This gene encodes a ubiquitously expressed magnesium cation transporter protein that localizes to the cell membrane. This protein also associates with N-oligosaccharyl transferase and therefore may have a role in N-glycosylation. Mutations in this gene cause a form of X-linked intellectual disability (XLID). This gene may have multiple in-frame translation initiation sites, one of which would encode a shorter protein with an N-terminus containing a signal peptide at amino acids 1-29. [provided by RefSeq, Jul 2017]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| MAGT1-20-RE | 20 (40 μL) | 200 μL |  |
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| MAGT1-20-OR | 20 (40 μL) | 200 μL |  |
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| MAGT1-20-GO | 20 (40 μL) | 200 μL |  |
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| MAGT1-20-GR | 20 (40 μL) | 200 μL |  |
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| MAGT1-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a ubiquitously expressed magnesium cation transporter protein that localizes to the cell membrane. This protein also associates with N-oligosaccharyl transferase and therefore may have a role in N-glycosylation. Mutations in this gene cause a form of X-linked intellectual disability (XLID). This gene may have multiple in-frame translation initiation sites, one of which would encode a shorter protein with an N-terminus containing a signal peptide at amino acids 1-29. [provided by RefSeq, Jul 2017]
Gene Symbol : MAGT1
Gene Name : Magnesium transporter 1
Chromosome : CHR X: 778,955,67-778,263,63
Locus : Xq21.1
Alt. Genes : HIPK3
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