{"symbol":"SYT14","synonyms":["SYTXIV","SCAR11"],"name":"synaptotagmin XIV","description":"This gene is a member of the synaptotagmin gene family and encodes a protein similar to other family members that mediate membrane trafficking in synaptic transmission. The encoded protein is a calcium-independent synaptotagmin. Mutations in this gene are a cause of autosomal recessive spinocerebellar ataxia-11 (SCAR11), and a t(1;3) translocation of this gene has been associated with neurodevelopmental abnormalities. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 4. [provided by RefSeq, Dec 2011]","ncbiEntrezGeneId":255928,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/255928","proteins":[{"symbol":"SYT14_HUMAN","href":"/api/1.0/protein/SYT14_HUMAN"}],"hgncRootFamilies":[{"name":"C2 domain containing","href":"/api/1.0/gene_family/C2+domain+containing"}]}