AKR1C4: Catalyzes the transformation of the potent androgen dihydrotestosterone (DHT) into the less active form, 5-alpha- androstan-3-alpha,17-beta-diol (3-alpha-diol). Also has some 20- alpha-hydroxysteroid dehydrogenase activity. The biotransformation of the pesticide chlordecone (kepone) to its corresponding alcohol leads to increased biliary excretion of the pesticide and concomitant reduction of its neurotoxicity since bile is the major excretory route. Defects in AKR1C4 are a cause of 46,XY sex reversal type 8 (SRXY8). A disorder of sex development. Affected individuals have a 46,XY karyotype but present as phenotypically normal females. AKR1C4 mutations may act as modifier of disease severity in SRXY8 patients. A splicing mutation resulting in loss of exon 2 has been found in affected individuals also carrying mutation Val-79 in AKR1C2 (PubMed:21802064). Belongs to the aldo/keto reductase family.
Protein type: Xenobiotic Metabolism - metabolism by cytochrome P450; Oxidoreductase; Lipid Metabolism - primary bile acid biosynthesis; Lipid Metabolism - C21-steroid hormone; EC 1.1.1.225; Lipid Metabolism - androgen and estrogen; EC 1.1.1.357
Chromosomal Location of Human Ortholog: 10p15.1
Cellular Component: cytoplasm; cytosol
Molecular Function: 3(or 17)-alpha-hydroxysteroid dehydrogenase activity; aldo-keto reductase activity; bile acid transmembrane transporter activity; chlordecone reductase activity; electron carrier activity; oxidoreductase activity, acting on NADH or NADPH, quinone or similar compound as acceptor; retinal dehydrogenase activity
Biological Process: androgen metabolic process; bile acid and bile salt transport; bile acid biosynthetic process; bile acid metabolic process; fat-soluble vitamin metabolic process; phototransduction, visible light; retinoid metabolic process; steroid metabolic process; vitamin metabolic process
Disease: 46,xy Sex Reversal 8
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