Amino Acid Metabolism, Inherited Disorders Gene Set

Dataset	DisGeNET Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
External Link	https://www.disgenet.org/browser/0/1/0/C0750905
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Genes

13 genes associated with the disease Amino Acid Metabolism, Inherited Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol	Name
AHCY	adenosylhomocysteinase
ALDH6A1	aldehyde dehydrogenase 6 family, member A1
ARG1	arginase 1
D2HGDH	D-2-hydroxyglutarate dehydrogenase
EIF2AK4	eukaryotic translation initiation factor 2 alpha kinase 4
GAMT	guanidinoacetate N-methyltransferase
GCLC	glutamate-cysteine ligase, catalytic subunit
MAT1A	methionine adenosyltransferase I, alpha
PRODH	proline dehydrogenase (oxidase) 1
PSPH	phosphoserine phosphatase
SECISBP2	SECIS binding protein 2
SLC7A7	solute carrier family 7 (amino acid transporter light chain, y+L system), member 7
XPC	xeroderma pigmentosum, complementation group C