Amino Acid Metabolism, Inborn Errors Gene Set
Genes
12 genes/proteins associated with the disease Amino Acid Metabolism, Inborn Errors from the curated CTD Gene-Disease Associations dataset.
| Symbol |
Name |
Standardized Value |
|
GAMT
|
guanidinoacetate N-methyltransferase
|
2.88009
|
|
EIF2AK4
|
eukaryotic translation initiation factor 2 alpha kinase 4
|
2.88009
|
|
GCLC
|
glutamate-cysteine ligase, catalytic subunit
|
2.88009
|
|
D2HGDH
|
D-2-hydroxyglutarate dehydrogenase
|
2.88009
|
|
SECISBP2
|
SECIS binding protein 2
|
2.88009
|
|
ALDH6A1
|
aldehyde dehydrogenase 6 family, member A1
|
2.88009
|
|
SLC7A7
|
solute carrier family 7 (amino acid transporter light chain, y+L system), member 7
|
2.88009
|
|
AHCY
|
adenosylhomocysteinase
|
2.88009
|
|
XPC
|
xeroderma pigmentosum, complementation group C
|
2.88009
|
|
ARG1
|
arginase 1
|
2.88009
|
|
MAT1A
|
methionine adenosyltransferase I, alpha
|
2.88009
|
|
PSPH
|
phosphoserine phosphatase
|
2.88009
|
