KEGG   ORTHOLOGY: K11588Help
Entry
K11588                      KO                                     
Name
MECP2
Definition
methyl CpG binding protein 2
Disease
H00440  
Rett syndrome
H00478  
Prader-Willi and Angelman syndromes
H00480  
Non-syndromic X-linked mental retardation
H01211  
MECP2-related severe neonatal encephalopathy
Brite
Chromosome [BR:ko03036]
 Eukaryotic Type
  Heterochromatin formation proteins
   MBPs (metylated DNA binding proteins)
    K11588  MECP2; methyl CpG binding protein 2
BRITE hierarchy
Genes
HSA: 
4204(MECP2)
PTR: 
465936(MECP2)
PPS: 
100968276(MECP2)
GGO: 
101132702(MECP2)
PON: 
100443011(MECP2)
MCC: 
700174(MECP2)
MMU: 
17257(Mecp2)
RNO: 
29386(Mecp2)
CFA: 
612973(MECP2)
AML: 
FCA: 
101082385(MECP2)
BTA: 
539629(MECP2)
SSC: 
100524967
ECB: 
100058125
MDO: 
100029536
SHR: 
100924168(MECP2)
OAA: 
100077487
ACS: 
100564173
XLA: 
398087(mecp2)
XTR: 
100216110(mecp2)
DRE: 
335250(mecp2)
 » show all
TaxonomyKoalaUniProt
Reference
  Authors
Guy J, Cheval H, Selfridge J, Bird A
  Title
The Role of MeCP2 in the Brain.
  Journal
Annu Rev Cell Dev Biol 27:631-52 (2011)
Reference
  Authors
Bogdanovic O, Veenstra GJ
  Title
DNA methylation and methyl-CpG binding proteins: developmental requirements and function.
  Journal
Chromosoma 118:549-65 (2009)
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