|
451
|
|
|
Receptor like tyrosine kinase |
D3S3195, JTK5, JTK5A, RYK1 |
|
|
452
|
|
|
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, Blepharoptosis, Renal cell carcinoma, Central core myopathy, Color vision deficiency, Lynch syndrome, Congenital clubfoot, Congenital myasthenic syndrome, 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 diseases, Osteoporosis, Pena-Shokeir syndrome type I, Sacral agenesis, Scoliosis, Intracranial vasospasmView all (16 more) |
|
453
|
|
|
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, Catecholaminergic polymorphic ventricular tachycardia, Central nervous system cancer, Acute lymphoblastic leukemia, Color vision deficiency, Congenital heart disease, Diabetic cardiomyopathy, Dilated cardiomyopathy, Diverticular disease, Eating disorder, Hypertrophic cardiomyopathy, 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 fibrillation, Ventricular hypertrophy, Polymorphic ventricular tachycardia, Wolff-parkinson-white syndromeView all (27 more) |
|
454
|
|
|
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 type I, Rheumatic fever, Schizophrenia, ScoliosisView all (1 more) |
|
455
|
|
|
Ring finger protein 123 |
FP1477, KPC1 |
|
|
456
|
|
|
RNA binding motif protein 26 |
ARRS2, C13orf10, PPP1R132, PRO1777, SE70-2, ZC3H17 |
|
|
457
|
|
|
Ribokinase |
RBSK, RK |
|
|
458
|
|
|
Ras related GTP binding C |
GTR2, LNGODS, LNGOS, RAGC, TIB929 |
|
|
459
|
|
|
Rabenosyn, RAB effector |
KAREVS, MFANDO, Rabenosyn-5, ZFYVE20 |
|
|
460
|
|
|
Roundabout guidance receptor 3 |
HGPPS, HGPPS1, HGPS, RBIG1, RIG1 |
|