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
RS2468435747 Health Risk Pathogenic Early-infantile DEE, Early-infantile DEE
RS2468436184 Health Risk Pathogenic Early-infantile DEE, Early-infantile DEE
RS2468437652 Health Risk Pathogenic Early-infantile DEE, Early-infantile DEE
RS2468437769 Health Risk Pathogenic Early-infantile DEE, Early-infantile DEE, Early-infantile DEE
RS2468493255 Health Risk Pathogenic Early-infantile DEE, Early-infantile DEE
RS2468493279 Health Risk Pathogenic Early-infantile DEE, Early-infantile DEE
RS2468494342 Health Risk Pathogenic Early-infantile DEE, Early-infantile DEE
RS2468495230 Health Risk Pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS2468512455 Health Risk Pathogenic Early-infantile DEE, Early-infantile DEE
RS2468513095 Health Risk Pathogenic Developmental and epileptic encephalopathy, 6A, Early-infantile DEE
RS2468531246 Health Risk Pathogenic Early-infantile DEE, Early-infantile DEE, Early-infantile DEE
RS2468531809 Health Risk Pathogenic Early-infantile DEE, Early-infantile DEE
RS2468532253 Health Risk Pathogenic Early-infantile DEE, Early-infantile DEE
RS2468548572 Health Risk Pathogenic Early-infantile DEE, Early-infantile DEE
RS2468548836 Health Risk Pathogenic Early-infantile DEE, Early-infantile DEE
RS2468550107 Health Risk Pathogenic Early-infantile DEE, Early-infantile DEE
RS35595680 Health Risk Pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS368609628 Health Risk Pathogenic Severe myoclonic epilepsy in infancy, Early-infantile DEE, Severe myoclonic epilepsy in infancy
RS372098964 Health Risk Pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS372425457 Health Risk Pathogenic Severe myoclonic epilepsy in infancy, Inborn genetic diseases, Early-infantile DEE
RS397514459 Health Risk Pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy, Early-infantile DEE
RS398123579 Health Risk Pathogenic
RS398123580 Health Risk Pathogenic
RS398123585 Health Risk Pathogenic Severe myoclonic epilepsy in infancy, Migraine, familial hemiplegic
RS398123588 Health Risk Pathogenic Autosomal dominant epilepsy, Seizure, Generalized epilepsy with febrile seizures plus
RS398123590 Health Risk Pathogenic Generalized epilepsy with febrile seizures plus, type 2, Generalized epilepsy with febrile seizures plus
RS398123593 Health Risk Pathogenic Severe myoclonic epilepsy in infancy, Inborn genetic diseases, SCN1A-related disorder
RS398123594 Health Risk Pathogenic Early-infantile DEE, Early-infantile DEE
RS398123595 Health Risk Pathogenic Seizure, Seizure
RS398123599 Health Risk Pathogenic
RS542420576 Health Risk Pathogenic Severe myoclonic epilepsy in infancy, Early-infantile DEE, Severe myoclonic epilepsy in infancy
RS547496777 Health Risk Pathogenic Early-infantile DEE, Early-infantile DEE
RS587781146 Health Risk Pathogenic
RS61741123 Health Risk Pathogenic Severe myoclonic epilepsy in infancy, Familial hemiplegic migraine, Generalized epilepsy with febrile seizures plus
RS727504136 Health Risk Pathogenic Severe myoclonic epilepsy in infancy, Inborn genetic diseases, Migraine
RS727504140 Health Risk Pathogenic Early-infantile DEE, Early-infantile DEE
RS727504142 Health Risk Pathogenic Severe myoclonic epilepsy in infancy, Early-infantile DEE, Early-infantile DEE
RS746718015 Health Risk Pathogenic Early-infantile DEE, Early-infantile DEE
RS748267258 Health Risk Pathogenic Early-infantile DEE, Epileptic encephalopathy, Early-infantile DEE
RS748508725 Health Risk Pathogenic Early-infantile DEE, Early-infantile DEE
RS749317646 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS750364705 Health Risk Pathogenic Early-infantile DEE, Developmental and epileptic encephalopathy, Early-infantile DEE
RS750997506 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases, Early-infantile DEE
RS751759887 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS760361423 Health Risk Pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS761333438 Health Risk Pathogenic Early-infantile DEE, Early-infantile DEE
RS763400390 Health Risk Pathogenic Early-infantile DEE, Early-infantile DEE
RS764037830 Health Risk Pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS764444350 Health Risk Pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS76921794 Health Risk Pathogenic Severe myoclonic epilepsy in infancy, Early-infantile DEE, Severe myoclonic epilepsy in infancy
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