This gene encodes a member of an evolutionarily conserved family of proteins that may function as methyltransferases. This gene is located in a larger region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. There are two pseudogenes for this gene located in the same region of chromosome 7. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| NSUN5-20-RE | 20 (40 μL) | 200 μL |  |
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| NSUN5-20-OR | 20 (40 μL) | 200 μL |  |
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| NSUN5-20-GO | 20 (40 μL) | 200 μL |  |
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| NSUN5-20-GR | 20 (40 μL) | 200 μL |  |
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| NSUN5-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a member of an evolutionarily conserved family of proteins that may function as methyltransferases. This gene is located in a larger region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. There are two pseudogenes for this gene located in the same region of chromosome 7. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]
Gene Symbol : NSUN5
Gene Name : NOP2/Sun RNA methyltransferase family member 5
Chromosome : CHR 7: 733,088,66-733,025,15
Locus : 7q11.23
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