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1001
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Calcium voltage-gated channel subunit alpha1 D |
CACH3, CACN4, CACNL1A2, CCHL1A2, Cav1.3, PASNA, SANDD |
Adenoma, Hyperaldosteronism, Adrenal hyperplasia, Atrioventricular block, Bipolar disorder, Cardiovascular diseases, Central visual impairment, Cerebral palsy, Congenital adrenal hyperplasia, Conn syndrome, Deafness, Developmental delay, Dyscognitive seizures, Focal myoclonic seizures, Heart block, Hypertension, Mental retardation, Left ventricular hypertrophy, Manic disorder, Metabolic alkalosis, Mood disorder, Movement disorders, Nephrolithiasis, Papillary adenoma, Aldosteronism, seizures, and neurologic abnormalities, Pulmonary arterial hypertension, Schizophrenia, Seizure, Sick sinus syndrome, Sinoatrial node dysfunction and deafness, Sinus node dysfunction, Sleep disorders, Spastic paraplegia, Supraventricular tachycardia, Ventricular hypertrophy, Ventricular septal defectView all (21 more) |
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1002
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Calcium voltage-gated channel subunit alpha1 E |
BII, CACH6, CACNL1A6, Cav2.3, DEE69, EIEE69, gm139 |
Arthrogryposis multiplex congenita, Atrophy of corpus callosum, Central visual impairment, Cerebral cortical atrophy, Congenital contracture, Developmental delay, Epileptic encephalopathy, Leukemia, Macrocephaly, Mental depression, Mental retardation, Nystagmus, Spastic quadriplegia, Status epilepticus |
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1003
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Calcium voltage-gated channel subunit alpha1 F |
AIED, COD3, COD4, CORDX, CORDX3, CSNB2, CSNB2A, CSNBX2, Cav1.4, Cav1.4alpha1, JM8, JMC8, OA2 |
Ocular albinism, Albinism, Astigmatism, Cone-rod dystrophy, Congenital stationary night blindness, Disorder of eye, Hypoplasia of optic disc, Myopia, Night blindness, Nyctalopia, Nystagmus, Progressive cone dystrophy, Retinal dystrophy, Schizophrenia, Strabismus, Congenital stationary night blindness, x-linkedView all (1 more) |
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1004
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Calcium voltage-gated channel subunit alpha1 S |
CACNL1A3, CCHL1A3, CMYO18, CMYP18, Cav1.1, DHPRM, HOKPP, HOKPP1, MHS5, TTPP1, hypoPP |
Adrenocortical adenoma, Anodontia, Atrioventricular block, Blood coagulation disorders, Congenital myopathy, Congestive heart failure, Graves disease, Hyperphosphatemia, Hyperthyroidism, Hypodontia, Hypodontia oligodontia with orofacial cleft, Hypokalemic periodic paralysis, Liver failure, Necrotizing myopathy, Obesity, Oligodontia, Periodic hypokalemic paresis, Periodic paralysis, Periodic paralysis with transient compartment-like syndrome, Quadriplegia, Respiratory failure, Schizophrenia, Supraventricular tachycardia, Thyrotoxic periodic paralysis, Thyrotoxicosis with toxic single thyroid nodule, Tooth agenesis, Tooth development and eruption disorder, Toxic goiter, Ventricular fibrillation, Ventricular tachycardiaView all (15 more) |
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1005
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Calcium voltage-gated channel auxiliary subunit alpha2delta 1 |
CACNA2, CACNL2A, CCHL2A, DEE110, LINC01112, lncRNA-N3 |
Atrial fibrillation, Atrioventricular block, Brugada syndrome, Bundle branch block, Cardiac conduction disease, Colonic neoplasms, Hypertension, Leukemia, Mental depression, Paroxysmal ventricular tachycardia, Short qt syndrome, Sick sinus syndrome, Sinus node dysfunction, Supraventricular tachycardia, Trifascicular block, Uveal melanoma, Ventricular fibrillationView all (2 more) |
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1006
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Cold shock domain containing E1 |
D1S155E, UNR |
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1007
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Calcium voltage-gated channel auxiliary subunit beta 1 |
CAB1, CACNLB1, CCHLB1 |
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1008
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Calcium voltage-gated channel auxiliary subunit beta 2 |
CAB2, CACNLB2, CAVB2, MYSB |
Atrial fibrillation, Atrioventricular block, Attention deficit hyperactivity disorder, Bipolar disorder, Brugada syndrome, Bundle branch block, Cardiac conduction disease, Cardiovascular diseases, Colorectal cancer, Coronary heart disease, Development disorder, Diverticular diseases, Hypertension, Hypertrophic cardiomyopathy, Mental depression, Paroxysmal ventricular tachycardia, Schizophrenia, Sick sinus syndrome, Sinus node dysfunction, Supraventricular tachycardia, Trifascicular block, Ventricular fibrillationView all (7 more) |
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1009
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Calcium voltage-gated channel auxiliary subunit beta 3 |
CAB3, CACNLB3 |
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1010
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Calcium voltage-gated channel auxiliary subunit beta 4 |
CAB4, CACNLB4, EA5, EIG9, EJM, EJM4, EJM6 |
Cardiomyopathy, Dysarthria, Epilepsy, Epilepsy with tonic-clonic seizures, Episodic ataxia, Febrile seizures, Mouth abnormalities, Myoclonic epilepsy, Nonconvulsive seizure disorder, Nystagmus, Photosensitive tonic-clonic seizures, Rubral tremor, Status epilepticus |
