Amino Acid 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:D000592
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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