glycine encephalopathy Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description An amino acid metabolic disorder that involves abnormally high levels of the amino acid glycine in bodily fluids and tissues. (Human Disease Ontology, DOID_9268)
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Genes

2 genes involed in the disease glycine encephalopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
AMT aminomethyltransferase
GLDC glycine dehydrogenase (decarboxylating)