Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 540
Gene Symbol: ATP7B
ATP7B 		0.300 Biomarker disease CTD_human Molecular diagnosis of Wilson disease using prevalent mutations and informative single-nucleotide polymorphism markers. 17634212 2007
Entrez Id: 540
Gene Symbol: ATP7B
ATP7B 		0.300 Biomarker disease CTD_human Selective divalent copper chelation for the treatment of diabetes mellitus. 22455587 2012
Entrez Id: 540
Gene Symbol: ATP7B
ATP7B 		0.300 Biomarker disease CTD_human Regulation of heme synthesis and proteasomal activity by copper: possible implications for Wilson's disease. 19888908 2009
Entrez Id: 3569
Gene Symbol: IL6
IL6 		0.300 Biomarker disease CTD_human A study of oxidative stress, cytokines and glutamate in Wilson disease and their asymptomatic siblings. 25002079 2014
Entrez Id: 540
Gene Symbol: ATP7B
ATP7B 		0.300 Biomarker disease CTD_human Mutation analysis of copper-transporting P-type adenosine triphosphatase (ATP7B) in human solid carcinomas. 12820478 2003
Entrez Id: 540
Gene Symbol: ATP7B
ATP7B 		0.300 Biomarker disease CTD_human Wilson's disease: an update. 16932613 2006
Entrez Id: 540
Gene Symbol: ATP7B
ATP7B 		0.300 Biomarker disease CTD_human Profound midbrain atrophy in patients with Wilson's disease and neurological symptoms? 16607473 2006
Entrez Id: 2
Gene Symbol: A2M
A2M 		0.300 Biomarker disease CTD_human The early molecular processes underlying the neurological manifestations of an animal model of Wilson's disease. 23519153 2013
Entrez Id: 540
Gene Symbol: ATP7B
ATP7B 		0.300 Biomarker disease CTD_human Haemolytic onset of Wilson disease in a patient with homozygous truncation of ATP7B at Arg1319. 11472373 2001
Entrez Id: 191
Gene Symbol: AHCY
AHCY 		0.300 Biomarker disease CTD_human The early molecular processes underlying the neurological manifestations of an animal model of Wilson's disease. 23519153 2013
Entrez Id: 540
Gene Symbol: ATP7B
ATP7B 		0.300 Biomarker disease CTD_human Copper transport and its defect in Wilson disease: characterization of the copper-binding domain of Wilson disease ATPase. 10830865 2000
Entrez Id: 4015
Gene Symbol: LOX
LOX 		0.300 Biomarker disease CTD_human Abnormal deposition of collagen around hepatocytes in Wilson's disease is associated with hepatocyte specific expression of lysyl oxidase and lysyl oxidase like protein-2. 16023247 2005
Entrez Id: 540
Gene Symbol: ATP7B
ATP7B 		0.300 Biomarker disease CTD_human Wilson's disease. 17276780 2007
Entrez Id: 540
Gene Symbol: ATP7B
ATP7B 		0.300 Biomarker disease CTD_human The plant decapeptide OSIP108 prevents copper-induced toxicity in various models for Wilson disease. 25134866 2014
Entrez Id: 57817
Gene Symbol: HAMP
HAMP 		0.300 Biomarker disease CTD_human The early molecular processes underlying the neurological manifestations of an animal model of Wilson's disease. 23519153 2013
Entrez Id: 540
Gene Symbol: ATP7B
ATP7B 		0.300 Biomarker disease CTD_human Urinary copper elevation in a mouse model of Wilson's disease is a regulated process to specifically decrease the hepatic copper load. 22802922 2012
Entrez Id: 540
Gene Symbol: ATP7B
ATP7B 		0.300 Biomarker disease CTD_human The impact of apolipoprotein E genotypes on age at onset of symptoms and phenotypic expression in Wilson's disease. 10686180 2000
Entrez Id: 540
Gene Symbol: ATP7B
ATP7B 		0.300 Biomarker disease CTD_human Genetic defects in Indian Wilson disease patients and genotype-phenotype correlation. 24094725 2014
Entrez Id: 7076
Gene Symbol: TIMP1
TIMP1 		0.300 Biomarker disease CTD_human Elevated copper impairs hepatic nuclear receptor function in Wilson's disease. 26241054 2015
Entrez Id: 540
Gene Symbol: ATP7B
ATP7B 		0.300 Biomarker disease CTD_human Copper transportion of WD protein in hepatocytes from Wilson disease patients in vitro. 11854914 2001
Entrez Id: 540
Gene Symbol: ATP7B
ATP7B 		0.300 Biomarker disease CTD_human ATP7B activity is stimulated by PKCɛ in porcine liver. 25003971 2014
Entrez Id: 4017
Gene Symbol: LOXL2
LOXL2 		0.300 Biomarker disease CTD_human Abnormal deposition of collagen around hepatocytes in Wilson's disease is associated with hepatocyte specific expression of lysyl oxidase and lysyl oxidase like protein-2. 16023247 2005
Entrez Id: 540
Gene Symbol: ATP7B
ATP7B 		0.300 Biomarker disease CTD_human Gene expression in the liver of Long-Evans cinnamon rats during the development of hepatitis. 14574444 2003
Entrez Id: 540
Gene Symbol: ATP7B
ATP7B 		0.300 Biomarker disease CTD_human The effect of zinc and D-penicillamine in a stable human hepatoma ATP7B knockout cell line. 24892424 2014
Entrez Id: 438
Gene Symbol: ASMT
ASMT 		0.300 Biomarker disease CTD_human The early molecular processes underlying the neurological manifestations of an animal model of Wilson's disease. 23519153 2013