Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23600
Gene Symbol: AMACR
AMACR 		0.700 GermlineCausalMutation disease ORPHANET Mechanisms of disease: Inborn errors of bile acid synthesis. 18577977 2008
Entrez Id: 23600
Gene Symbol: AMACR
AMACR 		0.700 Biomarker disease GENOMICS_ENGLAND Liver disease caused by failure to racemize trihydroxycholestanoic acid: gene mutation and effect of bile acid therapy. 12512044 2003
Entrez Id: 23600
Gene Symbol: AMACR
AMACR 		0.700 GeneticVariation disease UNIPROT Liver disease caused by failure to racemize trihydroxycholestanoic acid: gene mutation and effect of bile acid therapy. 12512044 2003
Entrez Id: 23600
Gene Symbol: AMACR
AMACR 		0.700 GeneticVariation disease UNIPROT Mutations in the gene encoding peroxisomal alpha-methylacyl-CoA racemase cause adult-onset sensory motor neuropathy. 10655068 2000
Entrez Id: 23600
Gene Symbol: AMACR
AMACR 		0.700 Biomarker disease GENOMICS_ENGLAND Mutations in the gene encoding peroxisomal alpha-methylacyl-CoA racemase cause adult-onset sensory motor neuropathy. 10655068 2000
Entrez Id: 23600
Gene Symbol: AMACR
AMACR 		0.700 CausalMutation disease CLINVAR
Entrez Id: 23600
Gene Symbol: AMACR
AMACR 		0.700 Biomarker disease CTD_human
Entrez Id: 100534612
Gene Symbol: C1QTNF3-AMACR
C1QTNF3-AMACR 		0.100 CausalMutation disease CLINVAR