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"
61 to 70 of 898 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

61
Mastermind like transcriptional coactivator 2
MAM-3, MAM2, MAM3, MLL-MAML2
Androgenetic alopecia, Juvenile arthritis, Central nervous system cancer, Obstructive pulmonary disease, Congenital heart disease, Corneal astigmatism, Crohn disease, Glioma, Inflammatory bowel disease, Juvenile idiopathic arthritis, Keratoconus, Metabolic syndrome, Osteoarthritis, Otosclerosis, Oligoarticular juvenile idiopathic arthritis
View all (5 more)

62
Mastermind like transcriptional coactivator 3
CAGH3, ERDA3, GDN, MAM-2, MAM2, TNRC3, mam-3
Alzheimer disease, Asthma, Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Bile duct disorder, Cancer, Cannabis abuse, Adenoid cystic carcinoma, Central nervous system cancer, Cholelithiasis, Obstructive pulmonary disease, Congenital heart defects, Congenital heart malformation, Coronary artery disease
View all (19 more)

63
Mastermind like domain containing 1
CG1, CXorf6, F18, HYSP2
Hypospadias, X-linked myotubular myopathy

64
MEF2 activating motif and SAP domain containing transcriptional regulator
MASTR
Alzheimer disease, Breast cancer, Cholecystolithiasis, Rhinosinusitis, Colorectal cancer, Crohn disease, Dental caries, Hyperlipidemia, Gastroesophageal reflux disease, Inflammatory bowel disease, Multiple sclerosis, Nasal disorder, Osteoarthritis, Sinusitis, Ulcerative colitis
View all (2 more)

65
Mannosidase alpha class 1A member 1
HUMM3, HUMM9, MAN9
Liver cirrhosis, Metabolic syndrome, Neurotic disorder, Systemic lupus erythematosus, Diabetes mellitus type 2, Vascular dementia

66
Mannosidase alpha class 1A member 2
MAN1B
Insomnia, Metabolic syndrome, Oligodendroglioma, Diabetes mellitus type 2

67
Mannosidase alpha class 1B member 1
ERMAN1, ERManI, MANA-ER, MRT15
Nonsyndromic intellectual disability, Carbohydrate deficient glycoprotein syndrome, Coronary aneurysm, Intellectual developmental disorder, Congenital disorder of glycosylation, Diabetes mellitus type 1, Diabetes mellitus type 2

68
Mannosidase alpha class 2A member 1
AMan II, GOLIM7, MANA2, MANII
Diabetic retinopathy, Hypothyroidism, Schizophrenia

69
Mannosidase alpha class 2A member 2
MANA2X, alpha-MIIx
Attention deficit hyperactivity disorder, Congenital disorder of glycosylation, Disorder of glycosylation, Hirschsprung disease

70
Mannosidase alpha class 2B member 1
LAMAN, MANB
Alpha-mannosidosis, Craniosynostosis, Alpha-mannosidase deficiency, Desbuquois syndrome, Iga nephropathy, Intellectual developmental disorder, Methylmalonic acidemia