Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "C"
1061 to 1070 of 1796 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1061
Cold inducible RNA binding protein
CIRP
Autism, Myocardial ischemia

1062
Ciliated left-right organizer metallopeptidase
HTX12, LMLN2
Lymphoblastic leukemia, Heterotaxy syndrome, Scoliosis, Situs ambiguus, Situs inversus

1063
Ciliated left-right organizer protein containing ZP-N domains
C1orf127, HTX14
Androgenetic alopecia, Ewing sarcoma, Heterotaxy syndrome, Oligodendroglioma, Visceral heterotaxy

1064
CDGSH iron sulfur domain 1
C10orf70, MDS029, ZCD1, mitoNEET
Alzheimer disease

1065
CDGSH iron sulfur domain 2
ERIS, Miner1, NAF-1, WFS2, ZCD2
Atrial fibrillation, Autism, Diabetes mellitus type 2, Schizophrenia, Wolfram syndrome

1066
CDGSH iron sulfur domain 3
MiNT, Miner2
Turnpenny-fry syndrome, Wolfram syndrome

1067
Cytokine inducible SH2 containing protein
BACTS2, CIS, CIS-1, G18, SOCS
Allergic contact dermatitis

1068
Citron rho-interacting serine/threonine kinase
CITK, CRIK, MCPH17, STK21
Atrial fibrillation, Primary microcephaly, Congenital microcephaly, Crohn disease, Inflammatory bowel disease, Long qt syndrome, Microcephaly, Migraine, Scoliosis, Diabetes mellitus type 2, Ulcerative colitis

1069
Cbp/p300 interacting transactivator with Glu/Asp rich carboxy-terminal domain 1
MSG1
Autism, Willis-ekbom disease

1070
Cbp/p300 interacting transactivator with Glu/Asp rich carboxy-terminal domain 2
ASD8, MRG-1, MRG1, P35SRJ, VSD2
Atrial septal defect, Congenital heart disease, Congenital septal defect of heart, Congenital heart septal defect, Obesity, Tetralogy of fallot, Ventricular septal defect