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"
481 to 490 of 893 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

481
Matrix metallopeptidase 12
HME, ME, MME, MMP-12
Alzheimer disease, Arteriosclerosis, Rheumatoid arthritis, Eczema, Barrett esophagus, Celiac disease, Cerebrovascular disorder, Ischemic heart disease, Obstructive pulmonary disease, Colonic neoplasms, Coronary aneurysm, Coronary artery disease, Large artery stroke, Multiple sclerosis, Myocardial ischemia
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482
Matrix metallopeptidase 13
CLG3, MANDP1, MDST, MMP-13
Aneurysm, Aortic aneurysm, Arteriosclerosis, Asthma, Cerebrovascular disorder, Coronary artery disease, Craniofacial abnormalities, Desbuquois syndrome, Tooth agenesis, Large artery stroke, Metaphyseal chondrodysplasia, Metaphyseal dysplasia, Prostatic neoplasms, Spondyloepimetaphyseal dysplasia

483
Matrix metallopeptidase 14
MMP-14, MMP-X1, MT-MMP, MT-MMP 1, MT1-MMP, MT1MMP, MTMMP1, WNCHRS
Aortic aneurysm, Eczema, Breast neoplasms, Hepatocellular carcinoma, Obstructive airway disease, Desbuquois syndrome, Dupuytren contracture, Esophageal neoplasms, Liver neoplasms, Myocardial infarction, Prostate cancer, Chronic obstructive pulmonary disease, Scoliosis, Torg-winchester syndrome, Winchester syndrome

484
Matrix metallopeptidase 15
MMP-15, MT2-MMP, MT2MMP, MTMMP2, SMCP-2
Obstructive pulmonary disease, Developmental disability

485
Matrix metallopeptidase 16
C8orf57, MMP-X2, MT-MMP2, MT-MMP3, MT3-MMP
Anorexia nervosa, Autism, Bipolar disorder, Schizophrenia

486
Matrix metallopeptidase 17
MMP-17, MT4-MMP, MT4MMP, MTMMP4
Migraine

487
Matrix metallopeptidase 19
CODA, MMP18, RASI-1
Cavitary optic disc anomalies, Cavitary optic disk anomaly, Interstitial lung disease

488
Matrix metallopeptidase 2
CLG4, CLG4A, MMP-2, MMP-II, MONA, TBE-1
Aortic aneurysm, Aortic disease, Aortic rupture, Arteriosclerosis, Rheumatoid arthritis, Osteonecrosis of the femoral head, Avascular necrosis of bone, Bone disease, Bone neoplasms, Breast neoplasms, Calcinosis, Hepatocellular carcinoma, Carotid artery disease, Cerebral hemorrhage, Ischemic stroke
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489
Matrix metallopeptidase 20
AI2A2, MMP-20
Amelogenesis imperfecta, Dentin dysplasia, Dentinogenesis imperfecta, Hypomaturation amelogenesis imperfecta, Intellectual developmental disorder, Neuroblastoma, Prostate cancer, Schizophrenia

490
Matrix metallopeptidase 21
HTX7, MMP-21
Dermatologic disorder, Heterotaxy syndrome, Situs ambiguus, Situs inversus, Skin disease, Tetralogy of fallot