Arginine:Glycine Amidinotransferase Deficiency Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An amino acid metabolic disorder that has_material_basis_in a mutation in the GATM gene resulting in deficiency of arginine:glycine amidinotransferase which then limits creatine synthesis. (Human Disease Ontology, DOID_0050712)
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1 genes/proteins associated with the disease Arginine:Glycine Amidinotransferase Deficiency from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
GATM glycine amidinotransferase (L-arginine:glycine amidinotransferase) 2.88009