Metabolism, Inborn Errors Gene Set
Genes
18 genes/proteins associated with the disease Metabolism, Inborn Errors from the curated CTD Gene-Disease Associations dataset.
| Symbol |
Name |
Standardized Value |
|
PLA2G7
|
phospholipase A2, group VII (platelet-activating factor acetylhydrolase, plasma)
|
2.88009
|
|
MYO5B
|
myosin VB
|
2.88009
|
|
SLC2A1
|
solute carrier family 2 (facilitated glucose transporter), member 1
|
2.88009
|
|
DHFR
|
dihydrofolate reductase
|
2.88009
|
|
SERPINA7
|
serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 7
|
2.88009
|
|
CES1
|
carboxylesterase 1
|
2.88009
|
|
LDHB
|
lactate dehydrogenase B
|
2.88009
|
|
LEPR
|
leptin receptor
|
2.88009
|
|
ADAMTSL2
|
ADAMTS-like 2
|
2.88009
|
|
DIO1
|
deiodinase, iodothyronine, type I
|
2.88009
|
|
ITPA
|
inosine triphosphatase (nucleoside triphosphate pyrophosphatase)
|
2.88009
|
|
ABCD4
|
ATP-binding cassette, sub-family D (ALD), member 4
|
2.88009
|
|
MUT
|
methylmalonyl CoA mutase
|
2.88009
|
|
PLA2G4A
|
phospholipase A2, group IVA (cytosolic, calcium-dependent)
|
2.88009
|
|
AGXT2
|
alanine--glyoxylate aminotransferase 2
|
2.88009
|
|
TPI1
|
triosephosphate isomerase 1
|
2.88009
|
|
APP
|
amyloid beta (A4) precursor protein
|
1.2818
|
|
MTR
|
5-methyltetrahydrofolate-homocysteine methyltransferase
|
1.01174
|
