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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:UBA2-CCL5 (FusionGDB2 ID:95806)

Fusion Gene Summary for UBA2-CCL5

check button Fusion gene summary
Fusion gene informationFusion gene name: UBA2-CCL5
Fusion gene ID: 95806
HgeneTgene
Gene symbol

UBA2

CCL5

Gene ID

10054

6352

Gene nameubiquitin like modifier activating enzyme 2C-C motif chemokine ligand 5
SynonymsARX|HRIHFB2115|SAE2D17S136E|RANTES|SCYA5|SIS-delta|SISd|TCP228|eoCP
Cytomap

19q13.11

17q12

Type of geneprotein-codingprotein-coding
DescriptionSUMO-activating enzyme subunit 2SUMO-1 activating enzyme subunit 2SUMO1 activating enzyme subunit 2UBA2, ubiquitin-activating enzyme E1 homologanthracycline-associated resistance ARXubiquitin-like 1-activating enzyme E1BC-C motif chemokine 5T-cell specific protein p288beta-chemokine RANTESchemokine (C-C motif) ligand 5eosinophil chemotactic cytokineregulated upon activation, normally T-expressed, and presumably secretedsmall inducible cytokine subfamily A (Cys-Cys)
Modification date2020031320200313
UniProtAcc.

P13501

Ensembl transtripts involved in fusion geneENST00000246548, ENST00000439527, 
ENST00000588585, ENST00000592791, 
ENST00000293272, ENST00000366113, 
Fusion gene scores* DoF score14 X 11 X 8=12322 X 2 X 2=8
# samples 183
** MAII scorelog2(18/1232*10)=-2.77493344436523
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/8*10)=1.90689059560852
Context

PubMed: UBA2 [Title/Abstract] AND CCL5 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointUBA2(34949372)-CCL5(34199311), # 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
HgeneUBA2

