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
14701 to 14710 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14701
WD repeat domain 49
CFAP337
Bipolar disorder, Prostate cancer

14702
WD repeat domain 5
BIG-3, BIG3, CFAP89, SWD3
Congenital heart disease, Neurodevelopmental disorder

14703
WD repeat domain 59
CDW12, FP977, p90-120
Dementia, Obesity, Pelvic organ prolapse, Scoliosis, Upper aerodigestive tract neoplasm, Venous thromboembolism

14704
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

14705
WD repeat domain 64
-
Obstructive pulmonary disease, Color vision deficiency, Depression

14706
WD repeat domain 7
TRAG
Alzheimer disease, Congenital heart septal defect, Metabolic syndrome, Obsessive-compulsive disorder, Tourette syndrome, Diabetes mellitus type 2

14707
WD repeat domain 70
-
Alzheimer disease, Digestive system disease, Diverticular disease

14708
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)

14709
WD repeat domain 73
GAMOS, GAMOS1, HSPC264
Camos syndrome, Color vision deficiency, Congenital neurologic anomalies, Dyskinesia, Galloway-mowat syndrome, Nephrotic syndrome, Periodontitis, Sarcoidosis

14710
WD repeat domain 74
Nsa1
Melanoma, Neurodevelopmental disorder