Genes | GeDiPNet - Gene Disease Pathway & Associations

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2091 to 2100 of 12229 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
2091	140468	COX11P1	COX11 pseudogene 1	COX11, COX11P	Schizophrenia
2092	140469	MYO3B	Myosin IIIB	-	Leukemia
2093	140578	CHODL	Chondrolectin	C21orf68, MT75, PRED12	Bulimia
2094	1406	CRX	Cone-rod homeobox	CORD2, CRD, LCA7, OTX3	Breast cancer, Cataract, Chorioretinal atrophy, Ciliopathies, Cone-rod dystrophy, Dysgenesis neuroepithelialis retinae, Congenital cerebral hernia, Congenital hypoplasia of penis, Developmental delay, Diabetes mellitus, Disorder of eye, Glaucoma, Hearing loss, Hemiplegia/hemiparesis, Hyperinsulinism View all (14 more)
2095	140609	NEK7	NIMA related kinase 7	-	Bipolar disorder, Ovarian serous adenocarcinoma
2096	140623	FAUP1	FAU pseudogene 1	FAU1P, RPS30_2_1613	Narcolepsy
2097	140628	GATA5	GATA binding protein 5	CHTD5, GATAS, bB379O24.1	Aneurysm of aortic arch, Aortic coarctation, Aortic valve calcification, Aortic valve disease, Aortic valve insufficiency, Aortic valve sclerosis, Atrial fibrillation, Atrial septal defect, Benign prostatic hyperplasia, Bicuspid aortic valve, Brachydactyly, Camptodactyly of fingers, Colorectal cancer, Colorectal neoplasms, Congenital heart defects View all (9 more)
2098	140660	RPL21P4	Ribosomal protein L21 pseudogene 4	RPL21_58_1548	Hereditary breast and ovarian cancer syndrome
2099	140685	ZBTB46	Zinc finger and BTB domain containing 46	BTBD4, BZEL, RINZF, ZNF340, dJ583P15.7, dJ583P15.8	Asthma, B-cell lymphoma, Eczema, Multiple sclerosis, Osteomyelitis
2100	140688	NOL4L	Nucleolar protein 4 like	C20orf112, C20orf113	Chronic obstructive pulmonary disease

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