Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "C"

461 to 470 of 1338 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
461	1500	CTNND1	Catenin delta 1	BCDS2, CAS, CTNND, P120CAS, P120CTN, p120, p120(CAS), p120(CTN)	Blepharocheilodontic syndrome, Cleft palate and bilateral cleft lip, Congenital euryblepharon, Hearing loss, Imperforate anus, Peg-shaped teeth, Syndactyly of fingers
462	1501	CTNND2	Catenin delta 2	GT24, NPRAP	5p partial monosomy syndrome, Amyotrophic lateral sclerosis, Autism, Benign myoclonic epilepsy, Colorectal cancer, Congenital epicanthus, Dwarfism, Giant cell glioblastoma, Glioblastoma, High palate, Mental retardation, Lateral sclerosis, Mental depression, Microcephaly, Monosomy 5p View all (7 more)
463	1503	CTPS1	CTP synthase 1	CTPS, GATD5, GATD5A, IMD24	Immunodeficiency, Immunologic deficiency syndromes, Lymphopenia, Severe combined immunodeficiency disease
464	150356	CHADL	Chondroadherin like	SLRR4B	Arthritis, Knee osteoarthritis, Osteoarthritis of hip
465	1504	CTRB1	Chymotrypsinogen B1	CTRB	Diabetes mellitus
466	150468	CKAP2L	Cytoskeleton associated protein 2 like	-	Accessory nipple, Aphasia, Camptodactyly of fingers, Cerebellar atrophy, Clinodactyly, Cryptorchidism, Developmental delay, Dwarfism, Dysphasia, Filippi syndrome, Frontal bossing, Liver carcinoma, Mental retardation, Microcephaly, Microdontia View all (8 more)
467	1506	CTRL	Chymotrypsin like	CTRL1	Schizophrenia
468	150684	COMMD1	Copper metabolism domain containing 1	C2orf5, MURR1	Liver cirrhosis, Copper-overload cirrhosis, Liver fibrosis, Proliferative diabetic retinopathy
469	1508	CTSB	Cathepsin B	APPS, CPSB, KWE, RECEUP	Chromophobe carcinoma, Giant cell glioblastoma, Glioblastoma, Hyperhidrosis palmaris et plantaris, Keratolytic winter erythema, Myopathy, Papillary renal carcinoma, Parkinson disease, Prostatic neoplasms, Prostate cancer, Renal carcinoma
470	1509	CTSD	Cathepsin D	CLN10, CPSD, HEL-S-130P	Amyotrophic lateral sclerosis, Arthritis, Cerebellar atrophy, Cerebral atrophy, Chromophobe carcinoma, Congenital neuronal ceroid lipofuscinosis, Disorder of eye, Mental retardation, Kidney disease, Lateral sclerosis, Liver carcinoma, Microcephaly, Neuronal ceroid lipofuscinosis, Osteoarthrosis deformans, Papillary renal carcinoma View all (7 more)

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