Genes | GeDiPNet - Gene Disease Pathway & Associations

Dataset:

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

14741 to 14750 of 15448 Genes

Show

	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
14741	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
14742	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)
14743	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
14744	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)
14745	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
14746	64743	WDR13	WD repeat domain 13	MG21	Esophageal atresia, Intellectual developmental disorder
14747	116966	WDR17	WD repeat domain 17	-	Insomnia, Liver neoplasms
14748	57728	WDR19	WD repeat domain 19	ATD5, CED4, CFAP66, DYF-2, FAP66, IFT144, NPHP13, ORF26, Oseg6, PWDMP, SPGF72, SRTD5	Jeune syndrome, Bardet-biedl syndrome, Breast cancer, Caroli disease, Lymphoblastic leukemia, Ciliopathy, Cone dystrophy, Connective tissue disease, Craniodiaphyseal dysplasia, Craniosynostosis, Desbuquois syndrome, Glaucoma, Intellectual developmental disorder, Jeune thoracic dystrophy, Nephronophthisis View all (8 more)
14749	91833	WDR20	WD repeat domain 20	Bun107, DMR	Atrial fibrillation, Obstructive pulmonary disease, Global developmental delay, Gout, Papillary thyroid cancer
14750	84219	WDR24	WD repeat domain 24	C16orf21, JFP7	Cerebellar ataxia, Spinocerebellar ataxia

«««...1473 147414751476 1477...»»»