Metabolism of nucleotides

Pathway network for the Metabolism of nucleotides SuperPath

Sources:
  • Reactome
  • PubChem

Pathways in the Metabolism of nucleotides SuperPath

#NameSourceGenes
1Metabolism of nucleotidesReactome
2Nucleotide catabolismReactome
3Purine catabolismReactome
4Nucleotide biosynthesisReactome
5superpathway of purine nucleotide salvagePubChem
6Pyrimidine catabolismReactome
7purine nucleotides degradationPubChem
8Purine ribonucleoside monophosphate biosynthesisReactome
9adenosine nucleotides degradationPubChem
10purine nucleotides degradation II (aerobic)PubChem
11Phosphate bond hydrolysis by NTPDase proteinsReactome
12superpathway of guanosine nucleotides de novo biosynthesis IPubChem
13Phosphate bond hydrolysis by NUDT proteinsReactome
14purine deoxyribonucleosides salvagePubChem
15superpathway of adenosine nucleotides de novo biosynthesis IPubChem
16adenosine nucleotides degradation IIPubChem
17guanosine ribonucleotides de novo biosynthesisPubChem
18adenosine ribonucleotides de novo biosynthesisPubChem
19oxidized GTP and dGTP detoxificationPubChem

Gene overlap in member pathways for Metabolism of nucleotides SuperPath

Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways

Disorders associated with Metabolism of nucleotides SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Adenosine monophosphate deaminase deficiencyEnrichmentAMPD1, AMPD34.29
2Severe combined immunodeficiencyEnrichmentADA, PNP4.24
3Adenylosuccinase deficiencyEnrichmentADSL3.83
4Calcification of joints and arteriesEnrichmentNT5E3.43
5Purine nucleoside phosphorylase deficiencyEnrichmentPNP3.43
6Retinitis pigmentosa 10EnrichmentIMPDH13.43
7Impdh2 enzyme activity, variation inEnrichmentIMPDH23.43
8Leber congenital amaurosis 11EnrichmentIMPDH13.43
9Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 6EnrichmentRRM13.35
10Thiopurines, poor metabolism of, 2EnrichmentNUDT153.29
11Anemia, congenital, nonspherocytic hemolytic, 8EnrichmentNT5C3A3.18
12Xanthinuria, type iEnrichmentXDH3.13
13Mitochondrial dna depletion syndrome 21EnrichmentGUK13.13
14Aica-ribosiduria due to atic deficiencyEnrichmentATIC3.09
15Myopathy, distal, 5EnrichmentADSS13.09
16Early myoclonic encephalopathyEnrichmentADSL3.05
17Dihydropyrimidinase deficiencyEnrichmentDPYS3.05
18Beta-aminoisobutyric aciduriaEnrichmentAGXT23.05
19Beta-ureidopropionase deficiencyEnrichmentUPB13.05
201p21.3 microdeletion syndromeEnrichmentDPYD3.05
21Hypermethioninemia due to adenosine kinase deficiencyEnrichmentADK3.02
22Orotic aciduriaEnrichmentUMPS2.99
23Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiencyEnrichmentADA2.96
24Xanthinuria, type iiEnrichmentXDH2.96
25Gtp cyclohydrolase 1-deficient dopa-responsive dystoniaEnrichmentIMPDH22.96
26Coenzyme q10 deficiency, primary, 6EnrichmentENTPD52.93
27Spastic paraplegia 64, autosomal recessiveEnrichmentENTPD12.93
28Mitochondrial dna depletion syndrome 3EnrichmentDGUOK2.88
29Portal hypertension, noncirrhotic, 1EnrichmentDGUOK2.88
30Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 4EnrichmentDGUOK2.88
31Spastic paraplegia 45, autosomal recessiveEnrichmentNT5C22.88
32Adenosine deaminase deficiencyEnrichmentADA2.83
33Phosphoribosylaminoimidazole carboxylase deficiencyEnrichmentPAICS2.79
34Portal hypertensionEnrichmentDGUOK2.75
35Mitochondrial neurogastrointestinal encephalomyopathyEnrichmentRRM2B, TYMP2.74
36Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-negativeEnrichmentADA2.73
37Developmental and epileptic encephalopathy 50EnrichmentCAD2.69
38Miller syndromeEnrichmentDHODH2.69
39Glomerulopathy with fibronectin deposits 2EnrichmentATIC2.61
40Cerebroretinal microangiopathy with calcifications and cysts 1EnrichmentPFAS2.61
41Dihydropyrimidine dehydrogenase deficiencyEnrichmentDPYD2.58
