Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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11441 to 11450 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11441
Relaxin family peptide receptor 3
GPCR135, RLN3R1, RXFPR3, SALPR
Basal cell carcinoma, Melanoma, Squamous cell carcinoma

11442
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

11443
Retinoid X receptor beta
DAUDI6, H-2RIIBP, NR2B2, RCoR-1, RXR-beta, RXRbeta
Breast neoplasms, Hypothyroidism, Rheumatoid arthritis, Stomach neoplasms

11444
Retinoid X receptor gamma
NR2B3, RXR-gamma, RXRC, RXRgamma
Atrial fibrillation, Attention deficit hyperactivity disorder, Bipolar disorder, Myocardial ischemia

11445
Ribitol xylosyltransferase 1
HP10481, MDDGA10, TMEM5
Muscle eye brain disease, Walker-warburg syndrome

11446
RING1 and YY1 binding protein
AAP1, APAP-1, DEDAF, YEAF1
Asthma, Eczema, Breast cancer, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Oligodendroglioma, Respiratory system disease, Hypertension

11447
Receptor like tyrosine kinase
D3S3195, JTK5, JTK5A, RYK1
Cardiovascular disease, Cleft palate, Coronary artery disease, Craniofacial abnormalities, Hypertension, Orofacial cleft, Vascular dementia, Venous thromboembolism

11448
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)

11449
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)

11450
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