401
|
|
|
CACNA1C intronic transcript 2 |
- |
Curated: N/A
Unreviewed: N/A
|
402
|
|
|
CACNA1C intronic transcript 3 |
- |
Curated: N/A
Unreviewed: N/A
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403
|
|
|
Calcium voltage-gated channel subunit alpha1 D |
CACH3, CACN4, CACNL1A2, CCHL1A2, Cav1.3, PASNA, SANDD |
Curated: Aldosterone-producing adenoma, Atrial fibrillation, Attention deficit hyperactivity disorder, Bipolar disorder, Bradycardia, Brain compression, Breast cyst, Cardiovascular disease, Obstructive pulmonary disease, Color vision deficiency, Neurodevelopmental disorder, Congenital disorder of glycosylation, Cushing syndrome, Deafness, Bipolar depression, Diabetes mellitus type 2, Edema, Hypertension, Long qt syndrome, Gastroesophageal reflux disease, Hearing loss, Heart failure, Hyperaldosteronism, Insomnia, Intellectual developmental disorder, Meniere disease, Metabolic syndrome, Mood disorder, Non-specific syndromic intellectual disability, Primary aldosteronism, Primary hyperaldosteronism-seizures-neurological abnormalities syndrome, Schizophrenia, Sick sinus syndrome, Substance abuse, sinoatrial node dysfunction and deafness, complex neurodevelopmental disorder
Unreviewed: Adenoma, Adrenal hyperplasia, Aldosteronism, Seizures, And Neurologic Abnormalities, Atrioventricular block, Autism, Autism spectrum disorder, Bipolar Disorder, Carcinogenesis, Cardiac arrhythmias, Cardiac conduction disease, Cardiovascular Diseases, Central Visual Impairment, Cerebral palsy, CNS Disorder, Colorectal neoplasm, Congenital adrenal hyperplasia, Congenital heart defect, Congenital hyperinsulinism, Conn Adenoma, Conn Syndrome, Cushing`s Syndrome, Developmental Delay, Developmental disability, Diabetes Mellitus, Diabetes mellitus, type 1, Diabetes mellitus, type 2, Down syndrome, Dyscognitive seizures, Dyslipidemias, Endocrine system disease, Endometriosis, Epilepsy, Focal myoclonic seizures, Heart Block, Hyperglycemia, Hyperinsulinemic hypoglycemia, Hyperplasia, Hypoglycemia, Insulinoma, Left Ventricular Hypertrophy, Long QT Syndrome, Lymphedema, Malignant Neoplasm, Manic Disorder, Mental Disorders, Mental retardation, Metabolic alkalosis, Microtia, Mood Disorder, Movement Disorders, Myopia, Neoplasms, Nephrolithiasis, Nervous System Disorder, Neurodegenerative disorder, Neurodevelopmental Disorders, Neuromuscular disease, Neuromuscular Diseases, Papillary Adenoma, Parkinson disease, Partial epilepsy, Prostate cancer, Prostatic neoplasm, Pulmonary arterial hypertension, Seizure, Seizures, Sick Sinus Syndrome, Sinoatrial Node Dysfunction And Deafness, Sinus Node Dysfunction, Sleep Disorders, Spastic Paraplegia, Stomach neoplasms, Supraventricular tachycardia, Tuberous sclerosis complex, Vascular malformation, Ventricular hypertrophy, Ventricular septal defect, Ventricular tachycardia
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404
|
|
|
Calcium voltage-gated channel subunit alpha1 E |
BII, CACH6, CACNL1A6, Cav2.3, DEE69, EIEE69, gm139 |
Curated: Alzheimer disease, Amblyopia, Bipolar disorder, Dementia, Developmental and epileptic encephalopathy, Major depressive disorder, Mood disorder, Neurodevelopmental disorder, Neurotic disorder, Post-traumatic stress disorder, Systemic mastocytosis, Van der woude syndrome, Wolff-parkinson-white syndrome, genetic developmental and epileptic encephalopathy
Unreviewed: Arthrogryposis multiplex congenita, Atrophy Of Corpus Callosum, Autism, Borderline personality disorder, Brain stem neoplasms, Breast Cancer, Breast Carcinoma, Breast neoplasm, Bronchopulmonary Dysplasia, Central Visual Impairment, Cerebral cortical atrophy, Cognition disorder, Colorectal neoplasm, Common Migraine, Congenital contracture, Contracture, Crohn Disease, Dental caries, Development Disorder, Developmental Delay, Diabetes, Diabetes Mellitus, Diabetes mellitus, type 1, Diabetes mellitus, type 2, Dyskinetic Syndrome, Epilepsy, Epileptic encephalopathy, Gastritis, Gastrointestinal stromal tumor, Hyperkinesia, Intellectual developmental disorder, Kawasaki disease, Language development disorders, Leukemia, Lung neoplasms, Lymphoma, Macrocephaly, Mental Depression, Mental retardation, Migraine, Migraine with Aura, Neoplasms, Neurodevelopmental Disorders, Nystagmus, Phobic Anxiety Disorder, Pulmonary hypertension, Seizures, Spastic Quadriplegia, Squamous cell carcinoma, Status Epilepticus, Stomach neoplasms
