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]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SYT14-20-RE | 20 (40 μL) | 200 μL |  |
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| SYT14-20-OR | 20 (40 μL) | 200 μL |  |
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| SYT14-20-GO | 20 (40 μL) | 200 μL |  |
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| SYT14-20-GR | 20 (40 μL) | 200 μL |  |
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| SYT14-20-AQ | 20 (40 μL) | 200 μL |  |
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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]
Gene Symbol : SYT14
Gene Name : Synaptotagmin 14
Chromosome : CHR 1: 209,938,164-210,171,314
Locus : 1q32.2
Alt. Genes : KIF20A
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