Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "C"

331 to 340 of 1338 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
331	1314	COPA	Coat protein complex I subunit alpha	AIAISD, AILJK, HEP-COP, alpha-COP	Arthritis, Autoimmune diseases, Autoimmune interstitial lung disease-arthritis syndrome, Autoimmune interstitial lung, joint, and kidney disease, Autoinflammatory disease, Lung diseases, Polyarthritis
332	132200	C3orf49	Chromosome 3 open reading frame 49	-	Schizophrenia
333	132321	C4orf33	Chromosome 4 open reading frame 33	-	Mental depression
334	1327	COX4I1	Cytochrome c oxidase subunit 4I1	COX IV-1, COX4, COX4-1, COXIV, COXIV-1, MC4DN16	Isolated cytochrome c oxidase deficiency, Leprosy, Mitochondrial diseases
335	132864	CPEB2	Cytoplasmic polyadenylation element binding protein 2	CPE-BP2, CPEB-2, hCPEB-2	Cardiovascular diseases
336	1329	COX5B	Cytochrome c oxidase subunit 5B	COXVB	Myocardial ischemia
337	1337	COX6A1	Cytochrome c oxidase subunit 6A1	CMTRID, COX6A, COX6AL	Charcot-marie-tooth disease, Peripheral neuropathy
338	1339	COX6A2	Cytochrome c oxidase subunit 6A2	COX6AH, COXVIAH, COXVIa-M, MC4DN18	Isolated cytochrome c oxidase deficiency
339	1340	COX6B1	Cytochrome c oxidase subunit 6B1	COX6B, COXG, COXVIb1, MC4DN7	Anemia, Cytochrome-c oxidase deficiency, Developmental delay, Fanconi syndrome, Hearing loss, High palate, Hypertrophic cardiomyopathy, Isolated cytochrome c oxidase deficiency, Leukoencephalopathy, Mental retardation, Mitochondrial diseases, Motor delay, Optic atrophy, Phosphate diabetes, Ptosis View all (2 more)
340	1345	COX6C	Cytochrome c oxidase subunit 6C	-	Cohen syndrome

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