MMP25

Gene Information
 
Gene Symbol
MMP25
 
Aliases
MMP-25, MMP20, MMP20A, MMPL1, MT-MMP 6, MT-MMP6, MT6-MMP, MT6MMP, MTMMP6
 
Entrez Gene ID
 
Gene Name
Matrix metallopeptidase 25
 
Chromosomal Location
16p13.3
 
HGNC ID
 
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]
  e!Ensembl
Gene
Transcript  
Protein

Gene Ontology (GO)

GO ID Ontology Function Evidence Reference
GO:0006508 Biological process Proteolysis NAS 10706098
GO:0006954 Biological process Inflammatory response NAS 10628838
GO:0030198 Biological process Extracellular matrix organization IBA 21873635
GO:0030574 Biological process Collagen catabolic process IBA 21873635
GO:0005615 Cellular component Extracellular space IBA 21873635
Protein Information
 
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
 
Function
May activate progelatinase A
 
UniProt
 
Pfam
Pfam Accession Pfam ID
PF00045 Hemopexin
PF00413 Peptidase_M10
PF01471 PG_binding_1
Pathways
 
KEGG
 
Reactome
 

Parathyroid hormone synthesis, secretion and action

 

Activation of Matrix Metalloproteinases
Neutrophil degranulation

Interactions
 
STRING MINT IntAct
ENSP00000337816 Q9NPA2
    View interactions
     

Associated Diseases

Disease groupDisease NameReferences
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital enamel hypoplasia
Endocrine System Diseases
PCOS
Musculoskeletal Diseases
Arthritis
Neoplasms
Colonic Neoplasms
Mouth Neoplasms
References
 
 
PubMed ID Associated gene/s Associated condition Genetic Mutation Diagnostic Criteria Association with PCOS Ethnicity Conclusion
 
PCOS, Inflammation 
 
Rotterdam Criteria 
Direct 
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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