Lipid Metabolism Disorders Gene Set

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

Genes

22 genes associated with the Lipid Metabolism Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ANGPTL3 angiopoietin-like 3
APOE apolipoprotein E
CELSR2 cadherin, EGF LAG seven-pass G-type receptor 2
CILP2 cartilage intermediate layer protein 2
ETFA electron-transfer-flavoprotein, alpha polypeptide
ETFB electron-transfer-flavoprotein, beta polypeptide
ETFDH electron-transferring-flavoprotein dehydrogenase
GALNT2 polypeptide N-acetylgalactosaminyltransferase 2
GCKR glucokinase (hexokinase 4) regulator
KCTD10 potassium channel tetramerization domain containing 10
LIPC lipase, hepatic
LPL lipoprotein lipase
LRPAP1 low density lipoprotein receptor-related protein associated protein 1
MLXIPL MLX interacting protein-like
PBX4 pre-B-cell leukemia homeobox 4
PNPLA2 patatin-like phospholipase domain containing 2
PPARG peroxisome proliferator-activated receptor gamma
PSRC1 proline/serine-rich coiled-coil 1
SORT1 sortilin 1
SREBF1 sterol regulatory element binding transcription factor 1
TBL2 transducin (beta)-like 2
TRIB1 tribbles pseudokinase 1