GCDH wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human GCDH wild-type allele is located in the vicinity of 19p13.13 and is approximately 24 kb in length. This allele, which encodes glutaryl-CoA dehydrogenase, mitochondrial protein, is involved in amino acid degradation. Mutations in the gene are associated with glutaric aciduria type 1.

**Synonyms:** - ACAD5 - GCD - Glutaryl-CoA Dehydrogenase wt Allele - Glutaryl-Coenzyme A Dehydrogenase Gene