Hepatolenticular Degeneration Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_893)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D006527
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14 genes/proteins associated with the disease Hepatolenticular Degeneration from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
ATP7B ATPase, Cu++ transporting, beta polypeptide 2.88009
CP ceruloplasmin (ferroxidase) 2.88009
LOX lysyl oxidase 2.88009
LOXL2 lysyl oxidase-like 2 2.88009
ANXA5 annexin A5 2.88009
PRNP prion protein 2.88009
APOE apolipoprotein E 2.88009
SOD1 superoxide dismutase 1, soluble 1.22436
HSPA1L heat shock 70kDa protein 1-like 1.20913
TP53 tumor protein p53 1.17728
APP amyloid beta (A4) precursor protein 1.16533
CASP3 caspase 3, apoptosis-related cysteine peptidase 1.09011
GPX1 glutathione peroxidase 1 1.07093
HMOX1 heme oxygenase 1 1.04427