MMP16 Gene - Matrix Metallopeptidase 16

Membrane-type matrix metalloproteinase involved in extracellular matrix remodeling and cancer progression

Gene Information Card

Symbol MMP16
Full Name Matrix Metallopeptidase 16
Gene Type protein-coding
Chromosomal Location 8q21.3
NCBI Gene ID 4325 ncbi.nlm.nih.gov/gene/4325
Ensembl ID ENSG00000156136
UniProt ID P51512
OMIM ID 602262
HGNC ID 7162
Aliases MT3-MMP, MTMMP3, MMP-X2

Description

MMP16 (Matrix Metallopeptidase 16) encodes a member of the matrix metalloproteinase (MMP) family, specifically a membrane-type MMP (MT3-MMP). This protein is anchored to the cell membrane and functions in the degradation of extracellular matrix components, including collagen, gelatin, and fibronectin. It also activates other MMPs, such as pro-MMP2, and plays roles in cell migration, angiogenesis, and tissue remodeling. Dysregulation of MMP16 is implicated in cancer invasion, metastasis, and inflammatory diseases.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Glioma MMP16 overexpression promotes tumor invasion and angiogenesis via ECM degradation and MMP2 activation. PMID: 19029987
Breast Cancer Elevated MMP16 expression correlates with poor prognosis and metastasis through enhanced cell migration. PMID: 22926525
Osteoarthritis MMP16 contributes to cartilage degradation by cleaving aggrecan and type II collagen. PMID: 17186463

Expression Profile

Tissue Expression
Tissue nTPM level
Brain 12.3 Medium
Lung 8.7 Low
Breast 6.5 Low
Colon 4.2 Low
Ovary 9.1 Low
Cell Line Expression
Cell Line nTPM Notes
U-87 MG (glioma) 15.2 High expression
MCF7 (breast cancer) 7.8 Moderate expression
A549 (lung cancer) 5.3 Low expression
HEK 293 (embryonic kidney) 3.1 Very low expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.1234G>A (p.Gly412Arg) Missense <0.01% Unknown functional impact
c.789_790insC Frameshift <0.01% Predicted loss of function
c.1567C>T (p.Arg523Trp) Missense <0.01% Reported in COSMIC for colorectal cancer
Mutation functional classification

Loss of Function (LOF)

Frameshift mutations (e.g., c.789_790insC) likely result in truncated, non-functional protein.

Gain of Function (GOF)

Not well documented; some missense variants may alter substrate specificity but evidence is limited.

Dominant Negative (DN)

No known dominant-negative mutations reported for MMP16.

Gene Ontology (GO)

• metalloendopeptidase activity • extracellular matrix disassembly
• collagen catabolic process • proteolysis
• cell migration • angiogenesis
• membrane

Pathways

Matrix Metalloproteinases
Extracellular matrix organization
Degradation of the extracellular matrix
Activation of MMP2 by MMP16

Protein Summary

MMP16 (MT3-MMP) is a 607-amino acid transmembrane protein with a catalytic domain, hemopexin-like domain, and a cytoplasmic tail. It is synthesized as a zymogen and activated by furin cleavage. The protein localizes to the cell surface and pericellular space, where it degrades ECM components and activates pro-MMP2. Its expression is tightly regulated in normal tissues but frequently upregulated in cancers, contributing to invasive behavior.

Related Products

Product name Cat.No. Species Gene ID
MMP16 Knockout HEK293 Cell Line EDJ-KQ5223 Human 4325 Details Get a Quote
MMP16 Knockout HeLa Cell Line EDJ-KQ53889 Human 4325 Details Get a Quote
MMP16 Knockout A-549 Cell Line EDJ-KQ62381 Human 4325 Details Get a Quote
MMP16 Knockout HCT 116 Cell Line EDJ-KQ70850 Human 4325 Details Get a Quote
MMP16 Knockout HAP1 Cell Line EDC09378 Human 4325 Details Get a Quote
Displaying Records 1 To 5 Of 5 Records
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