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 679 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

151
NDRG family member 2
SYLD
Cataract, Colonic neoplasms, Exostoses, Nonalcoholic fatty liver disease, Psoriasis, Transient ischemic attack

152
NDRG family member 3
-
Melanoma, Non-melanoma skin carcinoma

153
NDRG family member 4
BDM1, SMAP-8, SMAP8
Achromatopsia, Autism, Schizophrenia

154
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

155
N-deacetylase and N-sulfotransferase 2
HSST2, N-HSST 2, NST2
Myocardial infarction, Prostatic neoplasms, Schizophrenia

156
N-deacetylase and N-sulfotransferase 3
HSST3
Bipolar disorder, Kidney disease, Keratoconus, Metabolic syndrome, Neurotic disorder, Willis-ekbom disease, Schizophrenia, Diabetes mellitus type 2

157
N-deacetylase and N-sulfotransferase 4
N-HSST, N-HSST 4, NDST-4, NHSST4
Alzheimer disease, Liver cirrhosis, Dementia, Osteoarthritis, Prostatic neoplasms, Willis-ekbom disease

158
NADH:ubiquinone oxidoreductase subunit A1
CI-MWFE, MC1DN12, MWFE, ZNF183
Leigh syndrome, Mitochondrial complex deficiency

159
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

160
NADH:ubiquinone oxidoreductase subunit A11
B14.7, CI-B14.7, MC1DN14
Mitochondrial complex deficiency, Mitochondrial disease