Basic information

Full name
plasminogen
Ensembl
ENSG00000122194.18
Summary
The plasminogen protein encoded by this gene is a serine protease that circulates in blood plasma as an inactive zymogen and is converted to the active protease, plasmin, by several plasminogen activators such as tissue plasminogen activator (tPA), urokinase plasminogen activator (uPA), kallikrein, and factor XII (Hageman factor). The conversion of plasminogen to plasmin involves the cleavage of the peptide bond between Arg-561 and Val-562. Plasmin cleavage also releases the angiostatin protein which inhibits angiogenesis. Plasmin degrades many blood plasma proteins, including fibrin-containing blood clots. As a serine protease, plasmin cleaves many products in addition to fibrin such as fibronectin, thrombospondin, laminin, and von Willebrand factor. Plasmin is inactivated by proteins such as alpha-2-macroglobulin and alpha-2-antiplasmin in addition to inhibitors of the various plasminogen activators. Plasminogen also interacts with plasminogen receptors which results in the retention of plasmin on cell surfaces and in plasmin-induced cell signaling. The localization of plasminogen on cell surfaces plays a role in the degradation of extracellular matrices, cell migration, inflamation, wound healing, oncogenesis, metastasis, myogenesis, muscle regeneration, neurite outgrowth, and fibrinolysis. This protein may also play a role in acute respiratory distress syndrome (ARDS) which, in part, is caused by enhanced clot formation and the suppression of fibrinolysis. Compared to other mammals, the cluster of plasminogen-like genes to which this gene belongs has been rearranged in catarrhine primates. [provided by RefSeq, May 2020]
Annotation
Druggable target (Tier T2) Ligand

Protein product

Phosphosites on the primary protein product
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Tumor and normal comparison

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Signed p-values
Data type
Meta P
BRCA
CCRCC
COAD
GBM
HNSCC
LSCC
LUAD
OV
PDAC
UCEC
RNA-3.1e-59--1.3e-26---1.4e-6-6.3e-30-1.2e-14--0.087-
protein-7.8e-50--0.23-1.5e-8--7.2e-13-4.1e-23-9e-27-1.3e-74.1e-4-2.4e-8

* P-values are from Wilcoxon rank sum test and can be clicked to show the box plots. Positive values mean higher abundance in tumor. BRCA and GBM do not have normal samples.

mRNA expression at gene level
BRCACCRCCCOADGBMHNSCCLSCCLUADOVPDACUCEC0246810121416log2(RSEM+1)tumornormal
Protein expression
BRCACCRCCCOADGBMHNSCCLSCCLUADOVPDACUCEC2525.52626.52727.52828.52929.53030.531log2(MS1 intensity)tumornormal

* Mild outlier: filled circle; Extreme outlier: empty circle.

Phenotype and mutation association

Manhattan plot summarizing associations of phenotypes and mutations across all cohorts and omics data types

BRCACCRCCCOADGBMHNSCCLSCCLUADOVPDACUCEC02468101214160-2-4-6-8-10-12-14-16Pan-cancer05101520253035400-5-10-15-20-25-30-35-40proteinRNASCNVclinicalpathwaycell typegenomicmutation-log10 of P-value

* Data points of significant associations above and below the dotted lines can be hovered to show the phenotype.

Associations of the protein abundance of PLG with phenotypes and mutations

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Signed p-values
Phenotype
Meta P
BRCA
CCRCC
COAD
GBM
HNSCC
LSCC
LUAD
OV
PDAC
UCEC
HALLMARK_HYPOXIA4.2e-437.4e-60.0228.5e-82.2e-163.0e-65.3e-44.6e-60.031.3e-47.6e-6
HALLMARK_TNFA_SIGNALING_VIA_NFKB5.2e-290.0150.371.8e-72.2e-164.3e-60.149.2e-40.0042.2e-31.2e-3
HALLMARK_EPITHELIAL_MESENCHYMAL_TRANSITION6.4e-292.9e-48.0e-41.5e-62.6e-91.3e-30.0161.3e-30.0233.1e-34.5e-4
xcell: Endothelial cell1.1e-223.6e-82.7e-30.0940.040.0449.3e-51.1e-73.4e-30.342.7e-4
HALLMARK_MYOGENESIS8.1e-226.8e-51.3e-38.6e-48.0e-60.0918.2e-70.340.0270.0268.5e-4
PROGENy: TGFb8.6e-222.2e-41.1e-37.6e-52.0e-40.0370.0024.5e-30.0295.2e-37.2e-3
PROGENy: Hypoxia7.4e-216.1e-40.154.1e-92.4e-60.0192.8e-30.0180.325.1e-40.046
HALLMARK_TGF_BETA_SIGNALING2.6e-201.2e-55.8e-40.0171.2e-40.140.0380.0241.9e-33.9e-38.5e-4
HALLMARK_ANGIOGENESIS5.3e-207.9e-50.0122.7e-73.4e-62.2e-40.013.0e-40.034-0.140.027
HALLMARK_UV_RESPONSE_DN5.6e-191.2e-54.2e-49.5e-31.2e-30.182.8e-30.0591.6e-30.0226.1e-3
Showing 1 to 10 of 256 rows

* P-values could be from test for Spearman correlation, Wilcoxon rank sum test, Jonckheere-Terpstra trend test or Cox regression depending on the data type. P-values for individual cohorts can be clicked to show the data plots. The matrix icons in each row can be clicked to show a heatmap summary of associations across all cohorts and omics. The rows in the table can be expanded to show results from other omics.

Cis-association

Associations between omics data of PLG

BRCA0.10-0.080.08proteinmRNASCNVmethylationCCRCC0.150.160.16proteinmRNASCNVmethylationCOAD0.080.130.23proteinmRNASCNVmethylationGBM-0.010.050.13proteinmRNASCNVmethylationHNSCC-0.060.190.21proteinmRNASCNVmethylationLSCC0.110.100.08proteinmRNASCNVmethylationLUAD-0.190.030.11proteinmRNASCNVmethylationOV0.12-0.050.24proteinmRNASCNVmethylationPDAC0.100.020.21proteinmRNASCNVmethylationUCEC0.060.080.20proteinmRNASCNVmethylation

* The numbers are Spearman correlation coefficients and can be clicked to show the scatter plots. The color and size of the circles correlate with the coefficients.

Trans-association

Associations of the protein abundance of PLG and the protein abundance of other genes

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Signed p-values
Gene
Meta P
BRCA
CCRCC
COAD
GBM
HNSCC
LSCC
LUAD
OV
PDAC
UCEC
No matching records found

* P-values are from test for Spearman correlation. P-values for individual cohorts can be clicked to show the data plots. The matrix icons in each row can be clicked to show a heatmap summary of associations across all cohorts and omics. The rows in the table can be expanded to show results from other omics.

Gene set enrichment analysis

Submit genes and the common logarithm of the p-values of their association with to WebGestalt.