Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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14661 to 14670 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14661
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

14662
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

14663
WASH complex subunit 3
CCDC53, CGI-116
Prostate cancer

14664
WASH complex subunit 4
KIAA1033, MRT43, SWIP
Nonsyndromic intellectual disability, Intellectual developmental disorder, Schizophrenia

14665
WASH complex subunit 5
KIAA0196, RTSC, RTSC1, SPG8
Amyotrophic lateral sclerosis, Spastic paraplegia, Frontotemporal dementia, Ritscher-schinzler syndrome, Hereditary spastic paraplegia, Stress urinary incontinence

14666
WASP like actin nucleation promoting factor
N-WASP, NWASP, WASPB
Migraine

14667
WW domain binding protein 11
BUG13, CFAP90, FAP90, NPWBP, PPP1R165, SIPP1, VCTERL, VCTRL, WBP-11
Vertebral, cardiac, renal, and limb defects syndrome

14668
WW domain binding protein 1 like
C10orf26, OPA1L, OPAL1
Alzheimer disease, Anxiety disorder, Asthma, Colorectal adenoma, Coronary artery disease, Hypertension, Myocardial infarction, Parkinson disease, Schizophrenia, Diabetes mellitus type 2, Uterine fibroid

14669
WW domain binding protein 2
DFNB107, GRAMD6, WBP-2
Isolated sensorineural deafness, Deafness, Hearing loss

14670
WBP2 N-terminal like
GRAMD7, PAWP
Major depressive disorder