DNMT3A (NM_175630) - DNA methyltransferase 3 alpha
Dna (Cytosine-5)-Methyltransferase 3a Isoform C
Legend
Mutation impacts
Sites
- C-linked
- N-linked
- O-linked
- S-linked
- SARS-CoV-2
Others
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Mutations Visualisation
Protein summary
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 that is thought to function in de novo methylation, rather than maintenance methylation. The protein localizes to the cytoplasm and nucleus and its expression is developmentally regulated. [provided by RefSeq, Mar 2016].
Publication Note:
This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications.
Evidence data:
Transcript exon combination :: BC032392.1, SRR1163657.528386.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1966682, SAMEA1968189 [ECO:0000348]
- Strand
- -
- Chromosome
- 2
- Protein
- 166 residues
- All mutations
- 13
- PTM sites
- 5
- CDS
- 25,505,256 - 25,536,853
- Transcription
- 25,504,320 - 25,565,459