Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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11111 to 11120 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11111
Regulator of G protein signaling like 1
RGSL, RGSL2
Color vision deficiency, Venous thromboembolism

11112
Rh associated glycoprotein
CD241, OHS, OHST, RH2, RH50A, RHNR, Rh50, Rh50GP, SLC42A1
Hemolytic anemia, Carotid artery disease, Rh deficiency syndrome, Rh-null, regulator type

11113
Rhomboid domain containing 1
RHBDL4, RRP4
Kawasaki disease, Pancreatic neoplasms, Respiratory system infectious disease, Age-related macular degeneration

11114
Rhomboid 5 homolog 1
C16orf8, Dist1, EGFR-RS, gene-89, gene-90, hDist1
Central nervous system cancer, Glioblastoma, Glioma, Alzheimer disease, Wolff-parkinson-white syndrome

11115
Rhomboid like 1
RHBDL, RRP
Cerebellar ataxia, Spinocerebellar ataxia

11116
Rhomboid like 2
RRP2
Atrial fibrillation, Major depressive disorder, Diabetes mellitus type 2

11117
Rhomboid like 3
RHBDL4, VRHO
Schizophrenia, Scoliosis

11118
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

11119
Rh family C glycoprotein
C15orf6, PDRC2, RHGK, SLC42A3
Dental caries

11120
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