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 "O"
261 to 270 of 299 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

261
Oncostatin M receptor
IL-31R-beta, IL-31RB, OSMRB, OSMRbeta, PLCA1
Amyloidosis, Ankylosing spondylitis, Non-small-cell lung carcinoma, Crohn disease, Iga nephropathy, Inflammatory bowel disease, Mesothelioma, Psoriasis, Sclerosing cholangitis, Ulcerative colitis

262
Odd-skipped related transcription factor 1
ODD
Congenital heart disease, Nasopharyngeal neoplasms

263
Odd-skipped related transciption factor 2
-
Endometriosis

264
Oligosaccharyltransferase complex non-catalytic subunit
DC2
Central nervous system cancer, Glioblastoma, Glioma, Amyotrophic lateral sclerosis, Hypertension

265
Osteoclast stimulating factor 1
OSF, SH3P2, bA235O14.1
Asthma, Scoliosis

266
Osteoclastogenesis associated transmembrane protein 1
GIPN, GL, HSPC019, OPTB5
Osteopetrosis, Desbuquois syndrome, Psoriasis

267
Osteocrin
MUSCLIN
Alzheimer disease, Dementia, Immune system disease, Psoriasis

268
Ornithine transcarbamylase
OCTD, OTC1, OTCD, OTCase
Brain disease, Cognition disorder, Delirium, dementia, and cognitive disorders, Urea cycle disorder, Global developmental delay, Hyperammonemia

269
Otoancorin
CT108, DFNB22
Isolated sensorineural deafness, Nonsyndromic hearing loss, Deafness, Hearing impairment, Hearing loss, Hereditary hearing loss, Major depressive disorder, Schizophrenia, Usher syndrome

270
Otoferlin
AUNB1, DFNB6, DFNB9, FER1L2, NSRD9
Alzheimer disease, Arthrogryposis with ectodermal dysplasia, Auditory neuropathy, Isolated sensorineural deafness, Nonsyndromic intellectual disability, Congenital ear anomaly, Deafness, Hearing impairment, Hearing loss, Hereditary hearing loss, Pendred syndrome, Periodontitis, Nonsyndromic hearing loss