Automated description from the Alliance of Genome Resources (Release 3.1.1)
Predicted to have SUMO binding activity; ubiquitin protein ligase activity; and ubiquitin protein ligase binding activity. Involved in proteasome-mediated ubiquitin-dependent protein catabolic process and spermatogenesis. Localizes to mitochondrial inner membrane. Is expressed in several structures, including central nervous system; ganglia; and trunk. Human ortholog(s) of this gene implicated in autosomal recessive non-syndromic intellectual disability and pigmentation disease. Orthologous to human HERC2 (HECT and RLD domain containing E3 ubiquitin protein ligase 2).