2661
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|
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COX20 pseudogene 1 |
FAM36B, bA119F7.2 |
Curated: N/A
Unreviewed: N/A
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2662
|
|
|
COX20 pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
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2663
|
|
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Mitochondrially encoded cytochrome c oxidase III |
COIII, MTCO3 |
Curated: Spastic ataxia, Cerebellar ataxia, Cleft palate and bilateral cleft lip, Developmental delay, Epilepsy, Temporal lobe epilepsy, Hearing loss, Liver failure, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Mitochondrial encephalopathy, Nephrolithiasis, Neuropathy, ataxia, and retinitis pigmentosa, Leber hereditary optic neuropathy, Rod-cone dystrophy, Sleep apnea, Tetralogy of fallot, Postaxial polydactyly
Unreviewed: Addison`s Disease, Anorexia, Anxiety Disorder, Aortic Aneurysm, Aortic dissection, Aphasia, Arthrogryposis multiplex congenita, Attention Deficit Hyperactivity Disorder, Autism, Autoimmune Polyendocrinopathy, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinoma, Carcinoma Of The Head And Neck, Cardiomyopathy, Cataract, Central Visual Impairment, Cerebral cortical atrophy, Colon Carcinoma, Colonic Neoplasms, Congestive Heart Failure, Cytochrome c oxidase deficiency, Cytochrome-C Oxidase Deficiency, Dementia, Developmental regression, Diabetes and Hearing Loss, Diabetes Mellitus, Dwarfism, Dysarthria, Endometrial neoplasm, Epileptic encephalopathy, Fatty Liver, Gastroparesis, Gout, Hallucinations, Hearing Loss, Heart Block, Hematomas, Hemianopsia, Hereditary breast and ovarian cancer syndrome, Hereditary Leber Optic Atrophy, Hereditary spastic paraplegia, Hypertension, Hyperthyroidism, Hypertrophic cardiomyopathy, Hypoparathyroidism, Hypopituitarism, Hypothyroidism, Ichthyosis, Idiopathic pulmonary fibrosis, Iga nephropathy, Intestinal Obstruction, Keratoconus, Kidney Disease, Left Ventricular Hypertrophy, Leigh Syndrome, Liver carcinoma, Lymphoblastic Leukemia, Malabsorption Syndrome, Male infertility, Malformation of cortical development, Malignant Neoplasm, MELAS Syndrome, Mental Depression, Microcephaly, Migraine, Mitochondrial myopathy, Multiple Lipomata, Multiple polyposis syndrome, Multiple sclerosis, Myopathy, Neoplasms, Nephrotic Syndrome, Nervous System Diseases, Neuromuscular Diseases, Nyctalopia, Obesity, Optic Atrophy, Pancreatitis, Polyneuropathy, Proteinuria, Psychosis, Ptosis, Pulmonary arterial hypertension, Renal Glomerular Disease, Renal Insufficiency, Retinal telangiectasia, Seizure, Sensorineural hearing loss, Tetralogy of Fallot, Thyroiditis, Ventricular hypertrophy, Ventricular preexcitation, Wolff-Parkinson-White Syndrome
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2664
|
|
|
- |
- |
Curated: Spastic ataxia, Cerebellar ataxia, Cleft palate and bilateral cleft lip, Developmental delay, Epilepsy, Temporal lobe epilepsy, Hearing loss, Liver failure, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Mitochondrial encephalopathy, Nephrolithiasis, Neuropathy, ataxia, and retinitis pigmentosa, Leber hereditary optic neuropathy, Rod-cone dystrophy, Sleep apnea, Tetralogy of fallot, Postaxial polydactyly
Unreviewed: Addison`s Disease, Anorexia, Anxiety Disorder, Aortic Aneurysm, Aortic dissection, Aphasia, Arthrogryposis multiplex congenita, Attention Deficit Hyperactivity Disorder, Autism, Autoimmune Polyendocrinopathy, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinoma, Carcinoma Of The Head And Neck, Cardiomyopathy, Cataract, Central Visual Impairment, Cerebral cortical atrophy, Colon Carcinoma, Colonic Neoplasms, Congestive Heart Failure, Cytochrome c oxidase deficiency, Cytochrome-C Oxidase Deficiency, Dementia, Developmental regression, Diabetes and Hearing Loss, Diabetes Mellitus, Dwarfism, Dysarthria, Endometrial neoplasm, Epileptic encephalopathy, Fatty Liver, Gastroparesis, Gout, Hallucinations, Hearing Loss, Heart