151
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Potassium two pore domain channel subfamily K member 2 |
K2p2.1, TPKC1, TREK, TREK-1, TREK1, hTREK-1c, hTREK-1e |
Curated: Anhedonia, Breast cancer, Color vision deficiency, Major depressive disorder, Estrogen-receptor negative breast cancer
Unreviewed: Allergic rhinitis, Alzheimer disease, Amyotrophic Lateral Sclerosis, Atrial Fibrillation, Atrophy, Benign Prostatic Hyperplasia, Bipolar disorder, Bladder neck obstruction, Brain ischemia, Cardiac arrhythmias, Cerebral Infarction, Cerebral Ischemia, CNS Disorder, Cognition disorder, Congestive Heart Failure, Endometrial neoplasm, Epilepsy, Gestational diabetes, Heart Failure, Hepatocellular carcinoma, Impaired Cognition, Liver carcinoma, Liver cirrhosis, Malignant Neoplasm, Melancholia, Mental Depression, Migraine, MOHR-TRANEBJAERG SYNDROME, Myocardial Infarction, Neoplasms, Overactive bladder, Pancreatic cancer, Pancreatic carcinoma, Prostate cancer, Status Epilepticus, Stroke, Syndromic microphthalmia, Vascular dementia, Ventricular tachycardia
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152
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Potassium two pore domain channel subfamily K member 3 |
K2p3.1, OAT1, PPH4, TASK, TASK-1, TASK1, TBAK1 |
Curated: Cardiovascular disease, Cerebrovascular disorder, Corneal astigmatism, Coronary artery disease, Diverticular disease, Hypertension, Pulmonary hypertension, Heart failure, Pulmonary arterial hypertension, Major depressive disorder, Metabolic syndrome, Osteoarthritis, Potassium deficiency, Sarcoidosis, Stroke, Diabetes mellitus type 2
Unreviewed: Adenoma, Atrial Fibrillation, Basal cell carcinoma, Breast neoplasm, Cerebral Infarction, Cervical Cancer, Cervical Tumor, Cervix carcinoma, Cholelithiasis, Chronic Obstructive Pulmonary Disease, Congenital Long QT Syndrome, Congestive Heart Failure, Conn Syndrome, Cystic Fibrosis, Developmental disability, Diabetes Mellitus, Diverticular Diseases, Epilepsy, Heart Failure, Hereditary Hemorrhagic Telangiectasia, Heritable Pulmonary Arterial Hypertension, Hyperaldosteronism, Hyperuricemia, Hypocholesterolemia, Hypoxia, Ischemic Stroke, Long QT Syndrome, Lung adenocarcinoma, Lung Cancer, Lung carcinoma, Lung disease, Lymphedema, Lymphocytic Leukemia, Malignant Neoplasm, Motor neuron atrophy, Multiple Sclerosis, Obesity, Oligospermia, Periapical Periodontitis, Pulmonary Hypertension, Pulmonary Hypertension With Hereditary Hemorrhagic Telangiectasia, Pulmonary venoocclusive disease, Romano-Ward Syndrome, Skin neoplasm, Sleep Apnea, Squamous cell carcinoma, Torsades de Pointes, Ventricular Fibrillation, Ventricular hypertrophy
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153
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Potassium two pore domain channel subfamily K member 4 |
FHEIG, K2p4.1, TRAAK, TRAAK1 |
Curated: Facial dysmorphism syndrome, Intellectual developmental disorder
Unreviewed: Brachydactyly, Breast neoplasm, Camptodactyly of fingers, Developmental disability, Epilepsy, Facial dysmorphism, Gingival diseases, Hirschsprung Disease, HYPERTRICHOSIS, Imperforate anus, Macrostomia, Mental retardation, Micrognathism, Motor delay, Nystagmus, Synophrys, Zimmerman Laband Syndrome
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154
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KCNK4-CATSPERZ readthrough (NMD candidate) |
KCNK4-TEX40 |
Curated: N/A
Unreviewed: N/A
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155
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|
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Potassium two pore domain channel subfamily K member 5 |
