Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4340
Gene Symbol: MOG
MOG
0.510 SusceptibilityMutation disease ORPHANET A missense mutation in myelin oligodendrocyte glycoprotein as a cause of familial narcolepsy with cataplexy. 21907016 2011
Entrez Id: 4340
Gene Symbol: MOG
MOG
0.510 GeneticVariation disease BEFREE A missense mutation in myelin oligodendrocyte glycoprotein as a cause of familial narcolepsy with cataplexy. 21907016 2011
Entrez Id: 4340
Gene Symbol: MOG
MOG
0.510 Biomarker disease CTD_human