Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "W"
41 to 50 of 123 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

41
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
View all (2 more)

42
WD repeat domain 45B
NEDSBAS, WDR45L, WIPI-3, WIPI3
Intellectual developmental disorder, Neurodevelopmental disorder, Psoriasis, Diabetes mellitus type 2

43
WD repeat domain 46
BING4, C6orf11, FP221, UTP7
Inflammatory bowel disease, Multiple sclerosis, Rheumatoid arthritis, Stomach neoplasms

44
WD repeat domain 47
-
Neurodevelopmental disorder

45
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

46
WD repeat domain 49
CFAP337
Bipolar disorder, Prostate cancer

47
WD repeat domain 5
BIG-3, BIG3, CFAP89, SWD3
Congenital heart disease, Neurodevelopmental disorder

48
WD repeat domain 59
CDW12, FP977, p90-120
Dementia, Leprosy, Obesity, Pelvic organ prolapse, Scoliosis, Upper aerodigestive tract neoplasm, Venous thromboembolism

49
WD repeat domain 62
C19orf14, MCPH2
Atrial fibrillation, Primary microcephaly, Hepatocellular carcinoma, Congenital microcephaly, Congenital neurologic anomalies, Intellectual developmental disorder, Cortical development malformation, Microcephaly, Polymicrogyria, Skraban-deardorff syndrome

50
WD repeat domain 64
-
Obstructive pulmonary disease, Color vision deficiency, Depression