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"
291 to 299 of 299 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

291
OXA1L mitochondrial inner membrane insertase
OXA1, OXA1L1
Mitochondrial disease

292
3-oxoacid CoA-transferase 1
OXCT, SCOT
Bipolar disorder, Osteoporosis

293
Oxoeicosanoid receptor 1
GPCR, GPR170, TG1019
Major depressive disorder

294
Oxoglutarate receptor 1
CAON2, GPR80, GPR99, P2RY15, P2Y15, aKGR
Nephrolithiasis

295
Oxidoreductase NAD binding domain containing 1
RFTN1-AS1
Thoracic aortic aneurysm

296
Oxidation resistance 1
CHEGDD, Nbla00307, TLDC3
Breast cancer, Cerebellar atrophy, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Congenital cerebellar hypoplasia, Hearing impairment, Insomnia, Intellectual developmental disorder, Neurotic disorder, Peripheral arterial disease

297
Oxidative stress responsive kinase 1
OSR1
Astrocytoma, Hypertension, Schizophrenia

298
Oxytocin/neurophysin I prepropeptide
OT, OT-NPI, OXT-NPI
Anxiety disorder, Autism, Carcinoma, Colonic neoplasms, Major depressive disorder, Disseminated intravascular coagulation, Edema, Tonic-clonic epilepsy, Headache, Hyperkinesia, Hypertension, Hypotension, Mood disorder, Neurodevelopmental disorder, Prostatic disease
View all (4 more)

299
Oxytocin receptor
OT-R, OTR
Autism, Non-small-cell lung carcinoma, Cardiomyopathy, Chromosome 3p25 monosomy, Cognition disorder, Delirium, dementia, and cognitive disorders, Major depressive disorder, Disruptive impulse-control and conduct disorder, Long qt syndrome, Hypertrophic cardiomyopathy, Joubert syndrome, Rippling muscle disease, Schizophrenia, Tubular aggregate myopathy, Depression