Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
11491 to 11500 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11491
RWD domain containing 3
RSUME
Obsessive-compulsive disorder

11492
Relaxin family peptide receptor 1
LGR7, RXFPR1
Lymphoblastic leukemia, Color vision deficiency, Endometriosis

11493
Relaxin family peptide receptor 2
GPR106, GREAT, INSL3R, LGR8, LGR8.1, RXFPR2
Atrial fibrillation, Cardiovascular disease, Colorectal cancer, Cryptorchidism, Disorder of sexual differentiation, Hypertension, Gallbladder neoplasms, Hyperaldosteronism, Hyperplasia, Insomnia, Major depressive disorder, Potassium deficiency, Primary aldosteronism, Retinopathy

11494
Relaxin family peptide receptor 3
GPCR135, RLN3R1, RXFPR3, SALPR
Basal cell carcinoma, Melanoma, Squamous cell carcinoma

11495
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

11496
Retinoid X receptor beta
DAUDI6, H-2RIIBP, NR2B2, RCoR-1, RXR-beta, RXRbeta
Breast neoplasms, Hypothyroidism, Rheumatoid arthritis, Stomach neoplasms

11497
Retinoid X receptor gamma
NR2B3, RXR-gamma, RXRC, RXRgamma
Atrial fibrillation, Attention deficit hyperactivity disorder, Bipolar disorder, Myocardial ischemia

11498
Ribitol xylosyltransferase 1
HP10481, MDDGA10, TMEM5
Muscle eye brain disease, Walker-warburg syndrome

11499
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

11500
Receptor like tyrosine kinase
D3S3195, JTK5, JTK5A, RYK1
Cardiovascular disease, Cleft palate, Coronary artery disease, Craniofacial abnormalities, Hypertension, Orofacial cleft, Vascular dementia, Venous thromboembolism