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Gene Symbol |
MMP25 |
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Aliases |
MMP-25, MMP20, MMP20A, MMPL1, MT-MMP 6, MT-MMP6, MT6-MMP, MT6MMP, MTMMP6 |
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Entrez Gene ID |
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Gene Name |
Matrix metallopeptidase 25 |
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Chromosomal Location |
16p13.3 |
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HGNC ID |
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Summary |
Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. Most MMPs are secreted as inactive proproteins which are activated when cleaved by extracellular proteinases. However, the protein encoded by this gene is a member of the membrane-type MMP (MT-MMP) subfamily, attached to the plasma membrane via a glycosylphosphatidyl inositol anchor. In response to bacterial infection or inflammation, the encoded protein is thought to inactivate alpha-1 proteinase inhibitor, a major tissue protectant against proteolytic enzymes released by activated neutrophils, facilitating the transendothelial migration of neutrophils to inflammatory sites. The encoded protein may also play a role in tumor invasion and metastasis through activation of MMP2. The gene has previously been referred to as MMP20 but has been renamed MMP25. [provided by RefSeq, Jul 2008]
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e!Ensembl
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Protein Information |
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Protein Name |
Matrix metalloproteinase-25, leukolysin, matrix metallopeptidase-like 1, matrix metalloproteinase 20, matrix metalloproteinase-like 1, membrane-type 6 matrix metalloproteinase, membrane-type matrix metalloproteinase 6 |
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Function |
May activate progelatinase A |
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UniProt |
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Interactions |
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STRING |
MINT |
IntAct |
ENSP00000337816 |
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Q9NPA2 |
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View interactions
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Associated Diseases
Disease group | Disease Name | References |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
Congenital enamel hypoplasia |
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Endocrine System Diseases |
PCOS |
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Musculoskeletal Diseases |
Arthritis |
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Neoplasms |
Colonic Neoplasms |
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Mouth Neoplasms |
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Intraepithelial Neoplasia |
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Odontogenic neoplasm |
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Multiple Sclerosis |
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References |
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PubMed ID |
Associated gene/s |
Associated condition |
Genetic Mutation |
Diagnostic Criteria |
Association with PCOS |
Ethnicity |
Conclusion |
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PCOS, Inflammation |
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Rotterdam Criteria |
Direct
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8 PCOS Subjects and 8 Controls |
We conducted the peripheral-blood transcriptome in PCOS using microarray and identified dysregulated genes involved in inflammatory response. Our data strongly supported the notion that systemic rather than a local inflammatory response is implicated in the etiology of PCOS. |
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