91
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Potassium voltage-gated channel subfamily E regulatory subunit 1 |
ISK, JLNS, JLNS2, LQT2/5, LQT5, MinK |
Curated: Arrhythmogenic right ventricular cardiomyopathy, Atrial fibrillation, Cardiomyopathy, Dilated cardiomyopathy, Congenital hearing disorder, Long qt syndrome, Hereditary atrial fibrillation, Hypertrophic cardiomyopathy, Jervell and lange-nielsen syndrome, Long qt syndrome, digenic, Hearing loss, long qt syndrome 5
Unreviewed: Amelogenesis Imperfecta, Andersen Syndrome, Aortic dissection, Astrocytoma, Atrial Fibrillation, Atrophy, Brugada Syndrome, Cardiac arrhythmias, Cardiovascular Diseases, Catecholaminergic polymorphic ventricular tachycardia, Congenital Long QT Syndrome, Congenital Sensorineural Hearing Loss, Congestive Heart Failure, Deafness, Diabetes, Diabetes Mellitus, Diabetes mellitus, type 1, Down Syndrome, Dysautonomia, Endometrial Cancer, Endometrial carcinoma, Endometrial neoplasm, Epilepsy, Hearing Loss, Heart disease, Heart Diseases, Heart Failure, Heterotaxia, Heterotaxy syndrome, Hyperaldosteronism, Iron deficiency anemia, Jervell-Lange Nielsen Syndrome, Kidney Disease, Long QT Syndrome, Malignant Neoplasm, Meniere Disease, Myocardial Infarction, Myocardial ischemia, Nonsyndromic Deafness, Polymorphic catecholaminergic ventricular tachycardia, Propionic acidemia, Romano-Ward Syndrome, Russell-Silver Syndrome, Seborrheic keratosis, Seizures, Sensorineural hearing loss, Short QT Syndrome, Sleep apnea, Tic Disorder, Torsades de Pointes, Tourette syndrome, Ventricular arrhythmia, Ventricular ectopy, Ventricular Fibrillation, Ventricular tachycardia
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92
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Potassium voltage-gated channel subfamily E regulatory subunit 2 |
ATFB4, LQT5, LQT6, MIRP1 |
Curated: Alzheimer disease, Atrial fibrillation, Cardiac arrhythmia, Dilated cardiomyopathy, Cardiomyopathy, Cardiovascular disease, Ischemic heart disease, Obstructive pulmonary disease, Coronary artery disease, Long qt syndrome, Heart disease, Hereditary atrial fibrillation, Long qt syndrome, digenic, Migraine, Myocardial infarction, Myocardial ischemia, Diabetes mellitus type 2, Ventricular fibrillation
Unreviewed: Adenoma, Andersen Syndrome, Anemia, Arteriosclerosis, Atherosclerosis, Atrial Fibrillation, Brugada Syndrome, Cardiac arrhythmias, Catecholaminergic polymorphic ventricular tachycardia, Chronobiology disorder, Congenital Long QT Syndrome, Congestive Heart Failure, Diabetes Mellitus, Dysautonomia, Gastritis, Heart Failure, Hepatocellular carcinoma, Hypothyroidism, Hypoxia, Jervell-Lange Nielsen Syndrome, Liver carcinoma, Long QT Syndrome, LONG QT SYNDROME DIGENIC, Malignant Neoplasm, Myocardial Infarction, Neoplasms, Obesity, Paroxysmal atrial fibrillation, Romano-Ward Syndrome, Seizures, Sinus Node Dysfunction, Stomach Carcinoma, Stomach Neoplasms, Torsades de Pointes, Turner syndrome, Ventricular arrhythmia, Ventricular Fibrillation
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93
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|
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Potassium voltage-gated channel subfamily E regulatory subunit 3 |
BRGDA6, HOKPP, HYPP, MiRP2 |
Curated: Brugada syndrome, Corneal astigmatism, Long qt syndrome, Neurotic disorder, Oligodendroglioma, Ventricular fibrillation
Unreviewed: Adrenocortical adenoma, Atrial Fibrillation, Atrioventricular block, Brugada Syndrome, Bundle Branch Block, Cerebrovascular disorder, Colorectal neoplasm, Diarrhea, Heart disease, Hyperkalemic Periodic Paralysis, Hypokalemic Periodic Paralysis, Long QT Syndrome, Meniere Disease, Neoplasms, Neurodegenerative Disorders, Paramyotonia Congenita, Paroxysmal ventricular tachycardia, Periodic hypokalemic paresis, Periodic Paralysis, Proximal symphalangism, Sick Sinus Syndrome, Supraventricular tachycardia, Thyroid Gland Follicular Adenoma, Thyrotoxic Periodic Paralysis, Trifascicular block, Ulcerative colitis, Vascular malformation, Ventricular Fibrillation
