Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "C"

511 to 520 of 1338 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
511	157807	CLVS1	Clavesin 1	C6orf212L, CRALBPL, RLBP1L1	Atypical femoral fracture, Major depressive disorder, Metabolic syndrome, Migraine, Scoliosis, Amyotrophic lateral sclerosis, Squamous cell carcinoma, Diabetes mellitus, type 2, Venous thrombosis
512	1579	CYP4A11	Cytochrome P450 family 4 subfamily A member 11	CP4Y, CYP4A2, CYP4AII, CYPIVA11	Autism, Hepatocellular carcinoma, Hypertension, Liver cirrhosis
513	157922	CAMSAP1	Calmodulin regulated spectrin associated protein 1	CDCBM12	Alzheimer disease, Juvenile arthritis, Colorectal cancer, Cortical dysplasia with other brain malformations, Juvenile idiopathic arthritis, Oligoarticular juvenile idiopathic arthritis, Scoliosis
514	1580	CYP4B1	Cytochrome P450 family 4 subfamily B member 1	CYPIVB1, P-450HP	Autism, Urinary system disease
515	1581	CYP7A1	Cytochrome P450 family 7 subfamily A member 1	CP7A, CYP7, CYPVII	Autism, Cholecystolithiasis, Cholelithiasis, Esophageal squamous cell carcinoma, Hyperlipidemia, Gallstones, Hypercholesterolemia, Intrahepatic cholestasis of pregnancy, Liver disease, Metabolic syndrome
516	1582	CYP8B1	Cytochrome P450 family 8 subfamily B member 1	CP8B, CYP12, CYPVIIIB1	Alzheimer disease, Cholelithiasis, Lung cancer, Obesity, Squamous cell carcinoma
517	1583	CYP11A1	Cytochrome P450 family 11 subfamily A member 1	CYP11A, CYPXIA1, P450SCC	Autism, Congenital adrenal hyperplasia, Endometrial neoplasm, Seizures, Squamous cell carcinoma
518	1584	CYP11B1	Cytochrome P450 family 11 subfamily B member 1	CPN1, CYP11B, FHI, P450C11	Congenital adrenal hyperplasia, Cushing syndrome, Steroid 11-beta-monooxygenase deficiency, Hyperaldosteronism, Glucocorticoid-remediable aldosteronism
519	1585	CYP11B2	Cytochrome P450 family 11 subfamily B member 2	ALDOS, CPN2, CYP11B, CYP11BL, CYPXIB2, P-450C18, P450C18, P450aldo	Corticosterone methyl oxidase type i, Autism, Cardiomyopathy, Cardiovascular disease, Corticosterone methyloxidase deficiency, Cushing syndrome, Diabetes mellitus, Diabetes mellitus type 2, Hyperaldosteronism, Hyperreninemic hypoaldosteronism, Hypoaldosteronism, Glucocorticoid-remediable aldosteronism, Hypertension, Osteoarthritis, Prostatic neoplasm
520	1586	CYP17A1	Cytochrome P450 family 17 subfamily A member 1	CPT7, CYP17, P450C17, S17AH	17,20-lyase deficiency, 46,xy disorder of sex development, Amenorrhea, Anxiety disorder, Breast neoplasm, Stone disease, Hepatocellular carcinoma, Colorectal cancer, Congenital adrenal hyperplasia, Coronary artery disease, Steroid 17-alpha-monooxygenase deficiency, Genetic predisposition to disease, Hyperkalemia, Hypertension, Malignant hypertension View all (16 more)

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