| BioCyc:MTBH37RV_PWY-7221 |
guanosine ribonucleotides de novo biosynthesis |
| BioCyc:MTBH37RV_PWY-5695 |
inosine 5'-phosphate degradation |
| BioCyc:MTBCDC1551_PWY-7221 |
guanosine ribonucleotides de novo biosynthesis |
| BioCyc:MTBCDC1551_PWY-841 |
superpathway of purine nucleotides de novo biosynthesis I |
| BioCyc:MTBCDC1551_PWY-7228 |
superpathway of guanosine nucleotides de novo biosynthesis I |
| BioCyc:MTBH37RV_PWY-7228 |
superpathway of guanosine nucleotides de novo biosynthesis I |
| BioCyc:MTBCDC1551_PWY-5695 |
urate biosynthesis/inosine 5'-phosphate degradation |
| Reactome:R-HSA-9856651 |
MITF-M-dependent gene expression |
| Reactome:R-HSA-9854909 |
Regulation of MITF-M dependent genes involved in invasion |
| Reactome:R-HSA-9730414 |
MITF-M-regulated melanocyte development |
| Reactome:R-HSA-74217 |
Purine salvage |
| Reactome:R-MMU-1430728 |
Metabolism |
| Reactome:R-MMU-74217 |
Purine salvage |
| Reactome:R-RNO-74217 |
Purine salvage |
| Reactome:R-CEL-74217 |
Purine salvage |
| Reactome:R-HSA-1266738 |
Developmental Biology |
| Reactome:R-HSA-8956321 |
Nucleotide salvage |
| Reactome:R-MMU-8956321 |
Nucleotide salvage |
| Reactome:R-RNO-8956321 |
Nucleotide salvage |
| Reactome:R-CEL-15869 |
Nucleotide metabolism |
| Reactome:R-RNO-1430728 |
Metabolism |
| Reactome:R-CEL-1430728 |
Metabolism |
| Reactome:R-CEL-8956321 |
Nucleotide salvage |
| Reactome:R-HSA-1430728 |
Metabolism |
| Reactome:R-HSA-15869 |
Nucleotide metabolism |
| Reactome:R-MMU-15869 |
Nucleotide metabolism |
| Reactome:R-RNO-15869 |
Nucleotide metabolism |
| PathBank:SMP0120670 |
Adenylosuccinate Lyase Deficiency |
| PathBank:SMP0000167 |
Adenylosuccinate Lyase Deficiency |
| PathBank:SMP0000220 |
Xanthine Dehydrogenase Deficiency (Xanthinuria) |
| PathBank:SMP0000512 |
Xanthinuria Type I |
| PathBank:SMP0000536 |
Mitochondrial DNA Depletion Syndrome-3 |
| PathBank:SMP0120669 |
Adenosine Deaminase Deficiency |
| PathBank:SMP0120673 |
AICA-Ribosiduria |
| PathBank:SMP0120709 |
Gout or Kelley-Seegmiller Syndrome |
| PathBank:SMP0120717 |
Xanthine Dehydrogenase Deficiency (Xanthinuria) |
| PathBank:SMP0120797 |
Xanthinuria Type II |
| PathBank:SMP0120821 |
Myoadenylate Deaminase Deficiency |
| PathBank:SMP0000050 |
Purine Metabolism |
| PathBank:SMP0000144 |
Adenosine Deaminase Deficiency |
| PathBank:SMP0000203 |
Molybdenum Cofactor Deficiency |
| PathBank:SMP0000428 |
Mercaptopurine Action Pathway |
| PathBank:SMP0000535 |
Adenine Phosphoribosyltransferase Deficiency (APRT) |
| PathBank:SMP0120728 |
Lesch-Nyhan Syndrome (LNS) |
| PathBank:SMP0120752 |
Molybdenum Cofactor Deficiency |
| PathBank:SMP0120756 |
Purine Nucleoside Phosphorylase Deficiency |
| PathBank:SMP0120796 |
Xanthinuria Type I |
| PathBank:SMP0120820 |
Mitochondrial DNA Depletion Syndrome |
| PathBank:SMP0000365 |
Gout or Kelley-Seegmiller Syndrome |
| PathBank:SMP0000210 |
Purine Nucleoside Phosphorylase Deficiency |
| PathBank:SMP0000430 |
Thioguanine Action Pathway |
| PathBank:SMP0000513 |
Xanthinuria Type II |
| PathBank:SMP0000537 |
Myoadenylate Deaminase Deficiency |
| PathBank:SMP0087332 |
Purine Metabolism |
| PathBank:SMP0120819 |
Adenine Phosphoribosyltransferase Deficiency (APRT) |
| PathBank:SMP0000364 |
Lesch-Nyhan Syndrome (LNS) |
| PathBank:SMP0000168 |
AICA-Ribosiduria |
| PathBank:SMP0000427 |
Azathioprine Action Pathway |
| PathBank:SMP0087239 |
Purine Metabolism |