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