Estrone metabolism

Pathway network for the Estrone metabolism SuperPath

Sources:
  • GeneGo (Thomson Reuters)

Pathways in the Estrone metabolism SuperPath

#NameSourceGenes
1Estrone metabolismGeneGo (Thomson Reuters)
2Androstenedione and testosterone biosynthesis and metabolism p.1GeneGo (Thomson Reuters)
3Estrogen biosynthesisGeneGo (Thomson Reuters)

Gene overlap in member pathways for Estrone metabolism SuperPath

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

Disorders associated with Estrone metabolism SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Lipoid congenital adrenal hyperplasiaEnrichmentCYP17A1, HSD3B23.78
2Drug metabolism, poor, cyp2c19-relatedEnrichmentCYP2C193.09
3Drug metabolism, altered, cyp2c8-relatedEnrichmentCYP2C83.09
4Vitamin d-dependent rickets, type 3EnrichmentCYP3A43.09
5Ichthyosis, congenital, autosomal recessive 14EnrichmentSULT2B12.99
6Catechol-o-methyltransferase activity, variation inEnrichmentCOMT2.99
7Syndromic recessive x-linked ichthyosisEnrichmentSTS2.99
817-beta hydroxysteroid dehydrogenase iii deficiencyEnrichmentHSD17B32.79
9Ichthyosis, x-linkedEnrichmentSTS2.69
10Adrenal hyperplasia, congenital, due to steroid 11-beta-hydroxylase deficiencyEnrichmentCYP11B12.61
11Aromatase excess syndromeEnrichmentCYP19A12.61
12Coumarin resistanceEnrichmentCYP2C92.61
13Aromatase deficiencyEnrichmentCYP19A12.61
14Deficiency of steroid 11-beta-monooxygenaseEnrichmentCYP11B12.61
15Adrenal hyperplasia, congenital, due to 3-beta-hydroxysteroid dehydrogenase 2 deficiencyEnrichmentHSD3B22.55
16Hypospadias 1, x-linkedEnrichmentHSD3B22.55
173 beta-hydroxysteroid dehydrogenase deficiencyEnrichmentHSD3B22.55
18Ichthyosis, congenital, autosomal recessive 1EnrichmentSULT2B12.51
19PseudohermaphroditismEnrichmentHSD17B32.39
20Adrenal hyperplasia, congenital, due to 17-alpha-hydroxylase deficiencyEnrichmentCYP17A12.38
21Hyperaldosteronism, familial, type iEnrichmentCYP11B12.31
22Ichthyosis, congenital, autosomal recessive 2EnrichmentSULT2B12.29
23Difference of sex developmentEnrichmentHSD17B32.19
24Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiencyEnrichmentCYP17A12.08
2521-hydroxylase-deficient congenital adrenal hyperplasiaEnrichmentCYP17A12.08
26Epilepsy, myoclonic juvenileEnrichmentHSD17B32.05
27Congenital nonbullous ichthyosiform erythrodermaEnrichmentSULT2B11.99
28Digeorge syndromeEnrichmentCOMT1.91
29Autosomal recessive congenital ichthyosisEnrichmentSULT2B11.81
30Hypertension, essentialEnrichmentCYP3A51.76
31Bardet-biedl syndromeEnrichmentCOMT1.37
32Primary ovarian insufficiencyEnrichmentCYP19A11.33
33SchizophreniaEnrichmentCOMT1.23
34Breast cancerEnrichmentCYP17A11.00

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