Automated description from the Alliance of Genome Resources
Involved in actin cytoskeleton organization; cell migration; and negative regulation of protein depolymerization. Localizes to the filamentous actin and microtubule organizing center. Human ortholog(s) of this gene implicated in Opitz-GBBB syndrome. Is expressed in 1st branchial arch maxillary component; branchial arch; eye; fronto-nasal process; and limb. Orthologous to human SPECC1L (sperm antigen with calponin homology and coiled-coil domains 1 like).