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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:CCL24-CARD8 (FusionGDB2 ID:14043)

Fusion Gene Summary for CCL24-CARD8

check button Fusion gene summary
Fusion gene informationFusion gene name: CCL24-CARD8
Fusion gene ID: 14043
HgeneTgene
Gene symbol

CCL24

CARD8

Gene ID

6369

22900

Gene nameC-C motif chemokine ligand 24caspase recruitment domain family member 8
SynonymsCkb-6|MPIF-2|MPIF2|SCYA24CARDINAL|DACAR|DAKAR|NDPP|NDPP1|TUCAN
Cytomap

7q11.23

19q13.33

Type of geneprotein-codingprotein-coding
DescriptionC-C motif chemokine 24CK-beta-6chemokine (C-C motif) ligand 24eosinophil chemotactic protein 2eotaxin-2myeloid progenitor inhibitory factor 2small inducible cytokine subfamily A (Cys-Cys), member 24small-inducible cytokine A24caspase recruitment domain-containing protein 8CARD inhibitor of NF-kappaB-activating ligandsapoptotic protein NDPP1tumor up-regulated CARD-containing antagonist of CASP9tumor up-regulated CARD-containing antagonist of caspase nine
Modification date2020031320200320
UniProtAcc

O00175

Q9Y2G2

Ensembl transtripts involved in fusion geneENST00000222902, ENST00000416943, 
ENST00000359009, ENST00000391898, 
ENST00000447740, ENST00000357778, 
ENST00000519332, ENST00000519940, 
ENST00000520007, ENST00000520015, 
ENST00000520153, ENST00000520753, 
ENST00000521613, ENST00000522431, 
ENST00000600800, 
Fusion gene scores* DoF score1 X 1 X 1=16 X 5 X 4=120
# samples 16
** MAII scorelog2(1/1*10)=3.32192809488736log2(6/120*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CCL24 [Title/Abstract] AND CARD8 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCCL24(75440504)-CARD8(48712911), # 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
HgeneCCL24

GO:0001938

positive regulation of endothelial cell proliferation

19525930

HgeneCCL24

GO:0007010

cytoskeleton organization

10072545

HgeneCCL24

GO:0008360

regulation of cell shape

10072545

HgeneCCL24

GO:0030335

positive regulation of cell migration

19525930

HgeneCCL24

GO:0030838

positive regulation of actin filament polymerization

19525930

HgeneCCL24

GO:0043547

positive regulation of GTPase activity

19525930

HgeneCCL24

GO:0048245

eosinophil chemotaxis

10072545

TgeneCARD8

GO:0031665

negative regulation of lipopolysaccharide-mediated signaling pathway

11821383

TgeneCARD8

GO:0043124

negative regulation of I-kappaB kinase/NF-kappaB signaling

11551959

TgeneCARD8

GO:0043280

positive regulation of cysteine-type endopeptidase activity involved in apoptotic process

11821383|15030775

TgeneCARD8

GO:0050713

negative regulation of interleukin-1 beta secretion

11821383

TgeneCARD8

GO:0050718

positive regulation of interleukin-1 beta secretion

15030775

TgeneCARD8

GO:0097340

inhibition of cysteine-type endopeptidase activity

11821383


check buttonFusion gene breakpoints across CCL24 (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 CARD8 (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/ABM145926CCL24chr7

75440504

+CARD8chr19

48712911

+


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Fusion Gene ORF analysis for CCL24-CARD8

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-3UTRENST00000222902ENST00000359009CCL24chr7

75440504

+CARD8chr19

48712911

+
intron-3UTRENST00000222902ENST00000391898CCL24chr7

75440504

+CARD8chr19

48712911

+
intron-3UTRENST00000222902ENST00000447740CCL24chr7

75440504

+CARD8chr19

48712911

+
intron-3UTRENST00000416943ENST00000359009CCL24chr7

75440504

+CARD8chr19

48712911

+
intron-3UTRENST00000416943ENST00000391898CCL24chr7

75440504

+CARD8chr19

48712911

+
intron-3UTRENST00000416943ENST00000447740CCL24chr7

75440504

+CARD8chr19

48712911

+
intron-intronENST00000222902ENST00000357778CCL24chr7

75440504

+CARD8chr19

48712911

+
intron-intronENST00000222902ENST00000519332CCL24chr7

75440504

+CARD8chr19

48712911

+
intron-intronENST00000222902ENST00000519940CCL24chr7

75440504

+CARD8chr19

48712911

+
intron-intronENST00000222902ENST00000520007CCL24chr7

75440504

+CARD8chr19

48712911

+
intron-intronENST00000222902ENST00000520015CCL24chr7

75440504

+CARD8chr19

48712911

+
intron-intronENST00000222902ENST00000520153CCL24chr7

75440504

+CARD8chr19

48712911

+
intron-intronENST00000222902ENST00000520753CCL24chr7

75440504

+CARD8chr19

48712911

+
intron-intronENST00000222902ENST00000521613CCL24chr7

75440504

+CARD8chr19

48712911

+
intron-intronENST00000222902ENST00000522431CCL24chr7

75440504

+CARD8chr19

48712911

+
intron-intronENST00000222902ENST00000600800CCL24chr7

75440504

+CARD8chr19

48712911

+
intron-intronENST00000416943ENST00000357778CCL24chr7

75440504

+CARD8chr19

48712911

+
intron-intronENST00000416943ENST00000519332CCL24chr7

75440504

+CARD8chr19

48712911

+
intron-intronENST00000416943ENST00000519940CCL24chr7

75440504

+CARD8chr19

48712911

+
intron-intronENST00000416943ENST00000520007CCL24chr7

75440504

+CARD8chr19

48712911

+
intron-intronENST00000416943ENST00000520015CCL24chr7

75440504

+CARD8chr19

48712911

+
intron-intronENST00000416943ENST00000520153CCL24chr7

75440504

+CARD8chr19

48712911

+
intron-intronENST00000416943ENST00000520753CCL24chr7

75440504

+CARD8chr19

48712911

+
intron-intronENST00000416943ENST00000521613CCL24chr7

75440504

+CARD8chr19

48712911

+
intron-intronENST00000416943ENST00000522431CCL24chr7

75440504

+CARD8chr19

48712911

+
intron-intronENST00000416943ENST00000600800CCL24chr7

75440504

+CARD8chr19

48712911

+

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 CCL24-CARD8


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 CCL24-CARD8


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/:75440504/:48712911)
- 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
CCL24

O00175

CARD8

Q9Y2G2

FUNCTION: Chemotactic for resting T-lymphocytes, and eosinophils. Has lower chemotactic activity for neutrophils but none for monocytes and activated lymphocytes. Is a strong suppressor of colony formation by a multipotential hematopoietic progenitor cell line. Binds to CCR3.FUNCTION: Inhibits NF-kappa-B activation. May participate in a regulatory mechanism that coordinates cellular responses controlled by NF-kappa-B transcription factor. May be a component of the inflammasome, a protein complex which also includes PYCARD, NALP2 and CASP1 and whose function would be the activation of proinflammatory caspases.

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 CCL24-CARD8


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 CCL24-CARD8


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 CCL24-CARD8


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 CCL24-CARD8


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