Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "C"
1061 to 1070 of 1338 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1061
Centrosomal protein 63
SCKL6
Primary microcephaly, Desbuquois syndrome, Alzheimer disease, Microcephaly, Seckel syndrome, Hereditary spastic paraplegia

1062
CDK5 regulatory subunit associated protein 3
C53, HSF-27, IC53, LZAP, MST016, OK/SW-cl.114, PP1553
Astrocytoma, Bell's palsy, Epilepsy, Generalized epilepsy, Metabolic syndrome, Osteoarthritis, Prostate cancer, Diabetes mellitus, type 2

1063
Cubilin
IFCR, IGS, IGS1, MGA1, gp280
Amphetamine or related acting sympathomimetic abuse, Megaloblastic anemia, Autism, Bipolar disorder, Ischemic heart disease, Kidney disease, Colorectal cancer, Coronary artery disease, Deficiency anemia, Focal glomerulosclerosis, Gastroesophageal reflux disease, Gout, Imerslund-grasbeck syndrome, Melanoma, Kawasaki disease
View all (6 more)

1064
Coiled-coil domain containing 6
D10S170, H4, PTC, PTC1, TPC, TST1
Alzheimer disease, Differentiated thyroid carcinoma, Papillary thyroid cancer

1065
Cytoplasmic polyadenylation element binding protein 4
CPE-BP4, hCPEB-4
Ankylosing spondylitis, Atrial fibrillation, Atrial flutter, Attention deficit hyperactivity disorder, Cardiovascular disease, Obstructive pulmonary disease, Crohn disease, Hypertension, Gout, Heart failure, Inflammatory bowel disease, Multiple myeloma, Obesity, Peptic ulcer disease, Prion disease
View all (7 more)

1066
Centrosomal protein 70
BITE

1067
Coiled-coil domain containing 68
SE57-1
Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Coronary artery disease, Fuchs endothelial dystrophy, Hearing loss, Insomnia, Major depressive disorder, Mood disorder, Myocardial ischemia, Neurotic disorder, Obesity, Obsessive-compulsive disorder, Pancreatic cancer
View all (5 more)

1068
Coenzyme A synthase
DPCK, NBIA6, NBP, PCH12, PPAT, UKR1, pOV-2
Hallervorden spatz syndrome, Metabolic syndrome, Mucopolysaccharidosis, Neurodegeneration with brain iron accumulation, Pontocerebellar hypoplasia, Diabetes mellitus, type 2

1069
CD276 molecule
4Ig-B7-H3, B7-H3, B7H3, B7RP-2
Attention deficit hyperactivity disorder, Bipolar disorder, Hepatocellular carcinoma, Color vision deficiency, Dyslexia, Insomnia, Liver cirrhosis, Major depressive disorder, Metabolic syndrome, Post-traumatic stress disorder, Prostatic neoplasm, Substance abuse, Tourette syndrome, Diabetes mellitus, type 2

1070
Cysteine and glycine rich protein 3
CLP, CMD1M, CMH12, CRP3, LMO4, MLP
Cardiomyopathy, Dilated cardiomyopathy, Hypertrophic cardiomyopathy