Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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11171 to 11180 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11171
Receptor interacting serine/threonine kinase 3
RIP3
Calcinosis, Fatty liver, Fatty liver, alcoholic, Heart valve disease, Heart valve prolapse

11172
Receptor interacting serine/threonine kinase 4
ANKK2, ANKRD3, CHANDS, DIK, NKRD3, PKK, PPS2, RIP4
Atrial fibrillation, Bartsocas-papas syndrome, Breast cancer, Curly hair ankyloblepharon nail dysplasia syndrome, Ectodermal dysplasia, Venous thromboembolism

11173
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

11174
RIPOR family member 3
C20orf175, C20orf176, FAM65C
Colorectal adenoma, Colorectal cancer, Scoliosis

11175
Ripply transcriptional repressor 1
-
Cerebellar ataxia, intellectual disability, and dysequilibrium, Dysequilibrium syndrome

11176
Ripply transcriptional repressor 2
C6orf159, SCDO6, dJ237I15.1
Spondylocostal dysostosis, Color vision deficiency, Desbuquois syndrome, Jarcho-levin syndrome, Klippel-feil syndrome

11177
-
-
Klippel-feil syndrome, Spondylocostal dysostosis

11178
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, Liver cirrhosis, Noonan syndrome, Parkinson disease, Schizophrenia, Ulcerative colitis

11179
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

11180
Retinaldehyde binding protein 1
CRALBP
Retinitis pigmentosa, Bothnia retinal dystrophy, Eye disease, Macular degeneration, Night blindness, congenital stationary, Optic atrophy, Retinitis punctata albescens, Schizophrenia