Block, Hematomas, Hemianopsia, Hereditary breast and ovarian cancer syndrome, Hereditary Leber Optic Atrophy, Hereditary spastic paraplegia, Hypertension, Hyperthyroidism, Hypertrophic cardiomyopathy, Hypoparathyroidism, Hypopituitarism, Hypothyroidism, Ichthyosis, Idiopathic pulmonary fibrosis, Iga nephropathy, Intestinal Obstruction, Keratoconus, Kidney Disease, Left Ventricular Hypertrophy, Leigh Syndrome, Liver carcinoma, Lymphoblastic Leukemia, Malabsorption Syndrome, Male infertility, Malformation of cortical development, Malignant Neoplasm, MELAS Syndrome, Mental Depression, Microcephaly, Migraine, Mitochondrial myopathy, Multiple Lipomata, Multiple polyposis syndrome, Multiple sclerosis, Myopathy, Neoplasms, Nephrotic Syndrome, Nervous System Diseases, Neuromuscular Diseases, Nyctalopia, Obesity, Optic Atrophy, Pancreatitis, Polyneuropathy, Proteinuria, Psychosis, Ptosis, Pulmonary arterial hypertension, Renal Glomerular Disease, Renal Insufficiency, Retinal telangiectasia, Seizure, Sensorineural hearing loss, Tetralogy of Fallot, Thyroiditis, Ventricular hypertrophy, Ventricular preexcitation, Wolff-Parkinson-White Syndrome
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2665
|
|
|
- |
- |
Curated: Spastic ataxia, Cerebellar ataxia, Cleft palate and bilateral cleft lip, Developmental delay, Epilepsy, Temporal lobe epilepsy, Hearing loss, Liver failure, Melas syndrome, Mitochondrial complex deficiency, Mitochondrial disease, Mitochondrial encephalopathy, Nephrolithiasis, Neuropathy, ataxia, and retinitis pigmentosa, Leber hereditary optic neuropathy, Rod-cone dystrophy, Sleep apnea, Tetralogy of fallot, Postaxial polydactyly
Unreviewed: Addison`s Disease, Anorexia, Anxiety Disorder, Aortic Aneurysm, Aortic dissection, Aphasia, Arthrogryposis multiplex congenita, Attention Deficit Hyperactivity Disorder, Autism, Autoimmune Polyendocrinopathy, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinoma, Carcinoma Of The Head And Neck, Cardiomyopathy, Cataract, Central Visual Impairment, Cerebral cortical atrophy, Colon Carcinoma, Colonic Neoplasms, Congestive Heart Failure, Cytochrome c oxidase deficiency, Cytochrome-C Oxidase Deficiency, Dementia, Developmental regression, Diabetes and Hearing Loss, Diabetes Mellitus, Dwarfism, Dysarthria, Endometrial neoplasm, Epileptic encephalopathy, Fatty Liver, Gastroparesis, Gout, Hallucinations, Hearing Loss, Heart Block, Hematomas, Hemianopsia, Hereditary breast and ovarian cancer syndrome, Hereditary Leber Optic Atrophy, Hereditary spastic paraplegia, Hypertension, Hyperthyroidism, Hypertrophic cardiomyopathy, Hypoparathyroidism, Hypopituitarism, Hypothyroidism, Ichthyosis, Idiopathic pulmonary fibrosis, Iga nephropathy, Intestinal Obstruction, Keratoconus, Kidney Disease, Left Ventricular Hypertrophy, Leigh Syndrome, Liver carcinoma, Lymphoblastic Leukemia, Malabsorption Syndrome, Male infertility, Malformation of cortical development, Malignant Neoplasm, MELAS Syndrome, Mental Depression, Microcephaly, Migraine, Mitochondrial myopathy, Multiple Lipomata, Multiple polyposis syndrome, Multiple sclerosis, Myopathy, Neoplasms, Nephrotic Syndrome, Nervous System Diseases, Neuromuscular Diseases, Nyctalopia, Obesity, Optic Atrophy, Pancreatitis, Polyneuropathy, Proteinuria, Psychosis, Ptosis, Pulmonary arterial hypertension, Renal Glomerular Disease, Renal Insufficiency, Retinal telangiectasia, Seizure, Sensorineural hearing loss, Tetralogy of Fallot, Thyroiditis, Ventricular hypertrophy, Ventricular preexcitation, Wolff-Parkinson-White Syndrome
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2666
|
|
|
Cytochrome c oxidase subunit 4I1 |
COX IV-1, COX4, COX4-1, COXIV, COXIV-1, MC4DN16 |
Curated: Cytochrome c oxidase deficiency, Leigh syndrome, Mitochondrial complex deficiency, Mitochondrial disease
