Automated description from the Alliance of Genome Resources
Exhibits ephrin receptor binding activity. Involved in several processes, including axon guidance; neural crest cell migration; and positive regulation of T cell activation. Localizes to the cytoplasm; membrane raft; and nucleus. Used to study craniofrontonasal syndrome. Human ortholog(s) of this gene implicated in craniofrontonasal syndrome and dysostosis. Orthologous to human EFNB1 (ephrin B1).