# methyl-CpG binding protein 2

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21113404](https://www.wikidata.org/wiki/Q21113404)  
**Source**: https://4ort.xyz/entity/methyl-cpg-binding-protein-2-q21113404


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/P51608)
3. Q20641742
4. [Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation](http://www.ebi.ac.uk/QuickGO/annotations?protein=P51608&geneProductId=UniProtKB:P51608)
5. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=P51608&geneProductId=UniProtKB:P51608)
6. [Histone deacetylase-independent transcriptional repression by methyl-CpG-binding protein 2.](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P51608)
7. [The Ski protein family is required for MeCP2-mediated transcriptional repression](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P51608)
8. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P51608)
9. [Proteomic analyses reveal distinct chromatin-associated and soluble transcription factor complexes](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P51608)
10. [Brahma links the SWI/SNF chromatin-remodeling complex with MeCP2-dependent transcriptional silencing](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P51608)
11. [Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressor](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P51608)
12. [Methyl-CpG-binding protein 2 is phosphorylated by homeodomain-interacting protein kinase 2 and contributes to apoptosis](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P51608)
13. [Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex](http://www.ebi.ac.uk/QuickGO/annotations?protein=P51608&geneProductId=UniProtKB:P51608)
14. [Insights into RNA biology from an atlas of mammalian mRNA-binding proteins](http://www.ebi.ac.uk/QuickGO/annotations?protein=P51608&geneProductId=UniProtKB:P51608)
15. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P51608)
16. [Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P51608)
17. [Insights into RNA biology from an atlas of mammalian mRNA-binding proteins](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P51608)
18. [Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P51608)
19. [Histone deacetylase-independent transcriptional repression by methyl-CpG-binding protein 2.](http://www.ebi.ac.uk/QuickGO/annotations?protein=P51608&geneProductId=UniProtKB:P51608)
20. [The Ski protein family is required for MeCP2-mediated transcriptional repression](http://www.ebi.ac.uk/QuickGO/annotations?protein=P51608&geneProductId=UniProtKB:P51608)
21. [Mutations in ANKRD11 cause KBG syndrome, characterized by intellectual disability, skeletal malformations, and macrodontia](http://www.ebi.ac.uk/QuickGO/annotations?protein=P51608&geneProductId=UniProtKB:P51608)
22. [Comparison of tear protein levels in breast cancer patients and healthy controls using a de novo proteomic approach](http://www.ebi.ac.uk/QuickGO/annotations?protein=P51608&geneProductId=UniProtKB:P51608)
23. [Methyl-CpG binding protein 2 (MeCP2) localizes at the centrosome and is required for proper mitotic spindle organization](http://www.ebi.ac.uk/QuickGO/annotations?protein=P51608&geneProductId=UniProtKB:P51608)
24. [Methyl-CpG binding protein 2 (MeCP2) localizes at the centrosome and is required for proper mitotic spindle organization](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P51608)
25. [Comparison of tear protein levels in breast cancer patients and healthy controls using a de novo proteomic approach](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P51608)
26. [Mutations in ANKRD11 cause KBG syndrome, characterized by intellectual disability, skeletal malformations, and macrodontia](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P51608)
27. [MicroRNA-mediated epigenetic silencing of sirtuin1 contributes to impaired angiogenic responses](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P51608)
28. Ensembl Release 99
29. UMLS 2023