131
|
|
|
Sodium voltage-gated channel beta subunit 2 |
ATFB14 |
|
132
|
|
|
Sodium voltage-gated channel alpha subunit 3 |
DEE62, EIEE62, FFEVF4, NAC3, Nav1.3 |
|
133
|
|
|
Sodium voltage-gated channel beta subunit 3 |
ATFB16, BRGDA7, HSA243396, SCNB3 |
|
134
|
|
|
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) |
135
|
|
|
Sodium voltage-gated channel beta subunit 4 |
ATFB17, LQT10, Navbeta4 |
|
136
|
|
|
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) |
137
|
|
|
Sodium voltage-gated channel alpha subunit 7 |
NaG, Nav2.1, Nav2.2, SCN6A |
|
138
|
|
|
Sodium voltage-gated channel alpha subunit 8 |
BFIS5, CERIII, CIAT, DEE13, EIEE13, MED, MYOCL2, NaCh6, Nav1.6, PN4 |
Alzheimer disease, Arthrogryposis multiplex congenita, Ataxia, Autism, Nonsyndromic intellectual disability, Benign infantile epilepsy, Bipolar disorder, Cerebellar ataxia, Choreoathetosis, Cognitive impairment with or without cerebellar ataxia, Neurodevelopmental disorder, Developmental and epileptic encephalopathy, Developmental disability, Developmental regression, Digestive system disease, Partial epilepsy, Epilepsy, Febrile convulsion, Focal onset epileptic seizure, Global developmental delay, Intellectual developmental disorder, Major depressive disorder, Mood disorder, Nervous system disease, Non-specific syndromic intellectual disability, Pena-shokeir syndrome , Seizures, Intellectual disability, Spastic ataxia, Status epilepticus, Tremor, West syndromeView all (17 more) |
139
|
|
|
Sodium voltage-gated channel alpha subunit 9 |
ETHA, FEB3B, GEFSP7, HSAN2D, NE-NA, NENA, Nav1.7, PN1, SFNP |
Biliary atresia, Charcot-marie-tooth disease, Chronic pain, Congenital insensitivity to pain, Congenital pain insensitivity, Dental caries, Diverticular disease, Dravet syndrome, Epilepsy, Rolandic epilepsy, Primary erythromelalgia, Erythromelalgia, Febrile convulsion, Generalized epilepsy with febrile seizures plus, Global developmental delay, Hereditary sensory and autonomic neuropathy, Hypoglycemia, Paroxysmal extreme pain disorder, Pruritus, SchizophreniaView all (5 more) |
140
|
|
|
Sodium channel modifier 1 |
OFD19 |
|
