BAAT wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human BAAT wild-type allele is located in the vicinity of 9q31.1 and is approximately 31 kb in length. This allele, which encodes bile acid-CoA:amino acid N-acyltransferase protein, is involved in the synthesis of bile acid N-acyl amidates. Mutations in the gene are associated with familial hypercholanemia 3.

**Synonyms:** - BACAT - BACD1 - BAT - Bile Acid CoA: Amino Acid N-Acyltransferase (Glycine N-Choloyltransferase) Gene - Bile Acid Coenzyme A: Amino Acid N-Acyltransferase (Glycine N-Choloyltransferase) Gene - Bile Acid Coenzyme A:Amino Acid N-Acyltransferase (Glycine N-Choloyltransferase) Gene - Bile Acid-CoA:Amino Acid N-Acyltransferase wt Allele - FHCA3 - HCHO