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"
231 to 240 of 754 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

231
Retinol binding protein 3
D10S64, D10S65, D10S66, IRBP, RBPI, RP66
Ankylosing spondylitis, Autoimmune disease, Retinitis pigmentosa, Cone-rod dystrophy, Night blindness, congenital stationary, Optic atrophy, Uveitis

232
Retinol binding protein 4
MCOPCB10, RDCCAS
Anophthalmia, Anterior segment mesenchymal dysgenesis, Bilateral microphthalmos, Breast neoplasms, Carcinoma, Ischemic heart disease, Colobomatous microphthalmia, Colorectal cancer, Congenital ocular coloboma, Congestive heart failure, Coronary artery disease, Diabetes mellitus type 2, Heart failure, Kidney disease, Liver disease
View all (8 more)

233
Recombination signal binding protein for immunoglobulin kappa J region
AOS3, CBF-1, CBF1, IGKJRB, IGKJRB1, KBF2, RBP-J, RBP-J kappa, RBP-JK, RBPJK, RBPSUH, SUH, csl
Adams-oliver syndrome, Rheumatoid arthritis, Dilated cardiomyopathy, Color vision deficiency, Crohn disease, Desbuquois syndrome, Diabetes mellitus type 2, Endometriosis, Hypothyroidism, Inflammatory bowel disease, Metabolic syndrome, Multiple sclerosis, Obesity, Schizophrenia, Ulcerative colitis

234
Recombination signal binding protein for immunoglobulin kappa J region like
RBPL, RBPSUHL, SUHL
Bipolar disorder, Diabetes mellitus type 2

235
RNA binding protein, mRNA processing factor
HERMES
Atrial fibrillation, Kidney cancer, Myeloproliferative disorder, Oropharyngeal cancer, Tonsil cancer, Uterine fibroid

236
RNA binding protein, mRNA processing factor 2
-
Coronary artery disease

237
Rabenosyn, RAB effector
KAREVS, MFANDO, Rabenosyn-5, ZFYVE20
Congenital neutropenia, Insomnia, Congenital myelofibrosis with anemia, Severe congenital neutropenia

238
Ring-box 1
BA554C12.1, RNF75, ROC1
Crohn disease, Inflammatory bowel disease, Insomnia, Major depressive disorder, Neurotic disorder, Parkinson disease, Schizophrenia, Seasonal allergic rhinitis, Stevens-johnson syndrome

239
Ring finger and CCCH-type domains 1
FHL6, IMDSHY, RNF198, ROQUIN
Dyslexia, Hemophagocytic lymphohistiocytosis, Insomnia, Metabolic syndrome, Psychiatric disorders, Willis-ekbom disease, Diabetes mellitus type 2

240
Ring finger and CCCH-type domains 2
MNAB, RNF164
Insomnia, Osteoarthritis