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"
251 to 260 of 754 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

251
Reticulocalbin 2
E6BP, ERC-55, ERC55, TCBP49
Alzheimer disease, Gastroesophageal reflux disease, Gout, Intracranial hemorrhage, Peptic ulcer disease

252
Reticulocalbin 3
RLP49
Malunion fracture, Osteoarthritis, Diabetes mellitus type 2

253
REST corepressor 1
COREST, RCOR
Asthma, Eczema, Colonic neoplasms, Aplasia of the vermis, Insomnia, Multiple sclerosis, Prostate cancer, Sialolithiasis, Diabetes mellitus type 2

254
REST corepressor 2
-
Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Gout, Major depressive disorder, Obsessive-compulsive disorder, Schizophrenia, Tourette syndrome

255
RCSD domain containing 1
CAPZIP, MK2S4
Appendicitis, Astrocytoma, Central nervous system cancer, Kidney disease, Color vision deficiency, Glioma, Kidney failure, Sarcoidosis

256
RD3 regulator of GUCY2D
C1orf36, LCA12
Asthma, Kidney disease, Hypertension, Kidney failure, Leber congenital amaurosis, Lung cancer, Retinitis pigmentosa, Retinopathy, Squamous cell carcinoma

257
Retinol dehydrogenase 10
SDR16C4
Craniofacial abnormalities

258
Retinol dehydrogenase 11
ARSDR1, CGI82, HCBP12, MDT1, PSDR1, RALR1, RDJCSS, SCALD, SDR7C1
Optic atrophy, Retinitis pigmentosa, Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome, Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome

259
Retinol dehydrogenase 12
LCA13, RP53, SDR7C2
Cone-rod dystrophy, Leber congenital amaurosis, Macular dystrophy, Optic atrophy, Leber hereditary optic neuropathy, Retinal degeneration, Retinitis pigmentosa, Stargardt disease

260
Retinol dehydrogenase 13
SDR7C3
Aortic disease, Necrosis