391
|
|
|
Calcium voltage-gated channel subunit alpha1 A |
APCA, BI, CACNL1A4, CAV2.1, DEE42, EA2, EIEE42, FHM, HPCA, MHP, MHP1, SCA6 |
Curated: Alzheimer disease, Amyotrophic lateral sclerosis, Ataxia, Spinocerebellar ataxia, Auditory neuropathy, Benign paroxysmal torticollis of infancy, Bipolar disorder, Bulbar palsy, Cannabis abuse, Cerebellar ataxia, Cerebellar atrophy, Cerebral palsy, Chorea, Kidney disease, Color vision deficiency, Congenital neurologic anomalies, Cyclin-dependent kinase-like 5 deficiency, Vascular dementia, Developmental and epileptic encephalopathy, Dysarthria, Endometriosis, Absence epilepsy, Generalized epilepsy, Episodic ataxia, Gastroesophageal reflux disease, Global developmental delay, Gross motor development delay, Hemiplegic migraine, Intellectual developmental disorder, Lennox-gastaut syndrome, Major depressive disorder, Migraine, Neurodevelopmental disorder, Non-small cell lung carcinoma, Spastic ataxia, Strabismus, Substance abuse
Unreviewed: Absence Seizure, Adrenal Hypoplasia, X-Linked, Akinetic Petit Mal, Alagille Syndrome, Alternating Hemiplegia, Amyloidosis, Amyotrophic Lateral Sclerosis, Anxiety Disorder, Aphasia, Ataxia telangiectasia, Atrophy, Attention Deficit Hyperactivity Disorder, Autism, Autism Spectrum Disorder, Autoimmune Diseases, Benign Hereditary Chorea, Benign Paroxysmal Torticollis, Bipolar Disorder, Bladder carcinoma, Bladder Neoplasm, Blepharospasm, Brain disease, Brain edema, Brainstem Atrophy, Cadasil, CADASIL Syndrome, Calcium metabolism disorders, Cerebellar Ataxia, Cerebellar Diseases, Cerebellar Hypoplasia, Cerebral Atrophy, Choreoathetosis, Chronobiology disorder, Cognition disorder, Common Migraine, Congenital abnormalities, Congenital adrenal hypoplasia, Congenital disorder of glycosylation, Congenital hyperinsulinism, Craniocerebral trauma, CSF pleocytosis, Dentatorubral Pallidoluysian Atrophy, Developmental Delay, Developmental disability, Developmental regression, Diabetes Mellitus, Diabetes mellitus, type 1, Diastrophic dysplasia, Disorders of sex development, Dwarfism, Dyscalculia, Dyskinetic Syndrome, Dysmorphic Features, Dysphagia, Dysphasia, Dystonia, Ectodermal dysplasia, Epilepsy, Epilepsy And Migraine, Epileptic encephalopathy, Episodic Kinesigenic Dyskinesia, Esotropia, Exfoliation Syndrome, Febrile seizures, Friedreich Ataxia, Gastroesophageal Reflux Disease, Growth disorder, Guillain-Barre Syndrome, Hearing Loss, Heart disease, Hemiplegia, Hemiplegia/hemiparesis, Hemiplegic Migraine, Huntington Disease, Huntington Disease-Like, Hypercholesterolemia, Hyperopia, Hyperphenylalaninemia, Hypertension, Hypodontia, Impaired Cognition, Ischemic Stroke, Lambert-Eaton Myasthenic Syndrome, Learning disorders, Leiomyoma, Lennox-Gastaut Syndrome, Lung carcinoma, Lung Neoplasms, Lymphedema, Microcephaly And Chorioretinopathy Syndrome, Machado-Joseph Disease, Malan Overgrowth Syndrome, Marie Cerebellar Ataxia, Melanoma, Mental Depression, Mental retardation, Microcephaly, Migraine with Aura, Migraine, sporadic hemiplegic, Mitochondrial Diseases, Motor Disorders, Movement disorder, Movement Disorders, Multiple Congenital Anomalies, Myelodysplastic Syndrome, Myoclonic Epilepsy, Myotonic dystrophy, Neoplasms, Nervous System Disorder, Neurodegenerative Disorders, Neurodevelopmental