Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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14691 to 14700 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14691
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

14692
WDR4 tRNA N7-guanosine methyltransferase non-catalytic subunit
GAMOS6, MIGSB, TRM82, TRMT82, Wuho, hWH
Galloway-mowat syndrome, Microcephaly

14693
WD repeat domain 41
MSTP048
Alzheimer disease, Parkinson disease

14694
WD repeat domain 43
NET12, UTP5
Breast cancer, Estrogen-receptor negative breast cancer, Oligodendroglioma, Triple negative breast cancer

14695
WD repeat domain 44
RAB11BP, RPH11, SYM-4
Post-traumatic stress disorder

14696
WD repeat domain 45
JM5, NBIA4, NBIA5, WDRX1, WIPI-4, WIPI4
Autism, Beta-propeller protein-associated neurodegeneration, Developmental disability, X-linked optic atrophy, Epilepsy, Global developmental delay, Gross motor development delay, Hallervorden spatz syndrome, Heart failure, Hemiplegic migraine, Intellectual developmental disorder, Neurodegeneration with brain iron accumulation, Neurodevelopmental disorder, Oculocutaneous albinism, West syndrome
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14697
WD repeat domain 45B
NEDSBAS, WDR45L, WIPI-3, WIPI3
Intellectual developmental disorder, Neurodevelopmental disorder, Psoriasis, Diabetes mellitus type 2

14698
WD repeat domain 46
BING4, C6orf11, FP221, UTP7
Inflammatory bowel disease, Multiple sclerosis, Rheumatoid arthritis, Stomach neoplasms

14699
WD repeat domain 47
-
Neurodevelopmental disorder

14700
WD repeat domain 48
Bun62, P80, SPG60, UAF1
Spastic paraplegia, Cognition disorder, Delirium, dementia, and cognitive disorders, Metabolic syndrome, Hereditary spastic paraplegia, Diabetes mellitus type 2