Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "C"
1331 to 1340 of 1796 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1331
Collagen beta(1-O)galactosyltransferase 2
C1orf17, ColGalT 2, GLT25D2
Tourette syndrome, Osteoarthritis, Preeclampsia, Diabetes mellitus type 2

1332
Collagen like tail subunit of asymmetric acetylcholinesterase
CMS5, EAD
Alzheimer disease, Congenital myasthenic syndrome, Digestive system disease, Diverticular disease, Diverticulitis, Myasthenic syndrome, Pancreatic cancer

1333
Copper metabolism domain containing 1
C2orf5, MURR1
Alzheimer disease, Color vision deficiency, Copper overload cirrhosis, Coronary artery disease, Hypersensitivity, Liver cirrhosis, Nonalcoholic fatty liver disease, Parkinson disease, Proliferative diabetic retinopathy

1334
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, Major depressive disorder, Neurotic disorder, Schizophrenia

1335
COMM domain containing 4
-
Gout, Diabetes mellitus type 2

1336
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

1337
COMM domain containing 8
-
Hemolytic anemia, Uterine fibroid

1338
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

1339
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)

1340
COP1 E3 ubiquitin ligase
CFAP78, FAP78, RFWD2, RNF200
Alzheimer disease, Autism, Bipolar disorder, Endometriosis, Irritable bowel syndrome, Major depressive disorder, Obesity, Schizophrenia