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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:ECD-CXCL12 (FusionGDB2 ID:24842)

Fusion Gene Summary for ECD-CXCL12

check button Fusion gene summary
Fusion gene informationFusion gene name: ECD-CXCL12
Fusion gene ID: 24842
HgeneTgene
Gene symbol

ECD

CXCL12

Gene ID

11319

6387

Gene nameecdysoneless cell cycle regulatorC-X-C motif chemokine ligand 12
SynonymsGCR2|HSGT1|SGT1IRH|PBSF|SCYB12|SDF1|TLSF|TPAR1
Cytomap

10q22.2

10q11.21

Type of geneprotein-codingprotein-coding
Descriptionprotein ecdysoneless homologecdysoneless homologhuman suppressor of GCR twoprotein SGT1suppressor of GCR2suppressor of S. cerevisiae gcr2stromal cell-derived factor 1chemokine (C-X-C motif) ligand 12intercrine reduced in hepatomaspre-B cell growth-stimulating factor
Modification date2020031320200313
UniProtAcc.

P48061

Ensembl transtripts involved in fusion geneENST00000372979, ENST00000430082, 
ENST00000454759, ENST00000610256, 
ENST00000343575, ENST00000374426, 
ENST00000374429, ENST00000395793, 
ENST00000395794, ENST00000496375, 
ENST00000395795, 
Fusion gene scores* DoF score7 X 5 X 5=1756 X 4 X 4=96
# samples 76
** MAII scorelog2(7/175*10)=-1.32192809488736
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/96*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ECD [Title/Abstract] AND CXCL12 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointECD(74923491)-CXCL12(44793345), # samples:1
Anticipated loss of major functional domain due to fusion event.ECD-CXCL12 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
ECD-CXCL12 seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor due to the frame-shifted ORF.
* 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
HgeneECD

GO:0045944

positive regulation of transcription by RNA polymerase II

19919181

TgeneCXCL12

GO:0033622

integrin activation

29301984

TgeneCXCL12

GO:0045785

positive regulation of cell adhesion

23620790

TgeneCXCL12

GO:0060326

cell chemotaxis

18308860

TgeneCXCL12

GO:0070098

chemokine-mediated signaling pathway

20388803

TgeneCXCL12

GO:0090026

positive regulation of monocyte chemotaxis

18802065

TgeneCXCL12

GO:1902230

negative regulation of intrinsic apoptotic signaling pathway in response to DNA damage

20388803

TgeneCXCL12

GO:1903237

negative regulation of leukocyte tethering or rolling

18308860

TgeneCXCL12

GO:2000406

positive regulation of T cell migration

23620790

TgeneCXCL12

GO:2000669

negative regulation of dendritic cell apoptotic process

15059845


check buttonFusion gene breakpoints across ECD (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 CXCL12 (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
ChimerDB4BRCATCGA-E2-A1LA-01AECDchr10

74923491

-CXCL12chr10

44793345

-


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Fusion Gene ORF analysis for ECD-CXCL12

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
5CDS-intronENST00000372979ENST00000343575ECDchr10

