abnormal circulating vldl cholesterol level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the amount in the blood of the lipoprotein:cholesterol complex that transports triglycerides from the intestine and liver to muscle and adipose tissue (Mammalian Phenotype Ontology, MP_0005144)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005144
Similar Terms
Downloads & Tools

Genes

38 gene mutations causing the abnormal circulating vldl cholesterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADIPOR2 adiponectin receptor 2
ALOX5 arachidonate 5-lipoxygenase
ANGPTL3 angiopoietin-like 3
ANGPTL4 angiopoietin-like 4
APOA1 apolipoprotein A-I
APOA5 apolipoprotein A-V
APOB apolipoprotein B
APOC3 apolipoprotein C-III
APOE apolipoprotein E
BBS4 Bardet-Biedl syndrome 4
CES1 carboxylesterase 1
CPE carboxypeptidase E
GHR growth hormone receptor
GPIHBP1 glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1
LCAT lecithin-cholesterol acyltransferase
LDLR low density lipoprotein receptor
LEP leptin
LEPR leptin receptor
LPIN1 lipin 1
LPL lipoprotein lipase
LRP5 low density lipoprotein receptor-related protein 5
MALRD1 MAM and LDL receptor class A domain containing 1
MGAT4B mannosyl (alpha-1,3-)-glycoprotein beta-1,4-N-acetylglucosaminyltransferase, isozyme B
MIR122 microRNA 122
MOGAT2 monoacylglycerol O-acyltransferase 2
MTTP microsomal triglyceride transfer protein
NR0B2 nuclear receptor subfamily 0, group B, member 2
PLTP phospholipid transfer protein
PON1 paraoxonase 1
PON2 paraoxonase 2
PPARD peroxisome proliferator-activated receptor delta
PRKAR2B protein kinase, cAMP-dependent, regulatory, type II, beta
SCP2 sterol carrier protein 2
SEC14L2 SEC14-like 2 (S. cerevisiae)
SIRT3 sirtuin 3
SOAT2 sterol O-acyltransferase 2
TLR2 toll-like receptor 2
TXNIP thioredoxin interacting protein