PLG Gene (Plasminogen)

Key regulator of fibrinolysis and extracellular matrix remodeling

Gene Information Card

Symbol PLG
Full Name Plasminogen
Gene Type protein-coding
Chromosomal Location 6q26
NCBI Gene ID 5340 ncbi.nlm.nih.gov/gene/5340
Ensembl ID ENSG00000122194
UniProt ID P00747
OMIM ID 173350
HGNC ID 9071
Aliases PLG, plasminogen

Description

The PLG gene encodes plasminogen, a circulating zymogen that is converted to plasmin, a serine protease that degrades fibrin clots and extracellular matrix components. Plasminogen plays a central role in fibrinolysis, tissue remodeling, cell migration, and wound healing. Mutations in PLG cause plasminogen deficiency, leading to ligneous conjunctivitis and thrombosis.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Ligneous conjunctivitis Deficiency of plasminogen leads to impaired fibrinolysis and accumulation of fibrin-rich pseudomembranes on mucous membranes. ClinVar, OMIM
Plasminogen deficiency, type I (hypoplasminogenemia) Loss-of-function mutations reduce plasminogen activity, causing thrombotic and mucosal lesions. ClinVar, OMIM
Thrombophilia Reduced plasminogen activity predisposes to venous thrombosis. ClinVar

Expression Profile

Tissue Expression
Tissue nTPM level
Liver 12.5 High
Kidney 3.2 Medium
Lung 1.8 Low
Heart 0.9 Low
Cell Line Expression
Cell Line nTPM Notes
HepG2 15.0 Hepatocyte cell line, high expression
HEK293 2.1 Low expression
A549 1.5 Lung carcinoma cell line
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.2125G>A (p.Gly709Arg) Missense Rare Reduced plasminogen activity
c.112A>G (p.Lys38Glu) Missense Rare Impaired secretion
c.1468C>T (p.Arg490Cys) Missense Rare Loss of function
Mutation functional classification

Loss of Function (LOF)

Most PLG mutations are loss-of-function, reducing plasminogen activity or secretion.

Gain of Function (GOF)

Not reported for PLG.

Dominant Negative (DN)

Not reported for PLG.

Pathways

Plasminogen activating cascade (Reactome: R-HSA-75205)
Fibrinolysis (KEGG: hsa04610)

Protein Summary

Plasminogen is a 791-amino-acid glycoprotein synthesized primarily in the liver. It contains five kringle domains and a serine protease domain. Upon activation by tissue-type plasminogen activator (tPA) or urokinase, it is converted to plasmin, which degrades fibrin clots and extracellular matrix proteins. Plasminogen also regulates cell migration and wound healing.

Related Products

Product name Cat.No. Species Gene ID
PLG Knockout HEK293 Cell Line EDJ-KQ3711 Human 5340 Details Get a Quote
PLGRKT Knockout HEK293 Cell Line EDJ-KQ14803 Human 55848 Details Get a Quote
PLGRKT Knockout HeLa Cell Line EDJ-KQ43968 Human 55848 Details Get a Quote
PLG Knockout HeLa Cell Line EDJ-KQ24373 Human 5340 Details Get a Quote
PLG Knockout A-549 Cell Line EDJ-KQ25743 Human 5340 Details Get a Quote
PLGRKT Knockout A-549 Cell Line EDJ-KQ45227 Human 55848 Details Get a Quote
PLGRKT Knockout HCT 116 Cell Line EDJ-KQ45228 Human 55848 Details Get a Quote
PLGLB2 Knockout HEK293 Cell Line EDJ-KQ50516 Human 5342 Details Get a Quote
PLGLB1 Knockout HEK293 Cell Line EDJ-KQ50517 Human 5343 Details Get a Quote
SELPLG Knockout HEK293 Cell Line EDJ-KQ50621 Human 6404 Details Get a Quote
PLGLB2 Knockout HeLa Cell Line EDJ-KQ54154 Human 5342 Details Get a Quote
PLGLB1 Knockout HeLa Cell Line EDJ-KQ54155 Human 5343 Details Get a Quote
SELPLG Knockout HeLa Cell Line EDJ-KQ54441 Human 6404 Details Get a Quote
PLGLB2 Knockout A-549 Cell Line EDJ-KQ62649 Human 5342 Details Get a Quote
PLGLB1 Knockout A-549 Cell Line EDJ-KQ62650 Human 5343 Details Get a Quote
Displaying Records 1 To 15 Of 20 Records
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