Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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11281 to 11290 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11281
RNA binding protein with serine rich domain 1
E5.1
Mood disorder

11282
Roundabout guidance receptor 1
CPHD8, DUTT1, NORS, NYS8, SAX3
Alzheimer disease, Imperforate anus, Atrial septal defect, Autism, Congenital anomalies of the kidney and urinary tract, Hepatocellular carcinoma, Central hypothyroidism, Color vision deficiency, Renal agenesis, Congenital heart disease, Congenital nystagmus, Dementia, Dental caries, Dental enamel hypoplasia, Diverticular disease
View all (17 more)

11283
Roundabout guidance receptor 2
SAX3
Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Bell's palsy, Congenital anomalies of the kidney and urinary tract, Cholangiocarcinoma, Color vision deficiency, Deficiency anemia, Eating disorder, Endometriosis, Vesicoureteral reflux, Iga nephropathy, Insomnia, Liver cirrhosis, Liver disease
View all (14 more)

11284
Roundabout guidance receptor 3
HGPPS, HGPPS1, HGPS, RBIG1, RIG1
Autism, Horizontal gaze palsy with progressive scoliosis, Gestational diabetes, Retinopathy, Scoliosis

11285
Roundabout guidance receptor 4
AOVD3, ECSM4, MRB
Aortic aneurysm, Aortic valve disease, Autism, Bicuspid aortic valve, Congenital diaphragmatic hernia, Thoracic aortic aneurysm and aortic dissection, Tetralogy of fallot, Venous thromboembolism

11286
Rho associated coiled-coil containing protein kinase 1
P160ROCK, ROCK-I
Basal cell carcinoma, Promyelocytic leukemia

11287
Rho associated coiled-coil containing protein kinase 2
ROCK-II
Cardiomegaly, Congenital heart disease, Congestive heart failure, Dextrocardia, Heart failure, Non-immune hydrops fetalis, Ventricular remodeling

11288
Rogdi atypical leucine zipper
KTZS, RAV2, ROGD1
Amelocerebrohypohidrotic syndrome, Autism

11289
Retinal outer segment membrane protein 1
ROM, ROSP1, RP7, TSPAN23
Macular dystrophy, Optic atrophy, Retinitis pigmentosa, Retinitis pigmentosa, digenic

11290
Rhophilin associated tail protein 1 like
ASP, LINC01513, RSPH11, TCONS_00009352
Ankylosing spondylitis, Breast cancer, Coronary artery disease, Crohn disease, Dermatomyositis, Parkinson disease, Psoriasis, Sclerosing cholangitis, Ulcerative colitis