1811
|
|
|
Calsequestrin 2 |
PDIB2 |
Cardiac arrhythmias, Atrial fibrillation, Atrial flutter, Cardiomyopathy, Catecholaminergic polymorphic ventricular tachycardia, Conduction disorder of the heart, Dementia, Hereditary bundle branch system defect, Hypertrophic cardiomyopathy, Long qt syndrome, Polymorphic catecholaminergic ventricular tachycardia, Polymorphic ventricular tachycardia, Vesicoureteral reflux, Wolff-parkinson-white syndrome |
1812
|
|
|
Calcium sensing receptor |
CAR, EIG8, FHH, FIH, GPRC2A, HHC, HHC1, HYPOC1, NSHPT, PCAR1, hCasR |
Asthma, Hereditary chronic pancreatitis, Hypocalcemia, Bartter syndrome, Bladder calculus, Calcium metabolism disorders, Kidney and ureter calculus, Desbuquois syndrome, Epilepsy, Idiopathic generalized epilepsy, Benign hypercalcemia, Hypocalciuric hypercalcemia, Gitelman syndrome, Hypercalcemia, Hyperparathyroidism, Hypertrophic cardiomyopathy, Intellectual developmental disorder, Nephrolithiasis, Neurodevelopmental disorder, Psoriasis, Systemic lupus erythematosus, Diabetes mellitus type 2, UrolithiasisView all (8 more) |
1813
|
|
|
Cas scaffold protein family member 4 |
C20orf32, CAS4, HEFL, HEPL |
|
1814
|
|
|
Calpastatin |
BS-17, MIR583HG, PLACK |
Aneurysm, Anterior uveitis, Aortic aneurysm, Attention deficit hyperactivity disorder, Blood coagulation disorder, Gestational diabetes, Heart failure, Hodgkin lymphoma, Uveitis, Liver failure, Lung cancer, Systemic lupus erythematosus, Major depressive disorder, Metabolic syndrome, Obesity, Myasthenic syndrome, Myocarditis, Necrosis, Obstructive sleep apnea syndrome, Osteoarthritis, Parkinson disease, Peeling skin syndrome with leukonychia and acral punctate keratoses, Pemphigus, Psoriasis, Rheumatoid arthritis, Schizophrenia, Sjogren syndrome, Squamous cell carcinoma, Diabetes mellitus type 2, Vasculitis, Ventricular dysfunctionView all (16 more) |
1815
|
|
|
Cytosolic arginine sensor for mTORC1 subunit 1 |
GATSL3 |
|
1816
|
|
|
Cytosolic arginine sensor for mTORC1 subunit 2 |
GATSL1, GATSL2 |
|
1817
|
|
|
Castor zinc finger 1 |
CAS11, CST, SRG, ZNF693, dJ734G22.1 |
1p36 deletion syndrome, Anal polyp, Androgenetic alopecia, Atrial fibrillation, Breast cancer, Dilated cardiomyopathy, Cardiovascular disease, Cataract, Cerebrovascular disorder, Chromosome 1p36 deletion syndrome, Obstructive pulmonary disease, Color vision deficiency, Congenital heart disease, Coronary artery disease, Diabetic ketoacidosis, Hypertension, Heart failure, Major depressive disorder, Migraine, Potassium deficiency, Primary aldosteronism, Prostatic neoplasms, Small vessel stroke, Stroke, Diabetes mellitus type 2, Uterine fibroidView all (11 more) |
1818
|
|
|
Catalase |
- |
Acatalasia, Angle closure glaucoma, Aortic disease, Experimental arthritis, Rheumatoid arthritis, Osteonecrosis of the femoral head, Jeune syndrome, Asthma, Rhinitis, Autism, Avascular necrosis of bone, Behcet disease, Bonnevie-ullrich syndrome, Brain ischemia, Breast neoplasms, Hepatocellular carcinoma, Non-small-cell lung carcinoma, Renal cell carcinoma, Cardiomyopathy, Cholelithiasis, Persistent hepatitis, Congestive heart failure, Major depressive disorder, Diabetes mellitus, Experimental diabetes, Diabetes mellitus type 1, Diabetes mellitus type 2, Diabetic neuropathy, Dyskinesia, drug-induced, Edema, Hypertension, Fatty liver, Fatty liver, alcoholic, Gastric ulcer, Genetic predisposition to disease, Glioma, Heart failure, Hepatitis, Hyperemia, Hyperthyroidism, Hypotension, Keratosis, Kidney failure, Liver cirrhosis, Lung disease, Systemic lupus erythematosus, Diffuse large b-cell lymphoma, Marfan syndrome, Mesothelioma, Myocardial infarction, Necrosis, Nonalcoholic fatty liver disease, Optic neuritis, Osteonecrosis of medial femoral condyle, Osteoporosis, Psoriasis, Pulmonary edema, Pulmonary fibrosis, Retinitis pigmentosa, Seizures, Senile cataract, Status epilepticus, Turner syndrome, Depression, Ureteral calculi, Urinary bladder neoplasms, VitiligoView all (52 more) |
1819
|
|
|
Ciliogenesis associated TTC17 interacting protein |
C2orf62 |
|
1820
|
|
|
Cation channel sperm associated 1 |
CATSPER, SPGF7 |
|
