The protein encoded by this gene is a member of the SLC6 family of transporters, which are responsible for the presynaptic uptake of most neurotransmitters. The encoded vesicular transporter is selective for proline, glycine, leucine and alanine. In mouse, the strongest expression of this gene was in cortical and hippocampal tissues where expression increased during embryonic brain development and peaked postnatally. Defects in this gene cause a form of autosomal recessive intellectual disability. [provided by RefSeq, Jul 2017]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLC6A17-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC6A17-20-OR | 20 (40 μL) | 200 μL |  |
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| SLC6A17-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC6A17-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC6A17-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene is a member of the SLC6 family of transporters, which are responsible for the presynaptic uptake of most neurotransmitters. The encoded vesicular transporter is selective for proline, glycine, leucine and alanine. In mouse, the strongest expression of this gene was in cortical and hippocampal tissues where expression increased during embryonic brain development and peaked postnatally. Defects in this gene cause a form of autosomal recessive intellectual disability. [provided by RefSeq, Jul 2017]
Gene Symbol : SLC6A17
Gene Name : Solute carrier family 6 member 17
Chromosome : CHR 1: 110,150,509-110,202,201
Locus : 1p13.3
Alt. Genes : PREB
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