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"
161 to 170 of 682 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

161
NADH:ubiquinone oxidoreductase subunit A11
B14.7, CI-B14.7, MC1DN14
Mitochondrial complex deficiency, Mitochondrial disease

162
NADH:ubiquinone oxidoreductase subunit A12
B17.2, DAP13, MC1DN23
Alzheimer disease, Color vision deficiency, Coronary artery disease, Gallstones, Insomnia, Leigh syndrome, Mitochondrial complex deficiency, Myocardial infarction, Schizophrenia

163
NADH:ubiquinone oxidoreductase subunit A13
B16.6, CDA016, CGI-39, GRIM-19, GRIM19, MC1DN28
Differentiated thyroid carcinoma, Hypertrophic cardiomyopathy, Leigh syndrome, Mitochondrial complex deficiency, Nystagmus, Hurthle cell thyroid cancer, Thyroid carcinoma

164
NADH:ubiquinone oxidoreductase subunit A2
B8, CD14, CIB8, MC1DN13
Attention deficit hyperactivity disorder, Autism, Cystic leukoencephalopathy, Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Stomach neoplasms

165
NADH:ubiquinone oxidoreductase subunit A3
B9, CI-B9
Leigh syndrome

166
NADH:ubiquinone oxidoreductase subunit A6
B14, CI-B14, LYRM6, MC1DN33, NADHB14
Mitochondrial complex deficiency, Mitochondrial disease

167
NADH:ubiquinone oxidoreductase subunit A8
CI-19KD, CI-PGIV, MC1DN37, PGIV
Mitochondrial complex deficiency, Mitochondrial disease, Obesity, Scoliosis

168
NADH:ubiquinone oxidoreductase subunit A9
CC6, CI-39k, CI39k, COQ11, MC1DN26, NDUFS2L, SDR22E1
Alzheimer disease, Color vision deficiency, Leigh syndrome, Mitochondrial complex deficiency

169
NADH:ubiquinone oxidoreductase subunit AB1
ACP, ACP1, FASN2A, SDAP
Alzheimer disease

170
NADH:ubiquinone oxidoreductase complex assembly factor 1
CGI-65, CGI65, CIA30, MC1DN11
Mitochondrial complex deficiency, Mitochondrial disease