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Drug-Pathway
DRUGs and PATHWAYs
PATHWAY_NAME REACTOME_ID KEGG_ID DRUG_NAME PUBCHEM_CID Datasource
Adenylosuccinate Lyase Deficiency R-HSA-5602680 0 Glycine 3467 smpdb
Sarcosine Oncometabolite Pathway #N/A #N/A Glycine 3467 smpdb
gamma-Glutamyltranspeptidase Deficiency R-HSA-5602680 0 Glycine 3467 smpdb
Familial Hypercholanemia R-HSA-5682111 0 Glycine 3467 smpdb
Creatine Deficiency, Guanidinoacetate Methyltransferase Deficiency 0 0 Glycine 3467 smpdb
Hyperornithinemia with Gyrate Atrophy R-HSA-70666 0 Glycine 3467 smpdb
Xanthinuria Type II R-HSA-2127377 0 Glycine 3467 smpdb
Hyperprolinemia Type II R-HSA-2127377 0 Glycine 3467 smpdb
Myoadenylate Deaminase Deficiency R-HSA-5602680 0 Glycine 3467 smpdb
Homocarnosinosis 0 0 Glycine 3467 smpdb
27-Hydroxylase Deficiency R-HSA-5602680 0 Glycine 3467 smpdb
tRNA Charging: Glycine R-HSA-141679 0 Glycine 3467 smpdb
Thioguanine Action Pathway R-ALL-9679095 0 Glycine 3467 smpdb
Hyperornithinemia-Hyperammonemia-Homocitrullinuria [HHH-syndrome] 0 0 Glycine 3467 smpdb
Sarcosinemia R-HSA-6797913 0 Glycine 3467 smpdb
Homocystinuria-Megaloblastic Anemia Due to Defect in Cobalamin Metabolism, cblG Complementation Type 0 0 Glycine 3467 smpdb
Glutathione Metabolism R-HSA-156590 map00480 Glycine 3467 smpdb
Congenital Bile Acid Synthesis Defect Type II R-HSA-194068 0 Glycine 3467 smpdb
Adenine Phosphoribosyltransferase Deficiency R-ALL-83951 0 Glycine 3467 smpdb
Hereditary Coproporphyria R-HSA-5657560 0 Glycine 3467 smpdb