Unreviewed: Adrenocortical carcinoma, Anemia, Asthenozoospermia, Atrial fibrillation, Atrophy, Bone marrow failure syndromes, Brain disease, Breast Cancer, Breast Carcinoma, Cardiomyopathy, Congenital abnormalities, Coronary artery disease, Cytochrome-C Oxidase Deficiency, Developmental regression, Diabetes Mellitus, Dwarfism, Dysmorphic Features, Epilepsy, Fanconi Anemia, Glioma, Growth disorder, Hyperglycemia, Hypertension, Hypoxia, Intellectual developmental disorder, Isolated Cytochrome C Oxidase Deficiency, Leigh Syndrome, Leprosy, Lung disease, Mental Depression, Metabolic Syndrome, Microcephaly, Mitochondrial Diseases, Myocardial Ischemia, Myopathy, Neoplasms, Nervous system disease, Obesity, Ovarian neoplasm, Seizures
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2667
|
|
|
Cytochrome c oxidase subunit 4I1 pseudogene 1 |
COX4L1, COX4P1 |
Curated: N/A
Unreviewed: N/A
|
2668
|
|
|
Cytochrome c oxidase subunit 4I1 pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
|
2669
|
|
|
Cytochrome c oxidase subunit 4I2 |
COX4, COX4-2, COX4B, COX4L2, COXIV-2, dJ857M17.2 |
Curated: Alzheimer disease, Mitochondrial disease, Pancreatic insufficiency syndrome
Unreviewed: Adrenal Gland Pheochromocytoma, Allergic rhinitis, Anemia, Asthma, Atrial fibrillation, Cardiomyopathy, Cytochrome-C Oxidase Deficiency, Developmental Delay, Exocrine pancreatic insufficiency, Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, And Calvarial Hyperostosis, Hyperglycemia, Hypoxia, Malabsorption Syndrome, Malnutrition, Mitochondrial Diseases, Myocardial Ischemia, Myopathy, Neoplasms, Osteopenia, Pancreatic insufficiency-anemia-hyperostosis syndrome
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2670
|
|
|
Cytochrome c oxidase subunit 5A |
COX, COX-VA, MC4DN20, VA |
Curated: Alzheimer disease, Cytochrome c oxidase deficiency, Major depressive disorder, Mitochondrial complex deficiency, Myocardial infarction, Squamous cell carcinoma, Diabetes mellitus type 2, mitochondrial disease
Unreviewed: Adenoma, Arteriosclerosis, Arthritis, Asthma, Atherosclerosis, Autism Spectrum Disorder, Benign Prostatic Hyperplasia, Bipolar Disorder, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinoma, Cardiovascular Diseases, Catalepsy, Celiac disease, Cerebral Aneurysm, Cervical Cancer, Cervical Tumor, Cervix carcinoma, Chromophobe Carcinoma, Chronic Obstructive Pulmonary Disease, Colon Carcinoma, Colonic Neoplasms, Colorectal adenoma, Colorectal Cancer, Colorectal neoplasm, Complete Atrioventricular Block, Congenital Chromosomal Disease, Congenital lactic acidosis, Coronary artery disease, Cytochrome-C Oxidase Deficiency, Dermatitis, Diabetes Mellitus, Down Syndrome, Ductal carcinoma, Eosinophilia, Epithelioma, Esophagus Neoplasm, Gallbladder cancer, Glioblastoma, Glioma, Harderoporphyria, Head and neck cancer, Head And Neck Carcinoma, Hereditary Leber Optic Atrophy, Hypersensitivity, Hypertension, Inflammatory Bowel Disease, Ischemic Stroke, Isolated Cytochrome C Oxidase Deficiency, Kidney Disease, Kidney Failure, Knee osteoarthritis, Laryngeal Carcinoma, Leigh Syndrome, Leukoplakia, Lip and Oral Cavity Carcinoma, Lipoidosis, Liver carcinoma, Lung adenocarcinoma, Lung Cancer, Lung carcinoma, Lung Diseases, Lymphatic Metastasis, Lymphoblastic Leukemia, Lymphocytic Leukemia, Lymphoma, Malignant Neoplasm, Malignant neoplasm of mouth, Melanoma, MELAS Syndrome, Mental Depression, Mental Disorders, MERRF Syndrome, Metabolic Syndrome, Metastatic Melanoma, Mitochondrial Diseases, Mitochondrial myopathy, Mitochondrial trifunctional protein deficiency, Multiple myeloma, Multiple Sclerosis, Multiple Trichoepithelioma, Myocardial Infarction, Myofibrillar myopathy, Nasal polyposis, Nasopharyngeal Carcinoma, Neoplasms, Neurodegenerative Disorders, Non-Alcoholic Fatty Liver Disease, Optic Atrophy, Ovarian cancer, Ovarian Epithelial carcinoma, Ovarian neoplasm, Pancreatic adenocarcinoma, Pancreatic cancer, Pancreatic Neoplasm, Papillary thyroid carcinoma, Parkinson disease, Peptic Ulcer, Prostate cancer, Pulmonary arterial hypertension, Renal Carcinoma, Retinal Diseases, Rheumatoid arthritis, Schizophrenia, Stomach Carcinoma, Stomach Neoplasms, Stroke, Thyroid Carcinoma, Ulcerative colitis, Uveal Melanoma, Vascular Diseases
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