This website uses cookies to ensure you get the best experience on our website.
- Table of Contents
1 Citations 16 Q&As
Facts about Methyl-CpG-binding protein 2.
It is not influenced by sequences flanking the methyl-CpGs. Mediates transcriptional repression through interaction with histone deacetylase and the corepressor SIN3A.
Human | |
---|---|
Gene Name: | MECP2 |
Uniprot: | P51608 |
Entrez: | 4204 |
Belongs to: |
---|
No superfamily |
AUTSX3; DKFZp686A24160; MeCp-2 protein; mental retardation, X-linked 79; methyl CpG binding protein 2 (Rett syndrome); X-linked 16
Mass (kDA):
52.441 kDA
Human | |
---|---|
Location: | Xq28 |
Sequence: | X; NC_000023.11 (154021573..154097731, complement) |
Present in all adult somatic tissues tested.
Nucleus. Colocalized with methyl-CpG in the genome. Colocalized with TBL1X to the heterochromatin foci.
PMID: 9710633 by Kudo S.; Methyl-CpG-binding protein MeCP2 represses Sp1-activated transcription of the human leukosialin gene when the promoter is methylated.
PMID: 8976388 by Vilain A., et al. Assignment of the gene for methyl-CpG-binding protein 2 (MECP2) to human chromosome band Xq28 by in situ hybridization.
*More publications can be found for each product on its corresponding product page