Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "R"
751 to 754 of 754 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

751
Receptor like tyrosine kinase
D3S3195, JTK5, JTK5A, RYK1
Cardiovascular disease, Cleft palate, Coronary artery disease, Craniofacial abnormalities, Hypertension, Orofacial cleft, Vascular dementia, Venous thromboembolism

752
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
View all (22 more)

753
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
View all (31 more)

754
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 , Schizophrenia, Scoliosis