Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "C"
171 to 180 of 1338 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

171
Chromogranin A
CGA, PHE5, PHES
Basal cell carcinoma, Non-small-cell lung carcinoma, Hypertension, Iga nephropathy, Kidney failure, Pheochromocytoma, Schizophrenia

172
Calpain 10
CANP10, NIDDM1
Bipolar disorder, Diabetes mellitus type 2, Inflammatory bowel disease, Intellectual developmental disorder, Neurodevelopmental disorders, Obesity, Polycystic ovary syndrome, Ulcerative colitis

173
Chromogranin B
SCG1
Schizophrenia

174
Cell division cycle 37, HSP90 cochaperone
P50CDC37
Ankylosing spondylitis, Biliary cirrhosis, Crohn disease, Gastritis, Inflammatory bowel disease, Multiple sclerosis, Biliary cholangitis, Systemic lupus erythematosus, Ulcerative colitis

175
Coronin 1A
CLABP, CLIPINA, HCORO1, IMD8, TACO, p57
Ankylosing spondylitis, Atrial fibrillation, Autism, Carcinoma, Obstructive pulmonary disease, Color vision deficiency, Crohn disease, Dental caries, Epidermodysplasia verruciformis, Hodgkin lymphoma, Immunodeficiency, Insomnia, Multiple sclerosis, Ocular sarcoidosis, Osteoarthritis
View all (7 more)

176
Chitinase 3 like 1
ASRT7, CGP-39, GP-39, GP39, HC-gp39, HCGP-3P, YK-40, YKL-40, YKL40, YYL-40, hCGP-39
Asthma, Glioblastoma, Glioma, Osteoarthritis, Schizophrenia

177
Chitinase 1
CHI3, CHIT, CHITD
Gaucher disease

178
Choline kinase alpha
CHK, CK, CKI, EK, NEDMIMS
Nonsyndromic intellectual disability, Color vision deficiency, Neurodevelopmental disorder, Intellectual disability

179
Centrosomal protein 250
C-NAP1, CEP2, CNAP1, CRDHL2
Cone rod dystrophy and hearing loss, Optic atrophy, Retinitis pigmentosa, Usher syndrome

180
Choline kinase beta
CHETK, CHKL, CK, CKB, CKEKB, EK, EKB, MDCMC
Congenital myopathy, Cutaneous leishmaniasis, Intellectual developmental disorder, Muscular dystrophy, Narcolepsy