Automated description from the Alliance of Genome Resources
Predicted to have extracellular matrix structural constituent. Involved in several processes, including animal organ morphogenesis; generation of neurons; and regulation of synapse assembly. Localizes to the basement membrane and cytoplasm. Human ortholog(s) of this gene implicated in congenital mirror movement disorder. Is expressed in several structures, including alimentary system; central nervous system; integumental system; lung; and sensory organ. Orthologous to human NTN1 (netrin 1).