Genes | GeDiPNet - Gene Disease Pathway & Associations

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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

14731 to 14740 of 15448 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
14731	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
14732	8976	WASL	WASP like actin nucleation promoting factor	N-WASP, NWASP, WASPB	Migraine
14733	51729	WBP11	WW domain binding protein 11	BUG13, CFAP90, FAP90, NPWBP, PPP1R165, SIPP1, VCTERL, VCTRL, WBP-11	Vertebral, cardiac, renal, and limb defects syndrome
14734	54838	WBP1L	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
14735	23558	WBP2	WW domain binding protein 2	DFNB107, GRAMD6, WBP-2	Isolated sensorineural deafness, Deafness, Hearing loss
14736	164684	WBP2NL	WBP2 N-terminal like	GRAMD7, PAWP	Major depressive disorder
14737	11193	WBP4	WW domain binding protein 4	FBP21, NEDHFDB	Neurodevelopmental disorder
14738	80304	WDCP	WD repeat and coiled coil containing	C2orf44, MMAP, PP384	Alzheimer disease
14739	23001	WDFY3	WD repeat and FYVE domain containing 3	ALFY, BCHS, MCPH18, ZFYVE25	Autism, Color vision deficiency, Neurodevelopmental disorder, Intellectual developmental disorder, Microcephaly, Non-specific syndromic intellectual disability, Oropharyngeal cancer, Schizophrenia
14740	57705	WDFY4	WDFY family member 4	C10orf64	Autism, Biliary cirrhosis, Neurodevelopmental disorder, Developmental disability, Inflammatory bowel disease, Non-specific syndromic intellectual disability, Biliary cholangitis, Colorectal cancer, Rheumatoid arthritis, Scoliosis, Stroke, Systemic lupus erythematosus, Ulcerative colitis

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