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"
371 to 380 of 754 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

371
Rh blood group CcEe antigens
CD240CE, RH, RH30A, RHC, RHCe(152N), RHE, RHIXB, RHNA, RHPI, Rh4, RhIVb(J), RhVI, RhVIII, SLC42A4
Hemolytic anemia, Rh deficiency syndrome, Rh-null, amorph type

372
Rh family C glycoprotein
C15orf6, PDRC2, RHGK, SLC42A3
Dental caries

373
Rh blood group D antigen
CD240D, DIIIc, HDFNRH, RH, RH30, RHCED, RHDVA(TT), RHDel, RHPII, RHXIII, Rh4, RhDCw, RhII, RhK562-II, RhPI, SLC42A5
Hemolytic anemia, Alpha-1 antichymotrypsin deficiency, Hemolytic disease of fetus and newborn, Rh deficiency syndrome, Rh isoimmunization, Schizophrenia

374
Ras homolog, mTORC1 binding
RHEB2
Non-small-cell lung carcinoma, Central nervous system cancer, Neurodevelopmental disorder, Focal cortical dysplasia, Glioblastoma, Glioma, Hemimegalencephaly, Intellectual developmental disorder, Non-specific syndromic intellectual disability, Oligodendroglioma

375
RHEB like 1
RHEBL1c
Attention deficit hyperactivity disorder, Bipolar disorder

376
Rhodopsin
CSNBAD1, OPN2, RP4
Retinitis pigmentosa, Blindness, Cataract, Cone dystrophy, Cone-rod dystrophy, Congenital stationary night blindness, Exudative retinopathy, Microcephaly, Neuropathy, congenital hypomyelinating, Night blindness, congenital stationary, Nystagmus, Oguchi disease, Optic atrophy, Retinal degeneration, Retinal detachment
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377
Ras homolog family member A
ARH12, ARHA, EDFAOB, RHO12, RHOH12
Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Carcinoma, Congenital hemihypertrophy, Coronary artery disease, Craniofacial abnormalities, Ectodermal dysplasia, Gout, Inflammatory bowel disease, Myocardial infarction, Proteinuria, Stomach neoplasms, Substance abuse, Tooth disease
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378
Ras homolog family member B
ARH6, ARHB, MST081, MSTP081, RHOH6
Scleroderma, Systemic sclerosis, Venous thromboembolism

379
Rho related BTB domain containing 1
-
Juvenile arthritis, Juvenile idiopathic arthritis, Oligoarticular juvenile idiopathic arthritis

380
Rho related BTB domain containing 2
DBC2, DEE64, EIEE64, p83
Basal cell carcinoma, Chorea, Neurodevelopmental disorder, Developmental and epileptic encephalopathy, Non-neoplastic peripheral nervous system disease, Non-specific syndromic intellectual disability, Peripheral nervous system disease, Peripheral neuropathy, Rett syndrome