Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 540
Gene Symbol: ATP7B
ATP7B
0.440 GeneticVariation disease BEFREE SHED and SHED-Heps were transplanted into WD model Atp7b-mutated Long-Evans Cinnamon (LEC) rats received copper overloading to induce a lethal fulminant liver failure. 30733544 2019
Entrez Id: 540
Gene Symbol: ATP7B
ATP7B
0.440 Biomarker disease CTD_human Wilson disease (WD) is caused by accumulation of excess copper (Cu) due to a mutation in the gene encoding the liver Cu transporter ATP7B, and is characterized by acute liver failure or cirrhosis and neuronal cell death. 25134866 2014
Entrez Id: 540
Gene Symbol: ATP7B
ATP7B
0.440 Biomarker disease BEFREE Wilson disease (WD) is caused by accumulation of excess copper (Cu) due to a mutation in the gene encoding the liver Cu transporter ATP7B, and is characterized by acute liver failure or cirrhosis and neuronal cell death. 25134866 2014
Entrez Id: 540
Gene Symbol: ATP7B
ATP7B
0.440 GeneticVariation disease BEFREE High prevalence of fulminant hepatic failure among patients with mutant alleles for truncation of ATP7B in Wilson's disease. 20491539 2010
Entrez Id: 540
Gene Symbol: ATP7B
ATP7B
0.440 GeneticVariation disease BEFREE We examined the ATP7B gene in two Japanese sisters with Wilson's disease presenting with fulminant hepatic failure but who did not exhibit Kayser-Fleischer rings or abnormal neurological findings. 10777157 2000
Entrez Id: 540
Gene Symbol: ATP7B
ATP7B
0.440 Biomarker disease HPO