clinical features with the mutational status of GM-CSF signaling pathway-related genes in juvenile myelomonocytic leukemia. 19047918 2009
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
0.780 CausalMutation disease CLINVAR Hyperactive Ras in developmental disorders and cancer. 17384584 2007
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
0.780 CausalMutation disease CLINVAR Mutations of the PTPN11 and RAS genes in rhabdomyosarcoma and pediatric hematological malignancies. 16518851 2006
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
0.780 CausalMutation disease CLINVAR Repressible transgenic model of NRAS oncogene-driven mast cell disease in the mouse. 15831708 2005
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
0.780 CausalMutation disease CLINVAR Genetic evidence for lineage-related and differentiation stage-related contribution of somatic PTPN11 mutations to leukemogenesis in childhood acute leukemia. 14982869 2004
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
0.780 CausalMutation disease CLINVAR Constitutive activation of the Ras-Raf signaling pathway in metastatic melanoma is associated with poor prognosis. 15046639 2004
Entrez Id: 4893
Gene Symbol: NRAS
NRAS
0.780 CausalMutation disease CLINVAR Juvenile myelomonocytic leukemia and Noonan syndrome. 10598665 2000