PEX26 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human PEX26 wild-type allele is located in the vicinity of 22q11.21 and is approximately 27 kb in length. This allele, which encodes peroxisome assembly protein 26, plays a role in the localization of PEX1-PEX6 AAA ATPase complex. Mutation of the gene is associated with peroxisomal biogenesis disorder types 7A and 7B.

**Synonyms:** - FLJ20695 - PBD7A - PBD7B - PEX26M1T - Peroxin 26 Gene - Peroxisomal Biogenesis Factor 26 wt Allele - Peroxisome Biogenesis Disorder, Complementation Group 8 Gene - Peroxisome Biogenesis Disorder, Complementation Group A Gene - Peroxisome Biogenesis Factor 26 Gene - Pex26pM1T