Non-ketotic hyperglycinemia Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://www.omim.org/entry/605899
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Genes

3 genes associated with the Non-ketotic hyperglycinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
AMT aminomethyltransferase
GCSH glycine cleavage system protein H (aminomethyl carrier)
GLDC glycine dehydrogenase (decarboxylating)