lipid metabolism disorder Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description An inherited metabolic disorder that involves the creation and degradation of lipids. (Human Disease Ontology, DOID_3146)
Similar Terms
Downloads & Tools


14 genes involed in the disease lipid metabolism disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ABCA1 ATP-binding cassette, sub-family A (ABC1), member 1
ANGPTL3 angiopoietin-like 3
APOB apolipoprotein B
APOC2 apolipoprotein C-II
APOE apolipoprotein E
DHCR7 7-dehydrocholesterol reductase
LCAT lecithin-cholesterol acyltransferase
LDLRAP1 low density lipoprotein receptor adaptor protein 1
LPL lipoprotein lipase
MTTP microsomal triglyceride transfer protein
PCSK9 proprotein convertase subtilisin/kexin type 9
PEX7 peroxisomal biogenesis factor 7
PHYH phytanoyl-CoA 2-hydroxylase
TAZ tafazzin