Metabolism, Inborn Errors Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D008661
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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