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"
51 to 60 of 123 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

51
WD repeat domain 7
TRAG
Alzheimer disease, Congenital heart septal defect, Metabolic syndrome, Obsessive-compulsive disorder, Tourette syndrome, Diabetes mellitus type 2

52
WD repeat domain 70
-
Alzheimer disease, Digestive system disease, Diverticular disease

53
WD repeat domain 72
AI2A3
Amelogenesis imperfecta, Distal renal tubular acidosis, Kidney disease, Coronary artery disease, Dentin dysplasia, Dentinogenesis imperfecta, Diverticular disease, Hypertensive nephropathy, Hyperuricemia, Hypogonadism, Hypomaturation amelogenesis imperfecta, Hypophosphatemic rickets, Kidney failure, Nephrolithiasis, Proliferative diabetic retinopathy
View all (3 more)

54
WD repeat domain 73
GAMOS, GAMOS1, HSPC264
Camos syndrome, Color vision deficiency, Congenital neurologic anomalies, Dyskinesia, Galloway-mowat syndrome, Nephrotic syndrome, Periodontitis, Sarcoidosis

55
WD repeat domain 74
Nsa1
Melanoma, Neurodevelopmental disorder

56
WD repeat domain 75
NET16, UTP17
Breast cancer, Bronchial disease

57
WD repeat domain 76
CDW14, CMR1
Hepatocellular carcinoma, Lung cancer, Neutropenia, Squamous cell carcinoma

58
WD repeat domain 77
HKMT1069, MEP-50, MEP50, Nbla10071, p44, p44/Mep50
Ovarian neoplasms

59
WD repeat domain 81
CAMRQ2, CHMRQ, HYC3, PPP1R166, SORF-2
Alzheimer disease, Cerebellar ataxia, Cerebellar ataxia, impaired intellectual development, and dysequilibrium, Cerebellar ataxia, intellectual disability, and dysequilibrium, Cerebellar ataxia, mental retardation, and dysequilibrium, Congenital communicating hydrocephalus, Dysequilibrium syndrome, Developmental and epileptic encephalopathy, Fraser syndrome, Gout, Hydranencephaly, Hydrocephalus, Congenital hydrocephalus, Microlissencephaly, Omphalocele exstrophy imperforate anus

60
WD repeat domain 82
MST107, MSTP107, PRO2730, PRO34047, SWD2, TMEM113, WDR82A
Bipolar disorder, Color vision deficiency, Gout, Schizophrenia