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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:AKAP10-CCL3 (FusionGDB2 ID:3386)

Fusion Gene Summary for AKAP10-CCL3

check button Fusion gene summary
Fusion gene informationFusion gene name: AKAP10-CCL3
Fusion gene ID: 3386
HgeneTgene
Gene symbol

AKAP10

CCL3

Gene ID

11216

6348

Gene nameA-kinase anchoring protein 10C-C motif chemokine ligand 3
SynonymsAKAP-10|D-AKAP-2|D-AKAP2|PRKA10G0S19-1|LD78ALPHA|MIP-1-alpha|MIP1A|SCYA3
Cytomap

17p11.2

17q12

Type of geneprotein-codingprotein-coding
DescriptionA-kinase anchor protein 10, mitochondrialA kinase (PRKA) anchor protein 10A kinase anchor protein 10dual specificity A kinase-anchoring protein 2mitochondrial A kinase PPKA anchor protein 10protein kinase A anchoring protein 10C-C motif chemokine 3G0/G1 switch regulatory protein 19-1PAT 464.1SIS-betachemokine (C-C motif) ligand 3macrophage inflammatory protein 1-alphasmall inducible cytokine A3 (homologous to mouse Mip-1a)tonsillar lymphocyte LD78 alpha protein
Modification date2020031320200322
UniProtAcc.

P10147

Ensembl transtripts involved in fusion geneENST00000225737, ENST00000395536, 
ENST00000572155, 
ENST00000225245, 
Fusion gene scores* DoF score6 X 6 X 4=1441 X 1 X 1=1
# samples 61
** MAII scorelog2(6/144*10)=-1.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Context

PubMed: AKAP10 [Title/Abstract] AND CCL3 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointAKAP10(19880905)-CCL3(34416643), # samples:2
Anticipated loss of major functional domain due to fusion event.AKAP10-CCL3 seems lost the major protein functional domain in Hgene partner, which is a essential gene 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
TgeneCCL3

