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"
921 to 930 of 1806 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

921
Complement factor properdin
BFD, PFC, PFD, PROPERDIN
Hepatocellular carcinoma, Liver cirrhosis, Stevens-johnson syndrome

922
CF transmembrane conductance regulator
ABC35, ABCC7, CF, CFTR/MRP, MRP7, TNR-CFTR, dJ760C5.1
Asthma, Autism, Hereditary chronic pancreatitis, Polycystic kidney disease, Azoospermia, Barrett esophagus, Bronchiectasis, Cholecystolithiasis, Obstructive airway disease, Sinusitis, Colorectal neoplasms, Congenital bilateral absence of vas deferens, Connective tissue disease, Coronary artery disease, Cystic fibrosis
View all (15 more)

923
Glycoprotein hormones, alpha polypeptide
CG-ALPHA, FSHA, GPA1, GPHA1, GPHa, HCG, LHA, TSHA
Atrial fibrillation, Hemiplegia, Ovarian diseases, Follicular thyroid cancer, Uterine polyp

924
Chorionic gonadotropin subunit beta 1
-
Astrocytoma, Autism, Central nervous system cancer, Glioma

925
Chorionic gonadotropin subunit beta 3
CGB, CGB5, CGB7, CGB8, LHB, hCGB
Hypogonadism

926
Chorionic gonadotropin subunit beta 5
CGB, HCG, hCGB
Polycystic ovary syndrome

927
CGG triplet repeat binding protein 1
CGGBP, p20-CGGBP
Attention deficit hyperactivity disorder, Major depressive disorder, Metabolic syndrome, Orofacial cleft, Substance abuse, Diabetes mellitus type 2

928
Cingulin
-
Autism, Color vision deficiency, Venous thromboembolism

929
Cingulin like 1
JACOP, PCING
Atrial fibrillation, Autism, Bipolar disorder, Congenital esophageal anomaly, Diabetic neuropathy, Premature ovarian failure, Schizophrenia, Substance abuse, Hypertension, Diabetes mellitus type 2

930
Cell growth regulator with EF-hand domain 1
CGR11
Attention deficit hyperactivity disorder, Fructokinase deficiency, Liver neoplasms, Post-traumatic stress disorder, Diabetes mellitus type 2, Vascular dementia