101
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|
|
Potassium calcium-activated channel subfamily N member 2 |
DYT34, KCa2.2, NEDMAB, SK2, SKCA2, SKCa 2, hSK2 |
Alzheimer disease, Cardiac arrhythmias, Atrial fibrillation, Autism, Bipolar disorder, Hepatocellular carcinoma, Cardiac arrest, Cardiac arrhythmia, Cardioembolic stroke, Cardiovascular disease, Cerebellar ataxia, Congenital heart disease, Coronary aneurysm, Dyskinesia, Dystonia, Edema, Global developmental delay, Congenital heart septal defect, Intellectual developmental disorder, Juvenile idiopathic arthritis, Major depressive disorder, Intellectual disability, Neurodevelopmental disorder, Obesity, Psoriasis, Schizophrenia, Stroke, Diabetes mellitus type 1, Diabetes mellitus type 2View all (14 more) |
102
|
|
|
Potassium calcium-activated channel subfamily N member 3 |
KCa2.3, SK3, SKCA3, ZLS3, hSK3 |
Alzheimer disease, Atrial fibrillation, Atrial flutter, Bipolar disorder, Cardiac arrhythmia, Cardiac embolism, Cardioembolic stroke, Central nervous system cancer, Cholecystolithiasis, Paranoid schizophrenia, Dyslexia, Esophageal atresia, Glaucoma, Glioblastoma, Glioma, Obesity, Schizophrenia, Parkinson disease, Proliferative diabetic retinopathy, Prostate cancer, Squamous cell carcinoma, Zimmermann-laband syndromeView all (7 more) |
103
|
|
|
Potassium calcium-activated channel subfamily N member 4 |
DHS2, IK, IK1, IKCA1, KCA4, KCa3.1, SK4, SKCa4, hIK1, hIKCa1, hKCa4, hSK4 |
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104
|
|
|
Potassium voltage-gated channel subfamily Q member 1 |
ATFB1, ATFB3, JLNS1, KCNA8, KCNA9, KVLQT1, Kv1.9, Kv7.1, LQT, LQT1, RWS, SQT2, WRS |
Cardiac arrhythmias, Atrial fibrillation, Beckwith-wiedemann syndrome, Biliary tract cancer, Breast cancer, Brugada syndrome, Cancer, Cardiac arrhythmia, Cardiovascular abnormalities, Cervical cancer, Kidney disease, Clear cell renal cell carcinoma, Color vision deficiency, Colorectal cancer, Conduction disorder of the heart, Congenital ear anomaly, Congenital short qt syndrome, Coronary artery disease, Diabetes mellitus, Diabetes mellitus type 2, Diabetic eye disease, Diabetic neuropathy, Diabetic polyneuropathy, Diabetic retinopathy, Endometrial cancer, Esophageal cancer, Estrogen-receptor negative breast cancer, Long qt syndrome, Gastric cancer, Gestational diabetes, Gout, Hearing impairment, Hepatocellular carcinoma, Hereditary atrial fibrillation, Hypertrophic cardiomyopathy, Hyperuricemia, Intestinal neoplasms, Jervell and lange-nielsen syndrome, Kidney cancer, Long qt syndrome, digenic, Lung cancer, Metabolic syndrome, Non-hodgkins lymphoma, Ovarian cancer, Ovarian serous carcinoma, Pancreatic cancer, Paroxysmal atrial fibrillation, Prostate cancer, Short qt syndrome, Squamous cell carcinoma, Stroke, Hypertension, Diabetes mellitus type 1, Type 2 diabetes nephropathy, Polymorphic ventricular tachycardia, Wolff-parkinson-white syndromeView all (41 more) |
105
|
|
|
Potassium voltage-gated channel subfamily Q member 2 |
BFNC, DEE7, EBN, EBN1, ENB1, HNSPC, KCNA11, KV7.2 |
Alzheimer disease, Autism, Nonsyndromic intellectual disability, Benign infantile epilepsy, Benign neonatal-infantile seizures, Benign neonatal epilepsy, Bipolar disorder, Brain disease, Neurodevelopmental disorder, Congenital epicanthus, Developmental and epileptic encephalopathy, Developmental disability, Epilepsy, Epilepsy of infancy with migrating focal seizures, Global developmental delay, Intellectual developmental disorder, Major depressive disorder, Malignant migrating partial seizures of infancy, Nervous system disease, Non-specific syndromic intellectual disability, Schizophrenia, Seizures, West syndromeView all (8 more) |
106
|
|
|
Potassium voltage-gated channel subfamily Q member 3 |
BFNC2, EBN2, KV7.3 |
Autism, Benign infantile epilepsy, Benign neonatal epilepsy, Bipolar disorder, Neurodevelopmental disorder, Developmental and epileptic encephalopathy, Differentiated thyroid carcinoma, Rolandic epilepsy, Insomnia, Intellectual developmental disorder, Myoclonic epilepsy, Major depressive disorder, Nonalcoholic fatty liver disease, Non-specific syndromic intellectual disability, Schizophrenia, Seizures, Intellectual disability, Diabetes mellitus type 2View all (3 more) |
107
|
|
|
Potassium voltage-gated channel subfamily Q member 4 |
DFNA2, DFNA2A, KV7.4 |
|
108
|
|
|
Potassium voltage-gated channel subfamily Q member 5 |
Kv7.5, MRD46 |
Angioedema, Nonsyndromic intellectual disability, Cataract, Central nervous system cancer, Obstructive pulmonary disease, Color vision deficiency, Eye disease, Glioblastoma, Glioma, Global developmental delay, Hyperopia, Insomnia, Intellectual developmental disorder, Major depressive disorder, Metabolic syndrome, Myopia, Periodontitis, Primary angle closure glaucoma, Proliferative diabetic retinopathy, Schizophrenia, Diabetes mellitus type 2View all (6 more) |
109
|
|
|
Potassium voltage-gated channel modifier subfamily S member 1 |
Kv9.1, hKv9.1 |
|
110
|
|
|
Potassium voltage-gated channel modifier subfamily S member 3 |
KV9.3 |
Amyotrophic lateral sclerosis, Autism, Breast cancer, Obstructive pulmonary disease, Colorectal cancer, Conotruncal cardiac defect, Coronary artery disease, Gout, Ovarian epithelial cancer, Colorectal adenoma, Multinodular goiter, Oligodendroglioma, Ovarian cancer, Parkinson disease, Peptic ulcer disease, Schizophrenia, Scoliosis, Diabetes mellitus type 2View all (3 more) |
