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
14721 to 14730 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14721
Vexin
C8orf46
Color vision deficiency, Prostate cancer, Scoliosis

14722
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

14723
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

14724
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

14725
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

14726
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

14727
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

14728
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

14729
WASH complex subunit 3
CCDC53, CGI-116
Prostate cancer

14730
WASH complex subunit 4
KIAA1033, MRT43, SWIP
Nonsyndromic intellectual disability, Intellectual developmental disorder, Schizophrenia