Automated description from the Alliance of Genome Resources
Exhibits identical protein binding activity. Involved in circulatory system development and regulation of smoothened signaling pathway. Localizes to the ciliary basal body. Used to study acrocallosal syndrome; ciliopathy; congenital diaphragmatic hernia; and hydrolethalus syndrome. Human ortholog(s) of this gene implicated in acrocallosal syndrome; cleft lip; and hydrolethalus syndrome. Orthologous to human KIF7 (kinesin family member 7).