DNMT3B wt Allele

Human DNMT3B wild-type allele is located in the vicinity of 20q11.2 and is approximately 47 kb in length. This allele, which encodes DNA (cytosine-5)-methyltransferase 3B protein, plays a role in de novo methylation. Certain allelic variants of the DNMT3B gene cause immunodeficiency-centromeric instability-facial anomalies syndrome. (NCI Thesaurus)

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DNMT3B Gene

This gene plays a role in embryonic development, imprinting, and X-chromosome inactivation.

DNMT3A wt Allele

Human DNMT3A wt allele is located in the vicinity of 2p23 and is approximately 110 kb in length. This allele, which encodes…

DNMT3A Gene

This gene is involved in epigenetic modification of DNA.

DNMT1 wt Allele

Human DNMT1 wt allele is located in the vicinity of 19p13.2 and is approximately 62 kb in length. This allele, which encodes…

DNMT1 Gene

This gene is involved in epigenetic modification of DNA.

DNM2 wt Allele

Human DNM2 wild-type allele is located in the vicinity of 19p13.2 and is approximately 118 kb in length. This allele, which encodes…