61
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Kelch repeat and BTB domain containing 8 |
TA-KRP, TAKRP |
Curated: Alzheimer disease, Atherosclerosis, Color vision deficiency, Tourette syndrome, Migraine, Oligodendroglioma, Open angle glaucoma, Retinal detachment, Diabetes mellitus type 2
Unreviewed: Breast Cancer, Growth disorder, Mandibulofacial Dysostosis
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62
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- |
- |
Curated: N/A
Unreviewed: N/A
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63
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Potassium channel modulatory factor 1 |
DEBT91, FIGC, PCMF, ZZZ1 |
Curated: N/A
Unreviewed: Aneuploidy, Carcinogenesis, Carcinoma, Colon Carcinoma, Colonic Neoplasms, Colorectal neoplasm, Intellectual developmental disorder, Malignant Neoplasm, Mental retardation, Neoplasms, Pancreatic cancer, Pancreatic carcinoma, Renal cell carcinoma, Sarcoma, Squamous cell carcinoma, Stomach Neoplasms
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64
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|
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Potassium voltage-gated channel subfamily A member 1 |
AEMK, EA1, HBK1, HUK1, KV1.1, MBK1, MK1, RBK1 |
Curated: Color vision deficiency, Conduct disorder, Hereditary continuous muscle fiber activity, Dementia, Developmental and epileptic encephalopathy, Episodic ataxia, Episodic kinesigenic dyskinesia, Paroxysmal dystonic choreoathetosis, Paroxysmal dyskinesia, Paroxysmal nonkinesigenic dyskinesia, Schizophrenia, Scoliosis
Unreviewed: Acquired Kyphoscoliosis, Ataxia, Autism, Benign Epilepsy, Brain disease, Brain neoplasms, Breast Cancer, Breast Carcinoma, Carcinogenesis, Cataplexy, Cerebellar ataxia, Cerebellar atrophy, Cerebellar Diseases, Cervical Cancer, Cervical Tumor, Cervix carcinoma, Cholecystitis, Chorea, Choreoathetosis, Clonic Seizures, Colorectal neoplasm, Congenital diaphragmatic hernia, Congenital Exomphalos, Congenital kyphoscoliosis, Continuous Muscle Fiber Activity, Deafness, Developmental Delay, Developmental disability, Developmental regression, Dysarthria, Dyskinetic Syndrome, Dyspnea, Paroxysmal, Dyssomnia, Epilepsy, Epileptic encephalopathy, Episodic Kinesigenic Dyskinesia, Febrile seizures, Focal Seizures, Focal Sensory Seizure, Generalized Epilepsy With Febrile Seizures Plus, Hearing loss, Hereditary Continuous Muscle Fiber Activity, Huntington Disease, Hypocalcemia, Hypomagnesemia, Hypoplasia Of Corpus Callosum, Hypotonic seizures, Impaired Cognition, Isaacs Syndrome, Lymphatic metastasis, Lymphedema, Medulloblastoma, Mental retardation, Microcephaly, Migraine, Motor delay, Myokymia, Ovarian neoplasm, Pachygyria, Paroxysmal kinesigenic choreoathetosis, Paroxysmal Kinesigenic Dyskinesia, Partial epilepsy, Penis Agenesis, Precocious puberty, Pulmonary arterial hypertension, Renal dysplasia, Rheumatoid arthritis, Seizure, Seizures, Sleep Disorders, Specific Learning Disorder, Spinocerebellar Ataxia, Squamous cell carcinoma, Strabismus, Tetany, Ureterocele, Urinary bladder neoplasms, Ventricular septal defect, West Syndrome, Writer`s Cramp
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65
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|
|
Potassium voltage-gated channel subfamily A member 10 |
Kcn1, Kv1.8 |
Curated: Long qt syndrome
Unreviewed: Brain Neoplasms, Colorectal Cancer, Glioma, Neoplasms, Squamous cell carcinoma
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66
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|
|
Potassium voltage-gated channel subfamily A member 2 |
DEE32, EIEE32, HBK5, HK4, HUKIV, KV1.2, MK2, NGK1, RBK2 |
Curated: Developmental and epileptic encephalopathy, Global developmental delay, Intellectual developmental disorder, Language development disorders, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Prostate cancer, Seizures, genetic developmental and epileptic encephalopathy
Unreviewed: Ataxia, Attention Deficit Hyperactivity Disorder, Auditory processing disorder, Autism, Brain disease, Cerebellar ataxia, Cerebellar diseases, Cerebral Atrophy, Clonic Seizures, Congestive Heart Failure, Developmental Delay, Developmental disability, Developmental regression, Dwarfism, Dyskinetic Syndrome, Epilepsy, Epileptic encephalopathy, Episodic Ataxia, Gastroesophageal Reflux Disease, Growth disorder, Heart Failure, Henoch-Schonlein Nephritis, Hereditary spastic paraplegia, Hypodontia, Hypotonic seizures, Impaired Cognition, Jacksonian Seizure, Language Development Disorders, Liver carcinoma, Malignant Bone Neoplasm, Mental retardation, Microcephaly, Movement disorder, Movement Disorders, Myoclonic Epilepsy, Nervous system disease, Neurodevelopmental Disorders, Non-Specifi Epileptic Encephalopathy, Nystagmus, Optic Atrophy, Patent ductus arteriosus, Periodontitis, Ptosis, Rett Syndrome, Seizure, Spastic paraplegia, Speech Delay, Status Epilepticus, Ventricular arrhythmia