GO:0001775

cell activation

10706735

TgeneCCL3

GO:0002548

monocyte chemotaxis

10706735

TgeneCCL3

GO:0006816

calcium ion transport

10734056

TgeneCCL3

GO:0006874

cellular calcium ion homeostasis

10072545|10734056|21403648

TgeneCCL3

GO:0006887

exocytosis

10734056

TgeneCCL3

GO:0006935

chemotaxis

10679098

TgeneCCL3

GO:0006954

inflammatory response

10679098|10706735|21147091

TgeneCCL3

GO:0007010

cytoskeleton organization

10072545

TgeneCCL3

GO:0007267

cell-cell signaling

10679098

TgeneCCL3

GO:0008360

regulation of cell shape

10072545

TgeneCCL3

GO:0009636

response to toxic substance

10841574

TgeneCCL3

GO:0010628

positive regulation of gene expression

10706735

TgeneCCL3

GO:0010629

negative regulation of gene expression

21403648

TgeneCCL3

GO:0010818

T cell chemotaxis

10706735

TgeneCCL3

GO:0014808

release of sequestered calcium ion into cytosol by sarcoplasmic reticulum

19523456

TgeneCCL3

GO:0019722

calcium-mediated signaling

10072545|19523456

TgeneCCL3

GO:0030335

positive regulation of cell migration

7545673|10706735

TgeneCCL3

GO:0030502

negative regulation of bone mineralization

21403648

TgeneCCL3

GO:0030593

neutrophil chemotaxis

10706735

TgeneCCL3

GO:0031663

lipopolysaccharide-mediated signaling pathway

21147091

TgeneCCL3

GO:0043308

eosinophil degranulation

10706735

TgeneCCL3

GO:0043922

negative regulation by host of viral transcription

10841574

TgeneCCL3

GO:0045671

negative regulation of osteoclast differentiation

21403648

TgeneCCL3

GO:0048245

eosinophil chemotaxis

10072545

TgeneCCL3

GO:0048247

lymphocyte chemotaxis

10706735

TgeneCCL3

GO:0050795

regulation of behavior

20167378

TgeneCCL3

GO:0051928

positive regulation of calcium ion transport

8699119|15764707

TgeneCCL3

GO:0051930

regulation of sensory perception of pain

15764707

TgeneCCL3

GO:0070374

positive regulation of ERK1 and ERK2 cascade

21403648

TgeneCCL3

GO:0070723

response to cholesterol

19523456

TgeneCCL3

GO:0071407

cellular response to organic cyclic compound

21147091

TgeneCCL3

GO:0071621

granulocyte chemotaxis

10706735

TgeneCCL3

GO:2000503

positive regulation of natural killer cell chemotaxis

7545673


check buttonFusion gene breakpoints across AKAP10 (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 CCL3 (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
ChimerDB4SARCTCGA-FX-A3TO-01AAKAP10chr17

19880905

-CCL3chr17

34416643

-
ChimerDB4SARCTCGA-FX-A3TO-01AAKAP10chr17

19880905

-CCL3chr17

34416643

-


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Fusion Gene ORF analysis for AKAP10-CCL3

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
Frame-shiftENST00000225737ENST00000225245AKAP10chr17

19880905

-CCL3chr17

34416643

-
Frame-shiftENST00000395536ENST00000225245AKAP10chr17

19880905

-CCL3chr17

34416643

-
intron-3CDSENST00000572155ENST00000225245AKAP10chr17

19880905

-CCL3chr17

34416643

-

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 AKAP10-CCL3


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 AKAP10-CCL3


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
.CCL3

P10147

FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: Monokine with inflammatory and chemokinetic properties. Binds to CCR1, CCR4 and CCR5. One of the major HIV-suppressive factors produced by CD8+ T-cells. Recombinant MIP-1-alpha induces a dose-dependent inhibition of different strains of HIV-1, HIV-2, and simian immunodeficiency virus (SIV). {ECO:0000269|PubMed:8525373}.

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 AKAP10-CCL3


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 AKAP10-CCL3


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 AKAP10-CCL3


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 AKAP10-CCL3


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneAKAP10C0005586Bipolar Disorder1PSYGENET
TgeneCCL3C0007786Brain Ischemia2CTD_human
TgeneCCL3C0020517Hypersensitivity2CTD_human
TgeneCCL3C0034069Pulmonary Fibrosis2CTD_human
TgeneCCL3C0917798Cerebral Ischemia2CTD_human
TgeneCCL3C1527304Allergic Reaction2CTD_human
TgeneCCL3C4721507Alveolitis, Fibrosing2CTD_human
TgeneCCL3C0004153Atherosclerosis1CTD_human
TgeneCCL3C0017658Glomerulonephritis1CTD_human
TgeneCCL3C0021368Inflammation1CTD_human
TgeneCCL3C0035126Reperfusion Injury1CTD_human
TgeneCCL3C0038220Status Epilepticus1CTD_human
TgeneCCL3C0151744Myocardial Ischemia1CTD_human
TgeneCCL3C0270823Petit mal status1CTD_human
TgeneCCL3C0273115Lung Injury1CTD_human
TgeneCCL3C0311335Grand Mal Status Epilepticus1CTD_human
TgeneCCL3C0345967Malignant mesothelioma1CTD_human
TgeneCCL3C0393734Complex Partial Status Epilepticus1CTD_human
TgeneCCL3C0751522Status Epilepticus, Subclinical1CTD_human
TgeneCCL3C0751523Non-Convulsive Status Epilepticus1CTD_human
TgeneCCL3C0751524Simple Partial Status Epilepticus1CTD_human
TgeneCCL3C1563937Atherogenesis1CTD_human
TgeneCCL3C1704377Bright Disease1CTD_human
TgeneCCL3C2239176Liver carcinoma1CTD_human
TgeneCCL3C2350344Chronic Lung Injury1CTD_human