Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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7631 to 7640 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

7631
Methionine adenosyltransferase 2A
MATA2, MATII, SAMS2
Ischemic heart disease, Coronary artery disease, Thoracic aortic aneurysm and aortic dissection, Marfan syndrome, Myocardial ischemia, Prostate cancer, Combined deficiency of vitamin k-dependent clotting factors

7632
Methionine adenosyltransferase 2 non-catalytic beta subunit
MAT-II, MATIIbeta, Nbla02999, SDR23E1, TGR
Attention deficit hyperactivity disorder, Dementia, Oropharyngeal cancer, Substance abuse

7633
Megakaryocyte-associated tyrosine kinase
CHK, CTK, HHYLTK, HYL, HYLTK, Lsk
Obesity

7634
Matrilin 1
CMP, CRTM
Attention deficit hyperactivity disorder, Bipolar disorder, Color vision deficiency, Conduct disorder, Lung cancer, Oligodendroglioma, Periprosthetic osteolysis, Willis-ekbom disease, Scoliosis

7635
Matrilin 2
-
Eosinophilia, Erectile dysfunction

7636
Matrilin 3
DIPOA, EDM5, HOA, OADIP, OS2, SEMDBCD
Congenital cartilage disorder, Connective tissue disease, Desbuquois syndrome, Epiphyseal dysplasia, Osteoarthritis, Osteochondrodysplasias, Spondyloepimetaphyseal dysplasia

7637
Matrilin 4
-
Diabetes insipidus, Global developmental delay, Holoprosencephaly, Prostatic neoplasms

7638
Matrin 3
ALS21, MPD2, VCPDM
Amyotrophic lateral sclerosis, Distal muscular dystrophy, Distal myopathy, Hypertrophic cardiomyopathy, Vogt-koyanagi-harada disease

7639
MAU2 sister chromatid cohesion factor
KIAA0892, MAU2L, SCC4, mau-2
Alzheimer disease, Anorexia nervosa, Atrial fibrillation, Attention deficit hyperactivity disorder, Bipolar disorder, Breast cancer, Diabetes mellitus, Diabetic retinopathy, Hepatocellular carcinoma, Insomnia, Intrahepatic bile duct cancer, Liver cancer, Liver neoplasms, Migraine, Neurodevelopmental disorder
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7640
Mitochondrial antiviral signaling protein
CARDIF, IPS-1, IPS1, VISA
Alzheimer disease, Asthma