|
405
|
|
|
Calcium voltage-gated channel subunit alpha1 F |
AIED, COD3, COD4, CORDX, CORDX3, CSNB2, CSNB2A, CSNBX2, Cav1.4, Cav1.4alpha1, JM8, JMC8, OA2 |
Curated: Aland island eye disease, Amblyopia, Cone-rod dystrophy, Cone-rod dystrophy, x-linked, Congenital stationary night blindness, Macular dystrophy, Myopia, Night blindness, congenital stationary, Ocular albinism, Oguchi disease, Optic atrophy, Cone dystrophy, Retinitis pigmentosa, Schizophrenia, X-linked cone-rod dystrophy, CACNA1F-related retinopathy
Unreviewed: Achromatopsia, Albinism, Astigmatism, Astrocytoma, Atrophy, Colorectal Cancer, Colorectal neoplasm, Congenital stationary night blindness, X-Linked, Disorder Of Eye, Dysequilibrium Syndrome, Enhanced S-Cone Syndrome, Glioblastoma, Hyperopia, Hypophosphatasia, Hypoplasia Of Optic Disc, Leber congenital amaurosis, Malignant Neoplasm, Malignant Neoplasm Of Testis, Mixed Oligodendroglioma-Astrocytoma, Moyamoya disease, Multiple sclerosis, Nervous System Disorder, Night blindness, Nyctalopia, Nystagmus, Oligodendroglioma, Optic Atrophy, Progressive Cone Dystrophy, Retinal detachment, Retinal Diseases, Retinal Dystrophy, Retinitis Pigmentosa, Rod-cone dystrophy, Spinocerebellar Ataxia, Strabismus, Timothy Syndrome, Visual disorder
|
406
|
|
|
Calcium voltage-gated channel subunit alpha1 G |
Ca(V)T.1, Cav3.1, NBR13, SCA42, SCA42ND |
Curated: Alzheimer disease, Spinocerebellar ataxia, Cerebellar ataxia, Intellectual developmental disorder, Neurodevelopmental disorder, Schizophrenia, Intellectual disability, Spastic ataxia, spinocerebellar ataxia type 42
Unreviewed: Adenoma, Autism, Autism spectrum disorder, Brainstem Atrophy, Breast Cancer, Breast Carcinoma, Cerebellar atrophy, Cerebellar diseases, Cerebellar Hypoplasia, Clinodactyly, Cognition disorder, Colorectal Cancer, Colorectal neoplasm, Developmental and epileptic encephalopathy, Developmental Delay, Developmental disability, Diabetes mellitus, type 2, Dysarthria, Dysphagia, Epilepsy, Epileptic encephalopathy, Erectile Dysfunction, Essential tremor, Gastrointestinal Diseases, Generalized epilepsy, Glioma, Head and neck neoplasm, Hepatocellular carcinoma, Horizontal nystagmus, Hyperopia, Impaired Cognition, Kaposi Sarcoma, Learning Disorders, Leukemia, Liver carcinoma, Lung neoplasms, Lymphatic metastasis, Malignant Neoplasm, Malocclusion, Mental Depression, Mental retardation, Metastatic Prostate Carcinoma, Myoclonic Epilepsy, Neoplasms, Neurodegenerative Disorders, Oculomotor apraxia, Oculovestibuloauditory Syndrome, Osteoarthritis, Osteoporosis, Pancreatic neoplasm, Partial epilepsy, Prostatic neoplasm, Psoriasiform eczema, Pulmonary hypertension, Scoliosis, Seizures, Spastic Ataxia, Spinocerebellar Ataxia, Spinocerebellar Ataxia, WITH NEURODEVELOPMENTAL DEFICITS, Squamous cell carcinoma, Strabismus, Syndactyly, Tremor, Urinary bladder neoplasms
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407
|
|
|
CACNA1G antisense RNA 1 |
CAS1 |
Curated: N/A
Unreviewed: Anxiety Disorder, Colon Carcinoma, Glioblastoma, Liver carcinoma, Lung carcinoma, Mental Depression, Neoplasms, Pleural effusion
|
408
|
|
|
Calcium voltage-gated channel subunit alpha1 H |
CACNA1HB, Cav3.2, ECA6, EIG6, HALD4 |
