Automated description from the Alliance of Genome Resources (Release 3.1.1)
Predicted to have actin binding activity. Involved in several processes, including cytoskeleton organization; meiotic nuclear division; and oogenesis. Localizes to several cellular components, including cytoplasmic vesicle membrane; microvillus; and spindle. Predicted to colocalize with actin cytoskeleton. Is expressed in several structures, including brain; ganglia; neural ectoderm; otocyst; and testis. Human ortholog(s) of this gene implicated in autosomal recessive non-syndromic intellectual disability. Orthologous to human FMN2 (formin 2).