HSD17B4 Polyclonal Antibody

The protein encoded by this gene is a bifunctional enzyme that is involved in the peroxisomal beta-oxidation pathway for fatty acids. It also acts as a catalyst for the formation of 3-ketoacyl-CoA intermediates from both straight-chain and 2-methyl-branched-chain fatty acids. Defects in this gene that affect the peroxisomal fatty acid beta-oxidation activity are a cause of D-bifunctional protein deficiency (DBPD) . An apparent pseudogene of this gene is present on chromosome 8.

12-alpha-trihydroxy-5-beta-cholest-24-enoyl-CoA hydratase;17 beta HSD 4;17 beta HSD IV;17 beta hydroxysteroid dehydrogenase 4;17-beta-HSD 4;17-beta-hydroxysteroid dehydrogenase 4;17beta estradiol dehydrogenase type IV;3 alpha 7 alpha12 alpha trihydroxy 5 beta cholest 24 enoyl CoA hydratase;3-alpha;7-alpha; Beta hydroxyacyl dehydrogenase; Beta keto reductase; D 3 hydroxyacyl CoA dehydratase; D bifunctional protein; D bifunctional protein peroxisomal; D-3-hydroxyacyl CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein; D-bifunctional protein; D-bifunctional protein; peroxisomal; DBP; DBP; peroxisomal; DHB4; EDH17B4; Enoyl-CoA hydratase 2; Hsd17b4; MFE 2; MFE-2; MPF-2; Multifunctional protein 2; Peroxisomal multifunctional enzyme type 2; Peroxisomal multifunctional protein 2; PRLTS1; SDR8C1; Short chain dehydrogenase/reductase family 8C member 1