Aliases for KIF21A Gene
External Ids for KIF21A Gene
Previous Symbols for KIF21A Gene
This gene encodes a member of the KIF4 subfamily of kinesin-like motor proteins. The encoded protein is characterized by an N-terminal motor domain a coiled-coil stalk domain and a C-terminal WD-40 repeat domain. This protein may be involved in microtubule dependent transport. Mutations in this gene are the cause of congenital fibrosis of extraocular muscles-1. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Mar 2010]
GeneCards Summary for KIF21A Gene
KIF21A (Kinesin Family Member 21A) is a Protein Coding gene. Diseases associated with KIF21A include congenital fibrosis of the extraocular muscles and moebius syndrome. Among its related pathways are Reelin Pathway (Cajal-Retzius cells). GO annotations related to this gene include microtubule binding and microtubule motor activity. An important paralog of this gene is KIF5C.
UniProtKB/Swiss-Prot for KIF21A Gene
Microtubule-binding motor protein probably involved in neuronal axonal transport. In vitro, has a plus-end directed motor activity (By similarity).