Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "C"

1391 to 1400 of 1806 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1391	10063	COX17	Cytochrome c oxidase copper chaperone COX17	-	Hepatitis, Lung neoplasms
1392	285521	COX18	Cytochrome c oxidase assembly factor COX18	COX18HS, OXA1L2	Mitochondrial complex deficiency, Hearing loss
1393	90639	COX19	Cytochrome c oxidase assembly factor COX19	-	Bronchopulmonary dysplasia, Crohn disease, Hypertension, Inflammatory bowel disease, Leprosy, Ulcerative colitis, Urinary bladder cancer
1394	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
1395	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
1396	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
1397	116228	COX20	Cytochrome c oxidase assembly factor COX20	FAM36A, MC4DN11	Cytochrome c oxidase deficiency, Mitochondrial complex deficiency, Mitochondrial disease, Myocardial infarction
1398	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)
1399	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)
1400	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)

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