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- Table of Contents
Facts about 3-hydroxyacyl-CoA dehydrogenase type-2.
Carries out oxidative conversions of 7-alpha-OH and 7-beta-OH bile acids (PubMed:12917011). Also exhibits 20-beta- OH and 21-OH dehydrogenase activities with C21 steroids (PubMed:12917011).
Human | |
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Gene Name: | HSD17B10 |
Uniprot: | Q99714 |
Entrez: | 3028 |
Belongs to: |
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short-chain dehydrogenases/reductases (SDR) family |
17-beta-HSD 10; 17-beta-hydroxysteroid dehydrogenase 10; 17b-HSD10; 3-hydroxy-2-methylbutyryl-CoA dehydrogenase; ABAD; amyloid-beta peptide binding alcohol dehydrogenase; CAMR; DUPXp11.22; EC 1.1.1.178; EC 1.1.1.35; Endoplasmic reticulum-associated amyloid beta-peptide-binding protein; ERAB3-hydroxyacyl-CoA dehydrogenase type-2; HADH2AB-binding alcohol dehydrogenase; hydroxyacyl-Coenzyme A dehydrogenase, type II, hydroxyacyl-Coenzyme Adehydrogenase, type II; hydroxysteroid (17-beta) dehydrogenase 10; mental retardation, X-linked, syndromic 10; MHBD; Mitochondrial ribonuclease P protein 2,3-hyd
Mass (kDA):
26.923 kDA
Human | |
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Location: | Xp11.22 |
Sequence: | X; NC_000023.11 (53431258..53434376, complement) |
Ubiquitously expressed in normal tissues but is overexpressed in neurons affected in AD.
Mitochondrion.
PMID: 9338779 by Yan S.D., et al. An intracellular protein that binds amyloid-beta peptide and mediates neurotoxicity in Alzheimer's disease.
PMID: 9671743 by Miller A.P., et al. Chromosomal basis of X chromosome inactivation: identification of a multigene domain in Xp11.21-p11.22 that escapes X inactivation.