Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "C"

1111 to 1120 of 1338 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1111	834	CASP1	Caspase 1	ICE, IL1BC, P45	Amyotrophic lateral sclerosis, Grand mal status epilepticus, Hyperhomocysteinemia, Kidney disease, Lateral sclerosis, Multiple sclerosis, Nonconvulsive status epilepticus, Obesity, Petit mal status, Status epilepticus
1112	83461	CDCA3	Cell division cycle associated 3	GRCC8, TOME-1, TOME1	Liver carcinoma, Myopia, Night blindness, congenital stationary
1113	835	CASP2	Caspase 2	CASP-2, ICH1, MRT80, NEDD-2, NEDD2, PPP1R57	Chromophobe carcinoma, Mental retardation, Papillary renal carcinoma, Renal carcinoma
1114	83539	CHST9	Carbohydrate sulfotransferase 9	GALNAC4ST-2, GalNAc4ST2	Breast cancer, Breast carcinoma, Coronary artery disease, Mental depression
1115	83548	COG3	Component of oligomeric golgi complex 3	CDG2BB, SEC34	Breast cancer
1116	836	CASP3	Caspase 3	CPP32, CPP32B, SCA-1	Alzheimer disease, Asymmetric diabetic proximal motor neuropathy, Cardiac valvular disease, Cerebral ischemia, Cryptorchidism, Diabetes mellitus, Diabetic amyotrophy, Diabetic asymmetric polyneuropathy, Diabetic autonomic neuropathy, Diabetic cardiomyopathy, Diabetic mononeuropathy, Diabetic nephropathy, Diabetic neuralgia, Diabetic polyneuropathy, Diabetic retinopathy View all (16 more)
1117	83605	CCM2	CCM2 scaffold protein	C7orf22, OSM, PP10187	Capillary malformation-arteriovenous malformation, Cavernous angioma, central nervous system, Cavernous hemangioma, Cavernous hemangioma of retina, Cerebral cavernous hemangioma, Cerebral cavernous malformation, Venous malformation, Coronary artery disease, Hemangioma, Hemangioma of choroid, Hemangioma, cavernous, Impaired cognition, Meningioma, Neuroma, Scoliosis, Skin diseases, vascular, Stroke View all (2 more)
1118	83636	C19orf12	Chromosome 19 open reading frame 12	MPAN, NBIA3, NBIA4, SPG43	Bowel incontinence, Dementia, Developmental delay, Distal amyotrophy, Dysarthria, Dysphagia, Mental depression, Mitochondrial membrane protein-associated neurodegeneration, Mood swings, Neurodegeneration with brain iron accumulation, Night blindness, Optic atrophy, Ovarian neoplasm, Ovarian cancer, Parkinson disease, Spastic paraplegia View all (1 more)
1119	83638	C11orf68	Chromosome 11 open reading frame 68	BLES03, P5326	Melanoma
1120	83643	CCDC3	Coiled-coil domain containing 3	-	Leukemia

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