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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:JUP-CAMTA2 (FusionGDB2 ID:40875)

Fusion Gene Summary for JUP-CAMTA2

check button Fusion gene summary
Fusion gene informationFusion gene name: JUP-CAMTA2
Fusion gene ID: 40875
HgeneTgene
Gene symbol

JUP

CAMTA2

Gene ID

3728

23125

Gene namejunction plakoglobincalmodulin binding transcription activator 2
SynonymsCTNNG|DP3|DPIII|PDGB|PKGB-
Cytomap

17q21.2

17p13.2

Type of geneprotein-codingprotein-coding
Descriptionjunction plakoglobincatenin (cadherin-associated protein), gamma 80kDadesmoplakin IIIdesmoplakin-3calmodulin-binding transcription activator 2
Modification date2020031320200313
UniProtAcc

P14923

O94983

Ensembl transtripts involved in fusion geneENST00000540235, ENST00000393930, 
ENST00000393931, ENST00000310706, 
ENST00000358183, ENST00000414043, 
ENST00000361571, ENST00000572543, 
ENST00000381311, ENST00000348066, 
ENST00000571831, 
Fusion gene scores* DoF score22 X 25 X 12=66005 X 4 X 4=80
# samples 326
** MAII scorelog2(32/6600*10)=-4.36632221424582
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/80*10)=-0.415037499278844
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: JUP [Title/Abstract] AND CAMTA2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointJUP(39919235)-CAMTA2(4885455), # samples:1
Anticipated loss of major functional domain due to fusion event.JUP-CAMTA2 seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
JUP-CAMTA2 seems lost the major protein functional domain in Tgene partner, which is a transcription factor due to the frame-shifted ORF.
JUP-CAMTA2 seems lost the major protein functional domain in Tgene 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
HgeneJUP

GO:0002159

desmosome assembly

22889254

HgeneJUP

GO:0042127

regulation of cell proliferation

17924338

HgeneJUP

GO:0042307

positive regulation of protein import into nucleus

10825188|14661054

HgeneJUP

GO:0050982

detection of mechanical stimulus

18937352

HgeneJUP

GO:0051091

positive regulation of DNA-binding transcription factor activity

14661054

HgeneJUP

GO:0071681

cellular response to indole-3-methanol

10868478

HgeneJUP

GO:0098609

cell-cell adhesion

18937352

TgeneCAMTA2

GO:0006357

regulation of transcription by RNA polymerase II

16678093

TgeneCAMTA2

GO:0014898

cardiac muscle hypertrophy in response to stress

16678093


check buttonFusion gene breakpoints across JUP (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 CAMTA2 (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
ChimerDB4UCECTCGA-AP-A0LI-01AJUPchr17

39919235

-CAMTA2chr17

4885455

-


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Fusion Gene ORF analysis for JUP-CAMTA2

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-3CDSENST00000540235ENST00000358183JUPchr17

