Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "M"
171 to 180 of 898 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

171
MAS1 proto-oncogene, G protein-coupled receptor
MAS, MGRA
Coronary artery disease, Myocardial infarction, Thrombosis

172
MBL associated serine protease 1
3MC1, CRARF, CRARF1, MAP-1, MAP1, MASP, MASP-3, MASP3, MAp44, PRSS5, RaRF
3mc syndrome, Carnevale syndrome, Craniofacial abnormalities, Craniofacial ulnar renal syndrome, Hypertrophic cardiomyopathy, Malpuech facial clefting syndrome, Oculopalatosekeletal syndrome, Oligodendroglioma, Osteoarthritis, Amyotrophic lateral sclerosis, Diabetes mellitus type 2

173
MBL associated serine protease 2
MAP-2, MAP19, MASP-2, MASP1P1, sMAP
Amyotrophic lateral sclerosis, Ulcerative colitis, Masp2 deficiency

174
Microtubule associated serine/threonine kinase 1
MCCCHCM, SAST
Breast cancer, Metabolic syndrome, Diabetes mellitus type 2

175
Microtubule associated serine/threonine kinase 2
MAST205, MTSSK
Alzheimer disease, Breast cancer, Esophageal cancer, Gastric cancer, Hearing loss, Metabolic syndrome, Prostate cancer, Diabetes mellitus type 2

176
Microtubule associated serine/threonine kinase 3
DEE108
Attention deficit hyperactivity disorder, Autism, Biliary cirrhosis, Developmental and epileptic encephalopathy, Gout, Metabolic syndrome, Biliary cholangitis, Diabetes mellitus type 2

177
Microtubule associated serine/threonine kinase family member 4
-
Astrocytoma, Breast cancer, Bullous pemphigoid, Carotid artery disease, Central nervous system cancer, Lymphocytic leukemia, Colorectal cancer, Coronary artery disease, Epilepsy, Generalized epilepsy, Glioblastoma, Glioma, Metabolic syndrome, Moyamoya angiopathy, Oligodendroglioma
View all (7 more)

178
Microtubule associated serine/threonine kinase like
GREATWALL, GW, GWL, MAST-L, THC2
Thrombocytopenia with normal platelets, Squamous cell carcinoma, Thrombocytopenia

179
Methionine adenosyltransferase 1A
MAT, MATA1, SAMS, SAMS1
Amino acid metabolism disorder, Brain disease, Hepatocellular carcinoma, Colorectal cancer, S-adenosylhomocysteine hydrolase deficiency, Demyelinating diseases, Diabetes mellitus type 2, Diabetic neuropathy, Fatty liver, Fatty liver, alcoholic, Hepatic methionine adenosyltransferase deficiency, Hyperplasia, Open angle glaucoma

180
Methionine adenosyltransferase 2A
MATA2, MATII, SAMS2
Ischemic heart disease, Coronary artery disease, Thoracic aortic aneurysm and aortic dissection, Marfan syndrome, Myocardial ischemia, Prostate cancer, Combined vitamin k-dependent clotting factor deficiency