171
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Potassium calcium-activated channel subfamily N member 3 |
KCa2.3, SK3, SKCA3, ZLS3, hSK3 |
Curated: 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 syndrome
Unreviewed: Anorexia, Atrial Fibrillation, Bipolar Disorder, Bladder carcinoma, Bladder Neoplasm, Breast Cancer, Breast Carcinoma, Breast neoplasm, Cardiomyopathy, Cerebellar atrophy, Cholangiocarcinoma, Ciliary dyskinesia, Common Migraine, Developmental disability, Diabetes Mellitus, Dilated cardiomyopathy, Gingival diseases, Hemiplegic migraine, Hereditary xerocytosis, Heterotaxy syndrome, Hirschsprung Disease, Hypertension, Hypertrichosis, Hypoxia, Intrahepatic Cholangiocarcinoma, Major Affective Disorder, Malignant Neoplasm, Melanoma, Migraine, Myotonic dystrophy, Nervous system disease, Nonorganic Psychosis, Ovarian cancer, Ovarian Epithelial carcinoma, Ovarian neoplasm, Paroxysmal atrial fibrillation, Portal Hypertension, Proliferative Diabetic Retinopathy, Psychosis, Schizoaffective Disorder, Sjogren syndrome, Urinary bladder cancer, Urinary bladder neoplasms, Urothelial Carcinoma, Ventricular dysfunction, Ventricular tachycardia, Vulval varices, Zimmerman Laband Syndrome
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172
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Potassium calcium-activated channel subfamily N member 4 |
DHS2, IK, IK1, IKCA1, KCA4, KCa3.1, SK4, SKCa4, hIK1, hIKCa1, hKCa4, hSK4 |
Curated: Breast cancer, Ischemic stroke, Cystic fibrosis, Hereditary xerocytosis, Estrogen-receptor negative breast cancer, Myocardial infarction, Xerocytosis
Unreviewed: Abetalipoproteinemia, Alzheimer disease, Androgen insensitivity syndrome, Anemia, Anorexia, Arthritis, Asthma, Atherosclerosis, Brachial plexus neuralgia, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinogenesis, Cardiovascular Diseases, Cerebral Infarction, Cerebrovascular disorder, Cirrhosis, Colonic neoplasm, Color Blindness, Colorectal Cancer, Colorectal neoplasm, Common variable immunodeficiency, Congestive Heart Failure, Conjunctival disease, Craniofacial Dysostosis, Crohn Disease, Cystic Fibrosis, Dehydrated Hereditary Stomatocytosis, Diabetes, Diabetes Mellitus, Eating Disorders, Edema, Endometrial Cancer, Endometrial carcinoma, Endometrial Neoplasms, Esophageal squamous cell carcinoma, Fatty Liver, Glioma, Glycogen storage disease, Hamartoma, Hemolytic anemia, Heparin cofactor 2 deficiency, Hepatocellular carcinoma, Hyperbilirubinemia, Hypertension, Hypoxia, Idiopathic pulmonary fibrosis, Inflammatory Bowel Disease, Intracranial hypertension, Liver carcinoma, Liver failure, Liver neoplasms, Lung carcinoma, Lung disease, Lymphoma, Lynch syndrome, Malignant Neoplasm, Melanoma, Myocardial Infarction, Neoplasms, Neuralgic Amyotrophy, Ovarian neoplasm, Pancreatic cancer, Pancreatic carcinoma, Pancreatic ductal carcinoma, Pancreatic neoplasm, Papillary thyroid cancer, Prostate cancer, Renal cell carcinoma, Renal fibrosis, Sjogren syndrome, Spastic paraplegia, Squamous cell carcinoma, Stomach neoplasms, Stroke, Syndromic microphthalmia, Triple negative breast cancer, Uterine neoplasm, Vascular Diseases, Vascular malformation, Venous thromboembolism
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173
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Potassium voltage-gated channel subfamily Q member 1 |
ATFB1, ATFB3, JLNS1, KCNA8, KCNA9, KVLQT1, Kv1.9, Kv7.1, LQT, LQT1, RWS, SQT2, WRS |
Curated: Cardiac arrhythmia, Atrial fibrillation, Beckwith-wiedemann syndrome, Biliary tract cancer, Breast cancer, Brugada syndrome, Cancer, 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 loss, 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, Diabetic nephropathy type 2, Polymorphic ventricular tachycardia, Wolff-parkinson-white syndrome
