Gene: SHOC2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8036
Gene Symbol: SHOC2
SHOC2 		0.800 Biomarker disease BEFREE Germline mutations in genes encoding small GTPases of the RAS family (KRAS and NRAS), modulators of RAS function (PTPN11, SOS1 and SHOC2) or downstream signal transducers (RAF1) are causative for NS. 20673819 2011
Entrez Id: 8036
Gene Symbol: SHOC2
SHOC2 		0.800 GeneticVariation disease BEFREE To date, mutations in PTPN11, SOS1, KRAS, RAF1 and SHOC2 are known to cause NS and a small group of patients harbour mutations in BRAF, MEK1 or NRAS. 20302979 2010
Entrez Id: 8036
Gene Symbol: SHOC2
SHOC2 		0.800 Biomarker disease GENOMICS_ENGLAND Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair. 19684605 2009
Entrez Id: 8036
Gene Symbol: SHOC2
SHOC2 		0.800 Biomarker disease CTD_human Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair. 19684605 2009
Entrez Id: 8036
Gene Symbol: SHOC2
SHOC2 		0.800 CausalMutation disease CLINVAR Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair. 19684605 2009