K2p5.1, KCNK5b, TASK-2, TASK2 |
Curated: Eczema, Cardiovascular disease, Coronary artery disease, Eating disorder, Gout, Hypertension, Major depressive disorder, Migraine, Myocardial infarction, Nephrolithiasis, Obesity, Open angle glaucoma, Pancreatic cancer, Status epilepticus, Diabetes mellitus type 2, Urolithiasis, Vascular dementia
Unreviewed: Autoimmune Diseases, Balkan Nephropathy, Breast Cancer, Breast Carcinoma, Breast neoplasm, Congenital Central Hypoventilation, Conn Adenoma, Conn Syndrome, Coronary Heart Disease, Dyslipidemias, Epilepsy, Grand Mal Status Epilepticus, Intracranial aneurysm, Kidney Disease, Multiple Sclerosis, Myeloid Leukemia, Nonconvulsive status epilepticus, Petit Mal Status, Psychosis, Rheumatoid arthritis, Schizophrenia, Status Epilepticus, Urinary bladder neoplasms
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156
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Potassium two pore domain channel subfamily K member 6 |
K2p6.1, KCNK8, TOSS, TWIK-2, TWIK2 |
Curated: Focal segmental glomerulosclerosis
Unreviewed: Asthma, Atrophy, Endometrial neoplasm, Lung disease, Pulmonary arterial hypertension, Sarcoma, Sickle cell anemia
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157
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Potassium two pore domain channel subfamily K member 7 |
K2p7.1, TWIK3 |
Curated: Diabetes mellitus type 2
Unreviewed: Asthma, Atrial Fibrillation
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158
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|
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Potassium two pore domain channel subfamily K member 9 |
BIBARS, K2p9.1, KT3.2, TASK-3, TASK3, TASK32 |
Curated: Anxiety disorder, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Birk-barel syndrome, Color vision deficiency, Colorectal cancer, Dementia, Developmental disability, Absence epilepsy, Major depressive disorder, Mood disorder, Obesity, Psychiatric disorders, Schizophrenia, Scoliosis, Uterine fibroid
Unreviewed: Absence Seizure, Akinetic Petit Mal, Atrial Fibrillation, Basal cell carcinoma, Birk-Barel syndrome, Breast Cancer, Breast Carcinoma, Choroid Plexus Papilloma, Colorectal Cancer, Colorectal Neoplasms, Congenital finger flexion contractures, Conn Syndrome, Coronary artery disease, Development Disorder, Developmental Delay, Dolichocephaly, Dysphagia, Epilepsy, Glioblastoma, Hepatocellular carcinoma, High palate, Hyperaldosteronism, Hypertension, Hypotonia, Infertility, Liver carcinoma, Malignant Neoplasm, Mammary Neoplasms, Melanoma, Mental Depression, Mental retardation, Micrognathism, Mood Disorder, Motor nerve neuritis, Neoplasms, Pulmonary arterial hypertension, Skin neoplasm, Sleep apnea, Spinal Muscular Atrophy, Stomach Carcinoma, Stomach Neoplasms, Submucous cleft of soft and hard palate, Teratozoospermia, Tourette Syndrome, Ulcerative colitis
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159
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Potassium calcium-activated channel subfamily M alpha 1 |
BKTM, CADEDS, IEG16, KCa1.1, LIWAS, MaxiK, PNKD3, SAKCA, SLO, SLO-ALPHA, SLO1, bA205K10.1, hSlo, mSLO1 |
Curated: Alzheimer disease, Androgenetic alopecia, Angioedema, Autism, Bell's palsy, Bone disease, Renal cell carcinoma, Cerebellar atrophy with seizures and variable developmental delay, Color vision deficiency, Generalized epilepsy, Idiopathic generalized epilepsy, Eye disease, Gingival diseases, Global developmental delay, Growth disorder, Pulmonary hypertension, Hypospadias, Intellectual developmental disorder, Lung cancer, Metabolic bone disorder, Metabolic syndrome, Obesity, Nonalcoholic fatty liver disease, Non-melanoma skin carcinoma, Osteoarthritis, Osteonecrosis, Paroxysmal nonkinesigenic dyskinesia, Willis-ekbom disease, Schizophrenia, Spastic ataxia, Status epilepticus, Diabetes mellitus type 2, generalized epilepsy-paroxysmal dyskinesia syndrome
