Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "C"

1311 to 1320 of 1338 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1311	9662	CEP135	Centrosomal protein 135	CEP4, KIAA0635, MCPH8	Agenesis of corpus callosum, Developmental delay, Dwarfism, Mental retardation, Microcephaly, Neuronal heterotopia, Pachygyria, Renal aplasia, Vesicoureteral reflux
1312	968	CD68	CD68 molecule	GP110, LAMP4, SCARD1	Amyotrophic lateral sclerosis, Cholestasis, Compensatory hyperinsulinemia, Endogenous hyperinsulinism, Exogenous hyperinsulinism, Hyperinsulinism, Kidney failure, Lateral sclerosis, Miscarriage, Obesity, Psoriatic arthritis
1313	969	CD69	CD69 molecule	AIM, BL-AC/P26, CLEC2C, EA1, GP32/28, MLR-3	Arthritis, Autoimmune diabetes, Diabetes mellitus, Brittle diabetes mellitus, Miscarriage, Multiple sclerosis, Polyarthritis
1314	9696	CROCC	Ciliary rootlet coiled-coil, rootletin	CROCC1, ROLT, TAX1BP2	Retinitis pigmentosa
1315	970	CD70	CD70 molecule	CD27-L, CD27L, CD27LG, LPFS3, TNFSF7, TNLG8A	Lymphoproliferative disorder, Severe combined immunodeficiency disease
1316	9702	CEP57	Centrosomal protein 57	MVA2, PIG8, TSP57	Ambiguous genitalia, Aortic coarctation, Aortic valve insufficiency, Atrial septal defect, Cafe-au-lait spot, Camptodactyly of fingers, Cataract, Clinodactyly, Colonic neoplasms, Congenital epicanthus, Dandy-walker syndrome, Developmental delay, Dolichocephaly, Duodenal atresia, Dwarfism View all (21 more)
1317	972	CD74	CD74 molecule	CLIP, DHLAG, HLADG, II, Ia-GAMMA, p33	Breast cancer, Mammary neoplasms, Breast carcinoma, Liver failure, Lung carcinoma, Marfan syndrome
1318	9720	CCDC144A	Coiled-coil domain containing 144A	-	Leukemia
1319	973	CD79A	CD79a molecule	IGA, IGAlpha, MB-1, MB1	Agammaglobulinemia, Arthritis, Bronchiectasis, Bronchitis, Congenital epicanthus, Conjunctivitis, Diffuse lymphoma, High palate, Hypogammaglobulinemia, Immunologic deficiency syndromes, Non-hodgkin lymphoma, Malabsorption syndrome, Neutropenia, Osteomyelitis, Otitis media, Sinusitis View all (1 more)
1320	9731	CEP104	Centrosomal protein 104	CFAP256, GlyBP, JBTS25, KIAA0562, MRT77, ROC22	Cerebellar hypoplasia, Cerebellar vermis agenesis, Congenital cerebral hernia, Congenital coloboma of iris, Developmental delay, Hirschsprung disease, Hydrocephalus, Joubert syndrome, Mental retardation, Nystagmus, Oculomotor apraxia, Oculovestibuloauditory syndrome, Oral cleft, Polydactyly of toes, Polymicrogyria View all (4 more)

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