Male steroid hormones in cardiomyocyte energy metabolism

No Pathway Network information available for Male steroid hormones in cardiomyocyte energy metabolism

#	Name	Source	Genes
1	Male steroid hormones in cardiomyocyte energy metabolism	WikiPathways	CYP11A1 CYP17A1 CYP19A1 HSD17B14 HSD17B2 HSD17B3 SULT1A1 UGT1A1 (see all 8) (see less)

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

#	Symbol	Description	Category	# Related Pathways
1	HSD17B2	Hydroxysteroid 17-Beta Dehydrogenase 2	Protein Coding	1
2	CYP17A1	Cytochrome P450 Family 17 Subfamily A Member 1	Protein Coding	1
3	HSD17B14	Hydroxysteroid 17-Beta Dehydrogenase 14	Protein Coding	1
4	CYP11A1	Cytochrome P450 Family 11 Subfamily A Member 1	Protein Coding	1
5	HSD17B3	Hydroxysteroid 17-Beta Dehydrogenase 3	Protein Coding	1
6	CYP19A1	Cytochrome P450 Family 19 Subfamily A Member 1	Protein Coding	1
7	SULT1A1	Sulfotransferase Family 1A Member 1	Protein Coding	1
8	UGT1A1	UDP Glucuronosyltransferase Family 1 Member A1	Protein Coding	1

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency	Enrichment	CYP11A1, CYP17A1	5.34
2	21-hydroxylase-deficient congenital adrenal hyperplasia	Enrichment	CYP11A1, CYP17A1	5.34
3	Lipoid congenital adrenal hyperplasia	Enrichment	CYP11A1, CYP17A1	4.56
4	Primary ovarian insufficiency	Enrichment	CYP17A1, CYP19A1	3.29
5	Adrenal insufficiency, congenital, with 46,xy sex reversal, partial or complete	Enrichment	CYP11A1	3.23
6	Inherited isolated adrenal insufficiency due to partial cyp11a1 deficiency	Enrichment	CYP11A1	3.23
7	17-beta hydroxysteroid dehydrogenase iii deficiency	Enrichment	HSD17B3	2.93
8	Adrenal hyperplasia, congenital, due to 17-alpha-hydroxylase deficiency	Enrichment	CYP17A1	2.75
9	Aromatase excess syndrome	Enrichment	CYP19A1	2.75
10	Aromatase deficiency	Enrichment	CYP19A1	2.75
11	Pseudohermaphroditism	Enrichment	HSD17B3	2.53
12	Difference of sex development	Enrichment	HSD17B3	2.33
13	Crigler-najjar syndrome, type i	Enrichment	UGT1A1	2.23
14	Hyperbilirubinemia, transient familial neonatal	Enrichment	UGT1A1	2.23
15	Bilirubin, serum level of, quantitative trait locus 1	Enrichment	UGT1A1	2.23
16	Crigler-najjar syndrome, type ii	Enrichment	UGT1A1	2.23
17	Gilbert syndrome	Enrichment	UGT1A1	2.19
18	Epilepsy, myoclonic juvenile	Enrichment	HSD17B3	2.19
19	Bilirubin metabolic disorder	Enrichment	UGT1A1	2.19
20	Breast cancer	Enrichment	CYP17A1	1.36

¹ WikiPathways

² PubChem

³ R&D Systems

⁴ Reactome

⁵ GeneGo (Thomson Reuters)

⁶ QIAGEN

⁷ PharmGKB

⁹ Sino Biological

¹⁰ Tocris

¹¹ MalaCards

Pathway Network for Male steroid hormones in cardiomyocyte energy metabolism