{"symbol":"KLC2","synonyms":[],"name":"kinesin light chain 2","description":"The protein encoded by this gene is a light chain of kinesin, a molecular motor responsible for moving vesicles and organelles along microtubules. Defects in this gene are a cause of spastic paraplegia, optic atrophy, and neuropathy (SPOAN) syndrome. [provided by RefSeq, Mar 2016]","ncbiEntrezGeneId":64837,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/64837","proteins":[{"symbol":"KLC2_HUMAN","href":"/api/1.0/protein/KLC2_HUMAN"}],"hgncRootFamilies":[{"name":"Tetratricopeptide repeat domain containing (TTC)","href":"/api/1.0/gene_family/Tetratricopeptide+repeat+domain+containing+%28TTC%29"}]}