Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "C"

1381 to 1390 of 1796 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1381	1355	COX15	Cytochrome c oxidase assembly factor COX15	CEMCOX2, HAS, MC4DN6	Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency, Cardiomyopathy, Cytochrome c oxidase deficiency, Hypertrophic cardiomyopathy, Left ventricular noncompaction cardiomyopathy, Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease
1382	51241	COX16	Cytochrome c oxidase assembly factor COX16	C14orf112, HSPC203, MC4DN22, hCOX16	Mitochondrial complex deficiency, Obsessive-compulsive disorder, Prostate cancer
1383	10063	COX17	Cytochrome c oxidase copper chaperone COX17	-	Lung neoplasms
1384	285521	COX18	Cytochrome c oxidase assembly factor COX18	COX18HS, OXA1L2	Mitochondrial complex deficiency, Hearing loss
1385	90639	COX19	Cytochrome c oxidase assembly factor COX19	-	Bronchopulmonary dysplasia, Crohn disease, Hypertension, Inflammatory bowel disease, Ulcerative colitis, Urinary bladder cancer
1386	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
1387	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
1388	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
1389	116228	COX20	Cytochrome c oxidase assembly factor COX20	FAM36A, MC4DN11	Cytochrome c oxidase deficiency, Mitochondrial complex deficiency, Mitochondrial disease, Myocardial infarction
1390	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)

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