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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:SCARB2-SERPINE1 (FusionGDB2 ID:79056)

Fusion Gene Summary for SCARB2-SERPINE1

check button Fusion gene summary
Fusion gene informationFusion gene name: SCARB2-SERPINE1
Fusion gene ID: 79056
HgeneTgene
Gene symbol

SCARB2

SERPINE1

Gene ID

950

5054

Gene namescavenger receptor class B member 2serpin family E member 1
SynonymsAMRF|CD36L2|EPM4|HLGP85|LGP85|LIMP-2|LIMPII|SR-BIIPAI|PAI-1|PAI1|PLANH1
Cytomap

4q21.1

7q22.1

Type of geneprotein-codingprotein-coding
Descriptionlysosome membrane protein 285 kDa lysosomal membrane sialoglycoprotein85 kDa lysosomal sialoglycoprotein scavenger receptor class B, member 2CD36 antigen (collagen type I receptor, thrombospondin receptor)-like 2 (lysosomal integral membrane protein IIplasminogen activator inhibitor 1endothelial plasminogen activator inhibitorserine (or cysteine) proteinase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1serpin E1serpin peptidase inhibitor, clade E (nexin, plasminogen ac
Modification date2020031320200315
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000264896, ENST00000452464, 
ENST00000223095, ENST00000445463, 
Fusion gene scores* DoF score14 X 13 X 7=12747 X 7 X 1=49
# samples 167
** MAII scorelog2(16/1274*10)=-2.99322146736894
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/49*10)=0.514573172829758
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: SCARB2 [Title/Abstract] AND SERPINE1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointSCARB2(77091105)-SERPINE1(100777064), # samples:1
Anticipated loss of major functional domain due to fusion event.
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types
** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
TgeneSERPINE1

GO:0010469

regulation of signaling receptor activity

8837777

TgeneSERPINE1

GO:0010757

negative regulation of plasminogen activation

8508955

TgeneSERPINE1

GO:0010951

negative regulation of endopeptidase activity

1695900

TgeneSERPINE1

GO:0014912

negative regulation of smooth muscle cell migration

8837777

TgeneSERPINE1

GO:0030336

negative regulation of cell migration

10902815

TgeneSERPINE1

GO:0033629

negative regulation of cell adhesion mediated by integrin

8837777

TgeneSERPINE1

GO:0048260

positive regulation of receptor-mediated endocytosis

8626514

TgeneSERPINE1

GO:0051918

negative regulation of fibrinolysis

2503541

TgeneSERPINE1

GO:0097187

dentinogenesis

27046084

TgeneSERPINE1

GO:1901331

positive regulation of odontoblast differentiation

27046084

TgeneSERPINE1

GO:2000098

negative regulation of smooth muscle cell-matrix adhesion

8837777


check buttonFusion gene breakpoints across SCARB2 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across SERPINE1 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* All genome coordinats were lifted-over on hg19.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS5.0N/ABQ650179SCARB2chr4

77091105

-SERPINE1chr7

100777064

+


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Fusion Gene ORF analysis for SCARB2-SERPINE1

check button Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
intron-3CDSENST00000264896ENST00000223095SCARB2chr4

77091105

-SERPINE1chr7

100777064

+
intron-3CDSENST00000264896ENST00000445463SCARB2chr4

77091105

-SERPINE1chr7

100777064

+
intron-3CDSENST00000452464ENST00000223095SCARB2chr4

77091105

-SERPINE1chr7

100777064

+
intron-3CDSENST00000452464ENST00000445463SCARB2chr4

77091105

-SERPINE1chr7

100777064

+

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score

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Fusion Genomic Features for SCARB2-SERPINE1


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.

