Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "C"
161 to 170 of 1338 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

161
Cleavage and polyadenylation specific factor 6
CFIM, CFIM68, CFIM72, HPBRII-4, HPBRII-7
Attention deficit hyperactivity disorder, Carpal tunnel syndrome, Alzheimer disease, Major depressive disorder, Metabolic syndrome, Neurodevelopmental disorders, Osteoarthritis, Psychiatric disorders, Scoliosis, Severe acute respiratory syndrome, Substance abuse, Diabetes mellitus, type 2

162
Chromodomain helicase DNA binding protein 2
DEE94, EEOC
Alzheimer disease, Autism, Neurodevelopmental disorder, Coronary artery disease, Developmental and epileptic encephalopathy, Epilepsy, Epilepsy with myoclonic atonic seizures, Rolandic epilepsy, Glomerulonephritis, Intellectual developmental disorder, Lennox-gastaut syndrome, Lung cancer, Neurodevelopmental disorders, Non-specific syndromic intellectual disability, Osteoarthritis
View all (1 more)

163
Chromodomain helicase DNA binding protein 3
Mi-2a, Mi2-ALPHA, SNIBCPS, ZFH
Breast cancer, Cancer, Basal cell carcinoma, Colorectal cancer, Estrogen-receptor negative breast cancer, Global developmental delay, Gout, Intellectual developmental disorder, Lung cancer, Neurodevelopmental disorders, Ovarian cancer, Ovarian serous carcinoma, Prostate cancer, Prostatic neoplasm, Sezary syndrome
View all (2 more)

164
Chromodomain helicase DNA binding protein 4
CHD-4, Mi-2b, Mi2-BETA, SIHIWES
Atrial fibrillation, Autism, Developmental disability, Endometrial neoplasm, Genetic predisposition to disease, Global developmental delay, Lung neoplasms, Metabolic syndrome, Schizophrenia, Stomach neoplasms, Diabetes mellitus, type 2

165
Checkpoint kinase 1
CHK1, OZEMA21
Breast neoplasm, Male infertility testicular dysgenesis, Oocyte maturation defect, Schizophrenia, Squamous cell carcinoma

166
Citron rho-interacting serine/threonine kinase
CITK, CRIK, MCPH17, STK21
Atrial fibrillation, Primary microcephaly, Congenital microtia, Crohn disease, Inflammatory bowel disease, Long qt syndrome, Microcephaly, Migraine, Respiratory system infectious disease, Scoliosis, Diabetes mellitus, type 2, Ulcerative colitis

167
Centrosomal protein 43
FGFR1OP, FOP
Ankylosing spondylitis, Basal cell carcinoma, B-cell acute lymphoblastic leukemia, Biliary cirrhosis, Crohn disease, Melanoma, Graves disease, Hypothyroidism, Iga nephropathy, Immune system disease, Inflammatory bowel disease, Keratinocyte carcinoma, Lung cancer, Myasthenia gravis, Biliary cholangitis
View all (9 more)

168
CRYZL2P-SEC16B readthrough
-
Breast cancer, Color vision deficiency, Insomnia, Metabolic syndrome, Osteoarthritis, Scoliosis, Diabetes mellitus, type 2

169
CD160 molecule
BY55, NK1, NK28
Breast cancer, Gout, Moyamoya disease

170
CLK4 associating serine/arginine rich protein
CLASP, SFRS16, SWAP2
Alzheimer disease, Gastroesophageal reflux disease