Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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8031 to 8040 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

8031
Melanocortin 2 receptor accessory protein
B27, C21orf61, FALP, FGD2, GCCD2, MRAP1
Atrial fibrillation, Glucocorticoid deficiency, Hypertension

8032
Melanocortin 2 receptor accessory protein 2
C6orf117, bA51G5.2
Body mass index

8033
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
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8034
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

8035
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

8036
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

8037
Morf4 family associated protein 1 like 2
UPP
Preeclampsia

8038
MAS related GPR family member E
GPR167, MGRF, MRGE
Migraine, Multiple sclerosis

8039
MAS related GPR family member X2
MGRG3, MRGX2
Color vision deficiency

8040
Myoregulin
LINC00948, Linc-RAM, M1, MLN, MUSER1
Gout