This gene encodes a sodium/proton exchanger that is a member of the solute carrier 9 protein family. The encoded protein localizes the to the late recycling endosomes and may play an important role in maintaining cation homeostasis. Mutations in this gene are associated with autism susceptibility 16 and attention-deficit/hyperactivity disorder. [provided by RefSeq, Mar 2012]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLC9A9-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC9A9-20-OR | 20 (40 μL) | 200 μL |  |
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| SLC9A9-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC9A9-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC9A9-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a sodium/proton exchanger that is a member of the solute carrier 9 protein family. The encoded protein localizes the to the late recycling endosomes and may play an important role in maintaining cation homeostasis. Mutations in this gene are associated with autism susceptibility 16 and attention-deficit/hyperactivity disorder. [provided by RefSeq, Mar 2012]
Gene Symbol : SLC9A9
Gene Name : Solute carrier family 9 member A9
Chromosome : CHR 3: 143,848,530-143,265,221
Locus : 3q24
Alt. Genes : FAM13A
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