39919235

-CAMTA2chr17

4885455

-
intron-3CDSENST00000540235ENST00000414043JUPchr17

39919235

-CAMTA2chr17

4885455

-
intron-intronENST00000540235ENST00000361571JUPchr17

39919235

-CAMTA2chr17

4885455

-
intron-intronENST00000540235ENST00000572543JUPchr17

39919235

-CAMTA2chr17

4885455

-
intron-intronENST00000540235ENST00000381311JUPchr17

39919235

-CAMTA2chr17

4885455

-
intron-intronENST00000540235ENST00000348066JUPchr17

39919235

-CAMTA2chr17

4885455

-
intron-5UTRENST00000540235ENST00000571831JUPchr17

39919235

-CAMTA2chr17

4885455

-
Frame-shiftENST00000393930ENST00000358183JUPchr17

39919235

-CAMTA2chr17

4885455

-
Frame-shiftENST00000393930ENST00000414043JUPchr17

39919235

-CAMTA2chr17

4885455

-
5CDS-intronENST00000393930ENST00000361571JUPchr17

39919235

-CAMTA2chr17

4885455

-
5CDS-intronENST00000393930ENST00000572543JUPchr17

39919235

-CAMTA2chr17

4885455

-
5CDS-intronENST00000393930ENST00000381311JUPchr17

39919235

-CAMTA2chr17

4885455

-
5CDS-intronENST00000393930ENST00000348066JUPchr17

39919235

-CAMTA2chr17

4885455

-
5CDS-5UTRENST00000393930ENST00000571831JUPchr17

39919235

-CAMTA2chr17

4885455

-
Frame-shiftENST00000393931ENST00000358183JUPchr17

39919235

-CAMTA2chr17

4885455

-
Frame-shiftENST00000393931ENST00000414043JUPchr17

39919235

-CAMTA2chr17

4885455

-
5CDS-intronENST00000393931ENST00000361571JUPchr17

39919235

-CAMTA2chr17

4885455

-
5CDS-intronENST00000393931ENST00000572543JUPchr17

39919235

-CAMTA2chr17

4885455

-
5CDS-intronENST00000393931ENST00000381311JUPchr17

39919235

-CAMTA2chr17

4885455

-
5CDS-intronENST00000393931ENST00000348066JUPchr17

39919235

-CAMTA2chr17

4885455

-
5CDS-5UTRENST00000393931ENST00000571831JUPchr17

39919235

-CAMTA2chr17

4885455

-
Frame-shiftENST00000310706ENST00000358183JUPchr17

39919235

-CAMTA2chr17

4885455

-
Frame-shiftENST00000310706ENST00000414043JUPchr17

39919235

-CAMTA2chr17

4885455

-
5CDS-intronENST00000310706ENST00000361571JUPchr17

39919235

-CAMTA2chr17

4885455

-
5CDS-intronENST00000310706ENST00000572543JUPchr17

39919235

-CAMTA2chr17

4885455

-
5CDS-intronENST00000310706ENST00000381311JUPchr17

39919235

-CAMTA2chr17

4885455

-
5CDS-intronENST00000310706ENST00000348066JUPchr17

39919235

-CAMTA2chr17

4885455

-
5CDS-5UTRENST00000310706ENST00000571831JUPchr17

39919235

-CAMTA2chr17

4885455

-

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 JUP-CAMTA2


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 JUP-CAMTA2


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
JUP

P14923

CAMTA2

O94983

FUNCTION: Common junctional plaque protein. The membrane-associated plaques are architectural elements in an important strategic position to influence the arrangement and function of both the cytoskeleton and the cells within the tissue. The presence of plakoglobin in both the desmosomes and in the intermediate junctions suggests that it plays a central role in the structure and function of submembranous plaques. Acts as a substrate for VE-PTP and is required by it to stimulate VE-cadherin function in endothelial cells. Can replace beta-catenin in E-cadherin/catenin adhesion complexes which are proposed to couple cadherins to the actin cytoskeleton (By similarity). {ECO:0000250}.FUNCTION: Transcription activator. May act as tumor suppressor. {ECO:0000269|PubMed:11925432}.

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 JUP-CAMTA2


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 JUP-CAMTA2


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 JUP-CAMTA2


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneJUPP14923DB01593ZincSmall moleculeApproved|Investigational
HgeneJUPP14923DB01593ZincSmall moleculeApproved|Investigational
HgeneJUPP14923DB01593ZincSmall moleculeApproved|Investigational
HgeneJUPP14923DB14487Zinc acetateSmall moleculeApproved|Investigational
HgeneJUPP14923DB14487Zinc acetateSmall moleculeApproved|Investigational
HgeneJUPP14923DB14487Zinc acetateSmall moleculeApproved|Investigational

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Related Diseases for JUP-CAMTA2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneJUPC1832600Naxos disease5CTD_human;GENOMICS_ENGLAND
HgeneJUPC1969081Arrhythmogenic Right Ventricular Dysplasia, Familial, 124CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneJUPC0023895Liver diseases1CTD_human
HgeneJUPC0033578Prostatic Neoplasms1CTD_human
HgeneJUPC0086565Liver Dysfunction1CTD_human
HgeneJUPC0232347No-Reflow Phenomenon1CTD_human
HgeneJUPC0376358Malignant neoplasm of prostate1CTD_human
HgeneJUPC1864826Epidermolysis bullosa, lethal acantholytic1ORPHANET
HgeneJUPC2713615Slow-Flow Phenomenon1CTD_human