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"
171 to 180 of 679 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

171
NADH:ubiquinone oxidoreductase complex assembly factor 3
2P1, C3orf60, E3-3, MC1DN18
Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease

172
NADH:ubiquinone oxidoreductase complex assembly factor 4
C6orf66, HRPAP20, HSPC125, MC1DN15, My013, bA22L21.1
Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Prostate cancer, Stroke

173
NADH:ubiquinone oxidoreductase complex assembly factor 5
C20orf7, MC1DN16, bA526K24.2, dJ842G6.1
Leber hereditary optic neuropathy, Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease

174
NADH:ubiquinone oxidoreductase complex assembly factor 6
C8orf38, FRTS5, MC1DN17, lncREST
Alzheimer disease, Androgenetic alopecia, Cardiovascular disease, Coronary artery disease, De toni-debre-fanconi syndrome, Developmental regression, Diabetes mellitus, Fanconi renotubular syndrome, Gout, Hypertension, Keratoconus, Leigh syndrome, Metabolic syndrome, Mitochondrial complex deficiency, Mitochondrial disease
View all (8 more)

175
NADH:ubiquinone oxidoreductase complex assembly factor 7
C2orf56, MidA, PRO1853
Alzheimer disease, Bipolar disorder, Lymphocytic leukemia, Gastroesophageal reflux disease, Inflammatory bowel disease, Ulcerative colitis

176
NADH:ubiquinone oxidoreductase complex assembly factor 8
C17orf89, MC1DN34
Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease

177
NADH:ubiquinone oxidoreductase subunit B10
MC1DN35, PDSW
Mitochondrial complex deficiency, Mitochondrial disease

178
NADH:ubiquinone oxidoreductase subunit B11
CI-ESSS, ESSS, MC1DN30, NP17.3, Np15, P17.3
Microphthalmia, Mitochondrial complex deficiency, Mitochondrial disease, Neurodevelopmental disorder

179
NADH:ubiquinone oxidoreductase subunit B2
AGGG, CI-AGGG
Diabetes mellitus type 2

180
NADH:ubiquinone oxidoreductase subunit B3
B12, CI-B12, MC1DN25
Congenital cataract, Developmental regression, Mitochondrial complex deficiency, Mitochondrial disease