Genesⓘ

Dataset:
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
Extra-adrenal pheochromocytoma, Leukemia, Lung carcinoma, Pheochromocytoma, Schizophrenia

172
Calpain 10
CANP10, NIDDM1
Colorectal cancer, Diabetes mellitus, Mental retardation

173
Chromogranin B
SCG1
Schizophrenia

174
Cell division cycle 37, HSP90 cochaperone
P50CDC37
Ankylosing spondylitis, Crohn disease, Hypercholesterolemia, Inflammatory bowel disease, Multiple sclerosis

175
Coronin 1A
CLABP, CLIPINA, HCORO1, IMD8, TACO, p57
Anaplastic carcinoma, Carcinoma, Developmental delay, Immunodeficiency, Immunologic deficiency syndromes, Lymphopenia, Omenn syndrome, Severe combined immunodeficiency disease

176
Chitinase 3 like 1
ASRT7, CGP-39, GP-39, GP39, HC-gp39, HCGP-3P, YK-40, YKL-40, YKL40, YYL-40, hCGP-39
Arthritis, Delusions, Giant cell glioblastoma, Glioblastoma, Glioma, Hallucinations, Osteoarthrosis deformans, Schizophrenia

177
Chitinase 1
CHI3, CHIT, CHITD
Gaucher disease

178
Choline kinase alpha
CHK, CK, CKI, EK, NEDMIMS
Rachischisis, Spina bifida, Status dysraphicus

179
Centrosomal protein 250
C-NAP1, CEP2, CNAP1, CRDHL2
Hearing loss, Usher syndrome

180
Choline kinase beta
CHETK, CHKL, CK, CKB, CKEKB, EK, EKB, MDCMC
Cardiomyopathy, Congenital muscular dystrophy, Facial paralysis, Ichthyosis, Megaconial congenital muscular dystrophy, Mental retardation, Microcephaly, Motor delay, Muscular dystrophy, Myopathy, Narcolepsy, Narcolepsy-cataplexy syndrome, Hypotonia, Proximal myopathy with focal depletion of mitochondria