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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:CCL5-ZAP70 (FusionGDB2 ID:HG6352TG7535)

Fusion Gene Summary for CCL5-ZAP70

check button Fusion gene summary
Fusion gene informationFusion gene name: CCL5-ZAP70
Fusion gene ID: hg6352tg7535
HgeneTgene
Gene symbol

CCL5

ZAP70

Gene ID

6352

7535

Gene nameC-C motif chemokine ligand 5zeta chain of T cell receptor associated protein kinase 70
SynonymsD17S136E|RANTES|SCYA5|SIS-delta|SISd|TCP228|eoCPADMIO2|IMD48|SRK|STCD|STD|TZK|ZAP-70
Cytomap('CCL5')('ZAP70')

17q12

2q11.2

Type of geneprotein-codingprotein-coding
DescriptionC-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)tyrosine-protein kinase ZAP-7070 kDa zeta-associated protein70 kDa zeta-chain associated proteinsyk-related tyrosine kinasezeta chain of T cell receptor associated protein kinase 70kDazeta-chain (TCR) associated protein kinase 70kDazeta-chain associ
Modification date2020031320200327
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000293272, ENST00000366113, 
Fusion gene scores* DoF score1 X 1 X 1=12 X 2 X 2=8
# samples 12
** MAII scorelog2(1/1*10)=3.32192809488736log2(2/8*10)=1.32192809488736
Context

PubMed: CCL5 [Title/Abstract] AND ZAP70 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCCL5(34206530)-ZAP70(98351769), # 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
HgeneCCL5

