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
RS796053086 Health Risk Pathogenic Early-infantile DEE, Early-infantile DEE
RS796053087 Health Risk Pathogenic
RS796053091 Health Risk Pathogenic Generalized epilepsy with febrile seizures plus, type 2, Generalized epilepsy with febrile seizures plus
RS796053092 Health Risk Pathogenic
RS796053095 Health Risk Pathogenic Developmental and epileptic encephalopathy 6B, Early-infantile DEE, Developmental and epileptic encephalopathy 6B
RS796053103 Health Risk Pathogenic Early-infantile DEE, Early-infantile DEE
RS796053105 Health Risk Pathogenic
RS796053106 Health Risk Pathogenic
RS796053107 Health Risk Pathogenic
RS797044952 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS797044981 Health Risk Pathogenic
RS797044982 Health Risk Pathogenic
RS797044983 Health Risk Pathogenic Early-infantile DEE, Early-infantile DEE
RS797044984 Health Risk Pathogenic
RS797044985 Health Risk Pathogenic Migraine, familial hemiplegic, 3
RS863225030 Health Risk Pathogenic Severe myoclonic epilepsy in infancy, Early-infantile DEE, Severe myoclonic epilepsy in infancy
RS863225031 Health Risk Pathogenic Severe myoclonic epilepsy in infancy, Early-infantile DEE, Early-infantile DEE
RS863225032 Health Risk Pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS863225033 Health Risk Pathogenic Severe myoclonic epilepsy in infancy, Early-infantile DEE, Severe myoclonic epilepsy in infancy
RS863225034 Health Risk Pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS863225035 Health Risk Pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS863225036 Health Risk Pathogenic Severe myoclonic epilepsy in infancy, Early-infantile DEE, Severe myoclonic epilepsy in infancy
RS863225038 Health Risk Pathogenic Severe myoclonic epilepsy in infancy, Early-infantile DEE, Severe myoclonic epilepsy in infancy
RS866146696 Health Risk Pathogenic Early-infantile DEE, Early-infantile DEE
RS869312670 Health Risk Pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS869312684 Health Risk Pathogenic Severe myoclonic epilepsy in infancy, Generalized epilepsy with febrile seizures plus, type 2
RS878854263 Health Risk Pathogenic Early-infantile DEE, Early-infantile DEE
RS886039430 Health Risk Pathogenic Migraine, familial hemiplegic, 3
RS886039529 Health Risk Pathogenic Seizure, Seizure
RS886039705 Health Risk Pathogenic
RS886039712 Health Risk Pathogenic
RS886041442 Health Risk Pathogenic
RS886041501 Health Risk Pathogenic
RS886041562 Health Risk Pathogenic
RS886041604 Health Risk Pathogenic
RS886041644 Health Risk Pathogenic
RS886041733 Health Risk Pathogenic
RS886041852 Health Risk Pathogenic
RS886041926 Health Risk Pathogenic
RS886041937 Health Risk Pathogenic
RS886041939 Health Risk Pathogenic
RS886041961 Health Risk Pathogenic Developmental and epileptic encephalopathy 6B, Early-infantile DEE, Developmental and epileptic encephalopathy 6B
RS886041969 Health Risk Pathogenic
RS886041982 Health Risk Pathogenic
RS886042004 Health Risk Pathogenic Early-infantile DEE, Early-infantile DEE
RS886042528 Health Risk Pathogenic Severe myoclonic epilepsy in infancy, SCN1A-related disorder, Early-infantile DEE
RS886043532 Health Risk Pathogenic
RS886043864 Health Risk Pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS886044441 Health Risk Pathogenic Early-infantile DEE, Early-infantile DEE
RS922757507 Health Risk Pathogenic Early-infantile DEE, Early-infantile DEE, Early-infantile DEE
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