751
|
|
|
Retinoid X receptor alpha |
NR2B1, RXR-alpha, RXRalpha |
Amyotrophic lateral sclerosis, Congenital heart disease, Corneal disease, Corneal dystrophy, Crohn disease, Eye disease, Keratoconus, Mesothelioma, Motor neuron disease, Pelvic organ prolapse, Pericarditis, Prostatic neoplasms, Thyroid neoplasms |
752
|
|
|
Retinoid X receptor beta |
DAUDI6, H-2RIIBP, NR2B2, RCoR-1, RXR-beta, RXRbeta |
|
753
|
|
|
Retinoid X receptor gamma |
NR2B3, RXR-gamma, RXRC, RXRgamma |
|
754
|
|
|
Ribitol xylosyltransferase 1 |
HP10481, MDDGA10, TMEM5 |
|
755
|
|
|
RING1 and YY1 binding protein |
AAP1, APAP-1, DEDAF, YEAF1 |
|
756
|
|
|
Receptor like tyrosine kinase |
D3S3195, JTK5, JTK5A, RYK1 |
|
757
|
|
|
Ryanodine receptor 1 |
CCO, CMYO1A, CMYO1B, CMYP1A, CMYP1B, KDS, MHS, MHS1, PPP1R137, RYDR, RYR, RYR-1, SKRR |
Anterior segment dysgenesis, Arrhythmogenic right ventricular cardiomyopathy, Arthrogryposis multiplex congenita, Asthma, Centronuclear myopathy, Congenital myopathy, Central core disease, Benign samaritan congenital myopathy, Blepharoptosis, Renal cell carcinoma, Central core myopathy, Color vision deficiency, Lynch syndrome, Congenital clubfoot, Congenital fiber type disproportion myopathy, Congenital joint contractures, Congenital multicore myopathy with external ophthalmoplegia, Congenital muscular dystrophy, Congenital structural myopathy, Congestive heart failure, Distal arthrogryposis, Gross motor development delay, Heart failure, Hydrops fetalis, Pulmonary hypertension, Intellectual developmental disorder, Long qt syndrome, Lung cancer, Malignant hyperthermia, Myasthenic syndrome, Myopathy, Neuromuscular disease, Osteoporosis, Pena-shokeir syndrome , Sacral agenesis, Scoliosis, Intracranial vasospasmView all (22 more) |
758
|
|
|
Ryanodine receptor 2 |
ARVC2, ARVD2, RYR-2, RyR, VACRDS, VTSIP |
Cardiac arrhythmias, Arrhythmogenic right ventricular cardiomyopathy, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Brugada syndrome, Cardiac arrest, Cardiac arrhythmia, Cardiomyopathy, Dilated cardiomyopathy, Catecholaminergic polymorphic ventricular tachycardia, Central nervous system cancer, Lymphoblastic leukemia, Color vision deficiency, Conduction disorder of the heart, Congenital heart disease, Congestive heart failure, Diabetic cardiomyopathy, Diverticular disease, Eating disorder, Hypertrophic cardiomyopathy, Arrhythmogenic right ventricular dysplasia, Generalized epilepsy, Glioblastoma, Glioma, Heart disease, Hypotension, Left ventricular disease, Left ventricular noncompaction cardiomyopathy, Long qt syndrome, Mesothelioma, Myocardial ischemia, Obesity, Paroxysmal familial ventricular fibrillation, Polymorphic catecholaminergic ventricular tachycardia, Post-operative stroke, Rhabdomyolysis, Schizophrenia, Scoliosis, Substance abuse, Diabetes mellitus type 2, Ventricular arrhythmia, Ventricular fibrillation, Ventricular hypertrophy, Polymorphic ventricular tachycardia, Wolff-parkinson-white syndromeView all (31 more) |
759
|
|
|
Ryanodine receptor 3 |
CMYO20, CMYP20, RYR-3 |
Monomelic amyotrophy, Arthrogryposis multiplex congenita, Breast cancer, Carotid artery disease, Color vision deficiency, Congenital myopathy, Developmental and epileptic encephalopathy, Diabetic neuropathy, Hydrops fetalis, Hypotension, Premature ovarian failure, Parkinson disease, Pena-shokeir syndrome , Rheumatic fever, Schizophrenia, ScoliosisView all (1 more) |
