NCIt definition : Human ACOX1 wild-type allele is located in the vicinity of 17q25.1 and is approximately
38 kb in length. This allele, which encodes peroxisomal acyl-coenzyme A oxidase 1
protein, plays a role in fatty acid oxidation. Mutation of the gene is associated
with Mitchell syndrome and pseudoneonatal adrenoleukodystrophy (also called peroxisomal
acyl-CoA oxidase deficiency).;