Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "N"

331 to 340 of 533 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
331	4929	NR4A2	Nuclear receptor subfamily 4 group A member 2	HZF-3, IDLDP, NOT, NURR1, RNR1, TINUR	Arsenic encephalopathy, Arthritis, Autism, Bipolar disorder, Colorectal cancer, Colorectal neoplasms, Dementia, Dermatologic disorders, Dysarthria, Dysphagia, Dyssomnia, Juvenile arthritis, Language disorders, Mental depression, Mental retardation View all (7 more)
332	4931	NVL	Nuclear VCP like	NVL2	Leukemia
333	50507	NOX4	NADPH oxidase 4	KOX, KOX-1, RENOX	Colonic neoplasms, Congestive heart failure, Diabetes mellitus, Diabetic retinopathy, Heart failure, Hypertension, Kidney failure, Myocardial infarction, Narcolepsy, Renal insufficiency
334	50508	NOX3	NADPH oxidase 3	GP91-3, MOX-2	Prostatic neoplasms, Prostate cancer
335	50674	NEUROG3	Neurogenin 3	Atoh5, Math4B, NGN-3, bHLHa7, ngn3	Cholestatic liver disease, Diabetes mellitus, Malabsorption syndrome, Portal hypertension
336	50814	NSDHL	NAD(P) dependent 3-beta-hydroxysteroid dehydrogenase NSDHL	H105E3, SDR31E1, XAP104	Acquired kyphoscoliosis, Carcinoma of the head and neck, Child syndrome, Ck syndrome, Complete atrioventricular canal defect, Congenital epicanthus, Congenital exomphalos, Congenital hemidysplasia with ichthyosiform erythroderma and limb defects, Congenital kyphoscoliosis, Developmental delay, Dysphasia, Dyssomnia, Heart septal defects, High palate, Hydronephrosis View all (14 more)
337	50863	NTM	Neurotrimin	CEPU-1, HNT, IGLON2, NTRI	Attention deficit hyperactivity disorder, Leukemia, Mental depression, Myopia, Schizophrenia
338	51070	NOSIP	Nitric oxide synthase interacting protein	CGI-25	Schizophrenia
339	51079	NDUFA13	NADH:ubiquinone oxidoreductase subunit A13	B16.6, CDA016, CGI-39, GRIM-19, GRIM19, MC1DN28	Anemia, Cerebellar ataxia, Choreoathetosis, Developmental delay, Dysarthria, Dyskinetic syndrome, Thyroid carcinoma, Hypertrichosis, Hypertrophic cardiomyopathy, Mental retardation, Leigh syndrome with leukodystrophy, Leukodystrophy, Mitochondrial complex deficiency, Mitochondrial diseases, Mood swings View all (8 more)
340	51103	NDUFAF1	NADH:ubiquinone oxidoreductase complex assembly factor 1	CGI-65, CGI65, CIA30, MC1DN11	Congestive heart failure, Developmental delay, Diabetes mellitus, Epileptic encephalopathy, Hearing loss, Hypertrophic cardiomyopathy, Hypoglycemia, Isolated complex i deficiency, Leukodystrophy, Leukoencephalopathy, Microcephaly, Mitochondrial complex deficiency, Mitochondrial diseases, Mitochondrial myopathy, Myopathy View all (6 more)

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