kinesin family binding protein
The information on this page was automatically extracted from online scientific databases.
From NCBI Gene:
This gene encodes a kinesin family member 1 binding protein that is characterized by two tetratrico peptide repeats. The encoded protein localizes to the mitochondria and may be involved in regulating transport of the mitochondria. Mutations in this gene are associated with Goldberg-Shprintzen megacolon syndrome. [provided by RefSeq, Mar 2010]
Required for organization of axonal microtubules, and axonal outgrowth and maintenance during peripheral and central nervous system development.