Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "C"
1051 to 1060 of 1338 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1051
Calmodulin 1
CALML2, CAM2, CAM3, CAMB, CAMC, CAMI, CAMIII, CPVT4, DD132, LQT14, PHKD, PHKD1, caM
Alzheimer disease, Cardiac arrhythmias, Cannabis abuse, Catecholaminergic polymorphic ventricular tachycardia, Long qt syndrome, Polymorphic catecholaminergic ventricular tachycardia

1052
Coiled-coil domain containing 33
CC2D3, CT61, HP11097
Alzheimer disease, Asthma, Breast cancer, Central nervous system cancer, Color vision deficiency, Dementia, Glioblastoma, Glioma, Obesity, Osteoarthritis

1053
Coiled-coil domain containing 170
C6orf97, bA282P11.1
Atrial fibrillation, Biliary tract cancer, Bone disease, Bone fracture, Breast cancer, Breast neoplasm, Cancer, Cardiovascular disease, Cervical cancer, Myelogenous leukemia, Colorectal cancer, Endometrial cancer, Endometriosis, Esophageal cancer, Estrogen resistance
View all (16 more)

1054
Centromere protein T
C16orf56, CENP-T, SSMGA
Methylmalonic acidemia, Uterine fibroid

1055
Cell wall biogenesis 43 C-terminal homolog
CWH43-C, PGAP2IP
Hepatitis c virus infection, Interstitial lung disease, Lung neoplasms, Metabolic syndrome, Diabetes mellitus, type 2, Uterine fibroid

1056
CST telomere replication complex component 1
AAF-132, AAF132, C17orf68, CRMCC, tmp494178
Bone disease, Brain disease, Calcinosis, Cerebroretinal microangiopathy with calcifications and cysts, Dyskeratosis congenita, Interstitial lung disease, Metabolic bone disorder, Parkinson disease

1057
Centrosomal protein 290
3H11Ag, BBS14, CT87, JBTS5, LCA10, MKS4, NPHP6, POC3, SLSN6, rd16
Arima syndrome, Hemolytic uremic syndrome, Bardet-biedl syndrome, Blindness, Cone-rod dystrophy, Congenital kidney anomaly, Congenital disorder of glycosylation, Congenital neurologic anomalies , Cystic kidney disease, Desbuquois syndrome, Aplasia of the vermis, Global developmental delay, Intellectual developmental disorder, Joubert syndrome, Kidney disease
View all (12 more)

1058
Coiled-coil domain containing 92
-
Anorexia nervosa, Atrial fibrillation, Coronary artery disease, Diabetes mellitus, Diabetes mellitus type 2, Insomnia, Major depressive disorder, Metabolic syndrome, Myocardial infarction, Myocardial ischemia, Schizophrenia, Tourette syndrome, Diabetes mellitus, type 2

1059
Cilia and flagella associated protein 43
C10orf79, HYDNP1, SPGF19, WDR96, bA373N18.2
Attention deficit hyperactivity disorder, Ciliary dyskinesia, Gastroparesis, Normal pressure hydrocephalus, Insomnia, Spermatogenic failure, Uterine fibroid

1060
Coenzyme Q10B
-
Schizophrenia