BAIT

MECP2

1500041B07Rik, D630021H01Rik, Mbd5, WBP10, RP23-252M19.8
methyl CpG binding protein 2
GO Process (58)
GO Function (17)
GO Component (9)

Gene Ontology Biological Process

Mus musculus
PREY

GRIA2

GluA2, GluR-B, Glur-2, Glur2
glutamate receptor, ionotropic, AMPA2 (alpha 2)
GO Process (10)
GO Function (9)
GO Component (22)
Mus musculus

Co-localization

Interaction inferred from two proteins that co-localize in the cell by indirect immunofluorescence only when in addition, if one gene is deleted, the other protein becomes mis-localized. Also includes co-dependent association of proteins with promoter DNA in chromatin immunoprecipitation experiments.

Publication

Misregulation of Alternative Splicing in a Mouse Model of Rett Syndrome.

Li R, Dong Q, Yuan X, Zeng X, Gao Y, Chiao C, Li H, Zhao X, Keles S, Wang Z, Chang Q

Mutations in the human MECP2 gene cause Rett syndrome (RTT), a severe neurodevelopmental disorder that predominantly affects girls. Despite decades of work, the molecular function of MeCP2 is not fully understood. Here we report a systematic identification of MeCP2-interacting proteins in the mouse brain. In addition to transcription regulators, we found that MeCP2 physically interacts with several modulators of RNA ... [more]

PLoS Genet Dec. 01, 2015; 12(6);e1006129 [Pubmed: 27352031]

Throughput

  • Low Throughput

Additional Notes

  • ChIP

Curated By

  • BioGRID