Automated description from the Alliance of Genome Resources
Exhibits several functions, including RNA binding activity; translation initiation factor binding activity; and ubiquitin protein ligase activity. Involved in several processes, including cellular protein modification process; positive regulation of cell differentiation; and positive regulation of cytokine-mediated signaling pathway. Localizes to the nucleus and striated muscle myosin thick filament. Used to study autosomal recessive limb-girdle muscular dystrophy type 2H. Human ortholog(s) of this gene implicated in Bardet-Biedl syndrome; Bardet-Biedl syndrome 11; autosomal recessive limb-girdle muscular dystrophy type 2H; and muscular dystrophy. Orthologous to human TRIM32 (tripartite motif containing 32).