Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "C"

1341 to 1350 of 1806 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1341	150684	COMMD1	Copper metabolism domain containing 1	C2orf5, MURR1	Alzheimer disease, Color vision deficiency, Copper overload cirrhosis, Coronary artery disease, Dog diseases, Hepatitis, Hypersensitivity, Liver cirrhosis, Nonalcoholic fatty liver disease, Parkinson disease, Proliferative diabetic retinopathy
1342	51397	COMMD10	COMM domain containing 10	PTD002	Amyotrophic lateral sclerosis, Asthma, Bipolar disorder, Central nervous system cancer, Kidney disease, Obstructive pulmonary disease, Color vision deficiency, Glioblastoma, Glioma, Granulomatosis with polyangiitis, Kidney failure, Leprosy, Major depressive disorder, Neurotic disorder, Schizophrenia
1343	54939	COMMD4	COMM domain containing 4	-	Gout, Diabetes mellitus type 2
1344	149951	COMMD7	COMM domain containing 7	C20orf92, dJ1085F17.3	Ankylosing spondylitis, Crohn disease, Inflammatory bowel disease, Prostate cancer, Psoriasis, Sclerosing cholangitis, Toxic nodular goiter, Diabetes mellitus type 2, Ulcerative colitis
1345	54951	COMMD8	COMM domain containing 8	-	Hemolytic anemia, Uterine fibroid
1346	1311	COMP	Cartilage oligomeric matrix protein	CTS2, EDM1, EPD1, MED, PSACH, THBS5, TSP-5, TSP5	Attention deficit hyperactivity disorder, Carpal tunnel syndrome, Comp-related skeletal dysplasia, Congenital cartilage disorder, Connective tissue disease, Desbuquois syndrome, Epiphyseal dysplasia, Osteoarthritis, Osteochondrodysplasias
1347	1312	COMT	Catechol-O-methyltransferase	HEL-S-98n	22q11.2 deletion syndrome, Amphetamine or sympathomimetic abuse, Anhedonia, Attention deficit hyperactivity disorder, Autism, Bardet-biedl syndrome, Bipolar disorder, Breast neoplasms, Bulimia, Cannabis abuse, Hepatocellular carcinoma, Dilated cardiomyopathy, Cardiomyopathy, Cognition disorder, Delirium, dementia, and cognitive disorders View all (27 more)
1348	64326	COP1	COP1 E3 ubiquitin ligase	CFAP78, FAP78, RFWD2, RNF200	Alzheimer disease, Autism, Bipolar disorder, Endometriosis, Irritable bowel syndrome, Major depressive disorder, Obesity, Schizophrenia
1349	1314	COPA	Coat protein complex I subunit alpha	AIAISD, AILJK, HEP-COP, alpha-COP	Ankylosing spondylitis, Arthritis, Autoimmune disease, Autoimmune interstitial lung disease-arthritis syndrome, Autoinflammation and autoimmunity, systemic, with immune dysregulation 1, Lung disease
1350	1315	COPB1	Coat protein complex I subunit beta 1	BARMACS, COPB	Baralle-macken syndrome, Cataract, Intellectual developmental disorder dysmorphic microcephaly, Multiple sclerosis, Intellectual disability, Skeletal dysplasia, Diabetes mellitus type 2

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