Fmn2 - formin 2

Predicted to enable actin binding activity. Predicted to be involved in several processes, including cytoskeleton organization; meiotic nuclear division; and positive regulation of double-strand break repair. Predicted to act upstream of or within actin filament bundle assembly and meiotic chromosome movement towards spindle pole. Predicted to be located in several cellular components, including microvillus; nucleolus; and spindle. Predicted to colocalize with actin cytoskeleton. Human ortholog(s) of this gene implicated in autosomal recessive non-syndromic intellectual disability. Orthologous to human FMN2 (formin 2). [provided by Alliance of Genome Resources, Apr 2022]