Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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7651 to 7660 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

7651
MAP3K12 binding inhibitory protein 1
-
Attention deficit hyperactivity disorder, Differentiated thyroid carcinoma, Hypertension, Hypothyroidism, Multinodular goiter, Substance abuse, Thyroid cancer, Toxic nodular goiter

7652
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, Obstructive airway disease, Ciliary dyskinesia, with or without situs inversus, Common variable immunodeficiency, Coronary restenosis, Crohn disease, Cystic fibrosis
View all (26 more)

7653
Metallo-beta-lactamase domain containing 1
-
Long qt syndrome

7654
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

7655
Muscleblind like splicing regulator 2
MBLL, MBLL39, PRO2032
Atrial fibrillation, Attention deficit hyperactivity disorder, Breast cancer, Neurotic disorder, Obesity, Parkinson disease

7656
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

7657
Membrane bound glycerophospholipid O-acyltransferase 2
LPAAT, LPCAT, LPCAT4, LPEAT, LPLAT 2, LPLAT13, OACT2
Hepatomegaly, Lung cancer

7658
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

7659
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

7660
Mbt domain containing 1
SA49P01
Atrial fibrillation, Coronary artery disease