Known Diseases associated with this Protein: |  AUTISM, SUSCEPTIBILITY TO, X-LINKED 3, INCLUDED
| ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATION
| ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATION, INCLUDED
| MENTAL RETARDATION, X-LINKED, SYNDROMIC 13
| MENTAL RETARDATION, X-LINKED, SYNDROMIC, 13 (MRXS13)
| RETT SYNDROME
| RETT SYNDROME (RTT)
| RETT SYNDROME, ATYPICAL
| RETT SYNDROME, INCLUDED
| RETT SYNDROME, ZAPPELLA VARIANT
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|  | Tips: The Domains on the Default View are decided by the Domain's E-Value. Clicking a check box will display or hide the correlated domain. To view the Gene page, either click on the link to the left or the blue bar above the Protein's graphic. |
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1708973
MECP2_HUMAN RecName: Full=Methyl-CpG-binding protein 2; Short=MeCp-2 protein; Short=MeCp2
65
25
19
0
71