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Known Diseases associated with this Protein: |  DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND
| EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 16
| EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 16 (EIEE16)
| FAMILIAL INFANTILE MYOCLONIC EPILEPSY (FIME)
| MYOCLONIC EPILEPSY, INFANTILE, FAMILIAL
| SEIZURES SYNDROME
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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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TBC1D24
57465
12
0
8
0
4
