Genes | GeDiPNet - Gene Disease Pathway & Associations

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9301 to 9310 of 15380 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
9301	54726	OTUD4	OTU deubiquitinase 4	DUBA6, HIN1, HSHIN1	Obstructive pulmonary disease
9302	55593	OTUD5	OTU deubiquitinase 5	DUBA, MCAND	Dysgenesis of corpus callosum, Non-specific syndromic intellectual disability
9303	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
9304	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
9305	56957	OTUD7B	OTU deubiquitinase 7B	CEZANNE, ZA20D1	Bipolar disorder, Breast cancer, Obstructive pulmonary disease, Coronary artery disease, Glaucoma, Hypertension, Obesity, Open angle glaucoma, Schizophrenia
9306	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
9307	54491	OTULINL	OTU deubiquitinase with linear linkage specificity like	FAM105A, NET20	Asthma, Eczema, Obstructive pulmonary disease, Osteoarthritis, Respiratory system disease, Diabetes mellitus type 2
9308	5013	OTX1	Orthodenticle homeobox 1	-	Attention deficit hyperactivity disorder, Prostate cancer, Substance abuse, Vesicoureteral reflux
9309	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)
9310	341277	OVCH2	Ovochymase 2	OVTN	Contracture, Venous thromboembolism

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