Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "C"

1381 to 1390 of 1806 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1381	100529144	CORO7-PAM16	CORO7-PAM16 readthrough	CORO7, Coronin-7, Crn7	Chondrodysplasia, Coronary artery disease, Melanoma, Duodenitis, Gastroenteritis, Prostate cancer, Schizophrenia, Diabetes mellitus type 2
1382	23406	COTL1	Coactosin like F-actin binding protein 1	CLP	Breast neoplasms, Epilepsy, Liver cirrhosis, Hypertension
1383	4512	COX1	Mitochondrially encoded cytochrome c oxidase I	COI, MTCO1	Carcinoma, Cardiomyopathy, Cerebellar ataxia, Cleft palate and bilateral cleft lip, Deafness, aminoglycoside-induced, Deafness, nonsyndromic sensorineural, mitochondrial, Deafness, sensorineural, autosomal-mitochondrial type, Hypertrophy, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy, ataxia, and retinitis pigmentosa, Optic atrophy, Leber hereditary optic neuropathy, Rod-cone dystrophy View all (2 more)
1384	6775083	COX1	-	-	Carcinoma, Cardiomyopathy, Cerebellar ataxia, Cleft palate and bilateral cleft lip, Deafness, aminoglycoside-induced, Deafness, nonsyndromic sensorineural, mitochondrial, Deafness, sensorineural, autosomal-mitochondrial type, Hypertrophy, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy, ataxia, and retinitis pigmentosa, Optic atrophy, Leber hereditary optic neuropathy, Rod-cone dystrophy View all (2 more)
1385	8923218	COX1	-	-	Carcinoma, Cardiomyopathy, Cerebellar ataxia, Cleft palate and bilateral cleft lip, Deafness, aminoglycoside-induced, Deafness, nonsyndromic sensorineural, mitochondrial, Deafness, sensorineural, autosomal-mitochondrial type, Hypertrophy, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Neuropathy, ataxia, and retinitis pigmentosa, Optic atrophy, Leber hereditary optic neuropathy, Rod-cone dystrophy View all (2 more)
1386	1352	COX10	Cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10	MC4DN3	Conotruncal cardiac defect, Cytochrome c oxidase deficiency, Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease
1387	1353	COX11	Cytochrome c oxidase copper chaperone COX11	COX11P, MC4DN23	Mitochondrial complex deficiency, Obsessive-compulsive disorder
1388	84987	COX14	Cytochrome c oxidase assembly factor COX14	C12orf62, MC4DN10, PCAG1	Colorectal cancer, Cytochrome c oxidase deficiency, Mitochondrial complex deficiency, Mitochondrial disease
1389	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
1390	51241	COX16	Cytochrome c oxidase assembly factor COX16	C14orf112, HSPC203, MC4DN22, hCOX16	Mitochondrial complex deficiency, Obsessive-compulsive disorder, Prostate cancer

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