Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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11121 to 11130 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11121
RHO family interacting cell polarization regulator 2
C6orf32, DFNA21, DFNB104, DIFF40, DIFF48, FAM65B, MYONAP, PL48
Asthma, Isolated sensorineural deafness, Nonsyndromic hearing loss, Deafness, Dementia, Glaucoma, Gout, Hearing loss, Diabetes mellitus type 1, Diabetes mellitus type 2

11122
RIPOR family member 3
C20orf175, C20orf176, FAM65C
Colorectal adenoma, Colorectal cancer, Scoliosis

11123
Ripply transcriptional repressor 1
-
Cerebellar ataxia, intellectual disability, and dysequilibrium, Dysequilibrium syndrome

11124
Ripply transcriptional repressor 2
C6orf159, SCDO6, dJ237I15.1
Spondylocostal dysostosis, Color vision deficiency, Desbuquois syndrome, Jarcho-levin syndrome, Klippel-feil syndrome

11125
-
-
Klippel-feil syndrome, Spondylocostal dysostosis

11126
Ras like without CAAX 1
NS8, RIBB, RIT, ROC1
Cardiofaciocutaneous syndrome, Conduct disorder, Congenital heart disease, Congenital malformation syndromes associated with short stature, Crohn disease, Desbuquois syndrome, Non-immune hydrops fetalis, Hypertension, Inflammatory bowel disease, Noonan syndrome, Parkinson disease, Schizophrenia, Ulcerative colitis

11127
Ras like without CAAX 2
RIBA, RIN, ROC2
Attention deficit hyperactivity disorder, Lymphoblastic leukemia, Conduct disorder, Metabolic syndrome, Parkinson disease, Scoliosis, Substance abuse, Diabetes mellitus type 2, Venous thromboembolism

11128
Retinaldehyde binding protein 1
CRALBP
Retinitis pigmentosa, Bothnia retinal dystrophy, Eye disease, Macular degeneration, Night blindness, congenital stationary, Optic atrophy, Retinitis punctata albescens, Schizophrenia

11129
RLF zinc finger
ZN-15L, ZNF292L
Diabetes mellitus type 2

11130
RNA 5'-phosphate and 3'-OH ligase 1
C12orf29, Rnl
Bardet-biedl syndrome, Aplasia of the vermis, Global developmental delay, Joubert syndrome, Leber congenital amaurosis, Meckel-gruber syndrome, Micrognathism, Nephronophthisis, Rod-cone dystrophy, Senior-loken syndrome