Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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7621 to 7630 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

7621
MARVEL domain containing 3
MARVD3, MRVLDC3
Gout, Diabetes mellitus type 2

7622
MAS1 proto-oncogene, G protein-coupled receptor
MAS, MGRA
Coronary artery disease, Myocardial infarction, Thrombosis

7623
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

7624
MBL associated serine protease 2
MAP-2, MAP19, MASP-2, MASP1P1, sMAP
Amyotrophic lateral sclerosis, Ulcerative colitis, Masp2 deficiency

7625
Microtubule associated serine/threonine kinase 1
MCCCHCM, SAST
Breast cancer, Metabolic syndrome, Diabetes mellitus type 2

7626
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

7627
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

7628
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)

7629
Microtubule associated serine/threonine kinase like
GREATWALL, GW, GWL, MAST-L, THC2
Thrombocytopenia with normal platelets, Squamous cell carcinoma, Thrombocytopenia

7630
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