Unreviewed: Abducens palsy, Amnesia, Aphasia, Apraxia, Arthritis, Asymmetric crying face association, Ataxia, Atrophy, Autism Spectrum Disorder, Benign Prostatic Hyperplasia, Bilateral convulsive seizures, Blast crisis, Breast Cancer, Breast Carcinoma, Breast neoplasm, Cardiomyopathy, Cardiovascular Diseases, Cataplexy, Cerebellar atrophy, Cerebellar Atrophy, Developmental Delay, And Seizures, Cerebellar diseases, Cervical Intraepithelial Neoplasia, Chondrosarcoma, Chorea, Chromophobe Carcinoma, Chronic Obstructive Pulmonary Disease, Cognition disorder, Colonic neoplasm, Colorectal Cancer, Congenital abnormalities, Congenital Epicanthus, Congenital Malformation Syndrome, Connective tissue disease, Coronary artery disease, Craniosynostosis, Development Disorder, Developmental and epileptic encephalopathy, Developmental Delay, Developmental disability, Diabetes, Diabetes Mellitus, Diabetes mellitus transient neonatal, Diabetes mellitus, type 1, Dilated cardiomyopathy, Dysarthria, Dyskinesia, Dyskinetic Syndrome, Dystonia, Endometrial Cancer, Endometrial carcinoma, Endometrial neoplasm, Epilepsy, Epilepsy-Paroxysmal Dyskinesia Syndrome, Epiretinal Membrane, Epithelial ovarian carcinoma, Erectile Dysfunction, Esophageal squamous cell carcinoma, Esotropia, Fabry disease, Facial dysmorphism syndrome, Fundus Albipunctatus, Generalized Epilepsy and Paroxysmal Dyskinesia, Glioblastoma, Glioma, Grand Mal Status Epilepticus, Granulomatous Disease, Heart disease, Hydronephrosis, Hyperplasia, Hypertension, Hypoglycemia, Hypotonic seizures, Hypoxia, Immunologic Deficiency Syndromes, Impaired Cognition, Kidney Disease, Kidney Failure, Language development disorders, Laryngomalacia, Lung adenocarcinoma, Macular degeneration, Malignant Neoplasm, Melanoma, Meningioma, Mental Disorders, Mental retardation, Mesothelioma, Metabolic Bone Disorder, Movement disorder, Movement Disorders, Moyamoya disease, Multiple Sclerosis, Myocardial Infarction, Myopia, Myotonic dystrophy, Neoplasms, Nervous system disease, Neurodegenerative Disorders, Neurodevelopmental Disorders, Neuronal Ceroid Lipofuscinosis, Neutropenia, Nonconvulsive status epilepticus, Nystagmus, Osteopenia, Osteoporosis, Osteosarcoma, Ovarian cancer, Ovarian Epithelial carcinoma, Ovarian neoplasm, Ovarian serous adenocarcinoma, Papillary Renal Carcinoma, Parkinson disease, Petit Mal Status, Poikiloderma With Neutropenia, Progeria, Prostate cancer, Prostatic neoplasm, Prostatic Neoplasms, Pseudohypoaldosteronism, Pulmonary arterial hypertension, Pulmonary Cystic Fibrosis, Pulmonary Fibrosis, Renal Carcinoma, Rhabdoid Tumor, Rheumatoid arthritis, Seizure, Seizures, Septicemia, Smith-Lemli-Opitz Syndrome, Status Epilepticus, Stomach Carcinoma, Stomach Neoplasms, Stroke, Ulcerative colitis, Upgaze palsy, Vascular Diseases, Visual disorder
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160
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KCNMA1 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: Abducens palsy, Asymmetric crying face association, Cataplexy, Congenital Epicanthus, Generalized Epilepsy and Paroxysmal Dyskinesia, Hydronephrosis, Hypoglycemia, Hypospadias, Hypotonic seizures, Impaired Cognition, Laryngomalacia, Mental retardation, Myopia, Ovarian cancer, Ovarian Epithelial carcinoma, Upgaze palsy
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