abnormal prostaglandin level Gene Set
Genes
26 gene mutations causing the abnormal prostaglandin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Symbol |
Name |
ABCC4
|
ATP-binding cassette, sub-family C (CFTR/MRP), member 4
|
ACSL4
|
acyl-CoA synthetase long-chain family member 4
|
ALOX5
|
arachidonate 5-lipoxygenase
|
ALOX5AP
|
arachidonate 5-lipoxygenase-activating protein
|
APC
|
adenomatous polyposis coli
|
APOE
|
apolipoprotein E
|
CYSLTR2
|
cysteinyl leukotriene receptor 2
|
DUSP1
|
dual specificity phosphatase 1
|
FADS1
|
fatty acid desaturase 1
|
FADS2
|
fatty acid desaturase 2
|
HPGD
|
hydroxyprostaglandin dehydrogenase 15-(NAD)
|
LEPR
|
leptin receptor
|
LPAR3
|
lysophosphatidic acid receptor 3
|
MMP9
|
matrix metallopeptidase 9
|
NOS3
|
nitric oxide synthase 3 (endothelial cell)
|
PLA2G10
|
phospholipase A2, group X
|
PTGDR2
|
prostaglandin D2 receptor 2
|
PTGER4
|
prostaglandin E receptor 4 (subtype EP4)
|
PTGES
|
prostaglandin E synthase
|
PTGES3
|
prostaglandin E synthase 3 (cytosolic)
|
PTGIR
|
prostaglandin I2 (prostacyclin) receptor (IP)
|
PTGIS
|
prostaglandin I2 (prostacyclin) synthase
|
PTGS1
|
prostaglandin-endoperoxide synthase 1 (prostaglandin G/H synthase and cyclooxygenase)
|
PTGS2
|
prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)
|
SLCO2A1
|
solute carrier organic anion transporter family, member 2A1
|
XPA
|
xeroderma pigmentosum, complementation group A
|