Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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2391 to 2400 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2391
Cilia and flagella associated protein 92 (putative)
FAP92, KIAA1257
Dental caries, Mitochondrial complex deficiency

2392
Cilia and flagella associated protein 95
C9orf135
Stroke

2393
Cilia and flagella associated protein 96
C4orf47
Congenital neurologic anomalies, Developmental and epileptic encephalopathy, Intellectual developmental disorder, Seizures

2394
CFAP97 domain containing 1
C17orf105
Hyperlipidemia

2395
CFAP97 domain containing 2
-
Schizophrenia

2396
Cilia and flagella associated protein 99
-
Tourette syndrome

2397
Complement factor B
AHUS4, ARMD14, BF, BFD, CFAB, CFBD, FB, FBI12, GBG, H2-Bf, PBF2
Sickle cell anemia, Anterior uveitis, 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
View all (13 more)

2398
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

2399
Cryptic, EGF-CFC family member 1B
-
Heterotaxy syndrome, Tetralogy of fallot

2400
Complement factor D
ADIPSIN, ADN, DF, PFD
Asbestosis, Complement component deficiency, Congestive heart failure, Cyclic neutropenia, Endometriosis, Glomerulonephritis, Heart failure, Liver cirrhosis, Severe congenital neutropenia, Ovarian cysts, Pulmonary fibrosis