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Fusion Protein Features for SCARB2-SERPINE1


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
..
FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.

check buttonRetention analysis result of each fusion partner protein across 39 protein features of UniProt such as six molecule processing features, 13 region features, four site features, six amino acid modification features, two natural variation features, five experimental info features, and 3 secondary structure features. Here, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at

download page


* Minus value of BPloci means that the break pointn is located before the CDS.
- In-frame and retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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Fusion Gene Sequence for SCARB2-SERPINE1


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for SCARB2-SERPINE1


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page.


check button Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs for SCARB2-SERPINE1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for SCARB2-SERPINE1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSCARB2C0751779Action Myoclonus-Renal Failure Syndrome7CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneSCARB2C0751785Unverricht-Lundborg Syndrome1ORPHANET
HgeneSCARB2C1961835Gaucher Disease, Type 11ORPHANET
TgeneSERPINE1C0015695Fatty Liver2CTD_human
TgeneSERPINE1C0020538Hypertensive disease2CTD_human
TgeneSERPINE1C0040053Thrombosis2CTD_human
TgeneSERPINE1C0087086Thrombus2CTD_human
TgeneSERPINE1C2711227Steatohepatitis2CTD_human
TgeneSERPINE1C0002152Alloxan Diabetes1CTD_human
TgeneSERPINE1C0004153Atherosclerosis1CTD_human
TgeneSERPINE1C0004352Autistic Disorder1CTD_human
TgeneSERPINE1C0004943Behcet Syndrome1CTD_human
TgeneSERPINE1C0008370Cholestasis1CTD_human
TgeneSERPINE1C0011853Diabetes Mellitus, Experimental1CTD_human
TgeneSERPINE1C0011881Diabetic Nephropathy1CTD_human
TgeneSERPINE1C0017667Nodular glomerulosclerosis1CTD_human
TgeneSERPINE1C0017668Focal glomerulosclerosis1CTD_human
TgeneSERPINE1C0018801Heart failure1CTD_human
TgeneSERPINE1C0018802Congestive heart failure1CTD_human
TgeneSERPINE1C0022661Kidney Failure, Chronic1CTD_human
TgeneSERPINE1C0023212Left-Sided Heart Failure1CTD_human
TgeneSERPINE1C0023895Liver diseases1CTD_human
TgeneSERPINE1C0023903Liver neoplasms1CTD_human
TgeneSERPINE1C0024623Malignant neoplasm of stomach1CTD_human
TgeneSERPINE1C0027726Nephrotic Syndrome1CTD_human
TgeneSERPINE1C0027765nervous system disorder1CTD_human
TgeneSERPINE1C0028754Obesity1CTD_human
TgeneSERPINE1C0032914Pre-Eclampsia1CTD_human
TgeneSERPINE1C0033578Prostatic Neoplasms1CTD_human
TgeneSERPINE1C0035228Respiratory Hypersensitivity1CTD_human
TgeneSERPINE1C0038356Stomach Neoplasms1CTD_human
TgeneSERPINE1C0038433Streptozotocin Diabetes1CTD_human
TgeneSERPINE1C0041696Unipolar Depression1PSYGENET
TgeneSERPINE1C0041956Ureteral obstruction1CTD_human
TgeneSERPINE1C0086132Depressive Symptoms1PSYGENET
TgeneSERPINE1C0086432Hyalinosis, Segmental Glomerular1CTD_human
TgeneSERPINE1C0086565Liver Dysfunction1CTD_human
TgeneSERPINE1C0235527Heart Failure, Right-Sided1CTD_human
TgeneSERPINE1C0345904Malignant neoplasm of liver1CTD_human
TgeneSERPINE1C0376358Malignant neoplasm of prostate1CTD_human
TgeneSERPINE1C1269683Major Depressive Disorder1PSYGENET
TgeneSERPINE1C1563937Atherogenesis1CTD_human
TgeneSERPINE1C1708349Hereditary Diffuse Gastric Cancer1CTD_human
TgeneSERPINE1C1959583Myocardial Failure1CTD_human
TgeneSERPINE1C1961112Heart Decompensation1CTD_human
TgeneSERPINE1C2750067Plasminogen Activator Inhibitor-1 Deficiency1CTD_human;GENOMICS_ENGLAND;ORPHANET