hypertriglyceridemia Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An abnormal increase in the level of triglycerides in the blood. (Human Phenotype Ontology, HP_0002155)
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Genes

25 genes associated with the disease hypertriglyceridemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ACAT1 acetyl-CoA acetyltransferase 1
ADRB2 adrenoceptor beta 2, surface
ANGPTL3 angiopoietin-like 3
APOA1 apolipoprotein A-I
APOA2 apolipoprotein A-II
APOA4 apolipoprotein A-IV
APOA5 apolipoprotein A-V
APOB apolipoprotein B
APOC3 apolipoprotein C-III
APOE apolipoprotein E
APOL1 apolipoprotein L, 1
BAZ1B bromodomain adjacent to zinc finger domain, 1B
CETP cholesteryl ester transfer protein, plasma
CYP7A1 cytochrome P450, family 7, subfamily A, polypeptide 1
ENPP1 ectonucleotide pyrophosphatase/phosphodiesterase 1
FABP2 fatty acid binding protein 2, intestinal
GALNT2 polypeptide N-acetylgalactosaminyltransferase 2
GCKR glucokinase (hexokinase 4) regulator
LIPG lipase, endothelial
LPL lipoprotein lipase
MLXIPL MLX interacting protein-like
RP1 retinitis pigmentosa 1 (autosomal dominant)
TBL2 transducin (beta)-like 2
TRIB1 tribbles pseudokinase 1
ZPR1 ZPR1 zinc finger