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"
881 to 890 of 1806 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

881
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

882
Cilia and flagella associated protein 418
BBS21, C8orf37, CORD16, FAP418, MOT25, RP64, smalltalk
Retinitis pigmentosa, Bardet-biedl syndrome, Ciliopathy, Cone-rod dystrophy

883
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

884
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

885
Cilia and flagella associated protein 45
CCDC19, HTX11, NESG1
Crohn disease, Heterotaxy syndrome, Ileocolitis, Mesothelioma, Tetralogy of fallot

886
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

887
Cilia and flagella associated protein 47
CHDC2, CXorf22, CXorf30, CXorf59, SPGF52, SPGFX3
Kidney disease, Kidney failure, Male infertility large polyploid spermatozoa, Cortical development malformation, Polycystic kidney disease, Prostate cancer, Willis-ekbom disease, Spermatogenic failure, x-linked, Diabetes mellitus type 2

888
Cilia and flagella associated protein 52
HTX10, WDR16, WDRPUH
Heterotaxy syndrome, Situs inversus, Visceral heterotaxy

889
Cilia and flagella associated protein 53
CCDC11, HTX6
Dextrocardia, Heterotaxy syndrome, Hypoplastic left heart syndrome, Situs ambiguus, Situs inversus, Tetralogy of fallot

890
Cilia and flagella associated protein 54
C12orf55, C12orf63, CILD54, SPGF98
Ciliary dyskinesia, Frontotemporal dementia, Osteoarthritis, Post-traumatic stress disorder, Scoliosis, Spermatogenic failure