Unreviewed: Adenocarcinoma, Adrenocortical carcinoma, Andersen Syndrome, Andersen-tawil syndrome, Anemia, Arrhythmogenic right ventricular cardiomyopathy, Ataxia telangiectasia, Atrial Fibrillation, Atrioventricular block, Atrophy, Attention deficit hyperactivity disorder, Beckwith-Wiedemann Syndrome, Borderline personality disorder, Bradyarrhythmia, Brugada Syndrome, Carcinogenesis, Carcinoma, Cardiac arrhythmias, Cardiomyopathy, Cardiovascular disease, Cardiovascular Diseases, Cataract, Catecholaminergic polymorphic ventricular tachycardia, Clinodactyly, Colon Carcinoma, Colonic Neoplasms, Colorectal Cancer, Colorectal neoplasm, Complete Atrioventricular Block, Congenital disorder of glycosylation, Congenital Epicanthus, Congenital Hemihypertrophy, Congenital Long QT Syndrome, Congenital Microcephaly, Congenital omphalocele, Congenital Sensorineural Hearing Loss, Congestive Heart Failure, Coronary Heart Disease, Cryptorchidism, Cystic Fibrosis, Deafness, Development Disorder, Developmental Delay, Diabetes, Diabetes complications, Diabetes Mellitus, Diabetes mellitus, type 2, Diabetic Nephropathy, Diabetic Retinopathy, Diarrhea, Dilated cardiomyopathy, Dysautonomia, Ectodermal dysplasia, Endometriosis, Epilepsy, Gonadoblastoma, Gouty arthritis, Hearing Loss, Heart disease, Heart Diseases, Heart Failure, Hepatoblastoma, Hereditary bundle branch system defect, High palate, Hyperglycemia, Hyperinsulinism, Hyperparathyroidism, Hypoglycemia, Hypothyroidism, Hypotonia, Interstitial Cystitis, Intestinal Cancer, Intestinal Neoplasms, Iron deficiency anemia, Ischemic Stroke, Isolated Somatotropin Deficiency, Jervell-Lange Nielsen Syndrome, Kidney Disease, Kidney Failure, Left ventricular noncompaction, Leukemia, Liver carcinoma, Liver disease, Liver failure, Long QT Syndrome, LONG QT SYNDROME DIGENIC, Lung adenocarcinoma, Lung Cancer, Lung carcinoma, Lung Diseases, Lung neoplasms, Macroglossia, Major depressive disorder, Malignant gastrointestinal tract tumors, Malignant Neoplasm, Marfan Syndrome, Metabolic Syndrome, Microcephaly, Miscarriage, Mitochondrial disease, Mitochondrial encephalopathy, Multicystic renal dysplasia, Myocardial Infarction, Myofibrillar myopathy, Myotonic dystrophy, Neoplasms, Nephroblastoma, Nephrocalcinosis, Nephrolithiasis, Nervous System Disorder, Neural Tube Defect, Obesity, Osteosarcoma, Ovarian neoplasm, Pancreatic carcinoma, Pancreatic neoplasm, Paralysis, Paroxysmal ventricular fibrillation, Periodontitis, Phakomatosis pigmentovascularis, Primary microcephaly, Proptosis, Prostatic neoplasm, Pulmonary arterial hypertension, Renal cell carcinoma, Renal Insufficiency, Rhabdoid Tumor, Rheumatoid arthritis, Romano-Ward Syndrome, Rufous oculocutaneous albinism, Russell-Silver Syndrome, Schizophrenia, Seizures, Sensorineural hearing loss, Short QT Syndrome, Sick sinus syndrome, Sinus Node Dysfunction, Sleep apnea, Somatotropin Deficiency, Stomach Carcinoma, Stomach Neoplasms, Thromboembolic stroke, Timothy Syndrome, Torsades de Pointes, Trichohepatoenteric Syndrome, Ulcerative colitis, Ventricular arrhythmia, Ventricular dysfunction, Ventricular Fibrillation, Ventricular outflow obstruction, Ventricular tachycardia, Vesicoureteral Reflux, Vestibular disease, Wilms tumor, Wolff-Parkinson-White Syndrome
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174
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KCNQ1 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: Hyperuricemia, Jervell-Lange Nielsen Syndrome, Long QT Syndrome
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175
|
|
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KCNQ1 downstream neighbor |
BWRT, HSA404617 |
Curated: N/A
Unreviewed: Neoplasms, Renal Carcinoma, Wilms tumor
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176
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|
