decreased circulating vldl triglyceride level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description lower than average concentration in the blood of very low density lipoprotein, which normally transports triglycerides from the intestine and liver to muscle and adipose tissue (Mammalian Phenotype Ontology, MP_0003976)
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12 gene mutations causing the decreased circulating vldl triglyceride level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGRP agouti related neuropeptide
APOA4 apolipoprotein A-IV
APOE apolipoprotein E
CES1 carboxylesterase 1
FOXO1 forkhead box O1
GPAM glycerol-3-phosphate acyltransferase, mitochondrial
HIF1AN hypoxia inducible factor 1, alpha subunit inhibitor
MIA2 melanoma inhibitory activity 2
MTTP microsomal triglyceride transfer protein
PNPLA2 patatin-like phospholipase domain containing 2
SIK3 SIK family kinase 3
SIRT7 sirtuin 7