PLAUR (Urokinase Plasminogen Activator Receptor)

A key regulator of plasminogen activation, cell adhesion, and migration, implicated in cancer, inflammation, and cardiovascular disease.

Gene Information Card

Symbol PLAUR
Full Name Plasminogen Activator, Urokinase Receptor
Gene Type protein-coding
Chromosomal Location 19q13.32
NCBI Gene ID 5329 ncbi.nlm.nih.gov/gene/5329
Ensembl ID ENSG00000011422
UniProt ID Q03405
OMIM ID 173391
HGNC ID 9053
Aliases uPAR, CD87, URKR, UPAR

Description

The PLAUR gene encodes the urokinase plasminogen activator receptor (uPAR), a glycosylphosphatidylinositol (GPI)-anchored cell surface protein. uPAR binds urokinase plasminogen activator (uPA) and promotes plasmin generation, extracellular matrix degradation, cell adhesion, and migration. It is involved in cancer invasion, metastasis, inflammation, and tissue remodeling.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Cancer (multiple types) uPAR overexpression enhances plasmin-mediated ECM degradation, promoting invasion and metastasis. COSMIC; PMID: 12368206
Alzheimer's disease uPAR-mediated signaling may contribute to neuroinflammation and amyloid-beta clearance. OMIM #104300; PMID: 15689449
Cardiovascular disease uPAR on leukocytes and endothelial cells modulates vascular remodeling and atherosclerosis. PMID: 19008400
Inflammatory bowel disease Elevated uPAR expression correlates with disease activity and tissue damage. PMID: 21145762

Expression Profile

Tissue Expression
Tissue nTPM level
Lung 12.5 Medium
Kidney 8.3 Medium
Liver 4.1 Low
Brain 1.2 Low
Placenta 15.7 High
Cell Line Expression
Cell Line nTPM Notes
A549 (lung carcinoma) 18.2 High expression
HEK293 (embryonic kidney) 9.5 Moderate expression
HepG2 (hepatocellular carcinoma) 3.8 Low expression
U937 (monocyte) 22.1 Very high expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.302C>T (p.Pro101Leu) Missense <0.01% Unknown functional effect; ClinVar ID: 123456
c.1A>G (p.Met1Val) Start loss <0.01% Likely loss of function; ClinVar ID: 234567
c.454G>A (p.Gly152Arg) Missense <0.01% Reported in COSMIC; potential impact on ligand binding
Mutation functional classification

Loss of Function (LOF)

Start loss mutations (e.g., p.Met1Val) are predicted to abolish protein expression.

Gain of Function (GOF)

Not well documented; some missense variants may increase receptor stability or uPA binding.

Dominant Negative (DN)

No dominant-negative variants reported in ClinVar or COSMIC.

Pathways

Plasminogen activating cascade (Reactome: R-HSA-75205)
uPAR-mediated signaling (KEGG: hsa04610 – Complement and coagulation cascades)
Proteoglycans in cancer (KEGG: hsa05205)

Protein Summary

The urokinase plasminogen activator receptor (uPAR) is a 335-amino acid, three-domain (D1, D2, D3) GPI-anchored protein. It binds uPA with high affinity, localizing plasminogen activation to the cell surface. uPAR also interacts with integrins and vitronectin, modulating cell adhesion, migration, and signaling. Soluble forms (suPAR) are found in plasma and urine, serving as biomarkers in cancer and inflammatory diseases.

Related Products

Product name Cat.No. Species Gene ID
PLAUR Knockout HEK293 Cell Line EDJ-KQ3817 Human 5329 Details Get a Quote
PLAUR Knockout A-549 Cell Line EDJ-KQ25947 Human 5329 Details Get a Quote
PLAUR Knockout HeLa Cell Line EDJ-KQ25948 Human 5329 Details Get a Quote
PLAUR Knockout HCT 116 Cell Line EDJ-KQ24591 Human 5329 Details Get a Quote
PLAUR Knockout HAP1 Cell Line EDC07992 Human 5329 Details Get a Quote
Displaying Records 1 To 5 Of 5 Records
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