Curated: Alzheimer disease, Cerebral arteriovenous malformations, Autism, Beta thalassemia, Childhood absence epilepsy, Congenital arteriovenous malformation, Conn syndrome, Cushing syndrome, Partial epilepsy, Absence epilepsy, Hyperaldosteronism, Hyperalgesia, Epilepsy, Mastocytosis, Migraine, Non-neoplastic peripheral nervous system disease, Osteoarthritis, Pancreatic cancer, Peripheral nervous system disease, Peripheral neuropathy, Diabetes mellitus type 2, Urticaria
Unreviewed: Absence Seizure, Adenoma, Adrenocortical carcinoma, Akinetic Petit Mal, Amyotrophic Lateral Sclerosis, Anxiety Disorder, Aplasia Of Muscle, Arthrogryposis, Attention Deficit Hyperactivity Disorder, Autism Spectrum Disorder, beta Thalassemia, Breast Cancer, Breast Carcinoma, Breast neoplasm, Cardiac arrhythmias, Carotid artery stenosis, Chorea, Conn Adenoma, Conn Syndrome, Cooley`s Anemia, Developmental and epileptic encephalopathy, Developmental disability, Diabetes mellitus, type 1, Diabetes mellitus, type 2, Diabetic neuropathy, Dyslexia, Dystonia, Febrile seizures, Generalized epilepsy, Hearing loss, Hemoglobinopathy, Hyperglycemia, Hyperplasia, Hypertension, Language development disorders, Male infertility, Malignant Neoplasm, Mammary Neoplasms, Medulloblastoma, Mental Depression, Mental retardation, Multiple Sclerosis, Myoclonic epilepsy, Nervous System Diseases, Prostatic neoplasm, Prostatic Neoplasms, Pulmonary hypertension, Punding, Schizophrenia, Seizure, Seizures, Spinal muscular atrophy, Squamous cell carcinoma, Thalassemia, Trigeminal neuralgia
|
409
|
|
|
Calcium voltage-gated channel subunit alpha1 I |
Cav3.3, NEDSIS, ca(v)3.3 |
Curated: Anorexia nervosa, Astrocytoma, Attention deficit hyperactivity disorder, Autism, Nonsyndromic intellectual disability, Bipolar disorder, Neurodevelopmental disorder, Long qt syndrome, Global developmental delay, Hodgkin lymphoma, Juvenile idiopathic arthritis, Major depressive disorder, Metabolic syndrome, Non-specific syndromic intellectual disability, Obsessive-compulsive disorder, Oligodendroglioma, Prostate cancer, Schizophrenia, Tourette syndrome, Diabetes mellitus type 2
Unreviewed: N/A
|
410
|
|
|
Calcium voltage-gated channel subunit alpha1 S |
CACNL1A3, CCHL1A3, CMYO18, CMYP18, Cav1.1, DHPRM, HOKPP, HOKPP1, MHS5, TTPP1, hypoPP |
Curated: Biliary cirrhosis, Centronuclear myopathy, Congenital myopathy, Embryonal nuclear cataract, Long qt syndrome, Malignant hyperthermia, Periodic paralysis with transient compartment-like syndrome, Biliary cholangitis, Thyrotoxic periodic paralysis, Tooth agenesis
Unreviewed: Adrenocortical adenoma, Amyotrophic Lateral Sclerosis, Andersen Syndrome, Andersen-tawil syndrome, Anodontia, Arthrogryposis, Atrioventricular block, Autism, Blood Coagulation Disorders, Cardiac arrhythmias, Catecholaminergic polymorphic ventricular tachycardia, Clubfoot, Cognition disorder, Congenital adrenal hyperplasia, Congenital Thrombotic Thrombocytopenic Purpura, Congestive Heart Failure, Contracture, Epilepsy, Fatigue syndrome, Graves Disease, Heart failure, Hereditary pyropoikilocytosis, Hyperphosphatemia, Hypertension, Hyperthyroidism, Hypodontia, Hypodontia Oligodontia With Orofacial Cleft, Hypokalemic Periodic Paralysis, Kidney failure, Lipodystrophy, Lipoma, Liver carcinoma, Liver failure, Liver neoplasms, Major depressive disorder, Metabolic Myopathy, Myasthenia Gravis, Myopathy, Myotonia congenita, Necrotizing myopathy, Obesity, Oligodontia, Ophthalmoplegia, Paralysis, Parietal Foramina, Periodic hypokalemic paresis, Periodic Paralysis, Periodic Paralysis With Transient Compartment-Like Syndrome, Psoriatic arthritis, Quadriplegia, Respiratory Failure, Retinitis Pigmentosa, Rhabdomyolysis, Rheumatoid arthritis, Schizophrenia, Supraventricular tachycardia, Thrombotic thrombocytopenic purpura, Thyrotoxic Periodic Paralysis, Thyrotoxicosis with toxic single thyroid nodule, Tooth Agenesis, Tooth Development And Eruption Disorder, Toxic Goiter, Ventricular dysfunction, Ventricular Fibrillation, Ventricular tachycardia
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