Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "N"
171 to 180 of 533 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

171
Neurite extension and migration factor
KIAA2022, KIDLIA, MRX98, XLID98, XPN
Epilepsy, Epilepsy with myoclonic atonic seizures, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Neurodevelopmental disorders, X-linked intellectual disability, X-linked complex neurodevelopmental disorder

172
Nanos C2HC-type zinc finger 1
EC_Rep1a, NOS-1, NOS1, SPGF12, ZC2HC12A
Male infertility single gene azoospermia, Mesothelioma, Spermatogenic failure

173
Nanos C2HC-type zinc finger 3
NANOS1L, NOS3, ZC2HC12C
Breast cancer

174
NCK associated protein 5
ERIH1, ERIH2, NAP5
Alzheimer disease, Aneurysm, Aortic aneurysm, Eczema, Attention deficit hyperactivity disorder, Bipolar disorder, Bladder exstrophy, Hypertrophic cardiomyopathy, Male infertility, Intellectual developmental disorder, Metabolic syndrome, Multiple sclerosis, Oligodendroglioma, Premature ovarian failure, Pelvic organ prolapse
View all (7 more)

175
NME/NM23 family member 9
NM23-H9, NXL2, TXL-2, TXL2, TXNDC6
Alzheimer disease, Amyotrophic lateral sclerosis, Attention deficit hyperactivity disorder, Coronary artery disease, Dyslexia, Hypertension, Gout, Metabolic syndrome, Myocardial infarction, Diabetes mellitus, type 2

176
NPHP3 antisense RNA 1
NCRNA00119

177
NIPA like domain containing 4
ARCI6, ICHTHYIN, ICHYN, NIPA4, SLC57A6
Congenital ichthyosis, Congenital nonbullous ichthyosiform erythroderma, Erythrokeratodermia variabilis, Lamellar ichthyosis

178
Nanog homeobox pseudogene 9
NANOGP6

179
Nicotinamide nucleotide adenylyltransferase 3
FKSG76, PNAT-3, PNAT3
Polycystic ovary syndrome

180
NADH:ubiquinone oxidoreductase core subunit S7
CI-20, CI-20KD, MC1DN3, MY017, PSST
Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease