Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "C"

1271 to 1280 of 1338 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1271	929	CD14	CD14 molecule	-	Arthritis, Asthma, Eczema, Gout, Juvenile arthritis, Liver cirrhosis, Liver fibrosis, Non-alcoholic fatty liver disease, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Still disease
1272	930	CD19	CD19 molecule	B4, CVID3	Agammaglobulinemia, Anemia, Brachycephaly, Bronchiectasis, Bronchitis, Common variable immunodeficiency, Conjunctivitis, Gastrointestinal stromal tumor, Hypogammaglobulinemia, Immune thrombocytopenic purpura, Immunoglobulin deficiency, Immunologic deficiency syndromes, Imperforate anus, Lymphoma, Lymphopenia View all (4 more)
1273	9308	CD83	CD83 molecule	BL11, HB15	Arsenic encephalopathy, Arthritis, Dermatologic disorders, Juvenile arthritis, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Rheumatoid arthritis, Still disease
1274	9318	COPS2	COP9 signalosome subunit 2	ALIEN, CSN2, SGN2, TRIP15	Endometrioma, Endometriosis
1275	9332	CD163	CD163 molecule	M130, MM130, SCARI1	Carotid artery disease, Carotid atherosclerosis, Compensatory hyperinsulinemia, Endogenous hyperinsulinism, Exogenous hyperinsulinism, Glomerulonephritis, Hyperglycemia, Hyperinsulinism, Liver carcinoma, Miscarriage, Moyamoya disease, Obesity, Schizophrenia
1276	93589	CACNA2D4	Calcium voltage-gated channel auxiliary subunit alpha2delta 4	RCD4	Cone-rod dystrophy, Congenital stationary night blindness, Disorder of eye, Hypoplasia of optic disc, Myopia, Night blindness, Nyctalopia, Nystagmus, Retinal cone dystrophy, Strabismus
1277	93659	CGB5	Chorionic gonadotropin subunit beta 5	CGB, HCG, hCGB	Sclerocystic ovaries, Polycystic ovary syndrome
1278	93664	CADPS2	Calcium dependent secretion activator 2	CAPS2	Alzheimer disease, Autism, Cardiovascular diseases, Cholestasis, Schizophrenia
1279	9377	COX5A	Cytochrome c oxidase subunit 5A	COX, COX-VA, MC4DN20, VA	Cytochrome-c oxidase deficiency, Isolated cytochrome c oxidase deficiency
1280	9382	COG1	Component of oligomeric golgi complex 1	CDG2G, LDLB	Abnormal spinal segmentation, Acquired kyphoscoliosis, Anemia, Cerebellar atrophy, Cerebral atrophy, Congenital camptodactyly, Congenital clubfoot, Congenital disorder of glycosylation, Rib fusion, Congenital kyphoscoliosis, Cryptorchidism, Developmental delay, High palate, Hydronephrosis, Hypospadias View all (11 more)

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