3111
|
|
|
MPPED2 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: Asthma
|
3112
|
|
|
Myosin phosphatase Rho interacting protein |
M-RIP, MRIP, RHOIP3, RIP3, p116Rip |
Curated: Atrial fibrillation, Diabetic retinopathy, Obesity, Prostate cancer
Unreviewed: Aortic Aneurysm, Arteriosclerosis, Asthma, Astrocytoma, Atherosclerosis, Autoimmune hepatitis, Breast Cancer, Breast Carcinoma, Cardiac Neoplasms, Cerebral Ischemia, CNS Disorder, Colitis, Colorectal Cancer, Congestive Heart Failure, Coronary Arteriosclerosis, Coronary artery disease, Coronary Syndrome, Craniocerebral trauma, Creutzfeldt-Jakob disease, Crohn Disease, Diabetic Nephropathy, Disseminated intravascular coagulation, Dyslipidemias, Esophageal Carcinoma, Esophagus Neoplasm, Fatal Insomnia, Fatty Liver, Gaucher Disease, Glioblastoma, Glioma, Heart Failure, Hereditary Cancer Syndrome, Hyperuricemia, Inflammatory Bowel Disease, Intervertebral disc disease, Kashin-Beck Disease, Kidney Failure, Leukemia, Liver carcinoma, Liver Fibrosis, Lung Cancer, Lung carcinoma, Lupus Erythematosus, Lupus Nephritis, Lymphoblastic Leukemia, Lymphocytic Leukemia, Malignant Neoplasm, Mitochondrial disease, MOHR-TRANEBJAERG SYNDROME, Multiple Fibrofolliculomas, Myeloid leukemia, Myocardial Infarction, Myocardial Ischemia, Necrosis, Neoplasms, Non-Alcoholic Fatty Liver Disease, Ovarian neoplasm, Pancreatic cancer, Pancreatic carcinoma, Pancreatitis, Parkinson disease, Pneumothorax, Potocki-Lupski Syndrome, Prolactinoma, Pterygium, Radiation Syndrome, Renal Carcinoma, Retinitis pigmentosa, Sphingomyelinase deficiency, Squamous cell carcinoma, Status Epilepticus, Stevens-Johnson Syndrome, Subarachnoid hemorrhage, Thrombosis, Ulcerative colitis, Vascular Diseases, Vitiligo
|
3113
|
|
|
MPRIP antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
3114
|
|
|
Myosin phosphatase Rho interacting protein pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
3115
|
|
|
Mercaptopyruvate sulfurtransferase |
MST, TST2, TUM1 |
Curated: Melanoma, Psychiatric disorders
Unreviewed: Adenocarcinoma Of Colon, Arthritis, Astrocytoma, Borderline personality disorder, Brain Neoplasms, Breast Cancer, Breast Carcinoma, Carcinoma, Cognitive disorder, Colon Carcinoma, Colonic disease, Colonic Neoplasms, Colorectal neoplasm, Diabetes Mellitus, Down syndrome, Fatty Liver, Gastrointestinal neoplasm, Glioblastoma, Hypersensitivity, Hypertension, Hyperthyroidism, Kidney Neoplasm, Leukemia, Liver Cancer, Liver carcinoma, Lung carcinoma, Lymphoblastic Leukemia, Lymphocytic Leukemia, Malignant Neoplasm, Mesothelioma, Mitochondrial disease, Multiple myeloma, Myeloproliferative disorder, Neoplasms, Neuroblastoma, Neurodegenerative disorder, Neurodegenerative Disorders, Non-Alcoholic Fatty Liver Disease, Osteopenia, Osteosarcoma, Pancreatic cancer, Pancreatic carcinoma, Promyelocytic Leukemia, Pulmonary Fibrosis, Renal cell carcinoma, Rhabdomyosarcoma, Septicemia, Stress Disorder, Thymoma
|
3116
|
|
|
Mucosal pentraxin 1 (pseudogene) |
MPTX |
Curated: N/A
Unreviewed: N/A
|
3117
|
|
|
Mitochondrial inner membrane protein MPV17 |
CMT2EE, MTDPS6, SYM1 |
Curated: Charcot-marie-tooth disease, Cochlear diseases, Mitochondrial dna depletion syndrome, Focal glomerulosclerosis, Gout, Mitochondrial disease, Navajo neurohepatopathy, Proteinuria
Unreviewed: Alpers Syndrome, Amyloidosis, Arteriosclerosis, Ataxia, Brain disease, Cholestasis, Cirrhosis, Cochlear Diseases, Coenzyme Q10 Deficiency, Combined oxidative phosphorylation deficiency, Deoxyguanosine Kinase Deficiency, Developmental Delay, Distal amyotrophy, Distal lower limb amyotrophy, Dwarfism, Epileptic encephalopathy, Erosion Of Cornea, Glomerular Hyalinosis, Glomerulonephritis, Glomerulosclerosis, Gouty arthritis, Growth disorder, Hepatic encephalopathy, Hepatocellular carcinoma, Hereditary elliptocytosis, Hereditary folate malabsorption, Hypertension, Hypoglycemia, Incontinentia Pigmenti Achromians, Intracranial hypertension, Kidney Disease, Kidney Failure, Leukodystrophy, Leukoencephalopathy, Liver Cirrhosis, Liver disease, Liver failure, Metabolic syndrome, Miller Dieker Syndrome, Mitochondrial Diseases, Mitochondrial Electron Transport Chain Deficiencies, Mitochondrial myopathy, Mitochondrial Respiratory Chain Deficiencies, Multiple Synostoses Syndrome, Myelodysplastic Syndrome, Myoclonic Epilepsy, Myopathy, Navajo Familial Neurogenic Arthropathy, Navajo Neurohepatopathy, Nephrotic Syndrome, Nervous system disease, Nervous System Diseases, Neuropathy, Nystagmus, Oxidative Phosphorylation Deficiency, Peripheral axonal neuropathy, Peripheral nervous system disease, Peripheral Neuropathy, Pigmentation Disorders, Polyneuropathy, Proximal symphalangism, Ptosis, Renal Glomerular Disease, Scoliosis, Sensorimotor neuropathy, Sensory neuropathy, Visceral neuropathy
|
3118
|
|
|
MPV17 mitochondrial inner membrane protein like |
M-LPH, M-LPH1, M-LPH2, MLPH1, MLPH2, MPV17L1 |
Curated: N/A
Unreviewed: Hepatocellular carcinoma, Liver carcinoma, Liver neoplasms, Mitochondrial disease, Visceral neuropathy
|
3119
|
|
|
- |
- |
Curated: N/A
Unreviewed: N/A
|
3120
|
|
|
MPV17 mitochondrial inner membrane protein like 2 |
FKSG24 |
Curated: Multiple sclerosis
Unreviewed: Multiple Sclerosis
|