Genes | GeDiPNet - Gene Disease Pathway & Associations

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2871 to 2880 of 15380 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
2871	90639	COX19	Cytochrome c oxidase assembly factor COX19	-	Bronchopulmonary dysplasia, Crohn disease, Hypertension, Inflammatory bowel disease, Ulcerative colitis, Urinary bladder cancer
2872	4513	COX2	Mitochondrially encoded cytochrome c oxidase II	COII, MTCO2	Cerebellar ataxia, Cleft palate and bilateral cleft lip, Major depressive disorder, 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
2873	6775079	COX2	-	-	Cerebellar ataxia, Cleft palate and bilateral cleft lip, Major depressive disorder, 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
2874	8923202	COX2	-	-	Cerebellar ataxia, Cleft palate and bilateral cleft lip, Major depressive disorder, 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
2875	116228	COX20	Cytochrome c oxidase assembly factor COX20	FAM36A, MC4DN11	Cytochrome c oxidase deficiency, Mitochondrial complex deficiency, Mitochondrial disease, Myocardial infarction
2876	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)
2877	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)
2878	8923187	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)
2879	1327	COX4I1	Cytochrome c oxidase subunit 4I1	COX IV-1, COX4, COX4-1, COXIV, COXIV-1, MC4DN16	Cytochrome c oxidase deficiency, Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease
2880	84701	COX4I2	Cytochrome c oxidase subunit 4I2	COX4, COX4-2, COX4B, COX4L2, COXIV-2, dJ857M17.2	Alzheimer disease, Mitochondrial disease, Pancreatic insufficiency syndrome

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