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SYT14 Genesynaptotagmin XIV 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] |
syt14 Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term syt14 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
SYT14 Gene SetFrom Pathway Commons Protein-Protein Interactions interacting proteins for SYT14 from the Pathway Commons Protein-Protein Interactions dataset. |