1671
|
|
|
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 abuseView all (19 more) |
1672
|
|
|
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, Mood disorder, Neurodevelopmental disorder, Neurotic disorder, Post-traumatic stress disorder, Systemic mastocytosis, Van der woude syndrome, Wolff-parkinson-white syndrome |
1673
|
|
|
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, 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 |
1674
|
|
|
Calcium voltage-gated channel subunit alpha1 G |
Ca(V)T.1, Cav3.1, NBR13, SCA42, SCA42ND |
|
1675
|
|
|
Calcium voltage-gated channel subunit alpha1 H |
CACNA1HB, Cav3.2, ECA6, EIG6, HALD4 |
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, UrticariaView all (7 more) |
1676
|
|
|
Calcium voltage-gated channel subunit alpha1 I |
Cav3.3, NEDSIS, ca(v)3.3 |
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 2View all (5 more) |
1677
|
|
|
Calcium voltage-gated channel subunit alpha1 S |
CACNL1A3, CCHL1A3, CMYO18, CMYP18, Cav1.1, DHPRM, HOKPP, HOKPP1, MHS5, TTPP1, hypoPP |
|
1678
|
|
|
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 neoplasms, Colorectal cancer, Congenital short qt syndrome, Crohn disease, Developmental and epileptic encephalopathy, Head and neck neoplasm, Hyperalgesia, Hypertension, Intellectual developmental disorder, Long qt syndrome, Major depressive disorder, Multiple myeloma, Neurodevelopmental disorder, Nonalcoholic fatty liver disease, Obesity, Paroxysmal atrial fibrillation, Prostate cancer, Schizophrenia, Scoliosis, Short qt syndrome, Ulcerative colitis, Uveal melanoma, Ventricular fibrillationView all (13 more) |
1679
|
|
|
Calcium voltage-gated channel auxiliary subunit alpha2delta 2 |
CACNA2D, CASVDD |
Ataxia, Attention deficit hyperactivity disorder, Autism, Benign hereditary chorea, Bipolar disorder, Cerebellar atrophy with seizures and variable developmental delay, Chorea, Neurodevelopmental disorder, Developmental and epileptic encephalopathy, Absence epilepsy, Generalized epilepsy, Hearing impairment, Hearing loss, Female infertility, Insomnia, Non-specific syndromic intellectual disability, Post-traumatic stress disorder, Schizophrenia, Diabetes mellitus type 2View all (4 more) |
1680
|
|
|
Calcium voltage-gated channel auxiliary subunit alpha2delta 3 |
HSA272268 |
Alzheimer disease, Attention deficit hyperactivity disorder, Bipolar disorder, Central nervous system cancer, Obstructive pulmonary disease, Color vision deficiency, Endometrial cancer, Endometrial neoplasms, Glioblastoma, Glioma, Gout, Language development disorders, Lung cancer, Major depressive disorder, Neurodevelopmental disorder, Obsessive-compulsive disorder, Parkinson disease, Pelvic organ prolapse, Polycystic ovary syndrome, Schizophrenia, Substance abuse, Synovial disorder, Diabetes mellitus type 2View all (8 more) |
