11631
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Sodium voltage-gated channel alpha subunit 1 |
DEE6, DEE6A, DEE6B, DRVT, EIEE6, FEB3, FEB3A, FHM3, GEFSP2, HBSCI, NAC1, Nav1.1, SCN1, SMEI |
Arthrogryposis, Atrial fibrillation, Autism, Clinodactyly, Congenital joint contractures, Developmental and epileptic encephalopathy, Dravet syndrome, Myoclonic epilepsy, Epilepsy, Epilepsy of infancy with migrating focal seizures, Epilepsy with myoclonic atonic seizures, Generalized epilepsy, Rolandic epilepsy, Febrile convulsion, Focal onset epileptic seizure, Generalized epilepsy with febrile seizures plus, Global developmental delay, Hemiplegic migraine, Intellectual developmental disorder, Lennox-gastaut syndrome, Malignant migrating partial seizures of infancy, Migraine, Intellectual disability, Movement disorder, Neurodevelopmental disorder, Obesity, Partial epilepsy, Seizures, West syndromeView all (14 more) |
11632
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Sodium voltage-gated channel beta subunit 1 |
ATFB13, BRGDA5, DEE52, EIEE52, GEFSP1 |
Atrial fibrillation, Brugada syndrome, Cardiac arrhythmia, Cardiac conduction disease, Cardiomyopathy, Childhood absence epilepsy, Conduction disorder of the heart, Developmental and epileptic encephalopathy, Dravet syndrome, Rolandic epilepsy, Febrile convulsion, Generalized epilepsy with febrile seizures plus, Hereditary atrial fibrillation, Hereditary bundle branch system defect, Long qt syndrome, Seizures, Ventricular fibrillationView all (2 more) |
11633
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Sodium voltage-gated channel alpha subunit 2 |
BFIC3, BFIS3, BFNIS, DEE11, EA9, EIEE11, HBA, HBSCI, HBSCII, NAC2, Na(v)1.2, Nav1.2, SCN2A1, SCN2A2 |
Attention deficit hyperactivity disorder, Autism, Benign infantile epilepsy, Benign neonatal-infantile seizures, Benign neonatal epilepsy, Bipolar disorder, Neurodevelopmental disorder, Bipolar depression, Developmental and epileptic encephalopathy, Developmental disability, Dravet syndrome, Dystonia, Partial epilepsy, Epilepsy, Epilepsy of infancy with migrating focal seizures, Pyridoxine dependent epilepsy, Rolandic epilepsy, Episodic ataxia, Febrile convulsion, Generalized epilepsy with febrile seizures plus, Global developmental delay, Hemiplegia, Intellectual developmental disorder, Lennox-gastaut syndrome, Malignant migrating partial seizures of infancy, Metabolic syndrome, Movement disorder, Non-specific syndromic intellectual disability, Parkinson disease, Periodontitis, Seizures, Spastic ataxia, Substance abuse, Diabetes mellitus type 2, West syndromeView all (20 more) |
11634
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Sodium voltage-gated channel beta subunit 2 |
ATFB14 |
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11635
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Sodium voltage-gated channel alpha subunit 3 |
DEE62, EIEE62, FFEVF4, NAC3, Nav1.3 |
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11636
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|
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Sodium voltage-gated channel beta subunit 3 |
ATFB16, BRGDA7, HSA243396, SCNB3 |
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11637
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Sodium voltage-gated channel alpha subunit 4 |
CMS16, CMYO22A, CMYP22A, HOKPP2, HYKPP, HYPP, NAC1A, Na(V)1.4, Nav1.4, SkM1 |
Myotonia, Arthrogryposis multiplex congenita, Congenital myasthenic syndrome, Congenital myopathy, Hyperkalemic periodic paralysis, Gross motor development delay, Long qt syndrome, Male reproductive organ cancer, Myasthenic syndrome, Myopathy, Neuromuscular disease, Paralysis, Paramyotonia congenita, Pena-shokeir syndrome , Postsynaptic congenital myasthenic syndrome, Potassium-aggravated myotonia, Seizures, Sotos syndrome, TremorView all (4 more) |
11638
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|
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Sodium voltage-gated channel beta subunit 4 |
ATFB17, LQT10, Navbeta4 |
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11639
|
|
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Sodium voltage-gated channel alpha subunit 5 |
CDCD2, CMD1E, CMPD2, HB1, HB2, HBBD, HH1, ICCD, IVF, LQT3, Nav1.5, PFHB1, SSS1, VF1 |
Cardiac arrhythmias, Arrhythmogenic right ventricular cardiomyopathy, Arthrogryposis multiplex congenita, Atrial fibrillation, Atrial flutter, Atrial standstill, Autism, Brugada syndrome, Cardiac arrest, Cardiac arrhythmia, Cardiac conduction disease, Cardiac rhythm disease, Cardiomyopathy, Dilated cardiomyopathy, Conduction disorder of the heart, Congenital heart disease, Ectopic rhythm, Arrhythmogenic right ventricular dysplasia, Long qt syndrome, Sick sinus syndrome, Heart failure, Hereditary atrial fibrillation, Hereditary bundle branch system defect, Hypertrophic cardiomyopathy, Left ventricular noncompaction cardiomyopathy, Long qt syndrome, digenic, Migraine, Paroxysmal familial ventricular fibrillation, Paroxysmal tachycardia, Paroxysmal ventricular fibrillation, Pena-shokeir syndrome , Polymorphic catecholaminergic ventricular tachycardia, Short qt syndrome, Torsades de pointes, Ventricular fibrillation, Catecholaminergic polymorphic ventricular tachycardia, Wolff-parkinson-white syndromeView all (22 more) |
11640
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Sodium voltage-gated channel alpha subunit 7 |
NaG, Nav2.1, Nav2.2, SCN6A |
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