Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "C"
871 to 880 of 1796 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

871
Cilia and flagella associated protein 298
C21orf48, C21orf59, CILD26, DNAAF16, FBB18, Kur
Ciliary dyskinesia, Congenital nasopharyngeal atresia, Situs ambiguus

872
CFAP298-TCP10L readthrough
C21orf59-TCP10L, C21orf77, LINC00846
Cerebral amyloid angiopathy, Ciliary dyskinesia, Gastritis, Hepatocellular carcinoma, Neuroblastoma, Scoliosis, Situs ambiguus

873
Cilia and flagella associated protein 299
C4orf22
Androgenetic alopecia, Cataract, Colorectal cancer, Corneal astigmatism, Eye disease, Nonalcoholic fatty liver disease, Obesity, Retinal detachment, Diabetes mellitus type 2

874
Cilia and flagella associated protein 300
C11orf70, CILD38, DNAAF17, FBB5
Ciliary dyskinesia, Situs ambiguus

875
Cilia and flagella associated protein 410
C21orf2, LRRC76, RDMS, SMDAX, YF5/A2
Amyotrophic lateral sclerosis, Atrial fibrillation, Axial spondylometaphyseal dysplasia, Cone dystrophy, Cone-rod dystrophy, Desbuquois syndrome, Leber congenital amaurosis, Retinitis pigmentosa, Spondylometaphyseal dysplasia

876
Cilia and flagella associated protein 418
BBS21, C8orf37, CORD16, FAP418, MOT25, RP64, smalltalk
Retinitis pigmentosa, Bardet-biedl syndrome, Ciliopathy, Cone-rod dystrophy

877
Cilia and flagella associated protein 43
C10orf79, HYDNP1, SPGF19, WDR96, bA373N18.2
Attention deficit hyperactivity disorder, Ciliary dyskinesia, Congenital impairment of spermatozoa motility, Congenital left-sided heart lesions, Gastroparesis, Normal pressure hydrocephalus, Insomnia, Spermatogenic failure, Teratozoospermia, Uterine fibroid

878
Cilia and flagella associated protein 44
SPGF20, WDR52
Colorectal cancer, Congenital impairment of spermatozoa motility, Periodontal disease, Periodontitis, Prostate cancer, Spermatogenic failure, Diabetes mellitus type 2

879
Cilia and flagella associated protein 45
CCDC19, HTX11, NESG1
Crohn disease, Heterotaxy syndrome, Ileocolitis, Mesothelioma, Tetralogy of fallot

880
Cilia and flagella associated protein 46
C10orf123, C10orf124, C10orf92, C10orf93, TTC40, bA288G11.4, bA288G11.5, bB137A17.2, bB137A17.3
Alzheimer disease, Astrocytoma, Dementia, Psoriasis, Situs ambiguus