2171
|
|
|
ATP synthase peripheral stalk subunit d pseudogene 3 |
ATP5HP3 |
Curated: N/A
Unreviewed: N/A
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2172
|
|
|
ATP synthase peripheral stalk subunit d pseudogene 4 |
ATP5HP4 |
Curated: N/A
Unreviewed: N/A
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2173
|
|
|
ATP synthase peripheral stalk subunit F6 |
ATP5, ATP5A, ATP5J, ATPM, CF6, F6 |
Curated: Alzheimer disease, Heart disease
Unreviewed: Alopecia, B-Cell Lymphoma, Beta thalassemia, Carcinoma Of The Head And Neck, Cardiovascular Diseases, Colorectal Cancer, Colorectal neoplasm, Congestive Heart Failure, Coronary Heart Disease, Diabetes, Diabetes Mellitus, Heart Diseases, Hypertension, Kidney Failure, Leigh Syndrome, Myocardial Infarction, Myocardial Ischemia, Neoplasms, Vascular dementia
|
2174
|
|
|
ATP synthase peripheral stalk subunit F6 pseudogene 1 |
ATP5JP1 |
Curated: N/A
Unreviewed: N/A
|
2175
|
|
|
ATP5PF pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
|
2176
|
|
|
ATP5PF pseudogene 3 |
- |
Curated: N/A
Unreviewed: N/A
|
2177
|
|
|
ATP5PF pseudogene 4 |
- |
Curated: N/A
Unreviewed: N/A
|
2178
|
|
|
ATP synthase peripheral stalk subunit OSCP |
ATP5O, ATPO, HMC08D05, MC5DN7, OSCP |
Curated: Deglutition disorder, Mitochondrial complex deficiency, mitochondrial disease
Unreviewed: Autoimmune Diseases, Diabetes Mellitus, Diabetes mellitus, type 1, Diabetes mellitus, type 2, Down syndrome, Graves ophthalmopathy, Insomnia, Renal cell carcinoma, Stomach neoplasms, Venous thromboembolism
|
2179
|
|
|
ATP5PO pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
2180
|
|
|
Mitochondrially encoded ATP synthase 6 |
ATPase6, MTATP6 |
Curated: Ataxia with polyneuropathy, Bicuspid aortic valve, Cardiomyopathy, Cerebellar ataxia, Cerebellar atrophy, Charcot-marie-tooth disease, Cleft palate and bilateral cleft lip, Diabetes mellitus, Gonadal dysgenesis, Hypertrophy, Systemic lupus erythematosus, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Multiple sclerosis, Mitochondrial myopathy with sideroblastic anemia, Neuropathy, ataxia, and retinitis pigmentosa, Leber hereditary optic neuropathy, Optic neuropathy, Parkinson disease, Periodic paralysis, Rod-cone dystrophy, Postaxial polydactyly
Unreviewed: Acute Myeloid Leukemia, Adenocarcinoma, Amyotrophic Lateral Sclerosis, Asthenozoospermia, Ataxia, Ataxia and polyneuropathy, Ataxia Telangiectasia, Autism, Autoimmune disease, Autoimmune Diseases, Basal ganglia cysts, Brain disease, Brain neoplasms, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinogenesis, Cardiomyopathy, apical hypertrophic and neuropathy, Carnitine acetyltransferase deficiency, Cerebral cortical atrophy, Charcot-Marie-Tooth Disease, Childhood obesity, Choreoathetosis, Cleft Palate And Bilateral Cleft Lip, Coenzyme Q10 Deficiency, Colorectal neoplasm, Coronary artery disease, Dementia, Demyelinating neuropathy, Developmental Delay, Developmental regression, Diabetes Mellitus, Diabetes mellitus, type 2, Diarrhea, Distal hereditary motor neuropathy, Down Syndrome, Dwarfism, Dysarthria, Dyskinetic Syndrome, Dysphagia, Epilepsy, Episodic ataxia, Esophageal neoplasm, Gastroesophageal Reflux Disease, Glomerulonephritis, Hearing Loss, Hemiplegia, Hemolytic uremic syndrome, Hereditary breast and ovarian cancer syndrome, Hereditary Leber Optic Atrophy, Hereditary spastic paraplegia, High Altitude Pulmonary Edema, Histiocytoid Cardiomyopathy, Holocarboxylase Synthetase Deficiency, Horizontal pendular nystagmus, Huntington disease, Hyperlipidemia, Hypertension, Hypertrophic cardiomyopathy, Hypogonadism, Iga nephropathy, Intellectual developmental disorder, Irritable bowel syndrome, Isolated ATP Synthase Deficiency, Kearns Sayre Syndrome, Kidney Disease, Lactic acidosis, Language development disorders, Learning disorders, Leigh Syndrome, Leprosy, Liver failure, Lung disease, Lupus Erythematosus, Lymphoblastic Leukemia, Major depressive disorder, Male infertility, Maternally Inherited Leigh Syndrome, MELAS Syndrome, Mental retardation, MERRF Syndrome, Metabolic Syndrome, Microcephaly, Migraine, Mitochondrial Cardiomyopathy, Mitochondrial Complex Deficiency, Mitochondrial Diseases, Mitochondrial encephalomyopathy, Mitochondrial myopathy, Mitochondrial Myopathy And Sideroblastic Anemia, Mitochondrial Spastic Paraplegia, Mouth neoplasm, Multiple Sclerosis, Myocardial infarction, Myoclonic epilepsy with ragged red fibers, Myoclonic Seizures, Myopathy, Myopathy, lactic acidosis, and sideroblastic anemia, Neoplasms, Nervous system disease, Nervous System Diseases, Nervous System Disorder, Neurodegenerative disorder, Neurodegenerative Disorders, Neuropathy Ataxia And Retinis Pigmentosa, Nystagmus, Obesity, Ophthalmoplegia, Optic Atrophy, Osteoporosis, Osteosarcoma, Ovarian Failure, Paresis, Periodic Paralysis With Distal Motor Neuropathy, Peripheral axonal neuropathy, Peripheral nervous system disease, Peripheral Neuropathy, Polycystic ovary syndrome, Polyneuropathy, Postaxial hand polydactyly, Prostate cancer, Prostatic neoplasm, Pulmonary edema, Respiration Disorders, Respiratory Tract Diseases, Retinal Diseases, Retinal telangiectasia, Retinitis Pigmentosa, RHYNS Syndrome, Sarcoidosis, Schizophrenia, Seizure, Seizures, Sensorimotor neuropathy, Sensory neuropathy, Spastic ataxia, Spastic paraplegia, Spastic tetraparesis, Spinocerebellar Ataxia, Strabismus, Striatonigral Degeneration, Trichohepatoenteric Syndrome, Ventricular preexcitation, West Syndrome, Wolff-Parkinson-White Syndrome
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