Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "N"
151 to 160 of 682 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

151
N-myc downstream regulated 1
CAP43, CMT4D, DRG-1, DRG1, GC4, HMSNL, NDR1, NMSL, PROXY1, RIT42, RTP, TARG1, TDD5
Astrocytoma, Breast neoplasms, Non-small-cell lung carcinoma, Pancreatic ductal carcinoma, Renal cell carcinoma, Charcot-marie-tooth disease, Dejerine-sottas disease, Glioblastoma, Hereditary motor and sensory neuropathies, Hypertrophic neuropathy, Kidney neoplasms, Liver cirrhosis, Liver neoplasms, Melanoma, Mouth neoplasms
View all (8 more)

152
NDRG family member 2
SYLD
Cataract, Colonic neoplasms, Exostoses, Liver cirrhosis, Nonalcoholic fatty liver disease, Psoriasis, Transient ischemic attack

153
NDRG family member 3
-
Melanoma, Non-melanoma skin carcinoma

154
NDRG family member 4
BDM1, SMAP-8, SMAP8
Achromatopsia, Autism, Schizophrenia

155
N-deacetylase and N-sulfotransferase 1
HSST, MRT46, NST1
Nonsyndromic intellectual disability, Cleft lip and palate, Craniofacial abnormalities, Eye abnormalities, Gastrointestinal stromal tumor, Global developmental delay, Intellectual developmental disorder, Cortical development malformation, Osteoarthritis

156
N-deacetylase and N-sulfotransferase 2
HSST2, N-HSST 2, NST2
Myocardial infarction, Prostatic neoplasms, Schizophrenia

157
N-deacetylase and N-sulfotransferase 3
HSST3
Bipolar disorder, Kidney disease, Keratoconus, Metabolic syndrome, Neurotic disorder, Willis-ekbom disease, Schizophrenia, Diabetes mellitus type 2

158
N-deacetylase and N-sulfotransferase 4
N-HSST, N-HSST 4, NDST-4, NHSST4
Alzheimer disease, Laryngitis, Liver cirrhosis, Dementia, Osteoarthritis, Prostatic neoplasms, Willis-ekbom disease

159
NADH:ubiquinone oxidoreductase subunit A1
CI-MWFE, MC1DN12, MWFE, ZNF183
Leigh syndrome, Mitochondrial complex deficiency

160
NADH:ubiquinone oxidoreductase subunit A10
CI-42KD, CI-42k, MC1DN22
Alzheimer disease, Appendicitis, Obstructive pulmonary disease, Color vision deficiency, Colorectal cancer, Essential tremor, Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Obesity, Schizophrenia