Automated description from the Alliance of Genome Resources (Release 3.2)
Predicted to have protein homodimerization activity. Predicted to be involved in peroxisome fission and regulation of peroxisome size. Localizes to mitochondrion. Used to study Zellweger syndrome. Human ortholog(s) of this gene implicated in peroxisomal biogenesis disorder. Orthologous to human PEX11B (peroxisomal biogenesis factor 11 beta).