Automated description from the Alliance of Genome Resources
Exhibits serine-type endopeptidase activity. Involved in exocytosis and zymogen activation. Localizes to several cellular components, including the dendrite; synaptic cleft; and terminal bouton. Human ortholog(s) of this gene implicated in autosomal recessive non-syndromic intellectual disability and intellectual disability. Is expressed in several structures, including alimentary system; central nervous system; genitourinary system; immune system; and sensory organ. Orthologous to human PRSS12 (serine protease 12).