Hepatic Form Of Wilson Disease Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1527352
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Genes

24 genes associated with the disease Hepatic Form Of Wilson Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
A2M alpha-2-macroglobulin
AHCY adenosylhomocysteinase
ANKS1B ankyrin repeat and sterile alpha motif domain containing 1B
ANXA5 annexin A5
APOE apolipoprotein E
ASMT acetylserotonin O-methyltransferase
ATP7B ATPase, Cu++ transporting, beta polypeptide
BHMT betaine--homocysteine S-methyltransferase
CAMK2A calcium/calmodulin-dependent protein kinase II alpha
CP ceruloplasmin (ferroxidase)
CXCL8 chemokine (C-X-C motif) ligand 8
HAMP hepcidin antimicrobial peptide
IL10 interleukin 10
IL6 interleukin 6
LOX lysyl oxidase
LOXL2 lysyl oxidase-like 2
NDUFB7 NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 7, 18kDa
PPP3CA protein phosphatase 3, catalytic subunit, alpha isozyme
PPP3CB protein phosphatase 3, catalytic subunit, beta isozyme
PRNP prion protein
SDHAF2 succinate dehydrogenase complex assembly factor 2
SNCA synuclein, alpha (non A4 component of amyloid precursor)
TIMP1 TIMP metallopeptidase inhibitor 1
TNF tumor necrosis factor