hepatocellular carcinoma Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A liver carcinoma that has_material_basis_in undifferentiated hepatocytes. (Human Disease Ontology, DOID_684)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001402
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20 genes associated with the hepatocellular carcinoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCB11 ATP-binding cassette, sub-family B (MDR/TAP), member 11
APC adenomatous polyposis coli
AXIN1 axin 1
CASP8 caspase 8, apoptosis-related cysteine peptidase
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
FAH fumarylacetoacetate hydrolase (fumarylacetoacetase)
G6PC glucose-6-phosphatase, catalytic subunit
H19 H19, imprinted maternally expressed transcript (non-protein coding)
HFE hemochromatosis
HMBS hydroxymethylbilane synthase
IGF2R insulin-like growth factor 2 receptor
JAG1 jagged 1
MET MET proto-oncogene, receptor tyrosine kinase
PDGFRL platelet-derived growth factor receptor-like
PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
SERPINA1 serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 1
SLC25A13 solute carrier family 25 (aspartate/glutamate carrier), member 13
SLC37A4 solute carrier family 37 (glucose-6-phosphate transporter), member 4
TP53 tumor protein p53
UROD uroporphyrinogen decarboxylase