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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:BAG5-TPM4 (FusionGDB2 ID:HG9529TG7171)

Fusion Gene Summary for BAG5-TPM4

check button Fusion gene summary
Fusion gene informationFusion gene name: BAG5-TPM4
Fusion gene ID: hg9529tg7171
HgeneTgene
Gene symbol

BAG5

TPM4

Gene ID

9529

7171

Gene nameBAG cochaperone 5tropomyosin 4
SynonymsBAG-5HEL-S-108
Cytomap('BAG5')('TPM4')

14q32.33

19p13.12-p13.11

Type of geneprotein-codingprotein-coding
DescriptionBAG family molecular chaperone regulator 5BCL2 associated athanogene 5bcl-2-associated athanogene 5tropomyosin alpha-4 chainTM30p1epididymis secretory protein Li 108
Modification date2020031320200320
UniProtAcc.

P67936

Ensembl transtripts involved in fusion geneENST00000299204, ENST00000337322, 
ENST00000445922, 
Fusion gene scores* DoF score1 X 1 X 1=114 X 12 X 6=1008
# samples 114
** MAII scorelog2(1/1*10)=3.32192809488736log2(14/1008*10)=-2.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: BAG5 [Title/Abstract] AND TPM4 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointBAG5(104028952)-TPM4(16192722), # 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
HgeneBAG5

GO:0010977

negative regulation of neuron projection development

24510904

HgeneBAG5

GO:0031397

negative regulation of protein ubiquitination

25006867

HgeneBAG5

GO:0032435

negative regulation of proteasomal ubiquitin-dependent protein catabolic process

24475098

HgeneBAG5

GO:0050821

protein stabilization

25006867

HgeneBAG5

GO:1902176

negative regulation of oxidative stress-induced intrinsic apoptotic signaling pathway

24475098



check button Fusion gene information
* 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
ChimerDB4STADTCGA-BR-8372BAG5chr14

104028952

-TPM4chr19

16192722

+


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Fusion Gene ORF analysis for BAG5-TPM4

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
5UTR-3CDSENST00000299204ENST00000300933BAG5chr14

104028952

-TPM4chr19

16192722

+
5UTR-3CDSENST00000299204ENST00000344824BAG5chr14

104028952

-TPM4chr19

16192722

+
5UTR-3CDSENST00000299204ENST00000538887BAG5chr14

104028952

-TPM4chr19

16192722

+
5UTR-intronENST00000299204ENST00000591645BAG5chr14

104028952

-TPM4chr19

16192722

+
intron-3CDSENST00000337322ENST00000300933BAG5chr14

104028952

-TPM4chr19

16192722

+
intron-3CDSENST00000337322ENST00000344824BAG5chr14

104028952

-TPM4chr19

16192722

+
intron-3CDSENST00000337322ENST00000538887BAG5chr14

104028952

-TPM4chr19

16192722

+
intron-3CDSENST00000445922ENST00000300933BAG5chr14

104028952

-TPM4chr19

16192722

+
intron-3CDSENST00000445922ENST00000344824BAG5chr14

104028952

-TPM4chr19

16192722

+
intron-3CDSENST00000445922ENST00000538887BAG5chr14

104028952

-TPM4chr19

16192722

+
intron-intronENST00000337322ENST00000591645BAG5chr14

104028952

-TPM4chr19

16192722

+
intron-intronENST00000445922ENST00000591645BAG5chr14

104028952

-TPM4chr19

16192722

+

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 BAG5-TPM4


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)
BAG5chr14104028952-TPM4chr1916192722+1.75E-060.9999982
BAG5chr14104028952-TPM4chr1916192722+1.75E-060.9999982


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.
genomic feature of top 1%

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Fusion Protein Features for BAG5-TPM4


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/:104028952/:16192722)
- 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
.TPM4

P67936

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: Binds to actin filaments in muscle and non-muscle cells. Plays a central role, in association with the troponin complex, in the calcium dependent regulation of vertebrate striated muscle contraction. Smooth muscle contraction is regulated by interaction with caldesmon. In non-muscle cells is implicated in stabilizing cytoskeleton actin filaments (By similarity). Binds calcium (PubMed:1836432). {ECO:0000250|UniProtKB:P09495, ECO:0000269|PubMed:1836432}.

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 BAG5-TPM4


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 BAG5-TPM4


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 BAG5-TPM4


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 BAG5-TPM4


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneBAG5C0030567Parkinson Disease1CTD_human
TgeneC0001787Osteoporosis, Age-Related1CTD_human
TgeneC0003949Asbestosis1CTD_human
TgeneC0005818Blood Platelet Disorders1GENOMICS_ENGLAND
TgeneC0014859Esophageal Neoplasms1CTD_human
TgeneC0023893Liver Cirrhosis, Experimental1CTD_human
TgeneC0027627Neoplasm Metastasis1CTD_human
TgeneC0029456Osteoporosis1CTD_human
TgeneC0029459Osteoporosis, Senile1CTD_human
TgeneC0032927Precancerous Conditions1CTD_human
TgeneC0043094Weight Gain1CTD_human
TgeneC0282313Condition, Preneoplastic1CTD_human
TgeneC0334121Inflammatory Myofibroblastic Tumor1ORPHANET
TgeneC0546837Malignant neoplasm of esophagus1CTD_human
TgeneC0751406Post-Traumatic Osteoporosis1CTD_human
TgeneC0948089Acute Coronary Syndrome1CTD_human
TgeneC2751260Macrothrombocytopenia1GENOMICS_ENGLAND
TgeneC2930617Pulmonary Fibrosis - from Asbestos Exposure1CTD_human
TgeneC4304021Autosomal dominant macrothrombocytopenia1ORPHANET