macrovesicular hepatic steatosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A form of hepatic steatosis characterized by the presence of large, lipid-laden vesicles in the affected hepatocytes. (Human Phenotype Ontology, HP_0001403)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001403
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Genes

5 genes associated with the macrovesicular hepatic steatosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
COG6 component of oligomeric golgi complex 6
CPT2 carnitine palmitoyltransferase 2
EARS2 glutamyl-tRNA synthetase 2, mitochondrial
MPV17 MpV17 mitochondrial inner membrane protein
TRMU tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase