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Dataset:
Curated
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Showing genes starting with "W"
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91 to 96 of 96 Genes
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Entrez ID
Gene Symbol
Gene Name
Synonyms
Diseases
91
89780
WNT3A
Wnt family member 3A
-
Hirschsprung disease
,
Obesity
,
Osteoporosis
92
91833
WDR20
WD repeat domain 20
Bun107, DMR
Nonmedullary thyroid carcinoma
,
Chronic obstructive pulmonary disease
,
Papillary thyroid carcinoma
,
Thyroid cancer
93
9277
WDR46
WD repeat domain 46
BING4, C6orf11, FP221, UTP7
Gastric cancer
,
Stomach neoplasms
94
9671
WSCD2
WSC domain containing 2
-
Anxiety disorder
,
Diabetes mellitus
95
9897
WASHC5
WASH complex subunit 5
KIAA0196, RTSC, RTSC1, SPG8
3c syndrome
,
Amyotrophic lateral sclerosis
,
Aortic valve sclerosis
,
Atrial septal defect
,
Brachycephaly
,
Brachydactyly
,
Charcot-marie-tooth disease
,
Congenital coloboma of iris
,
Congenital hypoplasia of penis
,
Congenital malrotation of intestine
,
Congenital ocular coloboma
,
Dandy-walker syndrome
,
Developmental delay
,
Double outlet right ventricle
,
Dwarfism
,
Ectopic anus
,
Frontal bossing
,
Frontotemporal dementia
,
Fundus coloboma
,
Gastroesophageal reflux disease
,
Glaucoma
,
Hydrocephalus
,
Hydronephrosis
,
Hypoplastic left heart syndrome
,
Hypospadias
,
Imperforate anus
,
Isolated somatotropin deficiency
,
Macrocephaly
,
Malformation of cortical development
,
Mental retardation
,
Micrognathism
,
Optic atrophy
,
Peroneal muscle atrophy
,
Pulmonary stenosis
,
Retinal coloboma
,
Ritscher-schinzel syndrome
,
Scoliosis
,
Somatotropin deficiency
,
Spastic paraplegia
,
Speech disorders
,
Syndactyly
,
Syndactyly of fingers
,
Tetralogy of fallot
,
Ventricular septal defect
View all (29 more)
96
9948
WDR1
WD repeat domain 1
AIP1, HEL-S-52, NORI-1, PFITS
Atrial fibrillation
,
Gout
,
Gouty arthritis
,
Osteoporosis
,
Paroxysmal atrial fibrillation
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