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KCNQ1 opposite strand/antisense transcript 1 |
KCNQ1-AS2, KCNQ10T1, Kncq1, KvDMR1, KvLQT1-AS, LIT1, NCRNA00012 |
Curated: N/A
Unreviewed: Adenocarcinoma Of Colon, Adenocarcinoma Of Rectum, Adrenocortical adenoma, Adrenocortical carcinoma, Angelman syndrome, Atherosclerosis, Atrial Fibrillation, Autism, Beckwith-Wiedemann Syndrome, Bladder carcinoma, Bladder Neoplasm, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinogenesis, Carcinoma, Cardiomyopathy, Cardiovascular Diseases, Cataract, Cholangiocarcinoma, Chronic obstructive pulmonary disease, Colon Carcinoma, Colonic neoplasm, Colonic Neoplasms, Colorectal Cancer, Colorectal neoplasm, Colorectal Neoplasms, Congenital Chromosomal Disease, Congenital Contractural Arachnodactyly, Congenital Hemihypertrophy, Congenital Long QT Syndrome, Congenital omphalocele, Coronary Arteriosclerosis, Coronary artery disease, Coronary Heart Disease, Cryptorchidism, Diabetes, Diabetes Mellitus, Diabetes mellitus, type 2, Diabetic cardiomyopathy, Diabetic Retinopathy, Ductal carcinoma, Embryonal Neoplasm, Esophageal Carcinoma, Esophageal squamous cell carcinoma, Esophagus Neoplasm, Gestational diabetes, Glioma, Gonadoblastoma, Heart disease, Heart failure, Hemihyperplasia, Hepatoblastoma, Hepatocellular carcinoma, Hyperinsulinemic hypoglycemia, Hypertension, Hypoglycemia, Intellectual developmental disorder, Intervertebral Disc Disorder, Jervell-Lange Nielsen Syndrome, Kidney Disease, Klippel-Trenaunay-Weber Syndrome, Leukemia, Leukocyte adhesion deficiency, Liver carcinoma, Liver Cirrhosis, Liver neoplasms, Long QT Syndrome, Lung adenocarcinoma, Lung Cancer, Lung carcinoma, Lymphatic Metastasis, Macroglossia, Malignant Neoplasm, Malignant Neoplasm Of Tongue, Melanoma, Meningomyelocele, Mental retardation, Multiple sclerosis, Myelodysplastic syndrome, Myocardial Infarction, Neoplasms, Nephroblastoma, Nephrocalcinosis, Nephrolithiasis, Neural Tube Defect, Neuroblastoma, Obesity, Osteoarthritis, Osteomyelitis, Osteoporosis, Osteosarcoma, Ovarian cancer, Ovarian Epithelial carcinoma, Ovarian neoplasm, Pancreatic cancer, Papillary thyroid cancer, Pelizaeus-Merzbacher disease, Phakomatosis pigmentovascularis, Pituitary neoplasm, Promyelocytic leukemia, Proptosis, Prostatic neoplasm, Respiratory Distress Syndrome, Russell-Silver Syndrome, Scoliosis, Squamous cell carcinoma, Stomach neoplasms, Syndromic microphthalmia, Tarsal-Carpal Coalition Syndrome, Tongue cancer, Tongue carcinoma, Torsades de pointes, Trichohepatoenteric Syndrome, Tumors Of Adrenal Cortex, Urinary bladder cancer, Ventricular dysfunction, Vesicoureteral Reflux, Wilms tumor
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177
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Potassium voltage-gated channel subfamily Q member 2 |
BFNC, DEE7, EBN, EBN1, ENB1, HNSPC, KCNA11, KV7.2 |
Curated: 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 syndrome, neonatal-onset developmental and epileptic encephalopathy, neonatal encephalopathy with non-epileptic myoclonus, complex neurodevelopmental disorder
Unreviewed: Absence epilepsy, Alternating hemiplegia of childhood, Amyotrophic lateral sclerosis, Aphasia, Apraxia, Autism Spectrum Disorder, Benign Epilepsy, Benign Rolandic Epilepsy, Benign seizures and/or myokomia, Bipolar Disorder, Blast crisis, Borderline personality disorder, Bradycardia, Brain malformation, Bronchopulmonary Dysplasia, Cardiomyopathy, Carpal tunnel syndrome, Cerebral Atrophy, Cerebral palsy, CHARGE Syndrome, Choreoathetosis, Clonic Seizures, Cognition disorder, Cognitive disorder, Colorectal neoplasm, Congenital adrenal hyperplasia, Continuous spike and waves during slow sleep, Convulsions, Cortical development malformation, Crohn Disease, Demyelinating diseases, Development Disorder, Developmental Delay, Diabetes mellitus, Down