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Known Diseases associated with this Protein: |  DRAVET SYNDROME
| EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 6
| FEBRILE SEIZURES, FAMILIAL, 3A
| FEBRILE SEIZURES, FAMILIAL, 3A (FEB3A)
| GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS 2 (GEFS+2)
| GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2
| GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2, INCLUDED
| INTRACTABLE CHILDHOOD EPILEPSY WITH GENERALIZED TONIC-CLONIC SEIZURES (ICEGTC)
| MIGRAINE, FAMILIAL HEMIPLEGIC, 3
| MIGRAINE, FAMILIAL HEMIPLEGIC, 3 (FHM3)
| SEVERE MYOCLONIC EPILEPSY IN INFANCY (SMEI)
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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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SCN1A
6323
216
19
36
2
197
