HADHB wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human HADHB wild-type allele is located in the vicinity of 2p23.3 and is approximately 47 kb in length. This allele, which encodes trifunctional enzyme subunit beta, mitochondrial protein, is involved in fatty acid metabolism in the beta-oxidation pathway. Mutation of the gene is associated with mitochondrial trifunctional protein deficiency 2.

**Synonyms:** - 2-Enoyl-Coenzyme A (CoA) Hydratase, Beta Subunit Gene - 3-Ketoacyl-Coenzyme A (CoA) Thiolase of Mitochondrial Trifunctional Protein, Beta Subunit Gene - Acetyl-CoA Acyltransferase Gene - Beta-Ketothiolase Gene - ECHB - Hydroxyacyl-CoA Dehydrogenase Trifunctional Multienzyme Complex Subunit Beta wt Allele - Hydroxyacyl-CoA Dehydrogenase/3-Ketoacyl-CoA Thiolase/Enoyl-CoA Hydratase (Trifunctional Protein), Beta Subunit Gene - Hydroxyacyl-CoA Dehydrogenase/3-Ketoacyl-CoA Thiolase/Enoyl-CoA Hydratase, Beta Subunit Gene - Hydroxyacyl-Coenzyme A Dehydrogenase/3-Ketoacyl-Coenzyme A Thiolase/Enoyl-Coenzyme A Hydratase (Trifunctional Protein), Beta Subunit Gene - LCHAD - MSTP029 - MTPB - MTPD - MTPD2 - Mitochondrial Trifunctional Protein, Beta Subunit Gene - TP-BETA - Trifunctional Enzyme Subunit Beta, Mitochondrial Gene - Trifunctional Protein, Beta Subunit Gene