syndrome, Dysgraphia, Dyskinetic Syndrome, Dysmorphic Features, Dysphasia, Dystonia, Endometriosis, Epilepsy, Benign And/Or Myokymia, Epileptic encephalopathy, Episodic ataxia, Esophagus Neoplasm, Fabry disease, Febrile seizures, Focal Clonic Seizures, Fragile X Syndrome, Hallucinations, Hearing loss, Hypoplasia Of Corpus Callosum, Hypotonic seizures, Impaired Cognition, Infantile Spasms, Inflammatory Bowel Disease, Jacksonian Seizure, Language development disorders, Learning disorders, Long QT Syndrome, Major Affective Disorder, Mental retardation, Migraine, Migrating Partial Seizures In Infancy, Mitochondrial disease, Mitochondrial encephalopathy, Motor neuron disease, Movement Disorders, Myoclonic Encephalopathy, Myoclonic Epilepsy, Nervous System Disorder, Neurodegenerative disorder, Neurodevelopmental Disorders, Nocturnal Epilepsy, Paralysis, Paroxysmal extreme pain disorder, Partial epilepsy, Peripheral nervous system disease, Psychiatric disorders, Salaam Seizures, Seizure, Spasms X-Linked, Spastic tetraparesis, Sphingomyelinase deficiency, Status Epilepticus, Trichohepatoenteric Syndrome, Trigeminal neuralgia, Ulcerative colitis, Visual disorder, West Syndrome
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178
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|
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KCNQ2 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
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179
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|
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Potassium voltage-gated channel subfamily Q member 3 |
BFNC2, EBN2, KV7.3 |
Curated: 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 2, complex neurodevelopmental disorder, self-limited familial neonatal epilepsy, genetic developmental and epileptic encephalopathy
Unreviewed: Amyotrophic lateral sclerosis, Angelman Syndrome, Benign Epilepsy, Benign Rolandic Epilepsy, Bipolar Disorder, Borderline personality disorder, Brain disease, Bronchopulmonary Dysplasia, Carpal tunnel syndrome, Choreoathetosis, Convulsions, Coronary Arteriosclerosis, Development Disorder, Developmental Delay, Developmental disability, Diabetes Mellitus, Diabetic neuropathy, Dyskinetic Syndrome, Dysphasia, Epilepsy, Epileptic encephalopathy, Episodic ataxia, Fabry disease, Febrile seizures, Focal Clonic Seizures, Generalized Epilepsy With Febrile Seizures Plus, Hallucinations, Impaired Cognition, Learning disorders, Long QT Syndrome, Lymphatic metastasis, Mental retardation, Migraine, Migrating Partial Seizures In Infancy, Mood disorder, Mouth Abnormalities, Myocardial Ischemia, Myoclonic Epilepsy, Neurodevelopmental Disorders, Nocturnal Epilepsy, Paroxysmal extreme pain disorder, Peripheral nervous system disease, Photosensitive tonic-clonic seizures, Pulmonary arterial hypertension, Seizure, Status Epilepticus, Visual disorder
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180
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Potassium voltage-gated channel subfamily Q member 4 |
DFNA2, DFNA2A, KV7.4 |
Curated: Isolated sensorineural deafness, Nonsyndromic hearing loss, Colorectal cancer, Deafness, Hearing loss, Hereditary hearing loss, Inflammatory bowel disease, nonsyndromic genetic hearing loss
Unreviewed: Aortic aneurysm, Atrioventricular block, Atrophy, Branchiootic syndrome, Breast neoplasm, Cardiac arrhythmias, Classical Hodgkin lymphoma, Congenital diaphragmatic hernia, Diabetes mellitus, Dilated cardiomyopathy, Epilepsy, Hearing Impairment, Hearing Loss, Hyperkinesia, Irritable Bowel Syndrome, Jervell-Lange Nielsen Syndrome, Long QT Syndrome, Melnick-Fraser syndrome, Neuroblastoma, Non-Syndromic Sensorineural Deafness, Nonsyndromic Deafness, Polyneuropathy, Pulmonary arterial hypertension
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