Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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2361 to 2370 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

2361
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

2362
Cilia and flagella associated protein 418
BBS21, C8orf37, CORD16, FAP418, MOT25, RP64, smalltalk
Retinitis pigmentosa, Bardet-biedl syndrome, Ciliopathy, Cone-rod dystrophy

2363
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

2364
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

2365
Cilia and flagella associated protein 45
CCDC19, HTX11, NESG1
Crohn disease, Heterotaxy syndrome, Ileocolitis, Mesothelioma, Tetralogy of fallot

2366
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

2367
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

2368
Cilia and flagella associated protein 52
HTX10, WDR16, WDRPUH
Heterotaxy syndrome, Situs inversus, Visceral heterotaxy

2369
Cilia and flagella associated protein 53
CCDC11, HTX6
Dextrocardia, Heterotaxy syndrome, Hypoplastic left heart syndrome, Situs ambiguus, Situs inversus, Tetralogy of fallot

2370
Cilia and flagella associated protein 54
C12orf55, C12orf63, CILD54, SPGF98
Ciliary dyskinesia, Frontotemporal dementia, Osteoarthritis, Post-traumatic stress disorder, Scoliosis, Spermatogenic failure