hyperlipidemia Gene Set
Genes
16 gene mutations causing the hyperlipidemia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol |
Name |
|
ACOX1
|
acyl-CoA oxidase 1, palmitoyl
|
|
APC
|
adenomatous polyposis coli
|
|
APOE
|
apolipoprotein E
|
|
CPT1C
|
carnitine palmitoyltransferase 1C
|
|
CYB5R4
|
cytochrome b5 reductase 4
|
|
DLK1
|
delta-like 1 homolog (Drosophila)
|
|
KDM3A
|
lysine (K)-specific demethylase 3A
|
|
LEPR
|
leptin receptor
|
|
LPL
|
lipoprotein lipase
|
|
NOS3
|
nitric oxide synthase 3 (endothelial cell)
|
|
PPARG
|
peroxisome proliferator-activated receptor gamma
|
|
PTRF
|
polymerase I and transcript release factor
|
|
RASA3
|
RAS p21 protein activator 3
|
|
RRM2B
|
ribonucleotide reductase M2 B (TP53 inducible)
|
|
SLC37A4
|
solute carrier family 37 (glucose-6-phosphate transporter), member 4
|
|
WRN
|
Werner syndrome, RecQ helicase-like
|
