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"
851 to 860 of 1796 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

851
Ceramide synthase 5
LASS5, Trh4
Hypertension, Schizophrenia

852
Ceramide synthase 6
CERS5, LASS6
Bipolar disorder, Central nervous system cancer, Obstructive pulmonary disease, Glioblastoma, Glioma, Hyperthyroidism, Schizophrenia, Scoliosis, Diabetes mellitus type 2

853
Ceramide transporter 1
CERT, CERTL, COL4A3BP, GPBP, MRD34, NEDHSF, STARD11
Atrial fibrillation, Cancer, Non-small-cell lung carcinoma, Cardiovascular disease, Coronary artery disease, Diabetes mellitus, Epilepsy, Hyperlipidemia, Gallstones, Heart failure, Intellectual developmental disorder, Metabolic syndrome, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Stroke
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854
Carboxylesterase 1
ACAT, CE-1, CEH, CES2, HMSE, HMSE1, PCE-1, REH, SES1, TGH, hCE-1
Brain injuries, Hypercholesterolemia, Lung neoplasms, Obesity

855
Carboxylesterase 2
CE-2, CES2A1, PCE-2, iCE
Autism

856
Carboxylesterase 3
ES31
Autism, Myocardial ischemia

857
Carboxylesterase 5A
CAUXIN, CES4C1, CES5, CES7, HEL126
Alzheimer disease, Breast cancer, Ocular hypertension

858
Centrin 1
CEN1, CETN
Schizophrenia

859
Centrin 3
CDC31, CEN3
Bone disease, Cartilage disease

860
Cholesteryl ester transfer protein
BPIFF, HDLCQ10
Asthma, Atherosclerosis, Atrial fibrillation, Atrophic macular degeneration, Cancer, Hepatocellular carcinoma, Cardiovascular disease, Carotid artery disease, Cholesterol ester transfer protein deficiency, Coronary artery disease, Macular and posterior pole degeneration, Diabetes mellitus, Dyslexia, Hyperalphalipoproteinemia, Lipoprotein lipase deficiency
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