hdl cholesterol Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description disease cluster belonging to disease group metabolic (Genetic Association Database)
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35 genes associated with the disease hdl cholesterol in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ABCA1 ATP-binding cassette, sub-family A (ABC1), member 1
ACAA2 acetyl-CoA acyltransferase 2
ANGPTL4 angiopoietin-like 4
APOA1 apolipoprotein A-I
APOA4 apolipoprotein A-IV
APOA5 apolipoprotein A-V
APOB apolipoprotein B
APOC3 apolipoprotein C-III
APOE apolipoprotein E
CETP cholesteryl ester transfer protein, plasma
CMA1 chymase 1, mast cell
CTCF CCCTC-binding factor (zinc finger protein)
FADS1 fatty acid desaturase 1
FADS2 fatty acid desaturase 2
FADS3 fatty acid desaturase 3
FOLH1 folate hydrolase (prostate-specific membrane antigen) 1
GALNT2 polypeptide N-acetylgalactosaminyltransferase 2
HERPUD1 homocysteine-inducible, endoplasmic reticulum stress-inducible, ubiquitin-like domain member 1
HNF4A hepatocyte nuclear factor 4, alpha
LCAT lecithin-cholesterol acyltransferase
LDLR low density lipoprotein receptor
LIPC lipase, hepatic
LIPG lipase, endothelial
LPL lipoprotein lipase
MADD MAP-kinase activating death domain
MMAB methylmalonic aciduria (cobalamin deficiency) cblB type
MVK mevalonate kinase
NR1H3 nuclear receptor subfamily 1, group H, member 3
NUP93 nucleoporin 93kDa
PLTP phospholipid transfer protein
PRMT8 protein arginine methyltransferase 8
SLC12A3 solute carrier family 12 (sodium/chloride transporter), member 3
TOMM40 translocase of outer mitochondrial membrane 40 homolog (yeast)
TTC39B tetratricopeptide repeat domain 39B
UCP1 uncoupling protein 1 (mitochondrial, proton carrier)