74923491

-CXCL12chr10

44793345

-
5CDS-intronENST00000372979ENST00000374426ECDchr10

74923491

-CXCL12chr10

44793345

-
5CDS-intronENST00000372979ENST00000374429ECDchr10

74923491

-CXCL12chr10

44793345

-
5CDS-intronENST00000372979ENST00000395793ECDchr10

74923491

-CXCL12chr10

44793345

-
5CDS-intronENST00000372979ENST00000395794ECDchr10

74923491

-CXCL12chr10

44793345

-
5CDS-intronENST00000372979ENST00000496375ECDchr10

74923491

-CXCL12chr10

44793345

-
5CDS-intronENST00000430082ENST00000343575ECDchr10

74923491

-CXCL12chr10

44793345

-
5CDS-intronENST00000430082ENST00000374426ECDchr10

74923491

-CXCL12chr10

44793345

-
5CDS-intronENST00000430082ENST00000374429ECDchr10

74923491

-CXCL12chr10

44793345

-
5CDS-intronENST00000430082ENST00000395793ECDchr10

74923491

-CXCL12chr10

44793345

-
5CDS-intronENST00000430082ENST00000395794ECDchr10

74923491

-CXCL12chr10

44793345

-
5CDS-intronENST00000430082ENST00000496375ECDchr10

74923491

-CXCL12chr10

44793345

-
5CDS-intronENST00000454759ENST00000343575ECDchr10

74923491

-CXCL12chr10

44793345

-
5CDS-intronENST00000454759ENST00000374426ECDchr10

74923491

-CXCL12chr10

44793345

-
5CDS-intronENST00000454759ENST00000374429ECDchr10

74923491

-CXCL12chr10

44793345

-
5CDS-intronENST00000454759ENST00000395793ECDchr10

74923491

-CXCL12chr10

44793345

-
5CDS-intronENST00000454759ENST00000395794ECDchr10

74923491

-CXCL12chr10

44793345

-
5CDS-intronENST00000454759ENST00000496375ECDchr10

74923491

-CXCL12chr10

44793345

-
5UTR-3CDSENST00000610256ENST00000395795ECDchr10

74923491

-CXCL12chr10

44793345

-
5UTR-intronENST00000610256ENST00000343575ECDchr10

74923491

-CXCL12chr10

44793345

-
5UTR-intronENST00000610256ENST00000374426ECDchr10

74923491

-CXCL12chr10

44793345

-
5UTR-intronENST00000610256ENST00000374429ECDchr10

74923491

-CXCL12chr10

44793345

-
5UTR-intronENST00000610256ENST00000395793ECDchr10

74923491

-CXCL12chr10

44793345

-
5UTR-intronENST00000610256ENST00000395794ECDchr10

74923491

-CXCL12chr10

44793345

-
5UTR-intronENST00000610256ENST00000496375ECDchr10

74923491

-CXCL12chr10

44793345

-
Frame-shiftENST00000372979ENST00000395795ECDchr10

74923491

-CXCL12chr10

44793345

-
Frame-shiftENST00000430082ENST00000395795ECDchr10

74923491

-CXCL12chr10

44793345

-
Frame-shiftENST00000454759ENST00000395795ECDchr10

74923491

-CXCL12chr10

44793345

-

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 ECD-CXCL12


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 ECD-CXCL12


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/:74923491/:44793345)
- 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
.CXCL12

P48061

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 active on T-lymphocytes and monocytes but not neutrophils. Activates the C-X-C chemokine receptor CXCR4 to induce a rapid and transient rise in the level of intracellular calcium ions and chemotaxis. SDF-1-beta(3-72) and SDF-1-alpha(3-67) show a reduced chemotactic activity. Binding to cell surface proteoglycans seems to inhibit formation of SDF-1-alpha(3-67) and thus to preserve activity on local sites. Also binds to atypical chemokine receptor ACKR3, which activates the beta-arrestin pathway and acts as a scavenger receptor for SDF-1. Binds to the allosteric site (site 2) of integrins and activates integrins ITGAV:ITGB3, ITGA4:ITGB1 and ITGA5:ITGB1 in a CXCR4-independent manner (PubMed:29301984). Acts as a positive regulator of monocyte migration and a negative regulator of monocyte adhesion via the LYN kinase. Stimulates migration of monocytes and T-lymphocytes through its receptors, CXCR4 and ACKR3, and decreases monocyte adherence to surfaces coated with ICAM-1, a ligand for beta-2 integrins. SDF1A/CXCR4 signaling axis inhibits beta-2 integrin LFA-1 mediated adhesion of monocytes to ICAM-1 through LYN kinase. Inhibits CXCR4-mediated infection by T-cell line-adapted HIV-1. Plays a protective role after myocardial infarction. Induces down-regulation and internalization of ACKR3 expressed in various cells. Has several critical functions during embryonic development; required for B-cell lymphopoiesis, myelopoiesis in bone marrow and heart ventricular septum formation. Stimulates the proliferation of bone marrow-derived B-cell progenitors in the presence of IL7 as well as growth of stromal cell-dependent pre-B-cells (By similarity). {ECO:0000250|UniProtKB:P40224, ECO:0000269|PubMed:11069075, ECO:0000269|PubMed:11859124, ECO:0000269|PubMed:16107333, ECO:0000269|PubMed:18802065, ECO:0000269|PubMed:19255243, ECO:0000269|PubMed:29301984, ECO:0000269|PubMed:8752281}.

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 ECD-CXCL12


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 ECD-CXCL12


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 ECD-CXCL12


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 ECD-CXCL12


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