Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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2381 to 2390 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2381
Cilia and flagella associated protein 95
C9orf135
Stroke

2382
Cilia and flagella associated protein 96
C4orf47
Congenital neurologic anomalies, Developmental and epileptic encephalopathy, Intellectual developmental disorder, Seizures

2383
CFAP97 domain containing 1
C17orf105
Hyperlipidemia

2384
CFAP97 domain containing 2
-
Schizophrenia

2385
Cilia and flagella associated protein 99
-
Tourette syndrome

2386
Complement factor B
AHUS4, ARMD14, BF, BFD, CFAB, CFBD, FB, FBI12, GBG, H2-Bf, PBF2
Sickle cell anemia, Atrophic macular degeneration, Hemolytic uremic syndrome, Autoimmune thyroid disease, Brain injuries, C3 glomerulonephritis, Ulcerative colitis, Colorectal cancer, Complement component deficiency, Coronary artery disease, Crohn disease, Diabetes mellitus type 1, Diabetic retinopathy, Eye disease, Glaucoma
View all (12 more)

2387
Cryptic, EGF-CFC family member 1
CFC1B, CRYPTIC, DTGA2, HTX2
Biliary atresia, Congenitally uncorrected transposition of the great arteries, Double outlet right ventricle, Heterotaxy syndrome, Tetralogy of fallot, Transposition of the great arteries

2388
Cryptic, EGF-CFC family member 1B
-
Heterotaxy syndrome, Tetralogy of fallot

2389
Complement factor D
ADIPSIN, ADN, DF, PFD
Asbestosis, Complement component deficiency, Congestive heart failure, Cyclic neutropenia, Endometriosis, Glomerulonephritis, Heart failure, Severe congenital neutropenia, Ovarian cysts, Pulmonary fibrosis

2390
Craniofacial development protein 1
BCNT, BUCENTAUR, CENP-29, CP27, SWC5, Yeti, p97
Atherosclerosis, Brain aneurysm, Cardiovascular disease, Carotid atherosclerosis, Obstructive pulmonary disease, Coronary artery disease, Dupuytren contracture, Heart failure, Hypertension, Irritable bowel syndrome, Migraine, Moyamoya disease, Diabetes mellitus type 2