CpG methylation is an epigenetic modification that is important for embryonic development, imprinting, and X-chromosome inactivation. Studies in mice have demonstrated that DNA methylation is required for mammalian development. This gene encodes a DNA methyltransferase which is thought to function in de novo methylation, rather than maintenance methylation. The protein localizes primarily to the nucleus and its expression is developmentally regulated. Mutations in this gene cause the immunodeficiency-centromeric instability-facial anomalies (ICF) syndrome. Eight alternatively spliced transcript variants have been described. The full length sequences of variants 4 and 5 have not been determined. [provided by RefSeq, May 2011]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| DNMT3BBA-20-REGO | 20 (40 μL) | 200 μL |
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| DNMT3BBA-20-REGR | 20 (40 μL) | 200 μL |
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| DNMT3BBA-20-ORGR | 20 (40 μL) | 200 μL |
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| DNMT3BBA-20-GOGR | 20 (40 μL) | 200 μL |
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| DNMT3BBA-20-GRRE | 20 (40 μL) | 200 μL |
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| DNMT3BBA-20-GROR | 20 (40 μL) | 200 μL |
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| DNMT3BBA-20-GRGO | 20 (40 μL) | 200 μL |
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| DNMT3BBA-20-AQOR | 20 (40 μL) | 200 μL |
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CpG methylation is an epigenetic modification that is important for embryonic development, imprinting, and X-chromosome inactivation. Studies in mice have demonstrated that DNA methylation is required for mammalian development. This gene encodes a DNA methyltransferase which is thought to function in de novo methylation, rather than maintenance methylation. The protein localizes primarily to the nucleus and its expression is developmentally regulated. Mutations in this gene cause the immunodeficiency-centromeric instability-facial anomalies (ICF) syndrome. Eight alternatively spliced transcript variants have been described. The full length sequences of variants 4 and 5 have not been determined. [provided by RefSeq, May 2011]
Gene Symbol : DNMT3B
Gene Name : DNA methyltransferase 3 beta
Chromosome : CHR 20: 327,623,84-328,093,55
Locus : 20q11.21
Alt. Genes : FAM13A
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