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121
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|
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Potassium voltage-gated channel subfamily D member 3 |
BRGDA9, KCND3L, KCND3S, KSHIVB, KV4.3, SCA19, SCA22 |
Atrial fibrillation, Atrioventricular block, Brugada syndrome, Bundle branch block, Cardiac conduction disease, Cerebellar ataxia, Cerebellar atrophy, Colorectal cancer, Dysarthria, Dysphagia, Nystagmus, Paroxysmal atrial fibrillation, Paroxysmal ventricular tachycardia, Prostate cancer, Sick sinus syndrome, Sinus node dysfunction, Spinocerebellar ataxia, Supraventricular tachycardia, Trifascicular block, Ventricular fibrillationView all (5 more) |
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122
|
|
|
Potassium voltage-gated channel subfamily E regulatory subunit 1 |
ISK, JLNS, JLNS2, LQT2/5, LQT5, MinK |
Atrial fibrillation, Cardiomyopathy, Catecholaminergic polymorphic ventricular tachycardia, Congenital long qt syndrome, Congenital sensorineural hearing loss, Dysautonomia, Iron deficiency anemia, Jervell-lange nielsen syndrome, Long qt syndrome, Malignant neoplasm, Romano-ward syndrome, Sensorineural hearing loss, Torsades de pointes, Ventricular fibrillation |
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123
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|
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Potassium voltage-gated channel modifier subfamily G member 1 |
K13, KCNG, KV6.1, kH2 |
|
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124
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|
|
Potassium voltage-gated channel subfamily H member 1 |
EAG, EAG1, K(V)10.1, Kv10.1, TMBTS, ZLS1, h-eag, hEAG, hEAG1 |
Aneurysm of aortic arch, Breast cancer, Mammary neoplasms, Breast carcinoma, Cardiomyopathy, Cataract, Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Congenital epicanthus, Congenital exomphalos, Developmental delay, Epilepsy, Hearing loss, High palate, Hypodontia, Mental retardation, Leukemia, Lung carcinoma, Lung adenocarcinoma, Macroglossia, Macrostomia, Malocclusion, Marfan syndrome, Micrognathism, Myopia, Neurodevelopmental disorders, Osteosarcoma, Ovarian neoplasm, Ovarian serous adenocarcinoma, Ovarian endometrioid carcinoma, Patent ductus arteriosus, Posteriorly rotated ear, Prostate cancer, Scoliosis, Spina bifida occulta, Synophrys, Temple-baraitser syndrome, Zimmerman laband syndromeView all (24 more) |
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125
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|
|
Potassium voltage-gated channel subfamily H member 2 |
ERG-1, ERG1, H-ERG, HERG, HERG1, Kv11.1, LQT2, SQT1 |
Atrial fibrillation, Atrioventricular block, Benign neoplasm, Brugada syndrome, Cardiomyopathy, Colonic neoplasms, Congenital long qt syndrome, Dysautonomia, Dysmorphic features, Long qt syndrome, Long qt syndrome digenic, Malignant neoplasm, Multiple congenital anomalies, Neoplasms, Nonorganic psychosis, Obesity, Paroxysmal atrial fibrillation, Paroxysmal ventricular tachycardia, Psychosis, Romano-ward syndrome, Schizophrenia, Short qt syndrome, Torsades de pointes, Ventricular fibrillationView all (9 more) |
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126
|
|
|
Potassium inwardly rectifying channel subfamily J member 1 |
KIR1.1, ROMK, ROMK1 |
Amelogenesis imperfecta, Antenatal bartter syndrome, Bartter syndrome, Breast cancer, Chondrocalcinosis, Developmental delay, Dwarfism, Frontal bossing, Hyperaldosteronism, Hypertension, Hypochloremia, Hypokalemia, Macrocephaly, Macrotia, Mental retardation, Nephrocalcinosis, OsteopeniaView all (2 more) |
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127
|
|
|
Potassium inwardly rectifying channel subfamily J member 2 |
ATFB9, HHBIRK1, HHIRK1, IRK1, KIR2.1, LQT7, SQT3 |
Andersen syndrome, Andersen tawil syndrome, Arsenic encephalopathy, Atrial fibrillation, Atrioventricular block, Blepharophimosis, Brachydactyly, Camptodactyly of fingers, Catecholaminergic polymorphic ventricular tachycardia, Dental enamel hypoplasia, Dermatologic disorders, High palate, Hypodontia, Hypokalemic periodic paralysis, Hypoplasia of the maxilla, Mental depression, Microcephaly, Oligodontia, Paroxysmal atrial fibrillation, Periodic hypokalemic paresis, Periodic paralysis, Scoliosis, Short qt syndrome, Supraventricular tachycardia, Syndactyly of the toes, Ventricular fibrillation, Ventricular tachycardiaView all (12 more) |
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128
|
|
|
Potassium inwardly rectifying channel subfamily J member 3 |
GIRK1, KGA, KIR3.1 |
|
|
129
|
|
|
Potassium inwardly rectifying channel subfamily J member 4 |
HIR, HIRK2, HRK1, IRK-3, IRK3, Kir2.3 |
|
|
130
|
|
|
Potassium inwardly rectifying channel subfamily J member 5 |
CIR, GIRK4, KATP1, KIR3.4, LQT13 |
Adenoma, Hyperaldosteronism, Adrenal hyperplasia, Adrenocortical adenoma, Andersen syndrome, Andersen tawil syndrome, Atrial fibrillation, Atrioventricular block, Congenital adrenal hyperplasia, Congestive heart failure, Coronary arteriosclerosis, Dysautonomia, Glucocortocoid-insensitive hyperaldosteronism, Heart block, Hypertension, Left ventricular hypertrophy, Long qt syndrome, Metabolic alkalosis, Papillary adenoma, Paroxysmal atrial fibrillation, Romano-ward syndrome, Sick sinus syndrome, Sinus node dysfunction, Torsades de pointesView all (9 more) |
