This gene encodes a sodium- and chloride-dependent glycine neurotransmitter transporter. This integral membrane glycoprotein is responsible for the clearance of extracellular glycine during glycine-mediated neurotransmission. This protein is found in glycinergic axons and maintains a high presynaptic pool of neurotransmitter at glycinergic synapses. Mutations in this gene cause hyperekplexia; a heterogenous neurological disorder characterized by exaggerated startle responses and neonatal apnea. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2016]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLC6A5-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC6A5-20-OR | 20 (40 μL) | 200 μL |  |
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| SLC6A5-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC6A5-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC6A5-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a sodium- and chloride-dependent glycine neurotransmitter transporter. This integral membrane glycoprotein is responsible for the clearance of extracellular glycine during glycine-mediated neurotransmission. This protein is found in glycinergic axons and maintains a high presynaptic pool of neurotransmitter at glycinergic synapses. Mutations in this gene cause hyperekplexia; a heterogenous neurological disorder characterized by exaggerated startle responses and neonatal apnea. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2016]
Gene Symbol : SLC6A5
Gene Name : Solute carrier family 6 member 5
Chromosome : CHR 11: 205,993,99-206,592,84
Locus : 11p15.1
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