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"
51 to 60 of 301 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

51
Oligodendrocyte myelin glycoprotein
OMGP
Diverticular disease

52
One cut homeobox 1
HNF-6, HNF6, HNF6A
Insomnia, Metabolic syndrome, Neonatal diabetes mellitus, Polycystic liver disease, Schizophrenia, Diabetes mellitus type 2

53
One cut homeobox 2
OC-2, OC2
Migraine, Polycystic kidney disease, Polycystic liver disease, Prostatic neoplasms

54
One cut homeobox 3
OC3
Central nervous system cancer, Glioblastoma, Glioma

55
Oocyte expressed protein
C6orf156, FLOPED, HOEP19, KHDC2
Oocyte maturation defect

56
Oocyte secreted protein 1
-
Ocular sarcoidosis

57
Oocyte secreted protein family member 3
-
Deficiency anemia, Megaloblastic anemia, Vitamin b deficiency, Vitamin b12 deficiency, Vitamin deficiency disorder

58
OPA1 mitochondrial dynamin like GTPase
BERHS, MGM1, MTDPS14, NPG, NTG, largeG
Auditory neuropathy, Cerebellar ataxia, Optic atrophy, Blepharoptosis, Centronuclear myopathy, Cone-rod dystrophy, Dental caries, Dominant hereditary optic atrophy, Glaucoma, Leigh syndrome, Major depressive disorder, Mitochondrial disease, Mitochondrial dna depletion syndrome, Neurodevelopmental disorder, Osteoarthritis
View all (5 more)

59
Outer mitochondrial membrane lipid metabolism regulator OPA3
MGA3
3-methylglutaconic aciduria, Alzheimer disease, Optic atrophy, Costeff optic atrophy syndrome, Retinitis pigmentosa

60
Oligodendrocytic myelin paranodal and inner loop protein
HTMP10, TMEM10, TMP10
Dementia