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"
1 to 10 of 123 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1
WW domain containing adaptor with coiled-coil
BM-016, DESSH, PRO1741, Wwp4
Alzheimer disease, Desanto-shinawi syndrome, Facial dysmorphism syndrome, Multiple myeloma, Neurodevelopmental disorder, Prostatic neoplasms

2
WAPL cohesin release factor
FOE, KIAA0261, WAPAL
Cardiovascular disease, Color vision deficiency, Neurodevelopmental disorder, Congenital clubfoot, Hypertension, Migraine, Non-specific syndromic intellectual disability, Amyotrophic lateral sclerosis, Diabetes mellitus type 2, Ventricular septal defect

3
Tryptophanyl-tRNA synthetase 1
GAMMA-2, HMN9, HMND9, IFI53, IFP53, NEDMSBA, WARS
Primary microcephaly, Charcot-marie-tooth disease, Developmental delay, Distal hereditary motor neuropathy, Distal spinal muscular atrophy, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Obsessive-compulsive disorder, Schizophrenia, Scoliosis, Papillary thyroid cancer

4
Tryptophanyl tRNA synthetase 2, mitochondrial
NEMMLAS, PKDYS3, TrpRS, mtTrpRS
Androgenetic alopecia, Major depressive disorder, Mitochondrial disease, Neurodevelopmental disorder, Obstructive sleep apnea syndrome, Osteoarthritis, Parkinsonism-dystonia, Sialolithiasis, Combined oxidative phosphorylation defect

5
WASP actin nucleation promoting factor
IMD2, SCNX, THC, THC1, WASP, WASPA
Severe congenital neutropenia, Thrombocytopenia, Wiskott-aldrich syndrome, X-linked severe congenital neutropenia, X-linked thrombocytopenia

6
WASP family member 1
NEDALVS, SCAR1, WAVE, WAVE-1, WAVE1
Developmental and epileptic encephalopathy, Intellectual developmental disorder, Major depressive disorder, Neurodevelopmental disorder, Non-specific syndromic intellectual disability

7
WASP family member 3
Brush-1, SCAR3, WAVE3
Juvenile arthritis, Bipolar disorder, Cerebral atherosclerosis, Color vision deficiency, Coronary artery disease, Dupuytren contracture, Dyslexia, Eosinophilia, Juvenile idiopathic arthritis, Major depressive disorder, Osteoarthritis, Oligoarticular juvenile idiopathic arthritis, Prostatic neoplasms, Scoliosis

8
WASH complex subunit 3
CCDC53, CGI-116
Prostate cancer

9
WASH complex subunit 4
KIAA1033, MRT43, SWIP
Nonsyndromic intellectual disability, Intellectual developmental disorder, Schizophrenia

10
WASH complex subunit 5
KIAA0196, RTSC, RTSC1, SPG8
Amyotrophic lateral sclerosis, Spastic paraplegia, Frontotemporal dementia, Ritscher-schinzler syndrome, Hereditary spastic paraplegia, Stress urinary incontinence