GO:0016925

protein sumoylation

20164921

HgeneUBA2

GO:0033235

positive regulation of protein sumoylation

10187858

TgeneCCL5

GO:0006816

calcium ion transport

10734056

TgeneCCL5

GO:0006874

cellular calcium ion homeostasis

10734056

TgeneCCL5

GO:0006887

exocytosis

10734056

TgeneCCL5

GO:0006954

inflammatory response

21147091

TgeneCCL5

GO:0007159

leukocyte cell-cell adhesion

8558019

TgeneCCL5

GO:0007186

G protein-coupled receptor signaling pathway

17001303|23979485

TgeneCCL5

GO:0007267

cell-cell signaling

8558019

TgeneCCL5

GO:0009636

response to toxic substance

10841574

TgeneCCL5

GO:0010759

positive regulation of macrophage chemotaxis

16778803

TgeneCCL5

GO:0010820

positive regulation of T cell chemotaxis

1699135|7544376|16778803|18337562

TgeneCCL5

GO:0014068

positive regulation of phosphatidylinositol 3-kinase signaling

7544376

TgeneCCL5

GO:0014911

positive regulation of smooth muscle cell migration

21297082

TgeneCCL5

GO:0030335

positive regulation of cell migration

7545673

TgeneCCL5

GO:0031328

positive regulation of cellular biosynthetic process

18337562

TgeneCCL5

GO:0031584

activation of phospholipase D activity

9469451

TgeneCCL5

GO:0031663

lipopolysaccharide-mediated signaling pathway

21147091

TgeneCCL5

GO:0033634

positive regulation of cell-cell adhesion mediated by integrin

8558019

TgeneCCL5

GO:0034112

positive regulation of homotypic cell-cell adhesion

10488085

TgeneCCL5

GO:0042102

positive regulation of T cell proliferation

18832695

TgeneCCL5

GO:0042119

neutrophil activation

10488085

TgeneCCL5

GO:0042327

positive regulation of phosphorylation

18337562

TgeneCCL5

GO:0042531

positive regulation of tyrosine phosphorylation of STAT protein

9417081

TgeneCCL5

GO:0043922

negative regulation by host of viral transcription

10841574

TgeneCCL5

GO:0045071

negative regulation of viral genome replication

10490959

TgeneCCL5

GO:0045744

negative regulation of G protein-coupled receptor signaling pathway

10734056

TgeneCCL5

GO:0045785

positive regulation of cell adhesion

10910894

TgeneCCL5

GO:0048245

eosinophil chemotaxis

16778803

TgeneCCL5

GO:0048661

positive regulation of smooth muscle cell proliferation

21297082

TgeneCCL5

GO:0050796

regulation of insulin secretion

23979485

TgeneCCL5

GO:0050863

regulation of T cell activation

10488085

TgeneCCL5

GO:0051928

positive regulation of calcium ion transport

8699119

TgeneCCL5

GO:0070098

chemokine-mediated signaling pathway

17001303

TgeneCCL5

GO:0070233

negative regulation of T cell apoptotic process

10488085

TgeneCCL5

GO:0070234

positive regulation of T cell apoptotic process

10488085

TgeneCCL5

GO:0071407

cellular response to organic cyclic compound

21147091

TgeneCCL5

GO:0090026

positive regulation of monocyte chemotaxis

1699135|19779041

TgeneCCL5

GO:1901214

regulation of neuron death

17001303

TgeneCCL5

GO:2000406

positive regulation of T cell migration

23620790

TgeneCCL5

GO:2000503

positive regulation of natural killer cell chemotaxis

7545673


check buttonFusion gene breakpoints across UBA2 (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 CCL5 (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/ADL054536UBA2chr19

34949372

+CCL5chr17

34199311

-


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Fusion Gene ORF analysis for UBA2-CCL5

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-3UTRENST00000246548ENST00000293272UBA2chr19

34949372

+CCL5chr17

34199311

-
intron-3UTRENST00000246548ENST00000366113UBA2chr19

34949372

+CCL5chr17

34199311

-
intron-3UTRENST00000439527ENST00000293272UBA2chr19

34949372

+CCL5chr17

34199311

-
intron-3UTRENST00000439527ENST00000366113UBA2chr19

34949372

+CCL5chr17

34199311

-
intron-3UTRENST00000588585ENST00000293272UBA2chr19

34949372

+CCL5chr17

34199311

-
intron-3UTRENST00000588585ENST00000366113UBA2chr19

34949372

+CCL5chr17

34199311

-
intron-3UTRENST00000592791ENST00000293272UBA2chr19

34949372

+CCL5chr17

34199311

-
intron-3UTRENST00000592791ENST00000366113UBA2chr19

34949372

+CCL5chr17

34199311

-

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 UBA2-CCL5


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 UBA2-CCL5


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:34949372/:34199311)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
.CCL5

P13501

FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}.FUNCTION: Chemoattractant for blood monocytes, memory T-helper cells and eosinophils. Causes the release of histamine from basophils and activates eosinophils. May activate several chemokine receptors including CCR1, CCR3, CCR4 and CCR5. One of the major HIV-suppressive factors produced by CD8+ T-cells. Recombinant RANTES protein induces a dose-dependent inhibition of different strains of HIV-1, HIV-2, and simian immunodeficiency virus (SIV). The processed form RANTES(3-68) acts as a natural chemotaxis inhibitor and is a more potent inhibitor of HIV-1-infection. The second processed form RANTES(4-68) exhibits reduced chemotactic and HIV-suppressive activity compared with RANTES(1-68) and RANTES(3-68) and is generated by an unidentified enzyme associated with monocytes and neutrophils (PubMed:16791620, PubMed:1380064, PubMed:8525373, PubMed:9516414, PubMed:15923218). May also be an agonist of the G protein-coupled receptor GPR75, stimulating inositol trisphosphate production and calcium mobilization through its activation. Together with GPR75, may play a role in neuron survival through activation of a downstream signaling pathway involving the PI3, Akt and MAP kinases. By activating GPR75 may also play a role in insulin secretion by islet cells (PubMed:23979485). {ECO:0000269|PubMed:1380064, ECO:0000269|PubMed:15923218, ECO:0000269|PubMed:16791620, ECO:0000269|PubMed:17001303, ECO:0000269|PubMed:23979485, ECO:0000269|PubMed:8525373, ECO:0000269|PubMed:9516414}.

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 UBA2-CCL5


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 UBA2-CCL5


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 UBA2-CCL5


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 UBA2-CCL5


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource