agat deficiency Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
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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7 genes co-occuring with the disease agat deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
GAMT guanidinoacetate N-methyltransferase 2.94333
SLC6A8 solute carrier family 6 (neurotransmitter transporter), member 8 2.28421
GATM glycine amidinotransferase (L-arginine:glycine amidinotransferase) 2.19616
DDX21 DEAD (Asp-Glu-Ala-Asp) box helicase 21 1.0109
HTN3 histatin 3 0.873281
TAP1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) 0.826589
OAT ornithine aminotransferase 0.551686