Automated description from the Alliance of Genome Resources (Release 8.3.0)
Predicted to enable several functions, including ATP binding activity; ATP hydrolysis activity; and ubiquitin-modified protein reader activity. Predicted to be involved in protein import into peroxisome matrix, receptor recycling; protein targeting to peroxisome; and protein unfolding. Predicted to act upstream of or within microtubule-based peroxisome localization. Located in peroxisome. Used to study Zellweger syndrome. Human ortholog(s) of this gene implicated in Heimler syndrome 1; peroxisome biogenesis disorder 1A; and peroxisome biogenesis disorder 1B. Orthologous to human PEX1 (peroxisomal biogenesis factor 1).
This site uses cookies.
Some cookies are essential for site operations and others help us analyze use and utility of our web site.
Please refer to our
privacy policy
for more information.