42Inosine triphosphatase deficiencyEnrichmentITPA2.58
43Developmental and epileptic encephalopathy 35EnrichmentITPA2.58
44Chilblain lupus 2EnrichmentSAMHD12.58
45Aicardi-goutieres syndrome 5EnrichmentSAMHD12.58
46Lesch-nyhan syndromeEnrichmentHPRT12.54
47Hyperuricemia, hprt-relatedEnrichmentHPRT12.54
48Omenn syndromeEnrichmentADA2.43
49Mitochondrial dna depletion syndrome 1EnrichmentTYMP2.28
50Mitochondrial dna depletion syndrome 4bEnrichmentTYMP2.15
51Erythrocyte amp deaminase deficiencyEnrichmentAMPD32.14
52Immunodeficiency 24EnrichmentCTPS12.14
53Anemia, congenital, nonspherocytic hemolytic, 10EnrichmentGSR2.14
54Spermatogenic failure 27EnrichmentAK72.14
55Mitochondrial dna depletion syndrome 8bEnrichmentRRM2B2.14
56Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 3EnrichmentTK22.14
57Myopathy due to myoadenylate deaminase deficiencyEnrichmentAMPD12.14
58Bone marrow failure and diabetes mellitus syndromeEnrichmentDUT2.14
59Neurodegeneration, childhood-onset, with progressive microcephalyEnrichmentDTYMK2.14
60Rrm2b mitochondrial dna maintenance defectsEnrichmentRRM2B2.14
61Familial chilblain lupusEnrichmentSAMHD12.10
62Isolated tracheo-esophageal fistulaEnrichmentGART2.09
63Dyskeratosis congenitaEnrichmentPFAS, TYMS2.09
64Tooth agenesis, selective, 1EnrichmentITPA1.93
65DystoniaEnrichmentIMPDH21.89
66Developmental and epileptic encephalopathy 1EnrichmentCAD, ITPA1.86
67Fanconi renotubular syndrome 1EnrichmentRRM2B1.84
68Immunoerythromyeloid hypoplasiaEnrichmentAK21.84
69Reticular dysgenesisEnrichmentAK21.84
70Rod-cone dystrophy, sensorineural deafness, and fanconi-type renal dysfunctionEnrichmentRRM2B1.84
71Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 5EnrichmentRRM2B1.84
72Mitochondrial dna depletion syndrome 2EnrichmentTK21.84
73Mitochondrial dna depletion syndrome 8aEnrichmentRRM2B1.84
74Adenine phosphoribosyltransferase deficiencyEnrichmentAPRT1.84
75Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 2EnrichmentRRM2B1.84
76Spermatogenic failure 89EnrichmentAK91.84
77Anemia, congenital, nonspherocytic hemolytic, 3EnrichmentAK11.84
78Autosomal recessive progressive external ophthalmoplegiaEnrichmentTK21.84
79Dyskeratosis congenita, digenicEnrichmentTYMS1.84
80Esophageal atresia/tracheoesophageal fistulaEnrichmentGART1.82
81Severe covid-19EnrichmentENTPD21.77
82Pontocerebellar hypoplasia, type 9EnrichmentAMPD21.67
83Spastic paraplegia 63, autosomal recessiveEnrichmentAMPD21.67
84Idiopathic camptocormiaEnrichmentRRM2B1.67
85Aicardi-goutiares syndromeEnrichmentSAMHD11.63
86Aicardi-goutieres syndromeEnrichmentSAMHD11.58
87Tooth agenesisEnrichmentITPA1.54
88Fetal akinesia deformation sequence 1EnrichmentADSS11.53
89Distal arthrogryposisEnrichmentADSS11.47
90Nephrotic syndromeEnrichmentATIC1.46
91Leber plus diseaseEnrichmentIMPDH11.46
92Kearns-sayre syndromeEnrichmentRRM2B1.45
93Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 1EnrichmentRRM2B1.37
94Mitochondrial dna depletion syndromeEnrichmentTK21.37
95Developmental and epileptic encephalopathyEnrichmentITPA1.33
96Retinitis pigmentosaEnrichmentIMPDH11.12
97Postsynaptic congenital myasthenic syndromesEnrichmentAK91.08
98Cerebral palsyEnrichmentSAMHD11.01
99Hereditary retinal dystrophyEnrichmentIMPDH10.99
100Fundus dystrophyEnrichmentIMPDH10.99
101Pontocerebellar hypoplasiaEnrichmentAMPD20.91
102Mitochondrial diseaseEnrichmentRRM2B, TK20.88
103Myeloma, multipleEnrichmentSAMHD10.86
104Non-syndromic male infertility due to sperm motility disorderEnrichmentAK70.81
105MyopathyEnrichmentTK20.60
106Sensorineural hearing lossEnrichmentRRM2B0.53
107Spastic ataxiaEnrichmentAMPD20.50
108Congenital nervous system abnormalityEnrichmentAMPD20.27
109Nervous system diseaseEnrichmentAMPD20.27

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