The protein encoded by this gene may be a sodium-dependent transmembrane transport protein involved in the uptake of choline by cholinergic neurons. Defects in this gene can cause sialidosis, a lysosomal storage disease. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLC44A4-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC44A4-20-OR | 20 (40 μL) | 200 μL |  |
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| SLC44A4-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC44A4-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC44A4-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene may be a sodium-dependent transmembrane transport protein involved in the uptake of choline by cholinergic neurons. Defects in this gene can cause sialidosis, a lysosomal storage disease. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]
Gene Symbol : SLC44A4
Gene Name : Solute carrier family 44 member 4
Chromosome : CHR 6: 318,790,45-318,631,91
Locus : 6p21.33
Alt. Genes : OPTN
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