Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "O"

31 to 40 of 301 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
31	8481	OFD1	OFD1 centriole and centriolar satellite protein	71-7A, CXorf5, JBTS10, RP23, SGBS2	Bifid nail, Congenital anomalies of the kidney and urinary tract, Ciliary dyskinesia, Ciliopathy, Coach syndrome, Connective tissue disease, Desbuquois syndrome, Aplasia of the vermis, Joubert syndrome, Orofaciodigital syndrome, Osteoporosis, Otopalatodigital syndrome, Polydactyly, Polymicrogyria, Retinitis pigmentosa View all (3 more)
32	10724	OGA	O-GlcNAcase	MEA5, MGEA5, NCOAT	Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Epilepsy, Generalized epilepsy, Partial epilepsy
33	4967	OGDH	Oxoglutarate dehydrogenase	AKGDH, E1k, E1o, HsOGDH, KGD1, OGDC, OGDH-E1, OGDH2, OGDHD	Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Lung cancer, Metabolic syndrome, Diabetes mellitus type 2
34	55753	OGDHL	Oxoglutarate dehydrogenase L	YOBELN	Congestive heart failure, Major depressive disorder, Heart failure, Yoon-bellen neurodevelopmental syndrome
35	55239	OGFOD1	2-oxoglutarate and iron dependent oxygenase domain containing 1	TPA1	Bardet-biedl syndrome, Insomnia, Retinitis pigmentosa
36	4968	OGG1	8-oxoguanine DNA glycosylase	HMMH, HOGG1, MUTM, OGH1	Brain disease, Renal cell carcinoma, Discoid lupus erythematosus, Ischemic heart disease, Coronary artery disease, Dermatologic disorder, Developmental coordination disorder, Diabetes mellitus type 2, Esophageal squamous cell carcinoma, Genetic predisposition to disease, Graves disease, Heart disease, Huntington disease, Hyperplasia, Hypertension View all (12 more)
37	8473	OGT	O-linked N-acetylglucosamine (GlcNAc) transferase	HINCUT-1, HRNT1, MRX106, O-GLCNAC, OGT1, XLID106	Intellectual developmental disorder, x-linked
38	170392	OIT3	Oncoprotein induced transcript 3	LZP	Hepatocellular carcinoma, Coronary artery disease
39	29789	OLA1	Obg like ATPase 1	DOC45, GBP45, GTBP9, GTPBP9, PTD004	Astrocytoma, Glioma, Hypertension, Metabolic syndrome, Schizophrenia, Diabetes mellitus type 2
40	10439	OLFM1	Olfactomedin 1	AMY, NOE1, NOELIN1, OlfA	Alzheimer disease, Attention deficit hyperactivity disorder, Color vision deficiency, Colorectal cancer, Dementia, Insomnia, Liver disease, Major depressive disorder, Metabolic syndrome, Obesity, Oligodendroglioma, Ovarian cancer, Post-traumatic stress disorder, Prostatic neoplasms, Substance abuse, Diabetes mellitus type 2 View all (1 more)

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