Disorders, Non-Specifi Epileptic Encephalopathy, Nyctalopia, Nystagmus, Olivopontocerebellar Atrophies, Optic Atrophy, Ovarian neoplasm, Paranoia, Paresis, Parkinson disease, Paroxysmal Ataxia, Paroxysmal kinesigenic choreoathetosis, Peripheral nervous system disease, Phenylketonuria, Prostatic neoplasm, Psoriasis, Psychosis, Psychotic disorders, Ptosis, Retinitis Pigmentosa, Rett Syndrome, Rubral Tremor, Schizophrenia, Scoliosis, Seizure, Seizures, Senile Cardiac Amyloidosis, Sensory neuropathy, Skin Lesion, Sleep Apnea, Spastic paraplegia, Spinal muscular atrophy, Spinocerebellar Ataxia, Spinocerebellar Degeneration, Status Epilepticus, Stroke, Tremor, Trigeminal neuralgia, Urinary bladder cancer, Urinary bladder neoplasms, Vertical nystagmus
|
392
|
|
|
Calcium voltage-gated channel subunit alpha1 B |
BIII, CACNL1A5, CACNN, Cav2.2, DYT23, NEDNEH |
Curated: Bipolar disorder, Neurodevelopmental disorder, Dystonia, Gout, Non-neoplastic peripheral nervous system disease, Developmental and epileptic encephalopathy, Parkinson disease, Peripheral nervous system disease, Peripheral neuropathy, Schizophrenia, complex neurodevelopmental disorder with motor features
Unreviewed: Astrocytoma, Attention Deficit Hyperactivity Disorder, Autism, Autism Spectrum Disorder, Bipolar Disorder, Blepharospasm, Breast neoplasm, Cardiac arrhythmias, Central Visual Impairment, Cerebral Atrophy, Cerebral Infarction, Choreoathetosis, Cyst, Developmental Delay, Developmental regression, Dwarfism, Dyskinesia, Dyskinetic Syndrome, Edema, Epilepsy, Epileptic encephalopathy, Gastroesophageal Reflux Disease, Glioblastoma, Glioma, Hyperkinesia, Hypodontia, Ischemic stroke, Leukemia, Lung carcinoma, Major depressive disorder, Mental retardation, Microcephaly, Movement Disorders, Myoclonic Dystonia, Neoplasms, Nervous System Diseases, Non-Specifi Epileptic Encephalopathy, Nystagmus, Obesity, Optic Atrophy, Ptosis, Spinal muscular atrophy, Status Epilepticus, Strabismus
|
393
|
|
|
CACNA1B antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
394
|
|
|
CACNA1B antisense RNA 2 |
- |
Curated: N/A
Unreviewed: N/A
|
395
|
|
|
Calcium voltage-gated channel subunit alpha1 C |
CACH2, CACN2, CACNA1C-IT2, CACNL1A1, CCHL1A1, CaV1.2, LQT8, NEDHLSS, TS, TS. LQT8 |
Curated: Anhedonia, Anorexia nervosa, Anxiety disorder, Cardiac arrhythmia, Attention deficit hyperactivity disorder, Atypical femoral fracture, Timothy syndrome, Autism, Bipolar disorder, Brugada syndrome, Cardiomyopathy, Dilated cardiomyopathy, Cerebral palsy, Cognition disorder, Color vision deficiency, Concentric hypertrophic cardiomyopathy, Conduction disorder of the heart, Bipolar depression, Major depressive disorder, Epilepsy, Esophageal atresia, Long qt syndrome, Genetic predisposition to disease, Glomerulonephritis, Gout, Hypertension, Hypertrophic cardiomyopathy, Hypoglycemia, Inflammatory bowel disease, Intellectual developmental disorder, Congenital anomaly of limb, Metabolic syndrome, Mood disorder, Neurodevelopmental disorder, Non-organic psychosis, Non-specific syndromic intellectual disability, Obesity, Obsessive-compulsive disorder, Oligodendroglioma, Pancreatic cancer, Polymorphic catecholaminergic ventricular tachycardia, Psychiatric disorders, Psychotic disorders, Restrictive cardiomyopathy, Schizophrenia, Scoliosis, Short qt syndrome, Tetralogy of fallot, Tourette syndrome, Diabetes mellitus type 2, Ulcerative colitis, Depression, Ventricular fibrillation, Wolff-parkinson-white syndrome
