increased circulating vldl triglyceride level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description higher 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_0003975)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003975
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Genes

9 gene mutations causing the increased circulating vldl triglyceride level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCG5 ATP-binding cassette, sub-family G (WHITE), member 5
APOE apolipoprotein E
CAV1 caveolin 1, caveolae protein, 22kDa
CD36 CD36 molecule (thrombospondin receptor)
COL18A1 collagen, type XVIII, alpha 1
LDLR low density lipoprotein receptor
LPIN1 lipin 1
LPL lipoprotein lipase
TRA2B transformer 2 beta homolog (Drosophila)