eDiPNet

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Chromosome:

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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

Showing genes starting with "W"

1 to 10 of 123 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1	51322	WAC	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	23063	WAPL	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	7453	WARS1	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	10352	WARS2	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	7454	WAS	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	8936	WASF1	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	10810	WASF3	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	51019	WASHC3	WASH complex subunit 3	CCDC53, CGI-116	Prostate cancer
9	23325	WASHC4	WASH complex subunit 4	KIAA1033, MRT43, SWIP	Nonsyndromic intellectual disability, Intellectual developmental disorder, Schizophrenia
10	9897	WASHC5	WASH complex subunit 5	KIAA0196, RTSC, RTSC1, SPG8	Amyotrophic lateral sclerosis, Spastic paraplegia, Frontotemporal dementia, Ritscher-schinzler syndrome, Hereditary spastic paraplegia, Stress urinary incontinence, hereditary spastic paraplegia 8

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