member 7 (KIF7), also known as kinesin-4, is a human protein encoded by the gene KIF7. It is part of the kinesin family of motor proteins. KIF7 depolymerises...
The syndrome was first described by Albert Schinzel in 1979. Mutations in KIF7 are causative for ACLS, and mutations in GLI3 are associated with a similar...
signalling. A variant form, HLS2, with additional mutations to the KIF7 gene, is less common. KIF7 also ensures correct cilia formation and function, specifically...
BR, Silhavy JL, Akawi NA, Gleeson JG, Al-Gazali L (2012). "A mutation in KIF7 is responsible for the autosomal recessive syndrome of macrocephaly, multiple...