Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "C"

821 to 830 of 1338 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
821	54862	CC2D1A	Coiled-coil and C2 domain containing 1A	Aki-1, FREUD-1, Freud-1/Aki1, Lgd2, MRT3, TAPE	Autism, Nonsyndromic intellectual disability, Ciliopathies, Neurodevelopmental disorder, Intellectual developmental disorder, Major depressive disorder, Non-specific syndromic intellectual disability, Premature ovarian failure, Depression
822	54875	CNTLN	Centlein	C9orf101, C9orf39, bA340N12.1	Anorexia nervosa, Attention deficit hyperactivity disorder, Hemolytic anemia, Insomnia, Lung cancer, Major depressive disorder, Oligodendroglioma, Scoliosis
823	54897	CASZ1	Castor zinc finger 1	CAS11, CST, SRG, ZNF693, dJ734G22.1	1p36 deletion syndrome, Anal polyp, Androgenetic alopecia, Atrial fibrillation, Breast cancer, Cardiomyopathy, Cardiovascular disease, Cataract, Cerebrovascular disorder, Chromosome 1p36 deletion syndrome, Obstructive pulmonary disease, Color vision deficiency, Congenital hydrocephalus, Coronary artery disease, Diabetic ketoacidosis View all (11 more)
824	54901	CDKAL1	CDKAL1 threonylcarbamoyladenosine tRNA methylthiotransferase	-	Alzheimer disease, Androgenetic alopecia, Ankylosing spondylitis, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Body weight, Brain infarction, Breast cancer, Carcinoid tumor, Cardiovascular disease, Central nervous system cancer, Cerebral amyloid angiopathy, Clear cell renal cell carcinoma , Congenital esophageal anomaly View all (32 more)
825	54980	C2orf42	Chromosome 2 open reading frame 42	-	Alzheimer disease, Androgenetic alopecia
826	54982	CLN6	CLN6 transmembrane ER protein	CLN4A, CLN6A, HsT18960, nclf	Atrophy, Neuronal ceroid lipofuscinosis, Congenital neurologic anomalies�, Cystic fibrosis, Motor skills disorder, Neurodevelopmental disorders, Spastic ataxia, Visual disorder
827	55036	CCDC40	Coiled-coil domain 40 molecular ruler complex subunit	CFAP172, CILD15, FAP172	Autism, Autoimmune disease, Ciliary dyskinesia, with or without situs inversus, Ciliary dyskinesia, Congenital nasopharyngeal atresia, Glycogen storage disease, Hyperimmunoglobulin e syndrome, Lung cancer, Male infertility, Polynesian bronchiectasis, Situs ambiguus , Squamous cell carcinoma, Usher syndrome
828	55118	CRTAC1	Cartilage acidic protein 1	ASPIC, ASPIC1, CEP-68, CEP68, LOTUS	Central nervous system cancer, Coronary artery disease, Digestive system disease, Dyslexia, Glioblastoma, Glioma, Lung cancer, Metabolic syndrome, Myocardial infarction, Nasopharyngeal carcinoma, Diabetes mellitus, type 2
829	55125	CEP192	Centrosomal protein 192	PPP1R62	Breast cancer, Color vision deficiency
830	55143	CDCA8	Cell division cycle associated 8	BOR, BOREALIN, DasraB, MESRGP	Hepatocellular carcinoma

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