Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Showing genes starting with "M"
201 to 210 of 898 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

201
Mannose binding lectin 2
COLEC1, HSMBPC, MBL, MBL2D, MBP, MBP-C, MBP1, MBPD
Alzheimer disease, Aortic valve disease, Arterial occlusive disease, Asthma, Autoimmune thyroid disease, Behcet disease, Bipolar disorder, Bronchiolitis obliterans, Bronchopulmonary dysplasia, Cerebral cryptococcosis, Obstructive airway disease, Ciliary dyskinesia, with or without situs inversus, Common variable immunodeficiency, Coronary restenosis, Crohn disease
View all (34 more)

202
Metallo-beta-lactamase domain containing 1
-
Long qt syndrome

203
Muscleblind like splicing regulator 1
EXP, MBNL
Androgenetic alopecia, Kidney disease, Colorectal cancer, Major depressive disorder, Metabolic syndrome, Myotonic dystrophy, Neurotic disorder, Osteoarthritis, Prostate cancer, Sarcoidosis, Schizophrenia, Diabetes mellitus type 2

204
Muscleblind like splicing regulator 2
MBLL, MBLL39, PRO2032
Atrial fibrillation, Attention deficit hyperactivity disorder, Breast cancer, Neurotic disorder, Obesity, Parkinson disease

205
Membrane bound glycerophospholipid O-acyltransferase 1
LPEAT1, LPLAT, LPLAT 1, LPLAT14, LPSAT, OACT1, dJ434O11.1
Cholelithiasis, Iron metabolism disorder, Metabolic syndrome, Myocardial infarction, Obesity, Diabetes mellitus type 2

206
Membrane bound glycerophospholipid O-acyltransferase 2
LPAAT, LPCAT, LPCAT4, LPEAT, LPLAT 2, LPLAT13, OACT2
Hepatomegaly, Lung cancer

207
Membrane bound acylglycerophosphatidylinositol O-acyltransferase MBOAT7
BB1, LENG4, LPIAT, LPIAT1, LPLAT, LPLAT11, LRC4, MBOA7, MRT57, OACT7, hMBOA-7
Nonsyndromic intellectual disability, Neurodevelopmental disorder, Intellectual developmental disorder, Liver cirrhosis, Nonalcoholic fatty liver disease, Non-specific syndromic intellectual disability

208
Myelin basic protein
-
Atrophic macular degeneration, Cerebrovascular disorder, Demyelinating diseases, Iga nephropathy, Insomnia, Major depressive disorder, Multiple sclerosis, Obesity, Orofacial cleft, Periodontal disease, Periodontitis, Schizophrenia, Thoracic aortic aneurysm

209
Mbt domain containing 1
SA49P01
Atrial fibrillation, Coronary artery disease

210
Membrane bound transcription factor peptidase, site 1
CAOP, PCSK8, S1P, SEDKF, SKI-1
Hepatocellular carcinoma, Craniofacial abnormalities, Large artery stroke, Prostatic neoplasms, Schizophrenia, Scoliosis, Spondyloepiphyseal dysplasia