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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 HMMER's search E-Value of the Protein against the Domain model. Clicking a check box on the left will display or hide the corresponding domain(s). To view the Protein page, either click on the protein links in the box to the left or the blue bar above the Protein's graphic. |
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Domains found on the Proteins
Please Cite: Peterson, T.A., Adadey, A., Santana-Cruz ,I., Sun, Y., Winder A, Kann, M.G., (2010) DMDM: Domain Mapping of Disease Mutations. Bioinformatics 26 (19), 2458-2459.
| DMDM_info@umbc.edu | 1000 Hilltop Circle, Baltimore, MD
21250 | Department of Biological Sciences | Phone: 410-455-2258 |
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MECP2
4204
85
25
39
0
71
