Genes | GeDiPNet - Gene Disease Pathway & Associations

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14671 to 14680 of 15380 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
14671	11193	WBP4	WW domain binding protein 4	FBP21, NEDHFDB	Neurodevelopmental disorder
14672	80304	WDCP	WD repeat and coiled coil containing	C2orf44, MMAP, PP384	Alzheimer disease
14673	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
14674	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
14675	11169	WDHD1	WD repeat and HMG-box DNA binding protein 1	AND-1, AND1, CHTF4, CTF4	Alzheimer disease, Astrocytoma, Dry eye syndrome, Parkinson disease, Peripheral neuropathy, Schizophrenia
14676	51057	WDPCP	WD repeat containing planar cell polarity effector	BBS15, C2orf86, CHDTHP, CPLANE5, FRITZ, FRTZ	Alzheimer disease, Asthma, Astrocytoma, Attention deficit hyperactivity disorder, Bardet-biedl syndrome, Bipolar disorder, Ciliopathy, Congenital heart disease, Melanoma, Developmental and epileptic encephalopathy, Aplasia of the vermis, Heart defect, tongue hamartoma and polysyndactyly, Insomnia, Major depressive disorder, Neurotic disorder View all (7 more)
14677	9948	WDR1	WD repeat domain 1	AIP1, HEL-S-52, NORI-1, PFITS	Atrial fibrillation, Dementia, Gout, Hoarding disorder, Hyperuricemia, Intellectual developmental disorder, Neurotic disorder, Osteoporosis, Parkinson disease, Thrombocytopenia
14678	55717	WDR11	WD repeat domain 11	BRWD2, DR11, HH14, SRI1, WDR15	Anorexia nervosa, Nonsyndromic intellectual disability, Benign prostatic hyperplasia, Uinary system neoplasms, Breast cancer, Charge syndrome, Eating disorder, Hypogonadotropic hypogonadism, Hypopituitarism, Growth hormone deficiency, Intellectual developmental disorder, Kallmann syndrome, Panhypopituitarism, Pituitary dwarfism, Pituitary short stature View all (6 more)
14679	55759	WDR12	WD repeat domain 12	YTM1	Alzheimer disease, Dilated cardiomyopathy, Bronchitis, Ischemic heart disease, Coronary artery disease, Hemolytic anemia, Irritable bowel syndrome, Large artery stroke, Migraine, Myocardial infarction, Myocardial ischemia, Osteoarthritis, Small vessel stroke, Stroke
14680	64743	WDR13	WD repeat domain 13	MG21	Esophageal atresia, Intellectual developmental disorder

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