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"
341 to 350 of 1806 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

341
Caveolae associated protein 1
CAVIN, CGL4, FKSG13, PTRF, cavin-1
Eczema, Berardinelli-seip congenital lipodystrophy, Breast cancer, Congenital generalized lipodystrophy, Coronary artery disease, Crohn disease, Generalized lipodystrophy, Iga nephropathy, Inflammatory bowel disease, Lipodystrophy, Methylmalonic acidemia, Myocardial infarction, Psoriasis, Diabetes mellitus type 2

342
Caveolae associated protein 2
PS-p68, SDPR, SDR, cavin-2
Hirschsprung disease, Osteoarthritis, Parkinson disease

343
Caveolae associated protein 3
HSRBC, PRKCDBP, SRBC, cavin-3
Asthma, Insomnia, Ocular sarcoidosis, Willis-ekbom disease, Rheumatic heart disease, Smooth surface dental caries

344
Caveolae associated protein 4
MURC, cavin-4
Atrial fibrillation, Dilated cardiomyopathy, Scoliosis

345
CACN subunit beta associated regulatory protein
BARP, C19orf26, DOS
Androgenetic alopecia, Diabetes mellitus type 2

346
CBFA2/RUNX1 partner transcriptional co-repressor 2
EHT, MTGR1, ZMYND3, p85
Basal cell carcinoma, Benign prostatic hyperplasia, Breast cancer, Cancer, Colorectal cancer, Estrogen-receptor negative breast cancer, Lung cancer, Melanoma, Non-melanoma skin carcinoma, Ovarian cancer, Ovarian serous carcinoma, Prostate cancer, Squamous cell carcinoma, Diabetes mellitus type 2

347
CBFA2/RUNX1 partner transcriptional co-repressor 3
ETO2, MTG16, MTGR2, RUNX1T3, ZMYND4
Atherosclerosis, Color vision deficiency, Duodenal ulcer, Eye disease, Melanoma, Multiple sclerosis, Neurotic disorder, Non-melanoma skin carcinoma, Oligodendroglioma, Rheumatoid arthritis, Scoliosis, Diabetes mellitus type 1, Diabetes mellitus type 2, Vitiligo

348
Core-binding factor subunit beta
CLCD2, PEBP2B
Myeloid leukemia, Androgenetic alopecia, Bone disease, Cleft palate, Cleidocranial dysplasia, Congenital heart defects, Congenital heart defect

349
Cbl proto-oncogene
C-CBL, CBL2, FRA11B, NSLL, RNF55
Congestive heart failure, Cryptorchidism, Desbuquois syndrome, Developmental disability, Early onset vitamin b6 dependent epilepsy, Growth disorder, Heart failure, Male infertility, Myelomonocytic leukemia, Left ventricular noncompaction cardiomyopathy, Neurodevelopmental disorder, Noonan syndrome, Vasculitis

350
Cbl proto-oncogene B
ADMIO3, Cbl-b, Nbla00127, RNF56
Autoimmune disease, Autoimmune thyroid disease, Bronchopneumonia, Dementia, Diabetes mellitus type 1, Head and neck neoplasm, Hypothyroidism, Multiple sclerosis, Oropharyngeal cancer, Rheumatoid arthritis, Stroke, Upper aerodigestive tract neoplasm, Urticaria