Automated description from the Alliance of Genome Resources
Exhibits frizzled binding activity. Involved in several processes, including animal organ development; blood vessel morphogenesis; and embryonic limb morphogenesis. Localizes to several cellular components, including the Schaffer collateral - CA1 synapse; cell surface; and glutamatergic synapse. Used to study Fuhrmann syndrome. Human ortholog(s) of this gene implicated in Fuhrmann syndrome. Is expressed in several structures, including central nervous system; embryo ectoderm; reproductive system; sensory organ; and urinary system. Orthologous to human WNT7A (Wnt family member 7A).