Aliases for KIF13B Gene
External Ids for KIF13B Gene
Previous GeneCards Identifiers for KIF13B Gene
GeneCards Summary for KIF13B Gene
KIF13B (Kinesin Family Member 13B) is a Protein Coding gene. Diseases associated with KIF13B include Spastic Paraplegia 37, Autosomal Dominant and Muscular Dystrophy, Congenital, With Cataracts And Intellectual Disability. Among its related pathways are Response to elevated platelet cytosolic Ca2+ and Golgi-to-ER retrograde transport. Gene Ontology (GO) annotations related to this gene include protein kinase binding and microtubule motor activity. An important paralog of this gene is KIF13A.
UniProtKB/Swiss-Prot Summary for KIF13B Gene
Involved in reorganization of the cortical cytoskeleton. Regulates axon formation by promoting the formation of extra axons. May be functionally important for the intracellular trafficking of MAGUKs and associated protein complexes.