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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 14

FusionGeneSummary for A2M_EPN2

check button Fusion gene summary
Fusion gene informationFusion gene name: A2M_EPN2
Fusion gene ID: 14
HgeneTgene
Gene symbol

A2M

EPN2

Gene ID

2

22905

Gene namealpha-2-macroglobulinepsin 2
SynonymsA2MD|CPAMD5|FWP007|S863-7EHB21
Cytomap

12p13.31

17p11.2

Type of geneprotein-codingprotein-coding
Descriptionalpha-2-macroglobulinC3 and PZP-like alpha-2-macroglobulin domain-containing protein 5alpha-2-Mepsin-2EPS-15-interacting protein 2Eps15 binding protein
Modification date2018051920180522
UniProtAcc

P01023

O95208

Ensembl transtripts involved in fusion geneENST00000318602, ENST00000542567, 
ENST00000441293, ENST00000314728, 
ENST00000347697, ENST00000395618, 
ENST00000575595, ENST00000395620, 
ENST00000395626, ENST00000571254, 
Fusion gene scores* DoF score10 X 9 X 4=3609 X 9 X 5=405
# samples 1110
** MAII scorelog2(11/360*10)=-1.71049338280502
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(10/405*10)=-2.01792190799726
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: A2M [Title/Abstract] AND EPN2 [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotation
* 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
HgeneA2M

GO:0001869

negative regulation of complement activation, lectin pathway

12538697


check button Fusion gene information from three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* 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.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS3.1BF849872A2Mchr12

9243885

-EPN2chr17

19184805

+
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

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-intronENST00000318602ENST00000441293A2Mchr12

9243885

-EPN2chr17

19184805

+
intron-intronENST00000318602ENST00000314728A2Mchr12

9243885

-EPN2chr17

19184805

+
intron-intronENST00000318602ENST00000347697A2Mchr12

9243885

-EPN2chr17

19184805

+
intron-intronENST00000318602ENST00000395618A2Mchr12

9243885

-EPN2chr17

19184805

+
intron-intronENST00000318602ENST00000575595A2Mchr12

9243885

-EPN2chr17

19184805

+
intron-intronENST00000318602ENST00000395620A2Mchr12

9243885

-EPN2chr17

19184805

+
intron-intronENST00000318602ENST00000395626A2Mchr12

9243885

-EPN2chr17

19184805

+
intron-intronENST00000318602ENST00000571254A2Mchr12

9243885

-EPN2chr17

19184805

+
intron-intronENST00000542567ENST00000441293A2Mchr12

9243885

-EPN2chr17

19184805

+
intron-intronENST00000542567ENST00000314728A2Mchr12

9243885

-EPN2chr17

19184805

+
intron-intronENST00000542567ENST00000347697A2Mchr12

9243885

-EPN2chr17

19184805

+
intron-intronENST00000542567ENST00000395618A2Mchr12

9243885

-EPN2chr17

19184805

+
intron-intronENST00000542567ENST00000575595A2Mchr12

9243885

-EPN2chr17

19184805

+
intron-intronENST00000542567ENST00000395620A2Mchr12

9243885

-EPN2chr17

19184805

+
intron-intronENST00000542567ENST00000395626A2Mchr12

9243885

-EPN2chr17

19184805

+
intron-intronENST00000542567ENST00000571254A2Mchr12

9243885

-EPN2chr17

19184805

+

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FusionProtFeatures for A2M_EPN2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
A2M

P01023

EPN2

O95208

Is able to inhibit all four classes of proteinases by aunique 'trapping' mechanism. This protein has a peptide stretch,called the 'bait region' which contains specific cleavage sitesfor different proteinases. When a proteinase cleaves the baitregion, a conformational change is induced in the protein whichtraps the proteinase. The entrapped enzyme remains active againstlow molecular weight substrates (activity against high molecularweight substrates is greatly reduced). Following cleavage in thebait region, a thioester bond is hydrolyzed and mediates thecovalent binding of the protein to the proteinase. Plays a role in the formation of clathrin-coatedinvaginations and endocytosis. {ECO:0000269|PubMed:10567358}.

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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FusionGeneSequence for A2M_EPN2


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

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FusionGenePPI for A2M_EPN2


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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RelatedDrugs for A2M_EPN2


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneA2MP01023DB00515CisplatinAlpha-2-macroglobulinsmall moleculeapproved
HgeneA2MP01023DB08888OcriplasminAlpha-2-macroglobulinbiotechapproved
HgeneA2MP01023DB00102BecaplerminAlpha-2-macroglobulinbiotechapproved|investigational
HgeneA2MP01023DB01593ZincAlpha-2-macroglobulinsmall moleculeapproved|investigational
HgeneA2MP01023DB00626BacitracinAlpha-2-macroglobulinsmall moleculeapproved|vet_approved

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RelatedDiseases for A2M_EPN2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneA2MC0002395Alzheimer's Disease3CTD_human
HgeneA2MC0011570Mental Depression2PSYGENET
HgeneA2MC0011581Depressive disorder2PSYGENET
HgeneA2MC0024121Lung Neoplasms2CTD_human
HgeneA2MC0009375Colonic Neoplasms1CTD_human
HgeneA2MC0019202Hepatolenticular Degeneration1CTD_human
HgeneA2MC0023890Liver Cirrhosis1CTD_human
HgeneA2MC0023893Liver Cirrhosis, Experimental1CTD_human
HgeneA2MC0024115Lung diseases1CTD_human
HgeneA2MC0027726Nephrotic Syndrome1CTD_human
HgeneA2MC0206669Hepatocellular Adenoma1CTD_human
HgeneA2MC2239176Liver carcinoma1CTD_human
HgeneA2MC2609414Acute kidney injury1CTD_human