Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "C"

811 to 820 of 1338 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
811	53944	CSNK1G1	Casein kinase 1 gamma 1	CK1gamma1	Neurodevelopmental disorder, Major depressive disorder, Mood disorder, Neurodevelopmental disorders, Neurotic disorder, Non-specific syndromic intellectual disability
812	53981	CPSF2	Cleavage and polyadenylation specific factor 2	CPSF100	B-cell acute lymphoblastic leukemia, Kidney disease, Liver disease, Obesity
813	54205	CYCS	Cytochrome c, somatic	CYC, HCS, THC4	Alzheimer disease, Thrombocytopenia with normal platelets, Brain ischemia, Fatty liver, Fatty liver, alcoholic, Methylmalonic acidemia, Obesity, Systemic lupus erythematosus
814	54504	CPVL	Carboxypeptidase vitellogenic like	HVLP	Basal cell carcinoma, Color vision deficiency, Colorectal cancer, Melanoma, Cutaneous squamous cell carcinoma, Endometrial cancer, Keratinocyte carcinoma, Non-melanoma skin carcinoma, Obesity, Prostate cancer, Psoriasis, Psychotic disorders, Seborrheic keratosis, Skin cancer, Skin disease View all (3 more)
815	54520	CCDC93	CCC complex scaffolding subunit CCDC93	-	Central nervous system cancer, Glioblastoma, Glioma, Venous thromboembolism
816	54535	CCHCR1	Coiled-coil alpha-helical rod protein 1	C6orf18, HCR, SBP, pg8	Amphetamine or related acting sympathomimetic abuse, Breast cancer, Cancer, Colorectal cancer, Esophageal squamous cell carcinoma, Estrogen-receptor negative breast cancer, Head and neck cancer, Hypothyroidism, Lung cancer, Multiple myeloma, Myeloproliferative disorder, Non-hodgkins lymphoma, Ovarian cancer, Ovarian serous carcinoma, Preeclampsia View all (8 more)
817	54677	CROT	Carnitine O-octanoyltransferase	COT	Liver cirrhosis, Lung cancer, Squamous cell carcinoma
818	54714	CNGB3	Cyclic nucleotide gated channel subunit beta 3	ACHM1	Achromatopsia, Anxiety disorder, Color vision deficiency, Cone dystrophy, Cone-rod dystrophy, Leber congenital amaurosis, Macular dystrophy, Metabolic syndrome, Nystagmus, Optic atrophy, Retinitis pigmentosa, Stargardt disease, Diabetes mellitus, type 2
819	5476	CTSA	Cathepsin A	GLB2, GSL, NGBE, PPCA, PPGB	Cathepsin a-related arteriopathy, strokes, and leukoencephalopathy, Combined deficiency of sialidase and beta galactosidase, Desbuquois syndrome, Galactosialidosis, Non-immune hydrops fetalis
820	54805	CNNM2	Cyclin and CBS domain divalent metal cation transport mediator 2	ACDP2, HOMG6, HOMGSMR, SLC70A2	Anorexia nervosa, Cardiac arrhythmias, Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Brain aneurysm, Cardiac arrhythmia, Coronary artery disease, Hypertension, Gout, Insomnia, Kidney disease, Large artery stroke, Major depressive disorder View all (11 more)

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