Unreviewed: 22q13.3 deletion syndrome, Age-related macular degeneration, Alzheimer disease, Amelogenesis Imperfecta, Amyloidosis, Andersen Syndrome, Anemia, Antibody Deficiency Syndrome, Anxiety Disorder, Aortic Valve Disease, Arteriosclerosis, Arthrogryposis multiplex congenita, Ataxia, Atherosclerosis, Atrial Fibrillation, Atrial Septal Defect, Atrioventricular block, Attention Deficit Hyperactivity Disorder, Auditory perceptual disorder, Autism spectrum disorder, Behcet disease, Bipolar Disorder, Borderline personality disorder, Breast neoplasm, Bronchopulmonary Dysplasia, Brugada Syndrome, Bundle Branch Block, Cardiac arrhythmias, Cataract, Cerebellar ataxia, Choreoathetosis, Cognitive disorder, Common Migraine, Common Variable Immunodeficiency, Congenital heart defect, Congenital heart defects, Congenital heart septal defect, Congenital hyperinsulinism, Congenital Long QT Syndrome, Coronary Arteriosclerosis, Coronary artery disease, Coronary Heart Disease, Depressed bipolar disorder, Development Disorder, Developmental Delay, Developmental disability, Diabetes Mellitus, Diabetes mellitus, type 2, Diffuse Lymphoma, Dysmorphic Features, Dysphagia, Epileptic encephalopathy, Esophagus Neoplasm, Eye neoplasms, Facial dysmorphism syndrome, Glaucoma, Glioma, Heart disease, Hemiplegic Migraine, Hepatocellular carcinoma, High palate, Hydrops Fetalis, Hyperparathyroidism, Hypertrophy, Hypotension, Hypoxia, Immune system disease, Immunologic Deficiency Syndromes, Impaired Cognition, Infantile Spasms, Intestinal neoplasm, Involutional Depression, Involutional Paraphrenia, Ischemic myocardial dysfunction, Ischemic Stroke, Language development disorders, Learning disorders, Long QT Syndrome, Lung adenocarcinoma, Major Affective Disorder, Male infertility, Manic Disorder, Marfan syndrome, Memory disorders, Mental Depression, Mental Disorders, Microdontia, Migraine, Mood Disorder, Multiple system atrophy, Narcolepsy, Neck Neoplasms, Neoplasms, Neuroblastoma, Neurodevelopmental Disorders, Nonorganic Psychosis, Obsessive-Compulsive Disorder, Oculocerebrorenal syndrome, Optic Atrophy, Osteoarthritis, Ovarian neoplasm, Parkinson disease, Paroxysmal ventricular fibrillation, Paroxysmal ventricular tachycardia, Peripheral nervous system disease, Psychosis, Reactive hypoglycemia, Renal Carnitine Transport Defect, Rhabdomyolysis, Romano-Ward Syndrome, Salaam Seizures, Seizure, Seizures, Short QT Syndrome, Sick Sinus Syndrome, Sleep Disorders, Squamous cell carcinoma, Stress Disorder, Stroke, Supraventricular tachycardia, Syndactyly, Syndactyly of fingers, Timothy Syndrome, Torsades de pointes, Trifascicular block, Ventricular arrhythmia, Ventricular Fibrillation, Ventricular tachycardia
|
396
|
|
|
CACNA1C antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
397
|
|
|
CACNA1C antisense RNA 2 |
- |
Curated: N/A
Unreviewed: N/A
|
398
|
|
|
CACNA1C antisense RNA 3 |
- |
Curated: N/A
Unreviewed: N/A
|
399
|
|
|
CACNA1C antisense RNA 4 |
- |
Curated: N/A
Unreviewed: N/A
|
400
|
|
|
CACNA1C intronic transcript 1 |
- |
Curated: N/A
Unreviewed: N/A
|