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1001
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Calcium voltage-gated channel subunit alpha1 D |
CACH3, CACN4, CACNL1A2, CCHL1A2, Cav1.3, PASNA, SANDD |
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 impairment, 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, Diabetes mellitus, type 2View all (20 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 |
Alzheimer disease, Amblyopia, Bipolar disorder, Dementia, Developmental and epileptic encephalopathy, Major depressive disorder, Meningitis, Mood disorder, Neurodevelopmental disorders, Neurotic disorder, Post-traumatic stress disorder, Systemic mastocytosis, Van der woude syndrome, Wolff-parkinson-white syndrome |
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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 |
Aland island eye disease, Amblyopia, Cone-rod dystrophy, Cone-rod dystrophy, x-linked, Macular dystrophy, Myopia, Night blindness, congenital stationary, Ocular albinism, Oguchi disease, Optic atrophy, Cone dystrophy, Retinitis pigmentosa, Schizophrenia, X-linked cone-rod dystrophy |
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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 |
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1005
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Calcium voltage-gated channel auxiliary subunit alpha2delta 1 |
CACNA2, CACNL2A, CCHL2A, DEE110, LINC01112, lncRNA-N3 |
Asthma, Bipolar disorder, Brugada syndrome, Cardiac arrest, Liver cirrhosis, Colonic neoplasm, Colorectal cancer, Crohn disease, Developmental and epileptic encephalopathy, Head and neck neoplasm, Hyperalgesia, Hypertension, Intellectual developmental disorder, Long qt syndrome, Major depressive disorder, Multiple myeloma, Neurodevelopmental disorders, Nonalcoholic fatty liver disease, Obesity, Paroxysmal atrial fibrillation, Prostate cancer, Schizophrenia, Scoliosis, Severe acute respiratory syndrome, Short qt syndrome, Ulcerative colitis, Uveal melanoma, Ventricular fibrillationView all (13 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 |
Alzheimer disease, Anorexia nervosa, Arrhythmogenic right ventricular cardiomyopathy, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Brugada syndrome, Cardiac arrest, Cardiac conduction disease, Cardiogenetic disease, Cardiomyopathy, Cardiovascular disease, Color vision deficiency, Congenital cartilage disorder, Coronary artery disease, Digestive system disease, Diverticular disease, Repolarization syndrome, Hypertension, Heart failure, Hypertrophic cardiomyopathy, Long qt syndrome, Major depressive disorder, Intellectual developmental disorder, Obesity, Obsessive-compulsive disorder, Schizophrenia, Short qt syndrome, Small vessel stroke, Tourette syndrome, Ventricular fibrillationView all (16 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 |
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