hdl cholesterol Gene Set
Genes
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)
|
