Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "C"
1111 to 1120 of 1338 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1111
Caspase 1
ICE, IL1BC, P45
Amyotrophic lateral sclerosis, Hyperhomocysteinemia, Hypersensitivity, Diabetes mellitus, type 2, Kidney disease, Liver cirrhosis, Motor neuron disease, Multiple sclerosis, Obesity, Status epilepticus

1112
Cell division cycle associated 3
GRCC8, TOME-1, TOME1
Hepatocellular carcinoma, Hypertension, Eye disease, Night blindness, congenital stationary, Open angle glaucoma

1113
Caspase 2
CASP-2, ICH1, MRT80, NEDD-2, NEDD2, PPP1R57
Nonsyndromic intellectual disability, Renal cell carcinoma, Intellectual developmental disorder, Leprosy

1114
Carbohydrate sulfotransferase 9
GALNAC4ST-2, GalNAc4ST2
Breast cancer, Bronchopulmonary dysplasia, Dental caries, Dyslexia, Generalized anxiety disorder, Major depressive disorder, Scoliosis

1115
Component of oligomeric golgi complex 3
CDG2BB, SEC34
Congenital disorder of glycosylation

1116
Caspase 3
CPP32, CPP32B, SCA-1
Alzheimer disease, Brain ischemia, Calcinosis, Cerebral hemorrhage, Ulcerative colitis, Cryptorchidism, Experimental diabetes, Diabetes mellitus type 2, Diabetic angiopathies, Diabetic neuropathy, Diabetic peripheral angiopathy, Diabetic retinopathy, Edema, Heart valve disease, Heart valve prolapse
View all (9 more)

1117
CCM2 scaffold protein
C7orf22, OSM, PP10187
Cavernous malformations of cns, Cerebral cavernous malformation, Colorectal cancer, Coronary artery disease, Vascular dementia, Developmental venous anomaly, Cerebral cavernous malformations, Myocardial infarction, Diabetes mellitus, type 2, Vasculitis

1118
Chromosome 19 open reading frame 12
MPAN, NBIA3, NBIA4, SPG43
Spastic paraplegia, Breast cancer, Estrogen-receptor negative breast cancer, Global developmental delay, Hallervorden spatz syndrome, Intellectual developmental disorder, Urinary system cancer, Metabolic syndrome, Neurodegeneration with brain iron accumulation, Ovarian neoplasm, Ovarian serous carcinoma, Spastic ataxia, Hereditary spastic paraplegia, Diabetes mellitus, type 2, Urinary bladder cancer

1119
Chromosome 11 open reading frame 68
BLES03, P5326
Gout, Melanoma

1120
Coiled-coil domain containing 3
-
Attention deficit hyperactivity disorder, Color vision deficiency, Connective tissue disease, Oligodendroglioma, Open angle glaucoma