Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "C"

961 to 970 of 1338 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
961	708	C1QBP	Complement C1q binding protein	COXPD33, GC1QBP, HABP1, SF2AP32, SF2p32, gC1Q-R, gC1qR, p32	Breast neoplasm, Combined oxidative phosphorylation deficiency, Mitochondrial disease
962	712	C1QA	Complement C1q A chain	C1QD1	Systemic lupus erythematosus, C1q deficiency, Basal cell carcinoma, Exanthema, Glomerulonephritis, Iga nephropathy, Liver cirrhosis, Stevens-johnson syndrome
963	7122	CLDN5	Claudin 5	AWAL, BEC1, CPETRL1, TMDVCF, TMVCF	Major depressive disorder, Mesothelioma, Neurodevelopmental disorders, Schizophrenia
964	713	C1QB	Complement C1q B chain	C1QD2	C1q deficiency, Color vision deficiency, Iga nephropathy, Liver cirrhosis, Myocardial ischemia, Ovarian cysts, Schizophrenia, Diabetes mellitus, type 2
965	714	C1QC	Complement C1q C chain	C1Q-C, C1QD3, C1QG	C1q deficiency, Fatty liver, alcoholic, Hepatitis c, Liver cirrhosis, Nonalcoholic fatty liver disease, Stevens-johnson syndrome
966	715	C1R	Complement C1r	EDS8, EDSPD1	Systemic lupus erythematosus, Vascular dementia, Ehlers-danlos syndrome, Endometriosis, Paratuberculosis, Periodontal ehlers-danlos syndrome
967	716	C1S	Complement C1s	EDSPD2	Alzheimer disease, Ankylosing spondylitis, Autoimmune hepatitis, Autoimmune disease, Complement component deficiency, Coronary artery disease, Ehlers-danlos syndrome, Hashimoto disease, Hereditary angioedema, Lung cancer, Periodontal ehlers-danlos syndrome
968	717	C2	Complement C2	ARMD14, CO2	Alzheimer disease, Atrophic macular degeneration, Autism, C1 esterase inhibitor deficiency, Cancer, Interstitial cystitis, Complement component deficiency, Coronary artery disease, Irritant dermatitis, Dermatomyositis, Endometriosis, Glaucoma, Hepatocellular carcinoma, Hypertension, Hypothyroidism View all (16 more)
969	718	C3	Complement C3	AHUS5, ARMD9, ASP, C3a, C3b, CPAMD1, HEL-S-62p	Alzheimer disease, Sickle cell anemia, Asthma, Atrophic macular degeneration, Hemolytic uremic syndrome, C3 glomerulonephritis, Central nervous system cancer, Ulcerative colitis, Cold paroxysmal hemoglobinuria, Complement component deficiency, Macular and posterior pole degeneration, Diabetes mellitus type 2, Age-related macular degeneration, Glaucoma, Glioblastoma View all (14 more)
970	720	C4A	Complement C4A (Chido/Rodgers blood group)	C4, C4A2, C4A3, C4A4, C4A6, C4AD, C4S, CO4, CPAMD2, RG	Systemic lupus erythematosus, Behcet disease, Complement component deficiency, Graves disease, Vitiligo

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