Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "N"
161 to 170 of 533 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

161
NOP53 ribosome biogenesis factor
GLTSCR2, PICT-1, PICT1
Polycystic ovary syndrome

162
Neurexophilin 1
NPH1, Nbla00697
Bipolar disorder, Breast cancer, Color vision deficiency, Dilated cardiomyopathy, Exostoses, Gastric cancer, Internet addiction disorder, Lung cancer, Enterocolitis, Nervous system disease, Neurotic disorder, Obesity, Psychiatric disorders, Schizophrenia, Scoliosis
View all (4 more)

163
5', 3'-nucleotidase, cytosolic
DNT, DNT1, HEL74, P5N2, PN-I, PN-II, UMPH2, cdN, dNT-1
Colorectal neoplasm

164
Neuregulin 1
ARIA, GGF, GGF2, HGL, HRG, HRG1, HRGA, MST131, MSTP131, NDF, NRG1-IT2, SMDF
Amphetamine or related acting sympathomimetic abuse, Amyotrophic lateral sclerosis, Juvenile arthritis, Bipolar disorder, Breast neoplasm, Cannabis abuse, Chagas cardiomyopathy, Charcot-marie-tooth disease, Kidney disease, Contact dermatitis, Bipolar depression, Major depressive disorder, Differentiated thyroid carcinoma, Gastric ulcer, Gastroparesis
View all (34 more)

165
Nuclear receptor subfamily 4 group A member 1
GFRP1, HMR, N10, NAK-1, NGFIB, NP10, NUR77, TR3
Major depressive disorder, Endometriosis, Essential tremor, Diabetes mellitus, type 2, Kidney disease, Myocardial ischemia, Oligodendroglioma, Pancreatic neoplasm, Proteinuria

166
Nudix hydrolase 2
APAH1, IDDPN
Breast neoplasm, Gout, Intellectual developmental disorder peripheral neuropathy, Intellectual developmental disorder, Non-specific syndromic intellectual disability

167
N-deacetylase and N-sulfotransferase 1
HSST, MRT46, NST1
Osteopetrosis, Craniofacial abnormalities, Eye abnormalities, Gastrointestinal stromal tumor, Global developmental delay, Intellectual developmental disorder, Cortical development malformation, Osteoarthritis

168
NLR family pyrin domain containing 9
CLR19.1, NALP9, NOD6, PAN12
Major depressive disorder, Night blindness, congenital stationary

169
NLR family pyrin domain containing 14
CLR11.2, GC-LRR, NALP14, NOD5, PAN8

170
N-acetyltransferase 8 like
CML3, NACED, NAT8-LIKE