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      Open Access

      A closer look at the mysterious HSD17B13

      Journal of Lipid Research
      Vol. 61Issue 11p1361–1362Published online: October 2, 2020
      • X. Charlie Dong
      Cited in Scopus: 5
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        17-β hydroxysteroid dehydrogenase 13 (HSD17B13) belongs to a 15-member family that is involved in various metabolic processes, including steroid hormones, fatty acids, cholesterol, and bile acids (1). The human HSD17B13 gene is located on chromosome 4 (4q22.1), and its expression is highly restricted to the liver, specifically in hepatocytes but not other cell types in the liver (2, 3). The human HSD17B13 gene encodes a 300-amino-acid protein that is localized on lipid droplet (4). Interestingly, a few single-nucleotide polymorphisms (rs72613567, rs62305723, rs6834314, rs9992651, rs13118664, and rs4607179) of the human HSD17B13 gene have been linked to alcoholic and nonalcoholic fatty liver diseases by genome-wide association studies (5–12).
        A closer look at the mysterious HSD17B131
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