Automated description from the Alliance of Genome Resources
Predicted to have K63-linked polyubiquitin modification-dependent protein binding activity and phosphatidylinositol 3-kinase regulator activity. Involved in mitochondrion organization. Localizes to the mitochondrion. Human ortholog(s) of this gene implicated in cerebellar ataxia, mental retardation and dysequlibrium syndrome and hydrocephalus. Orthologous to human WDR81 (WD repeat domain 81).