331
|
|
|
Microtubule affinity regulating kinase 3 pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
|
332
|
|
|
Microtubule affinity regulating kinase 3 pseudogene 3 |
- |
Curated: N/A
Unreviewed: N/A
|
333
|
|
|
Microtubule affinity regulating kinase 4 |
MARK4L, MARK4S, MARKL1, MARKL1L, PAR-1D |
Curated: Alzheimer disease, Atrophic macular degeneration, Coronary artery disease, Gastroesophageal reflux disease, Hyperopia, Metabolic syndrome, Myocardial infarction, Neurodevelopmental disorder, Peptic ulcer disease, Scoliosis, Diabetes mellitus type 2, Age-related macular degeneration
Unreviewed: Anhydramnios, Arteriosclerosis, Atherosclerosis, Brain Neoplasms, Breast Cancer, Breast Carcinoma, Carcinogenesis, Colorectal Cancer, Congenital abnormalities, Dandy-Walker Syndrome, Developmental disability, Diabetes, Diabetes Mellitus, Exudative Macular Degeneration, Geographic Atrophy, Glioblastoma, Glioma, Hermansky-Pudlak Syndrome, Hyperlipidemia, Intellectual developmental disorder, Learning disorders, Liver carcinoma, Lung Cancer, Lung carcinoma, Macular degeneration, Malignant Neoplasm, Mammary Neoplasms, Meckel-Gruber Syndrome, Metabolic Syndrome, Neoplasms, Neurodegenerative Disorders, Obesity, Ovarian neoplasm, Peutz-Jeghers Syndrome, Polycystic kidney disease, Stomach neoplasms, Stroke, Tauopathies, Trichohepatoenteric Syndrome
|
334
|
|
|
Methionyl-tRNA synthetase 1 |
CMT2U, ILFS2, ILLD, MARS, METRS, MRS, MTRNS, SPG70, TTD9 |
Curated: Charcot-marie-tooth disease, Spastic paraplegia, Dejerine-sottas disease, Distal spinal muscular atrophy, Hereditary motor and sensory neuropathies, Hypertrophic neuropathy, Interstitial lung disease, Peroneal muscle atrophy, Roussy-levy syndrome, Hereditary spastic paraplegia, Trichothiodystrophy, Diabetes mellitus type 1, Diabetes mellitus type 2
Unreviewed: Alveolar proteinosis, Alzheimer disease, Anemia, Ataxia Telangiectasia, Breast neoplasm, Charcot-Marie-Tooth Disease, Colorectal Cancer, Developmental Delay, Epilepsy, Epileptic encephalopathy, Fatty Liver, Hyperlipoproteinemia, Hypothyroidism, Interstitial Lung And Liver Disease, Liver failure, Lung Cancer, Lung carcinoma, Lung Diseases, Malignant Neoplasm, Mental Depression, Mental retardation, Multiple myeloma, Nephrotic Syndrome, Nervous System Diseases, Pelger-Huet Anomaly, Peripheral axonal neuropathy, Polyneuropathy, Pulmonary alveolar proteinosis, Renal Aplasia, Spastic Paraplegia, Stroke, Subarachnoid hemorrhage
|
335
|
|
|
Methionyl-tRNA synthetase 2, mitochondrial |
COXPD25, MetRS, mtMetRS |
Curated: Ataxia, spastic, autosomal recessive, Spastic ataxia with leukoencephalopathy, Combined oxidative phosphorylation deficiency, Dilated cardiomyopathy, Mitochondrial disease, Rheumatoid arthritis, Spastic ataxia, Stroke, Systemic lupus erythematosus
Unreviewed: Ataxia, Breast neoplasm, Cerebellar Ataxia, Cerebellar atrophy, Cerebellar Hypoplasia, Cerebral Atrophy, Cerebral cortical atrophy, Combined Oxidative Phosphorylation Deficiency, Congenital Pectus Carinatum, Developmental Delay, Developmental disability, Dwarfism, Dysarthria, Hearing Loss, Horizontal nystagmus, Impaired Cognition, Isolated Somatotropin Deficiency, Leukoencephalopathy, Malnutrition, Mental retardation, Mesothelioma, Parkinson disease, Pulmonary alveolar proteinosis, Scoliosis, Sensorineural hearing loss, Somatotropin Deficiency, Spastic Ataxia, Spastic Ataxia With Leukoencephalopathy
|
336
|
|
|
MARVEL domain containing 1 |
GB14, MARVD1, MRVLDC1, bA548K23.8 |
Curated: Alzheimer disease
Unreviewed: Breast Cancer, Breast Carcinoma, Carcinogenesis, Epithelioma, Hepatocellular carcinoma, Impaired Cognition, Liver Cancer, Liver carcinoma, Lung Cancer, Lung carcinoma, Lung neoplasms, Neoplasms, Prostatic neoplasm
|
337
|
|
|
MARVEL domain containing 2 |
DFNB49, MARVD2, MRVLDC2, Tric |
Curated: Isolated sensorineural deafness, Nonsyndromic hearing loss, Congenital ear anomaly, Deafness, Hearing loss, Hereditary hearing loss, nonsyndromic genetic hearing loss
Unreviewed: Adenocarcinoma, Autism, Bardet-Biedl Syndrome, Cholesteatoma, Cockayne syndrome, Colorectal neoplasm, Crohn Disease, Hepatocellular carcinoma, Hereditary sensory and autonomic neuropathy, Hypertrophic cardiomyopathy, Leukemia, Lissencephaly, Lymphatic metastasis, Nasal polyposis, Neoplasms, Nervous system disease, Neurodegenerative disorder, Non-Syndromic Sensorineural Deafness, Nonsyndromic Deafness, Pancreatic neoplasm, Pancreatitis, Sensorineural hearing loss, Stomach Carcinoma, Stomach neoplasms, Ulcerative colitis, Whipple disease
|
338
|
|
|
MARVEL domain containing 3 |
MARVD3, MRVLDC3 |
Curated: Gout, Diabetes mellitus type 2
Unreviewed: Hepatocellular carcinoma, Lung adenocarcinoma, Lung Cancer, Lung carcinoma, Lung neoplasms, Pancreatic cancer, Pancreatic carcinoma
|
339
|
|
|
MAS1 proto-oncogene, G protein-coupled receptor |
MAS, MGRA |
Curated: Coronary artery disease, Myocardial infarction, Thrombosis
Unreviewed: N/A
|
340
|
|
|
MAS1 proto-oncogene like, G protein-coupled receptor |
MAS-L, MRG, dJ994E9.2 |
Curated: N/A
Unreviewed: Bullous pemphigoid, Colonic neoplasm, Diabetes mellitus, Esophageal squamous cell carcinoma, Hepatocellular carcinoma, Idiopathic pulmonary fibrosis, Lymphatic metastasis, Renal cell carcinoma
|