superpathway of cholesterol biosynthesis

Pathway network for the superpathway of cholesterol biosynthesis SuperPath

Sources:
  • PubChem
  • WikiPathways
  • Reactome

Pathways in the superpathway of cholesterol biosynthesis SuperPath

#NameSourceGenes
1superpathway of cholesterol biosynthesisPubChem
2Cholesterol metabolism with Bloch and Kandutsch-Russell pathwaysWikiPathways
3Cholesterol biosynthesisReactome
4Cholesterol biosynthesis pathwayWikiPathways
5Mevalonate arm of cholesterol biosynthesis pathwayWikiPathways
6superpathway of geranylgeranyldiphosphate biosynthesis I (via mevalonate)PubChem
7mevalonate pathway IPubChem
8mevalonate pathwayPubChem
9cholesterol biosynthesis III (via desmosterol)PubChem
10cholesterol biosynthesis IPubChem
11cholesterol biosynthesis II (via 24,25-dihydrolanosterol)PubChem
12Cholesterol biosynthesis via lathosterolReactome
13Cholesterol biosynthesis with skeletal dysplasiasWikiPathways
14Mevalonate pathwayWikiPathways
15Cholesterol biosynthesis via desmosterolReactome
16trans, trans-farnesyl diphosphate biosynthesisPubChem
17zymosterol biosynthesisPubChem
18Mevalonate arm of cholesterol biosynthesis pathway with inhibitorsWikiPathways
19epoxysqualene biosynthesisPubChem
20lanosterol biosynthesisPubChem

Gene overlap in member pathways for superpathway of cholesterol biosynthesis SuperPath

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

Disorders associated with superpathway of cholesterol biosynthesis SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1PorokeratosisEnrichmentFDPS, MVD, MVK9.43
2Porokeratosis 1, multiple typesEnrichmentMVK, PMVK6.64
3Alpha-methylacetoacetic aciduriaEnrichmentACAT1, ACAT26.31
4Linear porokeratosisEnrichmentMVD, PMVK6.16
5Palmoplantar keratoderma and congenital alopecia 2EnrichmentLSS4.13
6Hypotrichosis 14EnrichmentLSS4.13
7Porokeratosis 7, multiple typesEnrichmentMVD3.83
8Low density lipoprotein cholesterol level quantitative trait locus 3EnrichmentHMGCR3.83
9Muscular dystrophy, limb-girdle, autosomal recessive 28EnrichmentHMGCR3.83
10Alopecia-intellectual disability syndrome 4EnrichmentLSS3.83
11Alopecia - intellectual disability syndromeEnrichmentLSS3.66
12Squalene synthase deficiencyEnrichmentFDFT13.53
13DesmosterolosisEnrichmentDHCR243.53
14Chondrodysplasia punctata 2, x-linked dominantEnrichmentEBP3.53
15Mend syndromeEnrichmentEBP3.53
16Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndromeEnrichmentGGPS13.53
17Ck syndromeEnrichmentNSDHL3.53
18Congenital hemidysplasia with ichthyosiform erythroderma and limb defectsEnrichmentNSDHL3.53
19Greenberg dysplasiaEnrichmentLBR3.53
20Pelger-huet anomalyEnrichmentLBR3.53
21Rhizomelic skeletal dysplasia with or without pelger-huet anomalyEnrichmentLBR3.53
22Reynolds syndromeEnrichmentLBR3.53
23Congenital cataract-severe neonatal hepatopathy-global developmental delay syndromeEnrichmentCYP51A13.53
24Nsdhl-related disordersEnrichmentNSDHL3.53
25Porokeratosis 3, multiple typesEnrichmentMVK3.29
26Mevalonic aciduriaEnrichmentMVK3.29
27Acetyl-coa acetyltransferase-2 deficiencyEnrichmentACAT23.29
28LathosterolosisEnrichmentSC5D3.23
29Porokeratosis 9, multiple typesEnrichmentFDPS3.23
30Microcephaly, congenital cataract, and psoriasiform dermatitisEnrichmentMSMO13.23
31Hypotrichosis simplexEnrichmentLSS3.18
323-hydroxy-3-methylglutaryl-coa lyase deficiencyEnrichmentHMGCL3.02
33Hyper-igd syndromeEnrichmentMVK2.99
34Methylmalonic aciduria, cblb typeEnrichmentMVK2.99
35Porokeratosis 5, disseminated superficial actinic typeEnrichmentMVK2.99
36Smith-lemli-opitz syndromeEnrichmentDHCR72.93
37Cataract 44EnrichmentLSS2.90
38Limb-girdle muscular dystrophyEnrichmentHMGCR2.88
393-hydroxy-3-methylglutaryl-coa synthase-2 deficiencyEnrichmentHMGCS22.83
40Mucoepithelial dysplasia, hereditaryEnrichmentSREBF12.70
41Ifap syndrome 2EnrichmentSREBF12.70
42Myopathy, tubular aggregate, 1EnrichmentGGPS12.63
43Congenital myopathy 3 with rigid spineEnrichmentHMGCS12.59
44Perrault syndrome 2EnrichmentGGPS12.58
45Long-chain 3-hydroxyacyl-coa dehydrogenase deficiencyEnrichmentHMGCL2.54
46Intellectual developmental disorder, x-linked 63EnrichmentACSL42.54
47Cerebrotendinous xanthomatosisEnrichmentCYP27A12.54
48HypoalphalipoproteinemiaEnrichmentABCA12.54
49Isolated methylmalonic acidemiaEnrichmentMVK2.44
50Developmental and epileptic encephalopathy 38EnrichmentARV12.40
51Methylmalonic acidemiaEnrichmentMVK2.38
52Isolated congenital microcephalyEnrichmentDHCR72.33
53Perrault syndrome 1EnrichmentGGPS12.33
54Tangier diseaseEnrichmentABCA12.24
55Ifap syndrome 1, with or without bresheck syndromeEnrichmentSREBF12.22
56HepatoblastomaEnrichmentDHCR72.21
57Jeune thoracic dystrophyEnrichmentLBR2.13
58Hydrops fetalis, nonimmuneEnrichmentDHCR242.12
59Asphyxiating thoracic dystrophyEnrichmentLBR2.08
60Hypoalphalipoproteinemia, primary, 2EnrichmentABCA12.07
61Non-immune hydrops fetalisEnrichmentDHCR242.04
62Connective tissue diseaseEnrichmentEBP2.03
63Short-rib thoracic dysplasia 1 with or without polydactylyEnrichmentLBR2.01
64Hypoalphalipoproteinemia, primary, 1EnrichmentABCA11.94
65Amme complexEnrichmentACSL41.94
66Autoinflammatory diseaseEnrichmentMVK1.91
67Coronary heart disease 5EnrichmentABCA11.59
68Stroke, ischemicEnrichmentACSL41.55
69Pulmonary disease, chronic obstructiveEnrichmentCYP46A11.43
70Multiple sclerosisEnrichmentNR1H31.40
71Hirschsprung disease 1EnrichmentSREBF11.25
72Non-syndromic x-linked intellectual disabilityEnrichmentACSL41.01
73Hereditary retinal dystrophyEnrichmentMVK0.85
74Fundus dystrophyEnrichmentMVK0.85
75Congenital nervous system abnormalityEnrichmentARV10.72
76Nervous system diseaseEnrichmentARV10.72
77Breast cancerEnrichmentABCA10.71

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