Micronodular Cirrhosis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A type of cirrhosis characterized by the presence of small regenerative nodules. (Human Phenotype Ontology, HP_0001413)
External Link https://www.disgenet.org/browser/0/1/0/C0267812
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Genes

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

Symbol Name
ABHD5 abhydrolase domain containing 5
APC adenomatous polyposis coli
AXIN1 axin 1
CASP8 caspase 8, apoptosis-related cysteine peptidase
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
DGUOK deoxyguanosine kinase
IGF2R insulin-like growth factor 2 receptor
KRT18 keratin 18, type I
KRT8 keratin 8, type II
MET MET proto-oncogene, receptor tyrosine kinase
NGLY1 N-glycanase 1
PDGFRL platelet-derived growth factor receptor-like
PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
POLG polymerase (DNA directed), gamma
SLC30A10 solute carrier family 30, member 10
TALDO1 transaldolase 1
TP53 tumor protein p53
TREX1 three prime repair exonuclease 1