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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:ABHD17B-CCL25 (FusionGDB2 ID:405)

Fusion Gene Summary for ABHD17B-CCL25

check button Fusion gene summary
Fusion gene informationFusion gene name: ABHD17B-CCL25
Fusion gene ID: 405
HgeneTgene
Gene symbol

ABHD17B

CCL25

Gene ID

51104

6370

Gene nameabhydrolase domain containing 17B, depalmitoylaseC-C motif chemokine ligand 25
SynonymsC9orf77|CGI-67|FAM108B1Ckb15|SCYA25|TECK
Cytomap

9q21.13

19p13.2

Type of geneprotein-codingprotein-coding
Descriptionalpha/beta hydrolase domain-containing protein 17Babhydrolase domain containing 17Babhydrolase domain-containing protein 17Babhydrolase domain-containing protein FAM108B1epididymis secretory sperm binding proteinfamily with sequence similarity 108, mC-C motif chemokine 25Ck beta-15TECKvarchemokine (C-C motif) ligand 25chemokine TECKsmall inducible cytokine subfamily A (Cys-Cys), member 25small-inducible cytokine A25thymus expressed chemokine
Modification date2020031320200313
UniProtAcc

Q5VST6

O15444

Ensembl transtripts involved in fusion geneENST00000333421, ENST00000377041, 
ENST00000253451, ENST00000315626, 
ENST00000390669, 
Fusion gene scores* DoF score3 X 3 X 4=361 X 2 X 1=2
# samples 62
** MAII scorelog2(6/36*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(2/2*10)=3.32192809488736
Context

PubMed: ABHD17B [Title/Abstract] AND CCL25 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointABHD17B(74525550)-CCL25(8117884), # samples:1
ABHD17B(74525550)-CCL25(8117648), # 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
TgeneCCL25

GO:0001954

positive regulation of cell-matrix adhesion

18308860

TgeneCCL25

GO:0007186

G protein-coupled receptor signaling pathway

18308860

TgeneCCL25

GO:0060326

cell chemotaxis

18308860

TgeneCCL25

GO:1903237

negative regulation of leukocyte tethering or rolling

18308860


check buttonFusion gene breakpoints across ABHD17B (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 CCL25 (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
ChimerDB4PRADTCGA-XJ-A9DX-01AABHD17Bchr9

74525550

-CCL25chr19

8117884

+
ChimerDB4PRADTCGA-XJ-A9DXABHD17Bchr9

74525550

-CCL25chr19

8117648

+


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Fusion Gene ORF analysis for ABHD17B-CCL25

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
5UTR-3CDSENST00000333421ENST00000253451ABHD17Bchr9

74525550

-CCL25chr19

8117648

+
5UTR-3CDSENST00000377041ENST00000253451ABHD17Bchr9

74525550

-CCL25chr19

8117648

+
5UTR-5UTRENST00000333421ENST00000253451ABHD17Bchr9

74525550

-CCL25chr19

8117884

+
5UTR-5UTRENST00000333421ENST00000315626ABHD17Bchr9

74525550

-CCL25chr19

8117884

+
5UTR-5UTRENST00000333421ENST00000390669ABHD17Bchr9

74525550

-CCL25chr19

8117884

+
5UTR-5UTRENST00000377041ENST00000253451ABHD17Bchr9

74525550

-CCL25chr19

8117884

+
5UTR-5UTRENST00000377041ENST00000315626ABHD17Bchr9

74525550

-CCL25chr19

8117884

+
5UTR-5UTRENST00000377041ENST00000390669ABHD17Bchr9

74525550

-CCL25chr19

8117884

+
5UTR-intronENST00000333421ENST00000315626ABHD17Bchr9

74525550

-CCL25chr19

8117648

+
5UTR-intronENST00000333421ENST00000390669ABHD17Bchr9

74525550

-CCL25chr19

8117648

+
5UTR-intronENST00000377041ENST00000315626ABHD17Bchr9

74525550

-CCL25chr19

8117648

+
5UTR-intronENST00000377041ENST00000390669ABHD17Bchr9

74525550

-CCL25chr19

8117648

+

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 ABHD17B-CCL25


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)
ABHD17Bchr974525549-CCL25chr198117650+1.69E-060.99999833
ABHD17Bchr974525549-CCL25chr198117883+1.12E-091
ABHD17Bchr974525549-CCL25chr198117650+1.69E-060.99999833
ABHD17Bchr974525549-CCL25chr198117883+1.12E-091

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.
genomic feature of top 1%

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Fusion Protein Features for ABHD17B-CCL25


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/:74525550/:8117884)
- 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
ABHD17B

Q5VST6

CCL25

O15444

FUNCTION: Hydrolyzes fatty acids from S-acylated cysteine residues in proteins (PubMed:26701913). Has depalmitoylating activity towards DLG4/PSD95 (PubMed:26701913). Has depalmitoylating activity towards GAP43 (By similarity). Has depalmitoylating activity towards MAP6 (By similarity). Has depalmitoylating activity towards NRAS (PubMed:26701913). {ECO:0000250|UniProtKB:Q7M759, ECO:0000269|PubMed:26701913}.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.

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 ABHD17B-CCL25


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 ABHD17B-CCL25


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 ABHD17B-CCL25


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 ABHD17B-CCL25


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