GO:0006816

calcium ion transport

10734056

HgeneCCL5

GO:0006874

cellular calcium ion homeostasis

10734056

HgeneCCL5

GO:0006887

exocytosis

10734056

HgeneCCL5

GO:0006954

inflammatory response

21147091

HgeneCCL5

GO:0007159

leukocyte cell-cell adhesion

8558019

HgeneCCL5

GO:0007186

G protein-coupled receptor signaling pathway

17001303|23979485

HgeneCCL5

GO:0007267

cell-cell signaling

8558019

HgeneCCL5

GO:0009636

response to toxic substance

10841574

HgeneCCL5

GO:0010759

positive regulation of macrophage chemotaxis

16778803

HgeneCCL5

GO:0010820

positive regulation of T cell chemotaxis

1699135|7544376|16778803|18337562

HgeneCCL5

GO:0014068

positive regulation of phosphatidylinositol 3-kinase signaling

7544376

HgeneCCL5

GO:0014911

positive regulation of smooth muscle cell migration

21297082

HgeneCCL5

GO:0030335

positive regulation of cell migration

7545673

HgeneCCL5

GO:0031328

positive regulation of cellular biosynthetic process

18337562

HgeneCCL5

GO:0031584

activation of phospholipase D activity

9469451

HgeneCCL5

GO:0031663

lipopolysaccharide-mediated signaling pathway

21147091

HgeneCCL5

GO:0033634

positive regulation of cell-cell adhesion mediated by integrin

8558019

HgeneCCL5

GO:0034112

positive regulation of homotypic cell-cell adhesion

10488085

HgeneCCL5

GO:0042102

positive regulation of T cell proliferation

18832695

HgeneCCL5

GO:0042119

neutrophil activation

10488085

HgeneCCL5

GO:0042327

positive regulation of phosphorylation

18337562

HgeneCCL5

GO:0042531

positive regulation of tyrosine phosphorylation of STAT protein

9417081

HgeneCCL5

GO:0043922

negative regulation by host of viral transcription

10841574

HgeneCCL5

GO:0045071

negative regulation of viral genome replication

10490959

HgeneCCL5

GO:0045744

negative regulation of G protein-coupled receptor signaling pathway

10734056

HgeneCCL5

GO:0045785

positive regulation of cell adhesion

10910894

HgeneCCL5

GO:0048245

eosinophil chemotaxis

16778803

HgeneCCL5

GO:0048661

positive regulation of smooth muscle cell proliferation

21297082

HgeneCCL5

GO:0050796

regulation of insulin secretion

23979485

HgeneCCL5

GO:0050863

regulation of T cell activation

10488085

HgeneCCL5

GO:0051928

positive regulation of calcium ion transport

8699119

HgeneCCL5

GO:0070098

chemokine-mediated signaling pathway

17001303

HgeneCCL5

GO:0070233

negative regulation of T cell apoptotic process

10488085

HgeneCCL5

GO:0070234

positive regulation of T cell apoptotic process

10488085

HgeneCCL5

GO:0071407

cellular response to organic cyclic compound

21147091

HgeneCCL5

GO:0090026

positive regulation of monocyte chemotaxis

1699135|19779041

HgeneCCL5

GO:1901214

regulation of neuron death

17001303

HgeneCCL5

GO:2000406

positive regulation of T cell migration

23620790

HgeneCCL5

GO:2000503

positive regulation of natural killer cell chemotaxis

7545673

TgeneZAP70

GO:0006468

protein phosphorylation

12447358

TgeneZAP70

GO:0006955

immune response

1423621

TgeneZAP70

GO:0018108

peptidyl-tyrosine phosphorylation

22732588

TgeneZAP70

GO:0045059

positive thymic T cell selection

7630421

TgeneZAP70

GO:0045582

positive regulation of T cell differentiation

7630421



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/AAG266142CCL5chr17

34206530

-ZAP70chr2

98351769

+


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Fusion Gene ORF analysis for CCL5-ZAP70

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-3CDSENST00000293272ENST00000264972CCL5chr17

34206530

-ZAP70chr2

98351769

+
intron-3CDSENST00000366113ENST00000264972CCL5chr17

34206530

-ZAP70chr2

98351769

+
intron-3UTRENST00000293272ENST00000442208CCL5chr17

34206530

-ZAP70chr2

98351769

+
intron-3UTRENST00000293272ENST00000451498CCL5chr17

34206530

-ZAP70chr2

98351769

+
intron-3UTRENST00000293272ENST00000463643CCL5chr17

34206530

-ZAP70chr2

98351769

+
intron-3UTRENST00000366113ENST00000442208CCL5chr17

34206530

-ZAP70chr2

98351769

+
intron-3UTRENST00000366113ENST00000451498CCL5chr17

34206530

-ZAP70chr2

98351769

+
intron-3UTRENST00000366113ENST00000463643CCL5chr17

34206530

-ZAP70chr2

98351769

+

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 CCL5-ZAP70


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)


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Fusion Protein Features for CCL5-ZAP70


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/:34206530/:98351769)
- 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
..
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: 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}.

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 CCL5-ZAP70


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 CCL5-ZAP70


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 CCL5-ZAP70


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 CCL5-ZAP70


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCCL5C0004096Asthma1CTD_human
HgeneCCL5C0008312Primary biliary cirrhosis1CTD_human
HgeneCCL5C0011615Dermatitis, Atopic1CTD_human
HgeneCCL5C0017658Glomerulonephritis1CTD_human
HgeneCCL5C0019187Hepatitis, Alcoholic1CTD_human
HgeneCCL5C0020500Hyperoxaluria1CTD_human
HgeneCCL5C0023892Biliary cirrhosis1CTD_human
HgeneCCL5C0023893Liver Cirrhosis, Experimental1CTD_human
HgeneCCL5C0027626Neoplasm Invasiveness1CTD_human
HgeneCCL5C0034069Pulmonary Fibrosis1CTD_human
HgeneCCL5C0086196Eczema, Infantile1CTD_human
HgeneCCL5C0238065Secondary Biliary Cholangitis1CTD_human
HgeneCCL5C0241910Autoimmune Chronic Hepatitis1CTD_human
HgeneCCL5C0345967Malignant mesothelioma1CTD_human
HgeneCCL5C0524610Chronic Alcoholic Hepatitis1CTD_human
HgeneCCL5C1298681Oxalosis1CTD_human
HgeneCCL5C1704377Bright Disease1CTD_human
HgeneCCL5C4551595Biliary Cirrhosis, Primary, 11CTD_human
HgeneCCL5C4721507Alveolitis, Fibrosing1CTD_human
TgeneC2931299ZAP70 deficiency5CTD_human;GENOMICS_ENGLAND;UNIPROT
TgeneC0085110Severe Combined Immunodeficiency2CTD_human;GENOMICS_ENGLAND
TgeneC4310768AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 22CTD_human;GENOMICS_ENGLAND;UNIPROT
TgeneC0003257Antibody Deficiency Syndrome1CTD_human
TgeneC0021051Immunologic Deficiency Syndromes1CTD_human
TgeneC0242583Bare Lymphocyte Syndrome1CTD_human
TgeneC0700216Structural Clinical Interview for DSM-III1GENOMICS_ENGLAND
TgeneC2700553Omenn Syndrome1CTD_human
TgeneC2931320T cell immunodeficiency primary1CTD_human