Genes | GeDiPNet - Gene Disease Pathway & Associations

Dataset:

All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

Showing genes starting with "C"

1371 to 1380 of 1796 Genes

Show

	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1371	84940	CORO6	Coronin 6	ClipinE	Coronary artery disease
1372	79585	CORO7	Coronin 7	0610011B16Rik, CRN7, POD1	Coronary artery disease, Melanoma, Prostate cancer, Schizophrenia, Diabetes mellitus type 2
1373	100529144	CORO7-PAM16	CORO7-PAM16 readthrough	CORO7, Coronin-7, Crn7	Chondrodysplasia, Coronary artery disease, Melanoma, Duodenitis, Prostate cancer, Schizophrenia, Diabetes mellitus type 2
1374	23406	COTL1	Coactosin like F-actin binding protein 1	CLP	Breast neoplasms, Epilepsy, Hypertension
1375	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)
1376	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)
1377	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)
1378	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
1379	1353	COX11	Cytochrome c oxidase copper chaperone COX11	COX11P, MC4DN23	Mitochondrial complex deficiency, Obsessive-compulsive disorder
1380	84987	COX14	Cytochrome c oxidase assembly factor COX14	C12orf62, MC4DN10, PCAG1	Colorectal cancer, Cytochrome c oxidase deficiency, Mitochondrial complex deficiency, Mitochondrial disease

«««...136 137138139 140...»»»