This gene encodes a sodium-hydrogen exchanger that is amember of the solute carrier family 9. The encoded protein localizes to early and recycling endosomes and may be involved in regulating endosomal pH and volume. Defects in this gene are associated with X-linked syndromic cognitive disability, Christianson type. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Apr 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLC9A6-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC9A6-20-OR | 20 (40 μL) | 200 μL |  |
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| SLC9A6-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC9A6-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC9A6-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a sodium-hydrogen exchanger that is amember of the solute carrier family 9. The encoded protein localizes to early and recycling endosomes and may be involved in regulating endosomal pH and volume. Defects in this gene are associated with X-linked syndromic cognitive disability, Christianson type. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Apr 2010]
Gene Symbol : SLC9A6
Gene Name : Solute carrier family 9 member A6
Chromosome : CHR X: 135,974,596-136,047,268
Locus : Xq26.3
Alt. Genes : HIPK3
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