Gene: MAP2K1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5604
Gene Symbol: MAP2K1
MAP2K1 		0.100 CausalMutation phenotype CLINVAR Spectrum of MEK1 and MEK2 gene mutations in cardio-facio-cutaneous syndrome and genotype-phenotype correlations. 19156172 2009
Entrez Id: 5604
Gene Symbol: MAP2K1
MAP2K1 		0.100 CausalMutation phenotype CLINVAR Germline mutations of MEK in cardio-facio-cutaneous syndrome are sensitive to MEK and RAF inhibition: implications for therapeutic options. 17981815 2008
Entrez Id: 5604
Gene Symbol: MAP2K1
MAP2K1 		0.100 CausalMutation phenotype CLINVAR Mutation and phenotypic spectrum in patients with cardio-facio-cutaneous and Costello syndrome. 18042262 2008
Entrez Id: 5604
Gene Symbol: MAP2K1
MAP2K1 		0.100 CausalMutation phenotype CLINVAR Molecular and clinical characterization of cardio-facio-cutaneous (CFC) syndrome: overlapping clinical manifestations with Costello syndrome. 17366577 2007
Entrez Id: 5604
Gene Symbol: MAP2K1
MAP2K1 		0.100 CausalMutation phenotype CLINVAR Further delineation of the phenotype resulting from BRAF or MEK1 germline mutations helps differentiate cardio-facio-cutaneous syndrome from Costello syndrome. 17551924 2007
Entrez Id: 5604
Gene Symbol: MAP2K1
MAP2K1 		0.100 CausalMutation phenotype CLINVAR Hepatoblastoma and heart transplantation in a patient with cardio-facio-cutaneous syndrome. 17567882 2007
Entrez Id: 5604
Gene Symbol: MAP2K1
MAP2K1 		0.100 CausalMutation phenotype CLINVAR Germline mutations in genes within the MAPK pathway cause cardio-facio-cutaneous syndrome. 16439621 2006