Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "O"

281 to 290 of 301 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
281	55593	OTUD5	OTU deubiquitinase 5	DUBA, MCAND	Dysgenesis of corpus callosum, Non-specific syndromic intellectual disability
282	51633	OTUD6B	OTU deubiquitinase 6B	CGI-77, DUBA-5, DUBA5, IDDFSDA	Early-onset seizures-distal limb anomalies-facial dysmorphism-global developmental delay syndrome, Epilepsy, Intellectual developmental disorder dysmorphic seizures, Intellectual developmental disorder
283	161725	OTUD7A	OTU deubiquitinase 7A	C15orf16, C16ORF15, CEZANNE2, NEDHS, OTUD7	Color vision deficiency, Colorectal cancer, Neurodevelopmental disorder, Developmental and epileptic encephalopathy, Language development disorders, Non-specific syndromic intellectual disability, Orofacial cleft, Periprosthetic osteolysis, Specific learning disability, Venous thromboembolism
284	56957	OTUD7B	OTU deubiquitinase 7B	CEZANNE, ZA20D1	Bipolar disorder, Breast cancer, Obstructive pulmonary disease, Coronary artery disease, Glaucoma, Hypertension, Obesity, Open angle glaucoma, Schizophrenia
285	90268	OTULIN	OTU deubiquitinase with linear linkage specificity	AIPDS, AIPDSA, FAM105B, GUM, IMD107	Asthma, Autoinflammation, panniculitis, and dermatosis syndrome, Calcium metabolism disorders, Chondrocalcinosis, Craniometadiaphyseal dysplasia, Craniometaphyseal dysplasia, Immunodeficiency, Diabetes mellitus type 2
286	54491	OTULINL	OTU deubiquitinase with linear linkage specificity like	FAM105A, NET20	Asthma, Eczema, Obstructive pulmonary disease, Liver cirrhosis, Osteoarthritis, Respiratory system disease, Diabetes mellitus type 2
287	5013	OTX1	Orthodenticle homeobox 1	-	Attention deficit hyperactivity disorder, Prostate cancer, Substance abuse, Vesicoureteral reflux
288	5015	OTX2	Orthodenticle homeobox 2	CPHD6, MCOPS5	Anophthalmia/microphthalmia-esophageal atresia syndrome, Anophthalmia, Anxiety disorder, Attention deficit hyperactivity disorder, Bipolar disorder, Butterfly-shaped pigmentary macular dystrophy, Colobomatous microphthalmia, Combined pituitary hormone deficiency, Desbuquois syndrome, Diabetic neuropathy, Leber congenital amaurosis, Macular dystrophy, Male infertility single gene azoospermia, Medulloblastoma, Microphthalmia View all (11 more)
289	341277	OVCH2	Ovochymase 2	OVTN	Contracture, Venous thromboembolism
290	5017	OVOL1	Ovo like transcriptional repressor 1	HOVO1	Asthma, Eczema, Basal cell carcinoma, Bladder calculus, Breast cancer, Cardiovascular disease, Kidney disease, Atopic dermatitis, Gout, Hypertension, Hypertensive nephropathy, Iga nephropathy, Keratinocyte carcinoma, Kidney failure, Metabolic syndrome View all (8 more)

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