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"
1071 to 1080 of 1796 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1071
Cbp/p300 interacting transactivator with Glu/Asp rich carboxy-terminal domain 4
-
Androgenetic alopecia, Breast cancer

1072
CDKN1A interacting zinc finger protein 1
LSFR1, NP94, ZNF356
Cerebellar ataxia, Cervical dystonia, Developmental and epileptic encephalopathy, Dystonia, Global developmental delay, Prostatic neoplasms, Sarcoma, Torsion dystonia, Diabetes mellitus type 2

1073
Cytoskeleton associated protein 2 like
-
Hepatocellular carcinoma, Desbuquois syndrome, Endometriosis, Hypogonadism, Intellectual developmental disorder

1074
Cytoskeleton associated protein 4
CLIMP-63, CLIMP63, ERGIC-63, p63
Color vision deficiency

1075
Cytoskeleton associated protein 5
CHTOG, MSPS, TOG, TOGp, ch-TOG
Alzheimer disease, Aneuploidy, Chromosomal instability, Color vision deficiency, Polycystic ovary syndrome, Venous thromboembolism

1076
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

1077
Creatine kinase, M-type
CKMM, CPK-M, M-CK
Alzheimer disease, Colonic neoplasms, Hypertrophy, Left ventricular disease, Myocardial infarction

1078
Creatine kinase, mitochondrial 1B
CKMT, CKMT1, UMTCK
Diabetes mellitus type 2

1079
CDC28 protein kinase regulatory subunit 2
CKSHS2
Attention deficit hyperactivity disorder, Pelvic organ prolapse, Polycystic ovary syndrome, Substance abuse

1080
Cytoplasmic linker associated protein 1
MAST1
Bipolar disorder, Cardiomyopathy, Craniosynostosis, Partial epilepsy, Focal epilepsy, Non-specific syndromic intellectual disability, Oligodendroglioma, Roifman syndrome, Spondyloepiphyseal dysplasia