Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "M"
521 to 530 of 971 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

521
MPL proto-oncogene, thrombopoietin receptor
C-MPL, CD110, MPLV, THCYT2, THPOR, TPOR
Amegakaryocytic thrombocytopenia, Congenital amegakaryocytic thrombocytopenia, Essential thrombocythemia, Thrombocytosis, Aplastic anemia, Medulloblastoma, Myeloproliferative disorder

522
Myeloperoxidase
-
Alzheimer disease, Experimental arthritis, Rheumatoid arthritis, Asthma, Atherosclerosis, Brain disease, Brain injuries, Brain ischemia, Hepatocellular carcinoma, Cardiovascular disease, Cholelithiasis, Ulcerative colitis, Colitis, Cystic fibrosis, Major depressive disorder
View all (17 more)

523
MAGUK p55 scaffold protein 1
AAG12, DXS552E, EMP55, MRG1, PEMP
Lung neoplasms

524
Mercaptopyruvate sulfurtransferase
MST, TST2, TUM1
Melanoma, Psychiatric disorders

525
Mitochondrial inner membrane protein MPV17
CMT2EE, MTDPS6, SYM1
Charcot-marie-tooth disease, Mitochondrial dna depletion syndrome, Focal glomerulosclerosis, Gout, Mitochondrial disease, Navajo neurohepatopathy, Proteinuria

526
Myelin protein zero
CHM, CHN2, CMT1, CMT1B, CMT2I, CMT2J, CMT4E, CMTDI3, CMTDID, DSS, HMSNIB, MPP, P0
Charcot-marie-tooth disease, Dejerine-sottas disease, Distal hereditary motor neuropathy, Motor neuron disease, Hyperalgesia, Hypertrophic neuropathy, Intellectual developmental disorder, Peripheral neuropathy, Peroneal muscle atrophy, Roussy-levy syndrome, Sensory neuropathy

527
Mannose receptor C-type 1
CD206, CLEC13D, CLEC13DL, MMR, MRC1L1, bA541I19.1, hMR
Alzheimer disease, Rhinitis, Clonal hematopoiesis, Allergic contact dermatitis, Hyperinsulinism, Diabetes mellitus, type 2, Nonalcoholic fatty liver disease, Obesity, Psychiatric disorders

528
MRE11 double strand break repair nuclease
ATLD, HNGS1, MRE11A, MRE11B
Ataxia telangiectasia, Dementia, Major depressive disorder, Ovarian cancer, Hereditary breast and ovarian cancer syndrome, Hereditary breast cancer, Lynch syndrome, Parkinson disease, Preeclampsia

529
Mitochondrial contact site and cristae organizing system subunit 10
C1orf151, MINOS1, MIO10, Mic10
Hyperthyroidism, Hypothyroidism, Multinodular goiter, Thyroid disease, Toxic nodular goiter, Vascular dementia

530
Myocardial infarction associated transcript
C22orf35, GOMAFU, LINC00066, NCRNA00066, RNCR2, lncRNA-MIAT