Gene: SOS1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6654
Gene Symbol: SOS1
SOS1 		0.100 GeneticVariation disease CLINVAR NMR-based functional profiling of RASopathies and oncogenic RAS mutations. 23487764 2013
Entrez Id: 6654
Gene Symbol: SOS1
SOS1 		0.100 GeneticVariation disease CLINVAR SOS1 mutations in Noonan syndrome: molecular spectrum, structural insights on pathogenic effects, and genotype-phenotype correlations. 21387466 2011
Entrez Id: 6654
Gene Symbol: SOS1
SOS1 		0.100 CausalMutation disease CLINVAR SOS1 mutations in Noonan syndrome: molecular spectrum, structural insights on pathogenic effects, and genotype-phenotype correlations. 21387466 2011
Entrez Id: 6654
Gene Symbol: SOS1
SOS1 		0.100 CausalMutation disease CLINVAR Spectrum of mutations in Noonan syndrome and their correlation with phenotypes. 21784453 2011
Entrez Id: 6654
Gene Symbol: SOS1
SOS1 		0.100 GeneticVariation disease CLINVAR Effects of germline mutations in the Ras/MAPK signaling pathway on adaptive behavior: cardiofaciocutaneous syndrome and Noonan syndrome. 20186801 2010
Entrez Id: 6654
Gene Symbol: SOS1
SOS1 		0.100 CausalMutation disease CLINVAR Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome. 17143282 2007
Entrez Id: 6654
Gene Symbol: SOS1
SOS1 		0.100 CausalMutation disease CLINVAR SOS1 is the second most common Noonan gene but plays no major role in cardio-facio-cutaneous syndrome. 17586837 2007
Entrez Id: 6654
Gene Symbol: SOS1
SOS1 		0.100 GeneticVariation disease CLINVAR Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome. 17143282 2007