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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:COX11-JAM2 (FusionGDB2 ID:18755)

Fusion Gene Summary for COX11-JAM2

check button Fusion gene summary
Fusion gene informationFusion gene name: COX11-JAM2
Fusion gene ID: 18755
HgeneTgene
Gene symbol

COX11

JAM2

Gene ID

1353

58494

Gene namecytochrome c oxidase copper chaperone COX11junctional adhesion molecule 2
SynonymsCOX11PC21orf43|CD322|JAM-B|JAMB|PRO245|VE-JAM|VEJAM
Cytomap

17q22

21q21.3

Type of geneprotein-codingprotein-coding
Descriptioncytochrome c oxidase assembly protein COX11, mitochondrialCOX11 homolog, cytochrome c oxidase assembly proteinCOX11, cytochrome c oxidase copper chaperonecytochrome c oxidase subunit 11junctional adhesion molecule BJAM-2JAM-IT/VE-JAMvascular endothelial junction-associated molecule
Modification date2020031320200313
UniProtAcc.

P57087

Ensembl transtripts involved in fusion geneENST00000299335, ENST00000571584, 
ENST00000573912, 
ENST00000312957, 
ENST00000400532, ENST00000425221, 
ENST00000477351, ENST00000480456, 
Fusion gene scores* DoF score2 X 2 X 1=48 X 8 X 4=256
# samples 29
** MAII scorelog2(2/4*10)=2.32192809488736log2(9/256*10)=-1.50814690367033
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: COX11 [Title/Abstract] AND JAM2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCOX11(53038572)-JAM2(26986737), # 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
HgeneCOX11

GO:0055065

metal ion homeostasis

15840172

TgeneJAM2

GO:0045123

cellular extravasation

12239159

TgeneJAM2

GO:0050901

leukocyte tethering or rolling

19740376

TgeneJAM2

GO:0071593

lymphocyte aggregation

11823489

TgeneJAM2

GO:2000403

positive regulation of lymphocyte migration

12239159


check buttonFusion gene breakpoints across COX11 (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 JAM2 (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/ABF246394COX11chr17

53038572

-JAM2chr21

26986737

+


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Fusion Gene ORF analysis for COX11-JAM2

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-intronENST00000299335ENST00000312957COX11chr17

53038572

-JAM2chr21

26986737

+
5CDS-intronENST00000299335ENST00000400532COX11chr17

53038572

-JAM2chr21

26986737

+
5CDS-intronENST00000299335ENST00000425221COX11chr17

53038572

-JAM2chr21

26986737

+
5CDS-intronENST00000299335ENST00000477351COX11chr17

53038572

-JAM2chr21

26986737

+
5CDS-intronENST00000299335ENST00000480456COX11chr17

53038572

-JAM2chr21

26986737

+
intron-intronENST00000571584ENST00000312957COX11chr17

53038572

-JAM2chr21

26986737

+
intron-intronENST00000571584ENST00000400532COX11chr17

53038572

-JAM2chr21

26986737

+
intron-intronENST00000571584ENST00000425221COX11chr17

53038572

-JAM2chr21

26986737

+
intron-intronENST00000571584ENST00000477351COX11chr17

53038572

-JAM2chr21

26986737

+
intron-intronENST00000571584ENST00000480456COX11chr17

53038572

-JAM2chr21

26986737

+
intron-intronENST00000573912ENST00000312957COX11chr17

53038572

-JAM2chr21

26986737

+
intron-intronENST00000573912ENST00000400532COX11chr17

53038572

-JAM2chr21

26986737

+
intron-intronENST00000573912ENST00000425221COX11chr17

53038572

-JAM2chr21

26986737

+
intron-intronENST00000573912ENST00000477351COX11chr17

53038572

-JAM2chr21

26986737

+
intron-intronENST00000573912ENST00000480456COX11chr17

53038572

-JAM2chr21

26986737

+

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 COX11-JAM2


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 COX11-JAM2


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/:53038572/:26986737)
- 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
.JAM2

P57087

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: Junctional adhesion protein that mediates heterotypic cell-cell interactions with its cognate receptor JAM3 to regulate different cellular processes (PubMed:11590146, PubMed:11823489, PubMed:24357068). Plays a role in homing and mobilization of hematopoietic stem and progenitor cells within the bone marrow (PubMed:24357068). At the surface of bone marrow stromal cells, it contributes to the retention of the hematopoietic stem and progenitor cells expressing JAM3 (PubMed:11590146, PubMed:24357068). Plays a central role in leukocytes extravasation by facilitating not only transmigration but also tethering and rolling of leukocytes along the endothelium (PubMed:12239159). Tethering and rolling of leukocytes are dependent on the binding by JAM2 of the integrin alpha-4/beta-1 (PubMed:12070135). Plays a role in spermatogenesis where JAM2 and JAM3, which are respectively expressed by Sertoli and germ cells, mediate an interaction between both cell types and play an essential role in the anchorage of germ cells onto Sertoli cells and the assembly of cell polarity complexes during spermatid differentiation (By similarity). Also functions as an inhibitory somatodendritic cue that prevents the myelination of non-axonal parts of neurons (By similarity). During myogenesis, it is involved in myocyte fusion (By similarity). May also play a role in angiogenesis (By similarity). {ECO:0000250|UniProtKB:A0A0R4IGV4, ECO:0000250|UniProtKB:Q9JI59, ECO:0000269|PubMed:11590146, ECO:0000269|PubMed:11823489, ECO:0000269|PubMed:12070135, ECO:0000269|PubMed:12239159, ECO:0000269|PubMed:24357068}.

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 COX11-JAM2


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 COX11-JAM2


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 COX11-JAM2


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 COX11-JAM2


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