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94
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Potassium voltage-gated channel subfamily E regulatory subunit 4 |
MIRP3 |
Curated: Cardiac embolism, Cardioembolic stroke, Lymphoblastic leukemia, Oropharyngeal cancer
Unreviewed: Asthma, Atrial Fibrillation, Brugada syndrome, Heart disease, Long qt syndrome, Narcolepsy, Neoplasms, Vascular malformation
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95
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|
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Potassium voltage-gated channel subfamily E regulatory subunit 5 |
KCNE1L |
Curated: Brugada syndrome
Unreviewed: Alport Syndrome-Intellectual Disability-Midface Hypoplasia-Elliptocytosis Syndrome, Amme complex, Arrhythmogenic right ventricular cardiomyopathy, Atrial Fibrillation, Atrioventricular block, Brugada Syndrome, Bundle Branch Block, Congenital heart defects, Contiguous gene syndrome, Coronary Syndrome, Elliptocytosis, Heart disease, Long QT Syndrome, Mental retardation, Myopia, Paroxysmal ventricular fibrillation, Paroxysmal ventricular tachycardia, Patent ductus arteriosus, Renal Glomerular Disease, Renal Insufficiency, Sick Sinus Syndrome, Strabismus, Supraventricular tachycardia, Trifascicular block, Ventricular arrhythmia, Ventricular Fibrillation, Ventricular tachycardia
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96
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Potassium voltage-gated channel modifier subfamily F member 1 |
IK8, KCNF, KV5.1, kH1 |
Curated: Alzheimer disease, Anxiety disorder, Gastric ulcer, Gastritis, Major depressive disorder, Moyamoya angiopathy, Ocular hypotension
Unreviewed: Laryngeal neoplasm, Leukemia
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97
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|
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Potassium voltage-gated channel modifier subfamily G member 1 |
K13, KCNG, KV6.1, kH2 |
Curated: Alzheimer disease, Atypical femoral fracture, Bipolar disorder, Major depressive disorder, Schizophrenia, Diabetes mellitus type 2
Unreviewed: Depressed bipolar disorder, Laryngeal neoplasm, Triple negative breast cancer
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98
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|
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Potassium voltage-gated channel modifier subfamily G member 2 |
KCNF2, KV6.2 |
Curated: Amyotrophic lateral sclerosis, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Endometriosis, Insomnia, Major depressive disorder, Neurotic disorder, Obesity, Oligodendroglioma, Psychiatric disorders, Schizophrenia, Substance abuse
Unreviewed: Glioma
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99
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|
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Potassium voltage-gated channel modifier subfamily G member 3 |
KV10.1, KV6.3 |
Curated: Insomnia
Unreviewed: Brain disease, Brain neoplasms, Breast neoplasm, Carcinoma, Glioblastoma, Hirschsprung Disease, Imperforate anus, Prostatic hyperplasia, Prostatic neoplasm
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100
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|
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Potassium voltage-gated channel modifier subfamily G member 4 |
KV6.3, KV6.4 |
Curated: Alzheimer disease, Scoliosis
Unreviewed: Chronic Obstructive Pulmonary Disease, Complete Hydatidiform Mole, Hirschsprung Disease, Imperforate anus, Multiple sclerosis, Neurodegenerative disorder
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