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)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C567192
Similar Terms
Downloads & Tools

Genes

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