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"
61 to 70 of 301 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

61
Opioid binding protein/cell adhesion molecule like
IGLON1, OBCAM, OPCM
Androgenetic alopecia, Anorexia nervosa, Attention deficit hyperactivity disorder, Cardiomyopathy, Colorectal cancer, Coronary artery disease, Crohn disease, Developmental dysplasia of the hip, Diverticular disease, Eating disorder, Gastric cancer, Major depressive disorder, Metabolic syndrome, Migraine, Oligodendroglioma
View all (12 more)

62
Oligophrenin 1
ARHGAP41, MRX60, MRXSBL, OPN1
Androgenetic alopecia, Autism, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Congenital neurologic anomalies, Coronary artery disease, Craniofrontonasal dysplasia, Gross motor development delay, Hypogonadism, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Nystagmus, Prostate cancer, X-linked intellectual disability

63
5-oxoprolinase, ATP-hydrolysing
5-Opase, OPLA, OPLAHD
5-oxoprolinase deficiency, Alzheimer disease, Atrial fibrillation, Atrial flutter

64
Opsin 1, long wave sensitive
CBBM, CBP, COD5, RCP, ROP
Blue cone monochromatism, Color vision deficiency, Cone monochromatism, Cone-rod dystrophy, X-linked cone dysfunction syndrome with myopia

65
Opsin 1, medium wave sensitive
CBBM, CBD, COD5, GCP, GOP, OPN1MW1
Blue cone monochromatism, Color vision deficiency, Cone dystrophy, x-linked, Cone monochromatism, Cone-rod dystrophy, Deuteranomaly, X-linked cone dysfunction syndrome with myopia

66
Opsin 1, medium wave sensitive 2
GOP
Deuteranomaly

67
Opsin 1, short wave sensitive
BCP, BOP, CBT
Atrial fibrillation, Blue cone monochromatism, Cardioembolic stroke, Color vision deficiency, Hodgkin lymphoma, Hypertrophic cardiomyopathy, Retinitis pigmentosa, Systemic lupus erythematosus, Tritanopia

68
Opsin 3
ECPN, PPP1R116
Obesity, Pancreatic cancer, Depression

69
Opsin 4
MOP
Peripheral arterial disease, Seasonal affective disorder

70
Opsin 5
GPR136, GRP136, PGR12, TMEM13
Nephrotic syndrome, Peripheral arterial disease