Genes | GeDiPNet - Gene Disease Pathway & Associations

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2881 to 2890 of 15448 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
2881	51241	COX16	Cytochrome c oxidase assembly factor COX16	C14orf112, HSPC203, MC4DN22, hCOX16	Mitochondrial complex deficiency, Obsessive-compulsive disorder, Prostate cancer
2882	10063	COX17	Cytochrome c oxidase copper chaperone COX17	-	Hepatitis, Lung neoplasms
2883	285521	COX18	Cytochrome c oxidase assembly factor COX18	COX18HS, OXA1L2	Mitochondrial complex deficiency, Hearing loss
2884	90639	COX19	Cytochrome c oxidase assembly factor COX19	-	Bronchopulmonary dysplasia, Crohn disease, Hypertension, Inflammatory bowel disease, Leprosy, Ulcerative colitis, Urinary bladder cancer
2885	4513	COX2	Mitochondrially encoded cytochrome c oxidase II	COII, MTCO2	Cerebellar ataxia, Cleft palate and bilateral cleft lip, Major depressive disorder, Experimental diabetes, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Neuroblastoma, Neuropathy, ataxia, and retinitis pigmentosa, Leber hereditary optic neuropathy, Rod-cone dystrophy, Tetralogy of fallot, Postaxial polydactyly
2886	6775079	COX2	-	-	Cerebellar ataxia, Cleft palate and bilateral cleft lip, Major depressive disorder, Experimental diabetes, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Neuroblastoma, Neuropathy, ataxia, and retinitis pigmentosa, Leber hereditary optic neuropathy, Rod-cone dystrophy, Tetralogy of fallot, Postaxial polydactyly
2887	8923202	COX2	-	-	Cerebellar ataxia, Cleft palate and bilateral cleft lip, Major depressive disorder, Experimental diabetes, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Neuroblastoma, Neuropathy, ataxia, and retinitis pigmentosa, Leber hereditary optic neuropathy, Rod-cone dystrophy, Tetralogy of fallot, Postaxial polydactyly
2888	116228	COX20	Cytochrome c oxidase assembly factor COX20	FAM36A, MC4DN11	Cytochrome c oxidase deficiency, Mitochondrial complex deficiency, Mitochondrial disease, Myocardial infarction
2889	4514	COX3	Mitochondrially encoded cytochrome c oxidase III	COIII, MTCO3	Spastic ataxia, Cerebellar ataxia, Cleft palate and bilateral cleft lip, Developmental delay, Epilepsy, Temporal lobe epilepsy, Hearing impairment, Liver failure, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Mitochondrial encephalopathy, Nephrolithiasis, Neuropathy, ataxia, and retinitis pigmentosa, Leber hereditary optic neuropathy View all (4 more)
2890	6775073	COX3	-	-	Spastic ataxia, Cerebellar ataxia, Cleft palate and bilateral cleft lip, Developmental delay, Epilepsy, Temporal lobe epilepsy, Hearing impairment, Liver failure, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Mitochondrial encephalopathy, Nephrolithiasis, Neuropathy, ataxia, and retinitis pigmentosa, Leber hereditary optic neuropathy View all (4 more)

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