Copper-Overload Cirrhosis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1876165
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Genes

11 genes associated with the disease Copper-Overload Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACTA2 actin, alpha 2, smooth muscle, aorta
CASP3 caspase 3, apoptosis-related cysteine peptidase
COMMD1 copper metabolism (Murr1) domain containing 1
HGF hepatocyte growth factor (hepapoietin A; scatter factor)
KRT19 keratin 19, type I
KRT7 keratin 7, type II
MET MET proto-oncogene, receptor tyrosine kinase
MKI67 marker of proliferation Ki-67
SMAD2 SMAD family member 2
STAT3 signal transducer and activator of transcription 3 (acute-phase response factor)
TGFB1 transforming growth factor, beta 1