Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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11301 to 11310 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11301
Replication protein A1
HSSB, MST075, PFBMFT6, REPA1, RF-A, RP-A, RPA70
Bipolar disorder, Chloracne, Polycystic ovary syndrome, Prostate cancer, Telomere-related pulmonary fibrosis and/or bone marrow failure

11302
Replication protein A3
REPA3, RP-A p14
Interstitial lung disease, Neurotic disorder, Diabetes mellitus type 2

11303
RPA interacting protein
HRIP, RIP
Schizophrenia

11304
RNA polymerase II associated protein 1
-
Obstructive pulmonary disease, Diabetes mellitus type 2

11305
RNA polymerase II associated protein 2
C1orf82, Rtr1
Multiple sclerosis, Diabetes mellitus type 1, Diabetes mellitus type 2

11306
RNA polymerase II associated protein 3
Tah1, hSpagh
Dementia, Lung cancer, Obesity

11307
Retinoid isomerohydrolase RPE65
BCO3, LCA2, RP20, mRPE65, p63, rd12, sRPE65
Leber congenital amaurosis, Autism, Retinitis pigmentosa, Blindness, Cone-rod dystrophy, Congenital blindness, Congenital nystagmus, Eye disease, Glaucoma, Global developmental delay, Neurodevelopmental disorder, Nystagmus, Open angle glaucoma, Leber hereditary optic neuropathy, Retinal degeneration
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11308
Ribosome production factor 1 homolog
BXDC5
Prostate cancer, Psychiatric disorders

11309
Ribosome production factor 2 homolog
BXDC1, bA397G5.4
Dry eye syndrome

11310
Retinitis pigmentosa GTPase regulator
COD1, CORDX1, CRD, PCDX, RP15, RP3, XLRP3, orf15
Ciliary dyskinesia, Cone dystrophy, Cone dystrophy, x-linked, Cone-rod dystrophy, Cone-rod dystrophy, x-linked, Esophageal atresia, Hearing impairment, Hearing loss, Leber congenital amaurosis, Macular degeneration, Atrophic macular degeneration, Macular dystrophy, Night blindness, congenital stationary, Optic atrophy, Ciliary dyskinesia with retinitis pigmentosa
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