Sulfur amino acid metabolism

Pathway network for the Sulfur amino acid metabolism SuperPath

Sources:
  • Reactome
  • WikiPathways
  • PubChem

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

Disorders associated with Sulfur amino acid metabolism SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1HomocystinuriaEnrichmentCBS, MTR5.59
2Homocystinuria-megaloblastic anemia, cblg typeEnrichmentMTR, MTRR4.91
3Neural tube defects, folate-sensitiveEnrichmentMTR, MTRR4.61
4Sulfite oxidase deficiency, isolatedEnrichmentSUOX3.66
5Sulfide:quinone oxidoreductase deficiencyEnrichmentSQOR3.66
6Aspartate aminotransferase, serum level of, quantitative trait locus 1EnrichmentGOT13.43
7Encephalopathy, ethylmalonicEnrichmentETHE13.35
8Mitochondrial dna depletion syndrome 19EnrichmentSLC25A103.35
9Diaphyseal medullary stenosis with malignant fibrous histiocytomaEnrichmentMTAP3.13
10Diaphyseal medullary stenosis-bone malignancy syndromeEnrichmentMTAP3.13
11CystathioninuriaEnrichmentCTH3.02
12Glutathione synthetase deficiencyEnrichmentGSS3.02
13Anemia, congenital, nonspherocytic hemolytic, 6EnrichmentGSS3.02
14Hypermethioninemia with s-adenosylhomocysteine hydrolase deficiencyEnrichmentAHCY3.02
15HyperhomocysteinemiaEnrichmentCBS3.02
16Combined oxidative phosphorylation deficiency 29EnrichmentTXN22.96
17Disorders of intracellular cobalamin metabolismEnrichmentMTR2.72
18Homocystinuria without methylmalonic aciduriaEnrichmentMTRR2.69
19Bainbridge-ropers syndromeEnrichmentGADL12.66
20Developmental and epileptic encephalopathy 82EnrichmentGOT22.66
21Homocystinuria due to cystathionine beta-synthase deficiencyEnrichmentCBS2.54
22Homocystinuria-megaloblastic anemia, cble typeEnrichmentMTRR2.38
23Methionine adenosyltransferase i/iii deficiencyEnrichmentMAT1A2.38
24Methionine adenosyltransferase deficiencyEnrichmentMAT1A2.38
25Down syndromeEnrichmentMTRR2.08
26Mitochondrial complex i deficiency, nuclear type 1EnrichmentSLC25A101.78
27Congenital nervous system abnormalityEnrichmentETHE11.63
28Nervous system diseaseEnrichmentETHE11.63
29Connective tissue diseaseEnrichmentCBS1.52
30EpilepsyEnrichmentMTR1.42
31Developmental and epileptic encephalopathyEnrichmentGOT21.41
32Familial thoracic aortic aneurysm and aortic dissectionEnrichmentCBS1.38

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