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"
581 to 590 of 893 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

581
Melanocortin 2 receptor accessory protein 2
C6orf117, bA51G5.2
Body mass index

582
Muscle RAS oncogene homolog
M-RAs, NS11, R-RAS3, RRAS3
Attention deficit hyperactivity disorder, Cardiovascular disease, Carotid artery disease, Ischemic heart disease, Coronary artery disease, Desbuquois syndrome, Diabetes mellitus type 2, Dyslexia, Hypertension, Gout, Male infertility single gene azoospermia, Metabolic syndrome, Myocardial infarction, Myocardial ischemia, Noonan syndrome
View all (1 more)

583
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

584
Mannose receptor C-type 2
CD280, CLEC13E, ENDO180, UPARAP
Aneurysm, Aortic aneurysm, Carcinoma, Cardiac arrhythmia, Cardiac rhythm disease, Obstructive pulmonary disease, Coronary artery disease, Hoarding disorder, Migraine, Diabetes mellitus type 2

585
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

586
Morf4 family associated protein 1 like 2
UPP
Preeclampsia

587
MAS related GPR family member E
GPR167, MGRF, MRGE
Migraine, Multiple sclerosis

588
MAS related GPR family member X2
MGRG3, MRGX2
Color vision deficiency

589
Myoregulin
LINC00948, Linc-RAM, M1, MLN, MUSER1
Gout

590
Mitochondrial rRNA methyltransferase 1
-
Alzheimer disease, Dementia, Metabolic syndrome, Obstructive sleep apnea syndrome, Orofacial cleft, Diabetes mellitus type 2