| BioCyc:YEAST_PWY3O-697 |
folate interconversions |
| BioCyc:MOUSE_PWY-2201 |
folate transformations I |
| BioCyc:HUMAN_PWY-2201 |
folate transformations I |
| BioCyc:YEAST_PWY-2201 |
folate transformations |
| BioCyc:MOUSE_PWY-3841 |
folate transformations II (plants) |
| Reactome:R-HSA-196849 |
Metabolism of water-soluble vitamins and cofactors |
| Reactome:R-MMU-1430728 |
Metabolism |
| Reactome:R-MMU-196849 |
Metabolism of water-soluble vitamins and cofactors |
| Reactome:R-CEL-196849 |
Metabolism of water-soluble vitamins and cofactors |
| Reactome:R-HSA-196854 |
Metabolism of vitamins and cofactors |
| Reactome:R-HSA-196757 |
Metabolism of folate and pterines |
| Reactome:R-MMU-196854 |
Metabolism of vitamins and cofactors |
| Reactome:R-MMU-196757 |
Metabolism of folate and pterines |
| Reactome:R-SCE-1430728 |
Metabolism |
| Reactome:R-SCE-196849 |
Metabolism of water-soluble vitamins and cofactors |
| Reactome:R-CEL-1430728 |
Metabolism |
| Reactome:R-CEL-196854 |
Metabolism of vitamins and cofactors |
| Reactome:R-CEL-196757 |
Metabolism of folate and pterines |
| Reactome:R-HSA-1430728 |
Metabolism |
| Reactome:R-SCE-196854 |
Metabolism of vitamins and cofactors |
| Reactome:R-SCE-196757 |
Metabolism of folate and pterines |
| WikiPathways:WP4259 |
Disorders of folate metabolism and transport |
| PathBank:SMP0000177 |
Cystathionine beta-Synthase Deficiency |
| PathBank:SMP0000340 |
Methylenetetrahydrofolate Reductase Deficiency (MTHFRD) |
| PathBank:SMP0000432 |
Methotrexate Action Pathway |
| PathBank:SMP0000033 |
Methionine Metabolism |
| PathBank:SMP0000222 |
Glycine N-Methyltransferase Deficiency |
| PathBank:SMP0000543 |
Methylenetetrahydrofolate Reductase Deficiency (MTHFRD) |
| PathBank:SMP0087196 |
Folate Metabolism |
| PathBank:SMP0087249 |
Methionine Metabolism |
| PathBank:SMP0000341 |
Hypermethioninemia |
| PathBank:SMP0000221 |
Methionine Adenosyltransferase Deficiency |
| PathBank:SMP0000053 |
Folate Metabolism |
| PathBank:SMP0000214 |
S-Adenosylhomocysteine (SAH) Hydrolase Deficiency |
| PathBank:SMP0000570 |
Homocystinuria-Megaloblastic Anemia Due to Defect in Cobalamin Metabolism, cblG Complementation Type |
| PathBank:SMP0000724 |
Folate Malabsorption, Hereditary |