This gene encodes a member of the sodium:neurotransmitter symporter family. This member is a multi-pass membrane protein, which is responsible for reuptake of norepinephrine into presynaptic nerve terminals and is a regulator of norepinephrine homeostasis. Mutations in this gene cause orthostatic intolerance, a syndrome characterized by lightheadedness, fatigue, altered mentation and syncope. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.[provided by RefSeq, Feb 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLC6A2-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC6A2-20-OR | 20 (40 μL) | 200 μL |  |
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| SLC6A2-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC6A2-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC6A2-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a member of the sodium:neurotransmitter symporter family. This member is a multi-pass membrane protein, which is responsible for reuptake of norepinephrine into presynaptic nerve terminals and is a regulator of norepinephrine homeostasis. Mutations in this gene cause orthostatic intolerance, a syndrome characterized by lightheadedness, fatigue, altered mentation and syncope. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.[provided by RefSeq, Feb 2010]
Gene Symbol : SLC6A2
Gene Name : Solute carrier family 6 member 2
Chromosome : CHR 16: 556,556,03-557,061,91
Locus : 16q12.2
Alt. Genes : HIPK3
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