Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "C"

541 to 550 of 1338 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
541	170712	COX7B2	Cytochrome c oxidase subunit 7B2	-	Alzheimer disease, Hepatocellular carcinoma, Migraine
542	171425	CLYBL	Citramalyl-CoA lyase	CLB	Alzheimer disease, Attention deficit hyperactivity disorder, Color vision deficiency, Dementia, Large artery stroke, Lung cancer, Obesity, Pancreatic cancer, Rheumatoid arthritis, Squamous cell carcinoma, Substance abuse, Uterine fibroid, Vitamin b deficiency
543	1727	CYB5R3	Cytochrome b5 reductase 3	B5R, DIA1	Congenital myopathy, Cytochrome-b5 reductase deficiency, Dihydrolipoamide dehydrogenase deficiency, Intellectual developmental disorder, Methemoglobinemia, Osteoarthritis, Scoliosis, Diabetes mellitus, type 2, Venous thrombosis
544	192668	CYS1	Cystin 1	-	Atrial fibrillation, Polycystic kidney disease, Chronic bronchitis, Obstructive pulmonary disease, Gout
545	1951	CELSR3	Cadherin EGF LAG seven-pass G-type receptor 3	ADGRC3, CDHF11, EGFL1, FMI1, HFMI1, MEGF2, RESDA1	Anorexia nervosa, Hepatocellular carcinoma, Neurodevelopmental disorder, Crohn disease, Tourette syndrome, Hypertrophic cardiomyopathy, Inflammatory bowel disease, Major depressive disorder, Non-specific syndromic intellectual disability, Ulcerative colitis
546	1952	CELSR2	Cadherin EGF LAG seven-pass G-type receptor 2	ADGRC2, CDHF10, EGFL2, Flamingo1, MEGF3	Aneurysm, Aortic aneurysm, Aortic stenosis, Atrial fibrillation, Endometrial hyperplasia, Cancer, Cardiovascular disease, Cerebrovascular disorder, Ischemic heart disease, Coronary artery disease, Diabetes mellitus, Hyperlipidemia, Lipoprotein lipase deficiency, Global developmental delay, Heart disease View all (15 more)
547	196477	CCER1	Coiled-coil glutamate rich protein 1	C12orf12
548	1990	CELA1	Chymotrypsin like elastase 1	ELA1	Liver cirrhosis, Obesity
549	200373	CFAP221	Cilia and flagella associated protein 221	CILD55, FAP221, PCDP1	Attention deficit hyperactivity disorder, Bipolar disorder, Chronic bronchitis, Obstructive pulmonary disease, Ciliary dyskinesia, Young syndrome
550	200844	CFAP20DC	CFAP20 domain containing	C3orf67	Alzheimer disease, Obstructive sleep apnea syndrome, Rheumatoid arthritis, Scoliosis

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