Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "W"
61 to 70 of 96 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

61
WASP actin nucleation promoting factor
IMD2, SCNX, THC, THC1, WASP, WASPA
Severe congenital neutropenia, Wiskott-aldrich syndrome, X-linked severe congenital neutropenia, X-linked thrombocytopenia

62
WAS/WASL interacting protein family member 1
PRPL-2, WAS2, WASPIP, WIP
Atrial fibrillation, Atrial flutter, Cardioembolic stroke, Liver cirrhosis, Wiskott-aldrich syndrome

63
WEE1 G2 checkpoint kinase
WEE1A, WEE1hu
Alzheimer disease, Non-small-cell lung carcinoma, Cutaneous squamous cell carcinoma, Migraine, Skin cancer, Skin neoplasm, Squamous cell carcinoma, Diabetes mellitus, type 2

64
Wolframin ER transmembrane glycoprotein
CTRCT41, WFRS, WFS, WFSL
Auditory neuropathy, Autism, Isolated sensorineural deafness, Nonsyndromic hearing loss, Bipolar disorder, Cataract, Congenital cataract, Deafness, Major depressive disorder, Dermatomycosis, Dermatophytosis, Diabetes mellitus, Diabetes mellitus type 1, Diabetes mellitus type 2, Diabetic eye disease
View all (20 more)

65
-
PRDS

66
Wnt family member 1
BMND16, INT1, OI15
Attention deficit hyperactivity disorder, Autism, Bone disease, Bone fragility with contractures, arterial rupture, and deafness, Breast neoplasm, Connective tissue disease, Desbuquois syndrome, Osteoporosis, Keratoconus, Osteogenesis imperfecta, Osteoporosis-pseudoglioma syndrome

67
Wnt family member 2
INT1L1, IRP
Autism, Uterine neoplasm, Uterine fibroid

68
Wnt family member 3
INT4, TETAMS
Alzheimer disease, Androgenetic alopecia, Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Bladder exstrophy and epispadias complex, Breast cancer, Celiac disease, Coronary artery disease, Desbuquois syndrome, Estrogen-receptor negative breast cancer, Major depressive disorder, Mesothelioma, Mood disorder, Multiple system atrophy
View all (10 more)

69
Wnt family member 5A
hWNT5A
Robinow syndrome, Desbuquois syndrome, Female infertility, Idiopathic pulmonary fibrosis, Lung neoplasms, Scoliosis, Uterine neoplasm, Vesicoureteral reflux

70
Wnt family member 6
-
Androgenetic alopecia, Desbuquois syndrome, Diabetes mellitus, type 2