Chronic Liver Failure Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C2936476
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Genes

25 genes associated with the disease Chronic Liver Failure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ABCB4 ATP-binding cassette, sub-family B (MDR/TAP), member 4
AKR1D1 aldo-keto reductase family 1, member D1
ALB albumin
ALDOB aldolase B, fructose-bisphosphate
ALMS1 Alstrom syndrome protein 1
ARNTL2 aryl hydrocarbon receptor nuclear translocator-like 2
CC2D2A coiled-coil and C2 domain containing 2A
EIF2AK3 eukaryotic translation initiation factor 2-alpha kinase 3
GPR35 G protein-coupled receptor 35
HADHA hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), alpha subunit
HADHB hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), beta subunit
IFNA2 interferon, alpha 2
INPP5E inositol polyphosphate-5-phosphatase, 72 kDa
MAOA monoamine oxidase A
MST1 macrophage stimulating 1
NOS1 nitric oxide synthase 1 (neuronal)
PNPLA3 patatin-like phospholipase domain containing 3
PPP6R2 protein phosphatase 6, regulatory subunit 2
PTX3 pentraxin 3, long
RPGRIP1L RPGRIP1-like
SP110 SP110 nuclear body protein
TCF4 transcription factor 4
THPO thrombopoietin
TMEM67 transmembrane protein 67
TSPO translocator protein (18kDa)