Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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2371 to 2380 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2371
Cilia and flagella associated protein 300
C11orf70, CILD38, DNAAF17, FBB5
Ciliary dyskinesia, Situs ambiguus

2372
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

2373
Cilia and flagella associated protein 418
BBS21, C8orf37, CORD16, FAP418, MOT25, RP64, smalltalk
Retinitis pigmentosa, Bardet-biedl syndrome, Ciliopathy, Cone-rod dystrophy

2374
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

2375
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

2376
Cilia and flagella associated protein 45
CCDC19, HTX11, NESG1
Crohn disease, Heterotaxy syndrome, Ileocolitis, Mesothelioma, Tetralogy of fallot

2377
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

2378
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

2379
Cilia and flagella associated protein 52
HTX10, WDR16, WDRPUH
Heterotaxy syndrome, Situs inversus, Visceral heterotaxy

2380
Cilia and flagella associated protein 53
CCDC11, HTX6
Dextrocardia, Heterotaxy syndrome, Hypoplastic left heart syndrome, Situs ambiguus, Situs inversus, Tetralogy of fallot