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67
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|
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Potassium voltage-gated channel subfamily A member 3 |
HGK5, HLK3, HPCN3, HUKIII, KV1.3, MK3, PCN3 |
Curated: Lymphoblastic leukemia, Neurodevelopmental disorder, Panic disorder, Prostate cancer
Unreviewed: Alzheimer disease, Ataxia telangiectasia, Atherosclerosis, Autoimmune disease, Autoimmune Diseases, Autoimmune pancreatitis, Breast neoplasm, Colorectal Cancer, Colorectal neoplasm, Coronary restenosis, Crohn disease, Demyelinating diseases, Diabetes mellitus, type 1, Down Syndrome, Glioma, Granulomatosis with polyangiitis, Head and neck neoplasm, Hepatocellular carcinoma, Hyperplasia, Hypertension, Hypoxia, Immune system disease, Intermittent Porphyria, Lupus Erythematosus, Lymphatic Metastasis, Lymphoma, Multiple myeloma, Multiple Sclerosis, Neoplasms, Obesity, Parathyroid Gland Adenocarcinoma, Parathyroid neoplasm, Periodontitis, Psoriasis, Systemic lupus erythematosus, Ulcerative colitis, Vascular disease, Vascular system injury, Warburg micro syndrome
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68
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|
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Potassium voltage-gated channel subfamily A member 4 |
HBK4, HK1, HPCN2, HUKII, KCNA4L, KCNA8, KV1.4, MCIDDS, PCN2 |
Curated: Microcephaly, Preeclampsia
Unreviewed: Arthritis, Breast neoplasm, Cardiac arrhythmias, Congenital Long QT Syndrome, Dwarfism, Dysarthria, Epilepsy, Glioma, Graves ophthalmopathy, Hypothyroidism, Long QT Syndrome, Malignant Neoplasm, Microcystic meningioma, Motor delay, Pulmonary arterial hypertension, Rheumatoid arthritis, Romano-Ward Syndrome, Torsades de Pointes, Ventricular Fibrillation
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69
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Potassium voltage-gated channel subfamily A member 5 |
ATFB7, HCK1, HK2, HPCN1, KV1.5, PCN1 |
Curated: Atrial fibrillation, Neoplasms, Cardiac arrhythmia, Color vision deficiency, Atrioventricular block, Conduct disorder, Heart disease, Hereditary atrial fibrillation, Pulmonary hypertension, Mouth neoplasms, Nephrotic syndrome, Pulmonary arterial hypertension, Schizophrenia, Scoliosis
Unreviewed: Astrocytoma, Atrial Fibrillation, Atrial flutter, Benign Hereditary Chorea, Breast Cancer, Breast Carcinoma, Carcinogenesis, Carcinoma, Cardiac arrhythmias, Chorea, Choreoathetosis, Colon Carcinoma, Colonic Neoplasms, Colorectal Cancer, Colorectal neoplasm, Congenital Long QT Syndrome, Coronary artery disease, Coronary restenosis, Endometrial neoplasm, Episodic ataxia, Episodic Kinesigenic Dyskinesia, Ewing sarcoma, Glioblastoma, Glioma, Head and neck cancer, Head And Neck Carcinoma, Heart valve disease, Hepatocellular carcinoma, Huntington Disease, Hyperplasia, Hypertension, Hypoxia, Inflammatory bowel disease, Liver carcinoma, Long QT Syndrome, Lung carcinoma, Malignant Neoplasm, Myeloid leukemia, Oligodendroglioma, Osteosarcoma, Parkinson disease, Paroxysmal atrial fibrillation, Paroxysmal kinesigenic choreoathetosis, Pelvic Organ Prolapse, Polycystic ovary syndrome, Prostate cancer, Pulmonary Hypertension, Rheumatic Heart Disease, Romano-Ward Syndrome, Sarcoma, Scleroderma, Sleep apnea, Stomach Neoplasms, Systemic sclerosis, Torsades de Pointes, Vascular disease, Ventricular Fibrillation
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70
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|
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Potassium voltage-gated channel subfamily A member 6 |
HBK2, KV1.6, PPP1R96 |
Curated: Cerebellar ataxia, Neurodevelopmental disorder, Congenital epicanthus, Esophageal atresia, Seizures, Hyperopia, Non-specific syndromic intellectual disability
Unreviewed: Benign Hereditary Chorea, Chorea, Choreoathetosis, Developmental disability, Epilepsy, Episodic ataxia, Episodic Kinesigenic Dyskinesia, Heart disease, Hemolysis, Huntington Disease, Microcephaly, Paroxysmal kinesigenic choreoathetosis, Pulmonary arterial hypertension
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