Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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9321 to 9330 of 15435 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

9321
Oligosaccharyltransferase complex non-catalytic subunit
DC2
Central nervous system cancer, Glioblastoma, Glioma, Amyotrophic lateral sclerosis, Hypertension

9322
Osteoclast stimulating factor 1
OSF, SH3P2, bA235O14.1
Asthma, Scoliosis

9323
Osteoclastogenesis associated transmembrane protein 1
GIPN, GL, HSPC019, OPTB5
Osteopetrosis, Desbuquois syndrome, Psoriasis

9324
Osteocrin
MUSCLIN
Alzheimer disease, Dementia, Immune system disease, Psoriasis

9325
Ornithine transcarbamylase
OCTD, OTC1, OTCD, OTCase
Brain disease, Cognition disorder, Delirium, dementia, and cognitive disorders, Disorder of the urea cycle metabolism, Global developmental delay, Hyperammonemia, Liver cirrhosis

9326
Otoancorin
CT108, DFNB22
Isolated sensorineural deafness, Nonsyndromic hearing loss, Deafness, Hearing impairment, Hearing loss, Hereditary hearing loss, Major depressive disorder, Schizophrenia, Usher syndrome

9327
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

9328
Otogelin
DFNB18B, MLEMP, OTGN
Amyotrophic lateral sclerosis, Asthma, Isolated sensorineural deafness, Nonsyndromic hearing loss, Deafness, Hearing impairment, Hearing loss, Intellectual developmental disorder, Meniere disease

9329
Otogelin like
C12orf64, DFNB84B
Alzheimer disease, Isolated sensorineural deafness, Nonsyndromic intellectual disability, Central vertigo, Kidney disease, Deafness, Hearing impairment, Hearing loss, Meniere disease, Ocular hypertension, Oligodendroglioma, Peripheral vertigo, Nonsyndromic hearing loss, Skin disease, Vestibular disease

9330
Otolin 1
C1QTNF15, C1QTNF16
Alzheimer disease, Attention deficit hyperactivity disorder, Burkitt lymphoma, Coronary artery disease, Dementia, Eosinophilia, Eyelid disease, Glomerulonephritis, Kidney disease, Lung cancer, Major depressive disorder, Metabolic syndrome, Oligodendroglioma, Schizophrenia, Squamous cell carcinoma
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