Lipid Metabolism, Inborn Errors Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Similar Terms
Downloads & Tools

Genes

25 genes associated with the Lipid Metabolism, Inborn Errors phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ABCA1 ATP-binding cassette, sub-family A (ABC1), member 1
ABCG8 ATP-binding cassette, sub-family G (WHITE), member 8
ACADM acyl-CoA dehydrogenase, C-4 to C-12 straight chain
ACADS acyl-CoA dehydrogenase, C-2 to C-3 short chain
APOA1 apolipoprotein A-I
CETP cholesteryl ester transfer protein, plasma
CPT1A carnitine palmitoyltransferase 1A (liver)
GLA galactosidase, alpha
HADHA hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), alpha subunit
LCAT lecithin-cholesterol acyltransferase
LIPC lipase, hepatic
LIPG lipase, endothelial
LPL lipoprotein lipase
MCCC1 methylcrotonoyl-CoA carboxylase 1 (alpha)
MTTP microsomal triglyceride transfer protein
MYBPC3 myosin binding protein C, cardiac
MYH7 myosin, heavy chain 7, cardiac muscle, beta
MYL3 myosin, light chain 3, alkali; ventricular, skeletal, slow
PPARG peroxisome proliferator-activated receptor gamma
SCARB1 scavenger receptor class B, member 1
SLC22A4 solute carrier family 22 (organic cation/zwitterion transporter), member 4
SLC22A5 solute carrier family 22 (organic cation/carnitine transporter), member 5
TNNI3 troponin I type 3 (cardiac)
TNNT2 troponin T type 2 (cardiac)
UNC119B unc-119 homolog B (C. elegans)