Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "N"

171 to 180 of 533 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
171	340533	NEXMIF	Neurite extension and migration factor	KIAA2022, KIDLIA, MRX98, XLID98, XPN	Autism, Cerebral cortical atrophy, Continuous spike and waves during slow sleep, Developmental delay, Dysmorphic features, Epilepsy, Esotropia, Gastroesophageal reflux disease, Hypoplasia of corpus callosum, Macrotia, Mental retardation, Mental retardation, x-linked, Myoclonic seizures, Hypotonia, Neurodevelopmental disorders View all (2 more)
172	340719	NANOS1	Nanos C2HC-type zinc finger 1	EC_Rep1a, NOS-1, NOS1, SPGF12, ZC2HC12A	Azoospermia, Male infertility, Male infertility with teratozoospermia, Malignant mesothelioma, Non-obstructive azoospermia, Obstructive azoospermia, Spermatogenic failure
173	342977	NANOS3	Nanos C2HC-type zinc finger 3	NANOS1L, NOS3, ZC2HC12C	Ovarian failure
174	344148	NCKAP5	NCK associated protein 5	ERIH1, ERIH2, NAP5	Hypersomnia, Mental disorders, Psychosis
175	347736	NME9	NME/NM23 family member 9	NM23-H9, NXL2, TXL-2, TXL2, TXNDC6	Amyotrophic lateral sclerosis
176	348808	NPHP3-AS1	NPHP3 antisense RNA 1	NCRNA00119	Nephronophthisis
177	348938	NIPAL4	NIPA like domain containing 4	ARCI6, ICHTHYIN, ICHYN, NIPA4, SLC57A6	Alopecia, Congenital nonbullous ichthyosiform erythroderma, Corneal erosion, Dwarfism, Ectropion, Exfoliative dermatitis, Gangrene, Hyperkeratosis, Hypohidrosis, Hypotrichosis, Ichthyosis, Ichthyosis with hypotrichosis, Impaired cognition, Keratitis, Lamellar ichthyosis View all (4 more)
178	349386	NANOGP9	Nanog homeobox pseudogene 9	NANOGP6	Alopecia
179	349565	NMNAT3	Nicotinamide nucleotide adenylyltransferase 3	FKSG76, PNAT-3, PNAT3	Sclerocystic ovaries, Polycystic ovary syndrome
180	374291	NDUFS7	NADH:ubiquinone oxidoreductase core subunit S7	CI-20, CI-20KD, MC1DN3, MY017, PSST	Anemia, Cerebellar ataxia, Developmental delay, Developmental regression, Diabetes mellitus, Dysarthria, Epileptic encephalopathy, Hearing loss, Hypertrichosis, Hypertrophic cardiomyopathy, Hypoglycemia, Mental retardation, Isolated complex i deficiency, Leigh syndrome, Leigh syndrome with leukodystrophy View all (15 more)

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