Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23534
Gene Symbol: TNPO3
TNPO3
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.410 GeneticVariation GWASDB Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants. 22936693

2012
Entrez Id: 23534
Gene Symbol: TNPO3
TNPO3
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.410 GeneticVariation GWASDB Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000

2012
Entrez Id: 23534
Gene Symbol: TNPO3
TNPO3
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.410 GeneticVariation GWASCAT Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000

2012
Entrez Id: 23534
Gene Symbol: TNPO3
TNPO3
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.410 GeneticVariation GWASDB Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. 21399635

2011
Entrez Id: 23534
Gene Symbol: TNPO3
TNPO3
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.410 Biomarker BEFREE To examine the genetics of susceptibility to primary biliary cirrhosis (PBC), genome-wide association studies GWAS have been performed in patients of European ancestry and have shown the significant associations of IL12-related pathways, SPIB, IRF5-TNPO3, and 17q12-21. 21506939

2011
Entrez Id: 23534
Gene Symbol: TNPO3
TNPO3
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.410 GeneticVariation GWASCAT Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. 21399635

2011
Entrez Id: 23534
Gene Symbol: TNPO3
TNPO3
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.410 SusceptibilityMutation ORPHANET