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"
191 to 200 of 754 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

191
RBBP8 N-terminal like
C20orf151
Central serous retinopathy, Color vision deficiency, Colorectal cancer, Insomnia, Kidney cancer, Prostate cancer, Age-related macular degeneration

192
RANBP2-type and C3HC4-type zinc finger containing 1
C20orf18, HOIL-1, HOIL1, PBMEI, PGBM1, RBCK2, RNF54, UBCE7IP3, XAP3, XAP4, ZRANB4
Alzheimer disease, Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis, Cardiomegaly, Glycogen storage disease

193
RNA binding fox-1 homolog 1
2BP1, A2BP1, FOX-1, FOX1, HRNBP1
Alzheimer disease, Anorexia nervosa, Astrocytoma, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Brain aneurysm, Breast cancer, Cardiac embolism, Cardioembolic stroke, Cataract, Central nervous system cancer, Cervical cancer, Obstructive pulmonary disease, Color vision deficiency
View all (52 more)

194
RNA binding fox-1 homolog 2
FOX2, Fox-2, HNRBP2, HRNBP2, RBM9, RTA, dJ106I20.3, fxh
Alzheimer disease, Adenoid cystic carcinoma, Congenital heart disease, Dementia, Dyslexia, Hypoplastic left heart syndrome, Salivary gland neoplasms, Specific language disorder, Tetralogy of fallot

195
RNA binding fox-1 homolog 3
FOX-3, FOX3, HRNBP3, NEUN
Obstructive pulmonary disease, Endometriosis, Epilepsy, Rolandic epilepsy, Migraine, Oligodendroglioma, Osteoarthritis, Visual disorder

196
Ribokinase
RBSK, RK
Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Diverticular disease, Major depressive disorder, Obsessive-compulsive disorder, Psoriasis, Schizophrenia, Tourette syndrome

197
RB transcriptional corepressor like 1
CP107, PRB1, p107
Diabetic neuropathy

198
RB transcriptional corepressor like 2
BRUWAG, P130, Rb2
Attention deficit hyperactivity disorder, Autism, Brunet-wagner neurodevelopmental syndrome, Neurodevelopmental disorder, Insomnia, Lymphocytic b-cell leukemia, Non-specific syndromic intellectual disability, Ovarian neoplasms, Rheumatic disease, Diabetes mellitus type 2

199
RNA binding motif protein 12
HRIHFB2091, SCZD19, SWAN
Psychotic disorders, Schizophrenia

200
RBM14-RBM4 readthrough
COAZ, PSP2, RBM14, SIP
Insomnia, Migraine