Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4340
Gene Symbol: MOG
MOG 		0.600 Biomarker disease GENOMICS_ENGLAND A missense mutation in myelin oligodendrocyte glycoprotein as a cause of familial narcolepsy with cataplexy. 21907016 2011
Entrez Id: 4340
Gene Symbol: MOG
MOG 		0.600 GeneticVariation disease UNIPROT A missense mutation in myelin oligodendrocyte glycoprotein as a cause of familial narcolepsy with cataplexy. 21907016 2011
Entrez Id: 4340
Gene Symbol: MOG
MOG 		0.600 CausalMutation disease CLINVAR