Gene: SOS2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6655
Gene Symbol: SOS2
SOS2 		0.620 GeneticVariation disease BEFREE We identified two novel genes, SOS2 and LZTR1, associated with Noonan syndrome, thereby expanding the molecular spectrum of RASopathies. 25795793 2015
Entrez Id: 6655
Gene Symbol: SOS2
SOS2 		0.620 GeneticVariation disease BEFREE Similar to NS-causing SOS1 mutations, the phenotype associated with SOS2 defects is characterized by normal development and growth, as well as marked ectodermal involvement. 26173643 2015
Entrez Id: 6655
Gene Symbol: SOS2
SOS2 		0.620 Biomarker disease CLINGEN We identified two novel genes, SOS2 and LZTR1, associated with Noonan syndrome, thereby expanding the molecular spectrum of RASopathies. 25795793 2015
Entrez Id: 6655
Gene Symbol: SOS2
SOS2 		0.620 GermlineCausalMutation disease ORPHANET We identified two novel genes, SOS2 and LZTR1, associated with Noonan syndrome, thereby expanding the molecular spectrum of RASopathies. 25795793 2015
Entrez Id: 6655
Gene Symbol: SOS2
SOS2 		0.620 Biomarker disease CLINGEN Similar to NS-causing SOS1 mutations, the phenotype associated with SOS2 defects is characterized by normal development and growth, as well as marked ectodermal involvement. 26173643 2015
Entrez Id: 6655
Gene Symbol: SOS2
SOS2 		0.620 Biomarker disease CLINGEN The RASopathies. 23875798 2013
Entrez Id: 6655
Gene Symbol: SOS2
SOS2 		0.620 Biomarker disease CLINGEN Ras-guanine nucleotide exchange factor sos2 is dispensable for mouse growth and development. 10938118 2000
Entrez Id: 6655
Gene Symbol: SOS2
SOS2 		0.620 Biomarker disease GENOMICS_ENGLAND Ras-guanine nucleotide exchange factor sos2 is dispensable for mouse growth and development. 10938118 2000