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)
MCF: 
102135563(MECP2)
MMU: 
17257(Mecp2)
RNO: 
29386(Mecp2)
HGL: 
101700584(Mecp2)
TUP: 
102500435(MECP2)
CFA: 
612973(MECP2)
AML: 
FCA: 
101082385(MECP2)
PTG: 
BTA: 
539629(MECP2)
BOM: 
102279138(MECP2)
PHD: 
102321296(MECP2)
CHX: 
102174833(MECP2)
SSC: 
100524967(MECP2)
CFR: 
102504685(MECP2)
ECB: 
100058125(MECP2)
MYB: 
102245118(MECP2)
MYD: 
102765702(MECP2)
PALE: 
102894402(MECP2)
MDO: 
100029536(MECP2)
SHR: 
100924168(MECP2)
OAA: 
100077487(MECP2)
PHI: 
FPG: 
ASN: 
102374589(MECP2)
PSS: 
102462314(MECP2)
CMY: 
ACS: 
XLA: 
398087(mecp2)
XTR: 
100216110(mecp2)
DRE: 
335250(mecp2)
MZE: 
OLA: 
XMA: 
LCM: 
102357371(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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