Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "C"
1151 to 1160 of 1338 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1151
Cullin 1
-
Central nervous system cancer, Crohn disease, Glioblastoma, Glioma, Inflammatory bowel disease, Stevens-johnson syndrome, Diabetes mellitus, type 2, Ulcerative colitis

1152
Collagen type XXV alpha 1 chain
AMY, CFEOM5, CLAC, CLAC-P, CLACP
Alzheimer disease, Arthrogryposis, Arthrogryposis multiplex congenita, Clear cell renal cell carcinoma , Dementia, Kidney cancer, Pericarditis, Respiratory system disease, Schizophrenia, Systemic lupus erythematosus

1153
Calcium sensing receptor
CAR, EIG8, FHH, FIH, GPRC2A, HHC, HHC1, HYPOC1, NSHPT, PCAR1, hCasR
Asthma, Hereditary chronic pancreatitis, Hypocalcemia, Bartter syndrome, Bladder calculus, Calcium metabolism disorders, Stone disease, Desbuquois syndrome, Epilepsy, Idiopathic generalized epilepsy, Benign hypercalcemia, Hypocalciuric hypercalcemia, Gitelman syndrome, Hypercalcemia, Hyperparathyroidism
View all (9 more)

1154
Coiled-coil domain containing 62
CT109, ERAP75, SPGF67, TSP-NY
Atrial fibrillation, Insomnia, Parkinson disease, Schizophrenia, Spermatogenic failure, Diabetes mellitus, type 2

1155
Catalase
-
Acatalasia, Angle closure glaucoma, Aortic disease, Experimental arthritis, Rheumatoid arthritis, Osteonecrosis of the femoral head, Jeune syndrome, Asthma, Rhinitis, Autism, Avascular necrosis of bone, Behcet disease, Bonnevie-ullrich syndrome, Brain ischemia, Breast neoplasm
View all (51 more)

1156
Cytochrome c oxidase subunit 4I2
COX4, COX4-2, COX4B, COX4L2, COXIV-2, dJ857M17.2
Alzheimer disease, Mitochondrial disease, Pancreatic insufficiency syndrome

1157
Chromobox 2
CDCA6, M33, SRXY5
46,xy complete gonadal dysgenesis, 46,xy sex reversal

1158
Carnosine dipeptidase 1
CN1, CPGL2, HsT2308
Hepatocellular carcinoma, Carnosinase deficiency, Carnosinemia, Diabetic neuropathy, Glomerulonephritis, Intellectual developmental disorder, Liver cirrhosis

1159
Calcium release activated channel regulator 2A
EFCAB4B, RAB46
Liver cirrhosis, Combined immunodeficiency, Combined immunodeficiency disease, Male infertility, Nonalcoholic fatty liver disease, Periodontitis, Sialolithiasis

1160
Cartilage intermediate layer protein
CILP-1, CILP1, HsT18872
Atrial fibrillation, Intervertebral disc disease