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 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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12644229
SCN1A_HUMAN RecName: Full=Sodium channel protein type 1 subunit alpha; AltName: Full=Sodium channel protein brain I subunit alpha; AltName: Full=Sodium channel protein type I subunit alpha; AltName: Full=Voltage-gated sodium channel subunit alpha Nav1.1
198
18
18
1
197