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"
191 to 200 of 682 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

191
NADH:ubiquinone oxidoreductase subunit S4
AQDQ, CI-18, CI-18 kDa, CI-AQDQ, MC1DN1
Brain disease, Colorectal cancer, Developmental coordination disorder, Developmental regression, Gout, Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Motor skills disorder, Ovarian serous carcinoma, Schizophrenia, Diabetes mellitus type 2

192
NADH:ubiquinone oxidoreductase subunit S5
CI-15k, CI15K
Metabolic syndrome, Skin disease, Diabetes mellitus type 2

193
NADH:ubiquinone oxidoreductase subunit S6
CI-13kA, CI-13kD-A, CI13KDA, MC1DN9
Mitochondrial complex deficiency, Mitochondrial disease, Psychiatric disorders

194
NADH:ubiquinone oxidoreductase core subunit S7
CI-20, CI-20KD, MC1DN3, MY017, PSST
Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease

195
NADH:ubiquinone oxidoreductase core subunit S8
CI-23k, CI23KD, MC1DN2, TYKY
Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Osteoarthritis

196
NADH:ubiquinone oxidoreductase core subunit V1
CI-51K, CI51KD, MC1DN4, UQOR1
Bipolar disorder, Leigh syndrome, Major depressive disorder, Mitochondrial complex deficiency, Osteoarthritis, Schizophrenia, Stomach neoplasms, Depression

197
NADH:ubiquinone oxidoreductase core subunit V2
CI-24k, MC1DN7
Bipolar disorder, Cardiomyopathy, Bipolar depression, Epilepsy, Essential tremor, Leigh syndrome, Major depressive disorder, Mitochondrial complex deficiency, Mitochondrial disease, Mitochondrial encephalomyopathy, Parkinson disease, Schizophrenia, Depression

198
NADH:ubiquinone oxidoreductase subunit V3
CI-10k, CI-9KD
Bipolar disorder, Major depressive disorder, Psychotic disorders

199
Nebulin
AMC6, NEB177D, NEM2
Arthrogryposis multiplex congenita, Nebulin-related myopathy, Nemaline myopathy, Congenital neck anomaly, Congenital muscular dystrophy, Congenital structural myopathy, Deglutition disorder, Distal nebulin myopathy, Non-immune hydrops fetalis, Major depressive disorder, Muscular dystrophy, Peripheral neuropathy, Congenital nemaline myopathy, Squamous cell carcinoma, Diabetes mellitus type 2

200
Nebulette
C10orf113, LASP2, LNEBL, bA165O3.1
Atrial fibrillation, Breast cancer, Cardiac arrest, Cardiac arrhythmia, Cardiomyopathy, Dilated cardiomyopathy, Obstructive pulmonary disease, Color vision deficiency, Conotruncal cardiac defect, Coronary aneurysm, Digeorge syndrome, Eosinophilia, Heart failure, Hypertrophic cardiomyopathy, Metabolic syndrome
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