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"
1081 to 1090 of 1806 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1081
Cytoskeleton associated protein 5
CHTOG, MSPS, TOG, TOGp, ch-TOG
Alzheimer disease, Aneuploidy, Chromosomal instability, Color vision deficiency, Polycystic ovary syndrome, Venous thromboembolism

1082
Creatine kinase B
B-CK, BCK, CKBB, CPK-B, HEL-211, HEL-S-29
Attention deficit hyperactivity disorder, Autism, Basal cell carcinoma, Cardiovascular disease, Coronary artery disease, Hypertrophy, Left ventricular disease, Myocardial infarction, Pancreatic cancer, Schizophrenia, Small cell lung carcinoma, Stomach neoplasms

1083
Chemokine like factor
C32, CKLF1, CKLF2, CKLF3, CKLF4, HSPC224, UCK-1
Liver cirrhosis

1084
Creatine kinase, M-type
CKMM, CPK-M, M-CK
Alzheimer disease, Colonic neoplasms, Hypertrophy, Left ventricular disease, Myocardial infarction

1085
Creatine kinase, mitochondrial 1B
CKMT, CKMT1, UMTCK
Diabetes mellitus type 2

1086
CDC28 protein kinase regulatory subunit 2
CKSHS2
Attention deficit hyperactivity disorder, Pelvic organ prolapse, Polycystic ovary syndrome, Substance abuse

1087
Cytoplasmic linker associated protein 1
MAST1
Bipolar disorder, Cardiomyopathy, Craniosynostosis, Partial epilepsy, Focal epilepsy, Non-specific syndromic intellectual disability, Oligodendroglioma, Roifman syndrome, Spondyloepiphyseal dysplasia

1088
Cytoplasmic linker associated protein 2
-
Atherosclerosis

1089
CLK4 associating serine/arginine rich protein
CLASP, SFRS16, SWAP2
Alzheimer disease, Gastroesophageal reflux disease

1090
Clathrin binding box of aftiphilin containing 1
C14orf79
Oligodendroglioma, Diabetes mellitus type 2