Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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14681 to 14690 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14681
WD repeat domain 17
-
Insomnia, Liver neoplasms

14682
WD repeat domain 19
ATD5, CED4, CFAP66, DYF-2, FAP66, IFT144, NPHP13, ORF26, Oseg6, PWDMP, SPGF72, SRTD5
Jeune syndrome, Bardet-biedl syndrome, Breast cancer, Caroli disease, Lymphoblastic leukemia, Ciliopathy, Cone dystrophy, Connective tissue disease, Craniodiaphyseal dysplasia, Craniosynostosis, Desbuquois syndrome, Glaucoma, Intellectual developmental disorder, Jeune thoracic dystrophy, Nephronophthisis
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14683
WD repeat domain 20
Bun107, DMR
Atrial fibrillation, Obstructive pulmonary disease, Global developmental delay, Gout, Papillary thyroid cancer

14684
WD repeat domain 24
C16orf21, JFP7
Cerebellar ataxia, Spinocerebellar ataxia

14685
WD repeat domain 25
C14orf67
Eosinophilia

14686
WD repeat domain 26
CDW2, GID7, MIP2, SKDEAS
Intellectual developmental disorder, Intellectual developmental disorder seizures dysmorphic gait, Long qt syndrome, Scoliosis, Skraban-deardorff syndrome

14687
WD repeat domain 27
-
Attention deficit hyperactivity disorder, Corneal astigmatism, Endometriosis, Insomnia, Substance abuse

14688
WD repeat domain 33
NET14, WDC146
Coronary artery disease

14689
WD repeat domain 35
CED2, CFAP118, FAP118, IFT121, IFTA1, SRTD7
Jeune syndrome, Connective tissue disease, Craniodiaphyseal dysplasia, Craniosynostosis, Desbuquois syndrome, Ellis-van creveld syndrome, Jeune thoracic dystrophy, Majewski syndrome, Short rib dysplasia-polydactyly syndrome, Short-rib thoracic dysplasia

14690
WD repeat domain 36
GLC1G, TA-WDRP, TAWDRP, UTP21
Asthma, Eczema, Central nervous system cancer, Colorectal cancer, Eosinophilia, Glaucoma, Glioblastoma, Glioma, Nasal polyp, Nasal disorder, Periodontitis, Open angle glaucoma, Respiratory system disease, Rhinitis, Seasonal allergic rhinitis
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