This gene encodes a protein belonging to ubiE/COQ5 methyltransferase family. The gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.22-q11.23. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| METTL27-20-RE | 20 (40 μL) | 200 μL |  |
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| METTL27-20-OR | 20 (40 μL) | 200 μL |  |
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| METTL27-20-GO | 20 (40 μL) | 200 μL |  |
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| METTL27-20-GR | 20 (40 μL) | 200 μL |  |
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| METTL27-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a protein belonging to ubiE/COQ5 methyltransferase family. The gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.22-q11.23. [provided by RefSeq, Jul 2008]
Gene Symbol : METTL27
Gene Name : Methyltransferase like 27
Chromosome : CHR 7: 738,425,26-738,345,89
Locus : 7q11.23
Alt. Genes : LRPPRC
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