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 898 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

581
Myelin protein zero like 1
MPZL1b, PZR, PZR1b, PZRa, PZRb
Alzheimer disease, Carcinoma, Major depressive disorder, Schizophrenia

582
Myelin protein zero like 2
DFNB111, EVA, EVA1
Isolated sensorineural deafness, Crohn disease, Deafness, Hearing loss, Inflammatory bowel disease, Lung cancer, Squamous cell carcinoma

583
Myelin protein zero like 3
-
Lung cancer, Non-small cell lung carcinoma

584
Major histocompatibility complex, class I-related
HLALS
Insomnia

585
Melanocortin 2 receptor accessory protein
B27, C21orf61, FALP, FGD2, GCCD2, MRAP1
Atrial fibrillation, Glucocorticoid deficiency, Hypertension

586
Melanocortin 2 receptor accessory protein 2
C6orf117, bA51G5.2
Body mass index

587
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)

588
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

589
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

590
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