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  • 17 beta hydroxysteroid dehydrogenase
  • Zellweger s syndrome
  • Adrenoleukodystrophy
  • Fatty acids oxidation
  • Cholic acid
  • Peroxisomes
  • Refsum s disease
  • AMACR
  • Adrenomyeloneuropathy
  • Adrenoleukodystrophy X linked
  • Adrenoleukodystrophy pseudoneonatal ACOX1 deficiency
  • Racemase deficiency
  • Hypercholanemia familial
  • D bifunctional protein deficiency MFP2 deficiency SCPx deficiency
  • Ichthyosis prematurity syndrome FATP4 deficiency ACSVL5 deficiency
  • OMIM p603850
  • Rhizomelic chondrodysplasia punctata
  • PEX1
  • PEX2
  • PEX3
  • PEX5
  • PEX6
  • PEX10
  • PEX12
  • PEX13
  • PEX14
  • PEX16
  • PEX19
  • PEX26
  • ABCD1
  • ACOXI
  • BAAT
  • HSD17B4
  • PHYH
  • SCP2
  • SLC27A4
  • DNML1
  • ABCD2
  • ABCD3
  • ACAA1 Acetyl CoA Acyltransferase1
  • ACAD11 Acyl CoA dehydrogenase11
  • ACNAT1 Acyl CoA amino acid N acyltransferase
  • ACSL1 Acyl CoA synthetase long chain1
  • ACSL4 Acyl CoA synthetase long chain4
  • SLC27A2
  • ACOX1 Acyl CoA oxidase1a 1b
  • ACOX2 Acyl CoA oxidase2
  • ACOX3 Acyl CoA oxidase3
  • ACOXL Acyl CoA oxidase like
  • ACOT2 Acyl CoA thioesterase2
  • ACOT4 Acyl CoA thioesterase4
  • ACOT6 Acyl CoA thioesterase6
  • ACOT8 Acyl CoA thioesterase8
  • ACOT12 Acyl CoA thioesterase12
  • ALDH3A2 Aldehyde dehydrogenase3A2
  • CAT Catalase
  • CRAT Carnitine acetyltransferase
  • CROT Carnitine O octanoyltransferase
  • DECR2 2 4 Dienoyl CoA reductase 2 peroxisomal
  • DHRS4 Dehydrogenase reductase SDR family 4
  • ECH1 Enoyl CoA hydratase 1 peroxisomal
  • FAR1 Fatty acyl CoA reductase1
  • FAR2 Fatty acyl CoA Reductase2
  • HACL1 2 Hydroxyacyl CoA lyase 1
  • HAO2 Hydroxyacid oxidase 2 long chain
  • HSDL2 Hydroxysteroid dehydrogenase like2
  • IDH1 Isocitrate dehydrogenase1 NADP soluble
  • EHHADH Enoyl CoA hydratase 3 hydroxyacyl CoA dehydrogenase
  • NUDT7 Nudix type motif 7
  • NUDT12 Nudix type motif12
  • PECI Peroxisomal d3 d2 enoyl CoA isomerase
  • alpha Oxidation
  • beta oxidation
  • Phytanic acid
  • PTS1
  • PTS2
  • MFP1
  • TYSND1
  • Pristanic acid
  • 21 hydroxylase deficiency
  • Androgen insensitivity syndrome
  • Aromatase
  • Receptor (Estrogen)
  • Receptor (FSH)
  • Receptor (GnRH)
  • Leptin
  • Adrenal gland (Hyperplasia congenital)
  • StAR
  • McCune Albright s syndrome
  • Kallmann s syndrome
  • 5 alpha Reductase
  • Puberty (Precocious)
  • Congenital adrenal hyperplasia
  • KAL
  • Pituitary gland (Insufficiency Panhypopituitarism)
  • PROP1
  • Puberty (Delayed)
  • LH
  • Receptor (LH)
  • SF1
  • 3 beta hydroxysteroid dehydrogenase2
  • 17 alpha hydroxylase 17 20 lyase
  • Receptor (Androgen)
  • DAX1 NR0B1
  • PC1
  • 17 20 Desmolase
  • 20 22 Desmolase
  • HSD17B3
  • 11 hydoxylase
  • Receptor (Glucocorticoid)
  • GS alpha
  • Enzyme structure and chemistry
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    		Citation
    12008Design and validation of specific inhibitors of 17beta-hydroxysteroid dehydrogenases for therapeutic application in breast and prostate cancer, and in endometriosis.



    		+-nlEndocr Relat Cancer 15(3):665-92 (2008) Day JM
    22000Intracrinology: role of the family of 17 beta-hydroxysteroid dehydrogenases in human physiology and disease.



    		+-nlJ Mol Endocrinol 25(1):1-16 (2000)
    3199917beta-hydroxysteroid dehydrogenase (HSD)/17-ketosteroid reductase (KSR) family; nomenclature and main characteristics of the 17HSD/KSR enzymes.



    		+-nlJ Mol Endocrinol 23(1):1-11 (1999)
    41999Unique multifunctional HSD17B4 gene product: 17beta-hydroxysteroid dehydrogenase 4 and D-3-hydroxyacyl-coenzyme A dehydrogenase/hydratase involved in Zellweger syndrome.



    		+-nlJ Mol Endocrinol 22(3):227-40 (1999)
    52010Biochemistry and genetics of inherited disorders of peroxisomal fatty acid metabolism.



    		+-nlJ Lipid Res 51(10):2863-95 (2010)
    62002Clinical review 148: Monogenic disorders of puberty.



    		+-nlJ Clin Endocrinol Metab 87(6):2481-94 (2002)
    72010Insights in 17beta-HSD1 enzyme kinetics and ligand binding by dynamic motion investigation.



    		+-nlPLoS One 5(8):e12026 (2010)



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