Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
14751 to 14760 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14751
WD repeat domain 25
C14orf67
Eosinophilia

14752
WD repeat domain 26
CDW2, GID7, MIP2, SKDEAS
Intellectual developmental disorder, Intellectual developmental disorder seizures dysmorphic gait, Long qt syndrome, Scoliosis, Skraban-deardorff syndrome

14753
WD repeat domain 27
-
Attention deficit hyperactivity disorder, Corneal astigmatism, Endometriosis, Insomnia, Substance abuse

14754
WD repeat domain 33
NET14, WDC146
Coronary artery disease

14755
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

14756
WD repeat domain 36
GLC1G, TA-WDRP, TAWDRP, UTP21
Asthma, Eczema, Central nervous system cancer, Rhinosinusitis, Colorectal cancer, Eosinophilia, Glaucoma, Glioblastoma, Glioma, Nasal polyp, Nasal disorder, Periodontitis, Open angle glaucoma, Respiratory system disease, Rhinitis
View all (3 more)

14757
WD repeat domain 37
NOCGUS
Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Kidney disease, Congenital ocular coloboma, Developmental delay, Epilepsy, Intellectual developmental disorder, Neurooculocardio-genitourinary syndrome

14758
WDR4 tRNA N7-guanosine methyltransferase non-catalytic subunit
GAMOS6, MIGSB, TRM82, TRMT82, Wuho, hWH
Galloway-mowat syndrome, Microcephaly

14759
WD repeat domain 41
MSTP048
Alzheimer disease, Parkinson disease

14760
WD repeat domain 43
NET12, UTP5
Breast cancer, Estrogen-receptor negative breast cancer, Oligodendroglioma, Triple negative breast cancer