FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

Fusion Gene Summary

leaf

Fusion Gene ORF analysis

leaf

Fusion Genomic Features

leaf

Fusion Protein Features

leaf

Fusion Gene Sequence

leaf

Fusion Gene PPI analysis

leaf

Related Drugs

leaf

Related Diseases

Fusion gene:CCL25-AR (FusionGDB2 ID:14044)

Fusion Gene Summary for CCL25-AR

check button Fusion gene summary
Fusion gene informationFusion gene name: CCL25-AR
Fusion gene ID: 14044
HgeneTgene
Gene symbol

CCL25

AR

Gene ID

6370

374

Gene nameC-C motif chemokine ligand 25amphiregulin
SynonymsCkb15|SCYA25|TECKAR|AREGB|CRDGF|SDGF
Cytomap

19p13.2

4q13.3

Type of geneprotein-codingprotein-coding
DescriptionC-C motif chemokine 25Ck beta-15TECKvarchemokine (C-C motif) ligand 25chemokine TECKsmall inducible cytokine subfamily A (Cys-Cys), member 25small-inducible cytokine A25thymus expressed chemokineamphiregulinamphiregulin Bcolorectum cell-derived growth factorschwannoma-derived growth factor
Modification date2020031320200327
UniProtAcc

O15444

ARSK

Ensembl transtripts involved in fusion geneENST00000253451, ENST00000390669, 
ENST00000315626, 
ENST00000513847, 
ENST00000374690, ENST00000504326, 
ENST00000396043, ENST00000396044, 
Fusion gene scores* DoF score1 X 1 X 1=114 X 10 X 11=1540
# samples 116
** MAII scorelog2(1/1*10)=3.32192809488736log2(16/1540*10)=-3.2667865406949
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CCL25 [Title/Abstract] AND AR [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCCL25(8127459)-AR(66764976), # samples:2
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
HgeneCCL25

GO:0001954

positive regulation of cell-matrix adhesion

18308860

HgeneCCL25

GO:0007186

G protein-coupled receptor signaling pathway

18308860

HgeneCCL25

GO:0060326

cell chemotaxis

18308860

HgeneCCL25

GO:1903237

negative regulation of leukocyte tethering or rolling

18308860

TgeneAR

GO:0007173

epidermal growth factor receptor signaling pathway

12743035

TgeneAR

GO:0007186

G protein-coupled receptor signaling pathway

12743035


check buttonFusion gene breakpoints across CCL25 (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 AR (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
ChimerDB4THYMTCGA-4V-A9QR-01ACCL25chr19

8127459

+ARchrX

66764976

+
ChimerDB4THYMTCGA-4V-A9QRCCL25chr19

8127459

+ARchrX

66764976

+


Top

Fusion Gene ORF analysis for CCL25-AR

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
3UTR-3UTRENST00000253451ENST00000513847CCL25chr19

8127459

+ARchrX

66764976

+
3UTR-3UTRENST00000390669ENST00000513847CCL25chr19

8127459

+ARchrX

66764976

+
3UTR-5UTRENST00000253451ENST00000374690CCL25chr19

8127459

+ARchrX

66764976

+
3UTR-5UTRENST00000253451ENST00000504326CCL25chr19

8127459

+ARchrX

66764976

+
3UTR-5UTRENST00000390669ENST00000374690CCL25chr19

8127459

+ARchrX

66764976

+
3UTR-5UTRENST00000390669ENST00000504326CCL25chr19

8127459

+ARchrX

66764976

+
3UTR-intronENST00000253451ENST00000396043CCL25chr19

8127459

+ARchrX

66764976

+
3UTR-intronENST00000253451ENST00000396044CCL25chr19

8127459

+ARchrX

66764976

+
3UTR-intronENST00000390669ENST00000396043CCL25chr19

8127459

+ARchrX

66764976

+
3UTR-intronENST00000390669ENST00000396044CCL25chr19

8127459

+ARchrX

66764976

+
intron-3UTRENST00000315626ENST00000513847CCL25chr19

8127459

+ARchrX

66764976

+
intron-5UTRENST00000315626ENST00000374690CCL25chr19

8127459

+ARchrX

66764976

+
intron-5UTRENST00000315626ENST00000504326CCL25chr19

8127459

+ARchrX

66764976

+
intron-intronENST00000315626ENST00000396043CCL25chr19

8127459

+ARchrX

66764976

+
intron-intronENST00000315626ENST00000396044CCL25chr19

8127459

+ARchrX

66764976

+

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

Top

Fusion Genomic Features for CCL25-AR


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.

Top

Fusion Protein Features for CCL25-AR


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/:8127459/:66764976)
- 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
CCL25

O15444

AR

ARSK

FUNCTION: Potentially involved in T-cell development. Recombinant protein shows chemotactic activity on thymocytes, macrophages, THP-1 cells, and dendritics cells but is inactive on peripheral blood lymphocytes and neutrophils. Binds to CCR9. Isoform 2 is an antagonist of isoform 1. Binds to atypical chemokine receptor ACKR4 and mediates the recruitment of beta-arrestin (ARRB1/2) to ACKR4.536

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


Top

Fusion Gene Sequence for CCL25-AR


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.

Top

Fusion Gene PPI Analysis for CCL25-AR


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


Top

Related Drugs for CCL25-AR


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

Top

Related Diseases for CCL25-AR


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