micronodular cirrhosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A type of cirrhosis characterized by the presence of small regenerative nodules. (Human Phenotype Ontology, HP_0001413)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001413
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Genes

15 genes associated with the micronodular cirrhosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
APC adenomatous polyposis coli
AXIN1 axin 1
CASP8 caspase 8, apoptosis-related cysteine peptidase
COG6 component of oligomeric golgi complex 6
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
PDGFRL platelet-derived growth factor receptor-like
PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
POLG polymerase (DNA directed), gamma
TP53 tumor protein p53
TREX1 three prime repair exonuclease 1