431
|
|
|
NADH:ubiquinone oxidoreductase subunit B9 pseudogene 3 |
- |
Curated: N/A
Unreviewed: N/A
|
432
|
|
|
NADH:ubiquinone oxidoreductase subunit C1 |
KFYI |
Curated: N/A
Unreviewed: Adrenocortical carcinoma, Gestational diabetes
|
433
|
|
|
NADH:ubiquinone oxidoreductase subunit C2 |
B14.5b, CI-B14.5b, HLC-1, MC1DN36, NADHDH2 |
Curated: Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease
Unreviewed: Breast neoplasm, Carcinoma, Colon Carcinoma, Colorectal neoplasm, Coronary Syndrome, Diabetes mellitus, type 2, Ischemic Stroke, Lung adenocarcinoma, Ovarian diseases, Stable Angina, Stroke
|
434
|
|
|
NDUFC2-KCTD14 readthrough |
- |
Curated: Mitochondrial complex deficiency, Mitochondrial disease, Pelvic organ prolapse
Unreviewed: N/A
|
435
|
|
|
NADH:ubiquinone oxidoreductase core subunit S1 |
CI-75Kd, CI-75k, MC1DN5, PRO1304 |
Curated: Cardiomyopathy, Schizophrenia, Frontotemporal dementia, Hypertrophic cardiomyopathy, Leigh syndrome, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Stomach neoplasms
Unreviewed: Anemia, Arthrocutaneouveal granulomatosis, Autism spectrum disorder, Bipolar Disorder, Brain atrophy, Breast neoplasm, Carcinogenesis, Cerebellar Ataxia, Cerebellar atrophy, Cerebral Atrophy, Colorectal neoplasm, Cyanosis, Developmental Delay, Developmental regression, Diabetes Mellitus, Dysarthria, Dysphagia, Epileptic encephalopathy, Gastric Cancer, Hearing Loss, Heart failure, HYPERTRICHOSIS, Hypoglycemia, Isolated Complex I Deficiency, Leigh Syndrome, Leigh Syndrome With Leukodystrophy, Leukodystrophy, Leukoencephalopathy, Lung Cancer, Lung carcinoma, Lung neoplasms, Malignant Neoplasm, Malignant Neoplasm Of Testis, Malignant testicular germ cell tumor, MELAS Syndrome, Mental retardation, Microcephaly, Mitochondrial Complex Deficiency, Mitochondrial Diseases, Mitochondrial encephalopathy, Mitochondrial myopathy, Mood swings, Necrotizing encephalomyelopathy, Neoplasms, Nervous System Diseases, Neuroblastoma, Nystagmus, Optic Atrophy, Ovarian diseases, Parkinson Disease, Ptosis, Renal Carcinoma, Retinitis Pigmentosa, Stomach Neoplasms, Strabismus, Testicular neoplasm, Ventricular septal defect
|
436
|
|
|
NADH:ubiquinone oxidoreductase core subunit S2 |
CI-49, LHONAR2, MC1DN6 |
Curated: Asthma, Cardiomyopathy, Hypertrophic cardiomyopathy, Leber hereditary optic neuropathy, Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Mitochondrial encephalomyopathy, Multiple sclerosis, Optic atrophy
Unreviewed: Anemia, Arthrocutaneouveal granulomatosis, Brain atrophy, Cerebellar Ataxia, Cerebral Atrophy, Congestive Heart Failure, Coronary Heart Disease, Developmental Delay, Developmental regression, Diabetes Mellitus, Dysarthria, Dyskinetic Syndrome, Dysphagia, Epileptic encephalopathy, Hearing Loss, Hereditary Leber Optic Atrophy, HYPERTRICHOSIS, Hypoglycemia, Isolated Complex I Deficiency, Leigh Syndrome, Leigh Syndrome With Cardiomyopathy, Leigh Syndrome With Leukodystrophy, Leukodystrophy, Leukoencephalopathy, Lung Cancer, Lung carcinoma, Lung neoplasms, Malignant Neoplasm, Mental retardation, Microcephaly, Mitochondrial Complex Deficiency, Mitochondrial Diseases, Mitochondrial myopathy, Mood swings, Myocardial Diseases, Myopathy, Nervous System Diseases, Nystagmus, Optic Atrophy, Pancreatic neoplasm, Ptosis, Pulmonary Stenosis, Renal agenesis, Renal cell carcinoma, Renal dysplasia, Respiratory Failure, Retinal Diseases, Retinal telangiectasia, Retinitis Pigmentosa, Schizophrenia, Strabismus, Ventricular preexcitation, Ventricular septal defect, Wolff-Parkinson-White Syndrome
