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

Showing genes starting with "W"

21 to 30 of 96 Genes

Show

	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
21	23160	WDR43	WD repeat domain 43	NET12, UTP5	Breast carcinoma
22	23286	WWC1	WW and C2 domain containing 1	HBEBP3, HBEBP36, KIBRA, MEMRYQTL, PPP1R168	Behcet syndrome, Leukemia, Malignant mesothelioma, Mental depression, Nonorganic psychosis, Psychosis
23	23302	WSCD1	WSC domain containing 1	-	Liver neoplasms, Liver cancer
24	23325	WASHC4	WASH complex subunit 4	KIAA1033, MRT43, SWIP	Absence of septum pellucidum, Autism, Central visual impairment, Cerebral atrophy, Cortical dysplasia, Developmental delay, Dwarfism, Dyskinetic syndrome, Dyssomnia, Hypoplasia of corpus callosum, Mental retardation, Mental depression, Microcephaly, Motor delay, Non-syndromic intellectual disability View all (5 more)
25	23558	WBP2	WW domain binding protein 2	DFNB107, GRAMD6, WBP-2	Anxiety disorder, Deafness, Non-syndromic sensorineural deafness
26	253769	WDR27	WD repeat domain 27	-	Rheumatoid arthritis, Sleep disorders
27	256764	WDR72	WD repeat domain 72	AI2A3	Amelogenesis imperfecta, Diabetes, Diabetes mellitus, Distal renal tubular acidosis, Hyperuricemia, Hypomaturation amelogenesis imperfecta, Kidney disease, Kidney failure, Proliferative diabetic retinopathy, Renal tubular acidosis, distal, with hemolytic anemia
28	25861	WHRN	Whirlin	CIP98, DFNB31, PDZD7B, USH2D, WI	Anxiety disorder, Bipolar disorder, Cataract, Cerebral cortical atrophy, Ciliopathies, Deafness, Disorder of eye, Hallucinations, Hearing loss, Hemianopsia, Hereditary retinal dystrophy, Mental depression, Microdontia, Myopia, Non-syndromic sensorineural deafness View all (7 more)
29	25937	WWTR1	WW domain containing transcription regulator 1	TAZ	Agranulocytosis, Alveolar rhabdomyosarcoma, Cardiomyopathy, Congestive heart failure, Dilated cardiomyopathy, Disorder of skeletal muscle, Endocardial fibroelastosis, Epithelioid hemangioendothelioma, Hearing loss, Hypertrophic cardiomyopathy, Intermittent lactic acidemia, Lipoatrophy, Lipodystrophy, Macrotia, Malocclusion View all (4 more)
30	26100	WIPI2	WD repeat domain, phosphoinositide interacting 2	ATG18B, Atg21, CGI-50, IDDSSA, WIPI-2	Camptodactyly of fingers, Cerebral atrophy, Congenital camptodactyly, Developmental delay, Dwarfism, Dysarthria, Dyskinetic syndrome, Hypoplasia of thumb, Mental retardation

«««1 234 5...»»»