1671
|
|
|
Calcium binding tyrosine phosphorylation regulated |
CABYRa, CABYRc, CABYRc/d, CABYRe, CBP86, CT88, FSP-2, FSP2 |
|
1672
|
|
|
Calcium channel flower domain containing 1 |
C9orf7, D9S2135, FLOWER |
|
1673
|
|
|
Calcium voltage-gated channel subunit alpha1 A |
APCA, BI, CACNL1A4, CAV2.1, DEE42, EA2, EIEE42, FHM, HPCA, MHP, MHP1, SCA6 |
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 abuseView all (22 more) |
1674
|
|
|
Calcium voltage-gated channel subunit alpha1 B |
BIII, CACNL1A5, CACNN, Cav2.2, DYT23, NEDNEH |
|
1675
|
|
|
Calcium voltage-gated channel subunit alpha1 C |
CACH2, CACN2, CACNA1C-IT2, CACNL1A1, CCHL1A1, CaV1.2, LQT8, NEDHLSS, TS, TS. LQT8 |
Anhedonia, Anorexia nervosa, Anxiety disorder, Cardiac arrhythmias, Attention deficit hyperactivity disorder, Atypical femoral fracture, Timothy syndrome, Autism, Bipolar disorder, Brugada syndrome, Cardiac arrhythmia, 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 syndromeView all (40 more) |
1676
|
|
|
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) |
1677
|
|
|
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 |
1678
|
|
|
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 |
1679
|
|
|
Calcium voltage-gated channel subunit alpha1 G |
Ca(V)T.1, Cav3.1, NBR13, SCA42, SCA42ND |
|
1680
|
|
|
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) |