|
437
|
|
|
NADH:ubiquinone oxidoreductase core subunit S3 |
CI-30, MC1DN8 |
Curated: Anorexia nervosa, Attention deficit hyperactivity disorder, Breast neoplasms, Hypertension, Hypothyroidism, Insomnia, Leigh syndrome, Mitochondrial complex deficiency, Optic atrophy, Diabetes mellitus type 2, Venous thromboembolism, mitochondrial disease
Unreviewed: Acquired Kyphoscoliosis, Alzheimer disease, Amyloidosis, Anemia, Asthenozoospermia, Atherosclerosis, Breast Cancer, Breast Carcinoma, Breast neoplasm, Cerebellar Ataxia, Cognition disorder, Cognitive disorder, Congenital kyphoscoliosis, Dementia, Developmental Delay, Diabetes Mellitus, Down Syndrome, Ductal carcinoma, Dysarthria, Dysphagia, Encephalopathy, Epileptic encephalopathy, Graft-Vs-Host Disease, Hearing Loss, Hyperplasia, HYPERTRICHOSIS, Hypertrophic cardiomyopathy, Hypoglycemia, Hypoxia, Invasive Duct and Lobular Carcinoma, Isolated Complex I Deficiency, Kidney disease, Leigh Syndrome, Leigh Syndrome With Leukodystrophy, Leukodystrophy, Leukoencephalopathy, Mammary Neoplasms, Marfan Syndrome, Memory disorders, Mental retardation, Metabolic Syndrome, Microcephaly, Mitochondrial Complex Deficiency, Mitochondrial disease, Mitochondrial Diseases, Mitochondrial myopathy, Mood swings, Necrosis, Necrotizing encephalomyelopathy, Nervous System Diseases, Nystagmus, Optic Atrophy, Pancreatitis, Parkinson disease, Ptosis, Retinitis Pigmentosa, Rheumatoid arthritis, Schizophrenia, Senile Dementia, Septicemia, Stomach neoplasms, Strabismus, Venous thrombosis, Ventricular septal defect
|
438
|
|
|
NADH:ubiquinone oxidoreductase subunit S4 |
AQDQ, CI-18, CI-18 kDa, CI-AQDQ, MC1DN1 |
Curated: 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
Unreviewed: Alzheimer disease, Anemia, Ankylosing Spondylitis, Atrial Fibrillation, B-Cell Lymphoma, Breast Cancer, Breast Carcinoma, Cerebellar Ataxia, Cerebellar atrophy, Developmental Delay, Diabetes Mellitus, Dysarthria, Dyskinetic Syndrome, Dyslipidemias, Encephalopathy, Epileptic encephalopathy, Hearing Loss, Hypertension, HYPERTRICHOSIS, Hypertrophic cardiomyopathy, Hypoglycemia, Isolated Complex I Deficiency, Leigh Syndrome, Leigh Syndrome With Leukodystrophy, Leukodystrophy, Leukoencephalopathy, Liver failure, Lupus Erythematosus, Malnutrition, Mental Depression, Mental retardation, Microcephaly, Mitochondrial Complex Deficiency, Mitochondrial Diseases, Mitochondrial encephalomyopathy, Mitochondrial encephalopathy, Mitochondrial myopathy, Mood swings, Necrotizing encephalomyelopathy, Necrotizing Encephalopathy, Nervous System Diseases, Nervous System Disorder, Nystagmus, Optic Atrophy, Parkinson disease, Portal Hypertension, Ptosis, Respiration Disorders, Respiratory Failure, Respiratory Tract Diseases, Retinitis Pigmentosa, Strabismus, Systemic lupus erythematosus, Triple Negative Breast Neoplasms, Ventricular septal defect
|
439
|
|
|
NADH:ubiquinone oxidoreductase subunit S5 |
CI-15k, CI15K |
Curated: Metabolic syndrome, Skin disease, Diabetes mellitus type 2
Unreviewed: Alzheimer disease, Cognition disorder, Dilated cardiomyopathy, Glioma, Heart failure, Mitochondrial Diseases, Obesity, Ventricular remodeling
|
440
|
|
|
NADH:ubiquinone oxidoreductase subunit S5 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|