Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "C"
661 to 670 of 1338 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

661
Chromosome 17 open reading frame 58
-
Alzheimer disease, Insomnia, Lung disease, Prostate cancer, Respiratory system disease, Hypertension, Diabetes mellitus, type 2

662
Caveolae associated protein 1
CAVIN, CGL4, FKSG13, PTRF, cavin-1
Eczema, Berardinelli-seip congenital lipodystrophy, Breast cancer, Congenital generalized lipodystrophy, Coronary artery disease, Crohn disease, Generalized lipodystrophy, Iga nephropathy, Inflammatory bowel disease, Lipodystrophy, Methylmalonic acidemia, Myocardial infarction, Psoriasis, Diabetes mellitus, type 2

663
Chromosome 1 open reading frame 167
-
Ischemic heart disease, Coronary artery disease, Hypertension, Myocardial ischemia, Neural tube defect, Schizophrenia

664
Chromosome 1 open reading frame 185
-
Atrial fibrillation, Obstructive pulmonary disease, Hyperparathyroidism, Parathyroid disease

665
Cytochrome b561 family member D1
-
Dyslexia, Obesity, Schizophrenia

666
Coiled-coil domain containing 141
CAMDI
Atrioventricular block, Bundle branch block, Color vision deficiency, Colorectal cancer, Dental caries, Sick sinus syndrome, Heart disease, Heart failure, Hypertrophic cardiomyopathy, Hypogonadotropic hypogonadism, Hypopituitarism, Growth hormone deficiency, Kallmann syndrome, Panhypopituitarism, Pituitary dwarfism
View all (3 more)

667
CYP1B1 antisense RNA 1
C2orf58

668
Chromosome 3 open reading frame 38
-
Migraine

669
Coiled-coil domain containing 66
-
Gastritis, Nephrotic syndrome, Scoliosis

670
Cytochrome P450 family 4 subfamily V member 2
BCD, CYP4AH1
Bietti crystalline corneoretinal dystrophy, Choroideremia, Corneal dystrophy, Hereditary corneal dystrophy, Optic atrophy, Retinitis pigmentosa, Venous thromboembolism