Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "C"
801 to 810 of 1338 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

801
CYFIP related Rac1 interactor B
BM-009, CYRI, CYRI-B, FAM49B, L1
Alzheimer disease, Androgenetic alopecia, Colorectal cancer, Heart failure, Liver cirrhosis, Migraine, Parkinson disease, Post-traumatic stress disorder, Rheumatoid arthritis, Schizophrenia

802
CDK5RAP1 mitochondrial tRNA methylthiotransferase
C20orf34, C42, CGI-05, HSPC167
Biliary tract cancer, Breast cancer, Cancer, Cervical cancer, Colorectal cancer, Endometrial cancer, Esophageal cancer, Estrogen-receptor negative breast cancer, Gastric cancer, Hepatocellular carcinoma, Lung cancer, Non-hodgkins lymphoma, Non-melanoma skin carcinoma, Ovarian cancer, Ovarian serous carcinoma
View all (5 more)

803
Cleavage and polyadenylation specific factor 3
CPSF-73, CPSF73, NEDMHS, NEDMHSN
Neurodevelopmental disorder, Non-specific syndromic intellectual disability

804
CD244 molecule
2B4, NAIL, NKR2B4, Nmrk, SLAMF4
Ankylosing spondylitis, Rheumatoid arthritis, Crohn disease, Inflammatory bowel disease, Psoriasis, Sclerosing cholangitis, Ulcerative colitis

805
Cyclin dependent kinase 12
CRK7, CRKR, CRKRS
Asthma, Bladder calculus, Coronary artery disease, Diabetes mellitus, Diabetic neuropathy, Alzheimer disease, Tourette syndrome, Hyperopia, Nasopharyngeal carcinoma, Nephrolithiasis, Polycystic ovary syndrome, Prostatic neoplasm, Rheumatoid arthritis, Schizophrenia, Systemic lupus erythematosus
View all (2 more)

806
Complement factor properdin
BFD, PFC, PFD, PROPERDIN
Hepatocellular carcinoma, Liver cirrhosis, Meningitis, Stevens-johnson syndrome

807
Cyclin dependent kinase 14
PFTAIRE1, PFTK1
Attention deficit hyperactivity disorder, Hepatocellular carcinoma, Glomerulonephritis, Hepatitis b, Retinopathy of prematurity, Scoliosis, Substance abuse

808
Chloride intracellular channel 5
DFNB102, DFNB103, MST130, MSTP130
Alzheimer disease, Androgenetic alopecia, Isolated sensorineural deafness, Nonsyndromic hearing loss, Coronary artery disease, Deafness, Dementia, Glaucoma, Gout, Hearing impairment, Hearing loss, Hodgkin lymphoma, Intellectual developmental disorder, Open angle glaucoma, Osteoarthritis
View all (5 more)

809
Cadherin related family member 5
MLPCDH, MU-PCDH, MUCDHL, MUPCDH
Hypothyroidism, Systemic lupus erythematosus, Systemic sclerosis

810
Contactin 5
HNB-2s, NB-2
Anxiety disorder, Astrocytoma, Atrial fibrillation, Basal cell carcinoma, Behcet disease, Bipolar disorder, Central nervous system cancer, Obstructive pulmonary disease, Liver cirrhosis, Color vision deficiency, Colorectal cancer, Crohn disease, Dementia, Diabetic ketoacidosis, Digestive system disease
View all (19 more)