Regulation of pyruvate metabolism

Pathway network for the Regulation of pyruvate metabolism SuperPath

Sources:
  • Reactome
  • PubChem

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

Disorders associated with Regulation of pyruvate metabolism SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Pyruvate dehydrogenase e1-alpha deficiencyEnrichmentPDHA1, PDHX6.01
2Spermatogenic failure 70EnrichmentPDHA23.35
3Dihydrolipoamide dehydrogenase deficiencyEnrichmentDLD3.23
4Methemoglobinemia due to deficiency of methemoglobin reductaseEnrichmentDLD3.23
5Pyruvate dehydrogenase e2 deficiencyEnrichmentDLAT3.23
6Pyruvate dehydrogenase e1-beta deficiencyEnrichmentPDHB3.23
7Pyruvate dehydrogenase e3-binding protein deficiencyEnrichmentPDHX3.05
8Charcot-marie-tooth disease, x-linked dominant, 6EnrichmentPDK32.96
9Pyruvate dehydrogenase phosphatase deficiencyEnrichmentPDP12.96
10Maleylacetoacetate isomerase deficiencyEnrichmentGSTZ12.96
11Spermatogenic failure 1EnrichmentPDHA22.75
12AzoospermiaEnrichmentFAHD1, PDHA22.63
13Amyotrophic lateral sclerosis 24EnrichmentNEK12.61
14Renu syndromeEnrichmentSIRT42.48
15Lactic acidosisEnrichmentDLD2.45
16Adenosine triphosphate, elevated, of erythrocytesEnrichmentPKLR2.44
17Anemia, congenital, nonspherocytic hemolytic, 2EnrichmentPKLR2.44
18Hydroxyacyl glutathione hydrolase deficiencyEnrichmentHAGH2.44
19Lactate dehydrogenase b deficiencyEnrichmentLDHB2.44
20Mitochondrial pyruvate carrier deficiencyEnrichmentMPC12.44
21Myeloproliferative disorder, chronic, with eosinophiliaEnrichmentMAEA2.31
22Fanconi-bickel syndromeEnrichmentLDHA2.31
23Orofaciodigital syndrome iiEnrichmentNEK12.31
24Dyskeratosis congenita, autosomal recessive 2EnrichmentRMND5B2.31
25Skraban-deardorff syndromeEnrichmentWDR262.31
26Submucosal cleft palateEnrichmentUBB2.31
27Cleft hard palateEnrichmentUBB2.31
28Sudden infant death syndromeEnrichmentPDHA12.30
29Spermatogenic failure 22EnrichmentFAHD12.14
30Premature ovarian failure 23EnrichmentFAHD12.14
31Uvula, bifidEnrichmentUBB2.14
32Cleft soft palateEnrichmentUBB2.14
33Pyruvate carboxylase deficiencyEnrichmentPC1.97
34Short rib-polydactyly syndromeEnrichmentNEK11.84
35Motor neuron diseaseEnrichmentNEK11.77
36Short-rib thoracic dysplasia 12EnrichmentNEK11.71
37Male infertility with azoospermia or oligozoospermia due to single gene mutationEnrichmentPDHA21.61
38Hemolytic anemiaEnrichmentPKLR1.60
39Short-rib thoracic dysplasia 6 with or without polydactylyEnrichmentNEK11.54
40Short-rib thoracic dysplasia 3 with or without polydactylyEnrichmentNEK11.54
41Mitochondrial diseaseEnrichmentPDHX1.42
42Connective tissue diseaseEnrichmentNEK11.12
43Frontotemporal dementia and/or amyotrophic lateral sclerosis 7EnrichmentNEK10.88

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