SCN1A Chromosome 2

Sodium voltage-gated channel alpha subunit 1
1884 variants 1 Drug Response 1883 Health Risk

Upload your DNA to see your personal genotypes for variants in SCN1A.

What This Gene Does
Voltage-dependent sodium channels are heteromeric complexes that regulate sodium exchange between intracellular and extracellular spaces and are essential for the generation and propagation of action potentials in muscle cells and neurons. Each sodium channel is composed of a large pore-forming, glycosylated alpha subunit and two smaller beta subunits. This gene encodes a sodium channel alpha subunit, which has four homologous domains, each of which contains six transmembrane regions. Allelic variants of this gene are associated with generalized epilepsy with febrile seizures and epileptic encephalopathy. Alternative splicing results in multiple transcript variants. The RefSeq Project has decided to create four representative RefSeq records. Three of the transcript variants are supported by experimental evidence and the fourth contains alternate 5' untranslated exons, the exact combination of which have not been experimentally confirmed for the full-length transcript. [provided by RefSeq, Oct 2015]
Gene Info
Gene Group
Sodium voltage-gated channel alpha subunits
Locus Type
gene with protein product
Location
2q24.3
Ensembl
ENSG00000144285
Associated Conditions (56)
Febrile seizures
familial
3a
carbamazepine response - Dosage
Early-infantile DEE
Inborn genetic diseases
Developmental and epileptic encephalopathy 6B
Migraine
familial hemiplegic
3
Generalized epilepsy with febrile seizures plus
type 2
SCN1A-related disorder
type 1
Severe myoclonic epilepsy in infancy
Focal epilepsy
Autosomal dominant epilepsy
Seizure
Developmental and epileptic encephalopathy
Bilateral tonic-clonic seizure
+36 more conditions
Key Variants
All Variants (1884)
RSID Category Clinical Significance Conditions
RS2105867534 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS2105867993 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS2105868016 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS2105868295 Health Risk Likely pathogenic Generalized epilepsy with febrile seizures plus, type 2, Severe myoclonic epilepsy in infancy
RS2105874284 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS2105874493 Health Risk Likely pathogenic Generalized epilepsy with febrile seizures plus, type 2, Generalized epilepsy with febrile seizures plus
RS2105888708 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS2105890296 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS2105890375 Health Risk Likely pathogenic Generalized epilepsy with febrile seizures plus, type 2, Developmental and epileptic encephalopathy 6B
RS2105890879 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS2105917940 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS2105918428 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS2105918665 Health Risk Likely pathogenic Generalized epilepsy with febrile seizures plus, type 2, Generalized epilepsy with febrile seizures plus
RS2468080465 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS2468095824 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS2468096330 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS2468096854 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS2468098342 Health Risk Likely pathogenic Migraine, familial hemiplegic, 3
RS2468098623 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS2468101174 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS2468115612 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS2468115658 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS2468115681 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS2468130270 Health Risk Likely pathogenic
RS2468130287 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS2468131676 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS2468140689 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS2468141601 Health Risk Likely pathogenic Seizure, Seizure
RS2468156232 Health Risk Likely pathogenic Generalized epilepsy with febrile seizures plus, type 2, Generalized epilepsy with febrile seizures plus
RS2468156607 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS2468169093 Health Risk Likely pathogenic Generalized epilepsy with febrile seizures plus, type 2, Generalized epilepsy with febrile seizures plus
RS2468169278 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS2468180474 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS2468181767 Health Risk Likely pathogenic Generalized epilepsy with febrile seizures plus, type 2, Generalized epilepsy with febrile seizures plus
RS2468181816 Health Risk Likely pathogenic Early-infantile DEE, Epilepsy, Early-infantile DEE
RS2468182008 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS2468188957 Health Risk Likely pathogenic Generalized epilepsy with febrile seizures plus, type 2, Generalized epilepsy with febrile seizures plus
RS2468189109 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS2468189894 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE, Early-infantile DEE
RS2468190770 Health Risk Likely pathogenic Inborn genetic diseases, Inborn genetic diseases
RS2468224333 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS2468224941 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS2468224999 Health Risk Likely pathogenic Generalized epilepsy with febrile seizures plus, type 2, Generalized epilepsy with febrile seizures plus
RS2468225315 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS2468225401 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Neonatal developmental and epileptic encephalopathy with movement disorders and arthrogryposis (NDEEMA), Severe myoclonic epilepsy in infancy
RS2468225592 Health Risk Likely pathogenic
RS2468233753 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 6A, Early-infantile DEE
RS2468247712 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS2468257958 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS2468258442 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
« Prev 1 ... 9 10 11 12 13 14 15 ... 38 Next »
Sign Up to Analyze Your DNA Log In