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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:MSRB3-BCL2L14 (FusionGDB2 ID:HG253827TG79370)

Fusion Gene Summary for MSRB3-BCL2L14

check button Fusion gene summary
Fusion gene informationFusion gene name: MSRB3-BCL2L14
Fusion gene ID: hg253827tg79370
HgeneTgene
Gene symbol

MSRB3

BCL2L14

Gene ID

253827

79370

Gene namemethionine sulfoxide reductase B3BCL2 like 14
SynonymsDFNB74BCLG
Cytomap('MSRB3')('BCL2L14')

12q14.3

12p13.2

Type of geneprotein-codingprotein-coding
Descriptionmethionine-R-sulfoxide reductase B3methionine-R-sulfoxide reductase B3, mitochondrialapoptosis facilitator Bcl-2-like protein 14BCL2-like 14 (apoptosis facilitator)apoptosis regulator BCL-Gbcl2-L-14testicular tissue protein Li 26
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000538725, ENST00000355192, 
ENST00000540804, ENST00000308259, 
ENST00000535664, 
Fusion gene scores* DoF score7 X 5 X 4=1406 X 6 X 2=72
# samples 76
** MAII scorelog2(7/140*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0		log2(6/72*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: MSRB3 [Title/Abstract] AND BCL2L14 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointMSRB3(65672645)-BCL2L14(12204730), # 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
HgeneMSRB3

GO:0030091

protein repair

14699060

TgeneBCL2L14

GO:0006915

apoptotic process

17280616



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
ChimerDB4LUSCTCGA-85-6175-01AMSRB3chr12

65672645

-BCL2L14chr12

12204730

+


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Fusion Gene ORF analysis for MSRB3-BCL2L14

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
3UTR-3UTRENST00000538725ENST00000484949MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
3UTR-5UTRENST00000538725ENST00000586576MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
3UTR-5UTRENST00000538725ENST00000589718MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
3UTR-intronENST00000538725ENST00000266434MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
3UTR-intronENST00000538725ENST00000308721MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
3UTR-intronENST00000538725ENST00000396367MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
3UTR-intronENST00000538725ENST00000396369MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
5CDS-3UTRENST00000355192ENST00000484949MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
5CDS-3UTRENST00000540804ENST00000484949MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
5CDS-5UTRENST00000355192ENST00000586576MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
5CDS-5UTRENST00000355192ENST00000589718MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
5CDS-5UTRENST00000540804ENST00000586576MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
5CDS-5UTRENST00000540804ENST00000589718MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
5CDS-intronENST00000355192ENST00000266434MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
5CDS-intronENST00000355192ENST00000308721MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
5CDS-intronENST00000355192ENST00000396367MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
5CDS-intronENST00000355192ENST00000396369MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
5CDS-intronENST00000540804ENST00000266434MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
5CDS-intronENST00000540804ENST00000308721MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
5CDS-intronENST00000540804ENST00000396367MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
5CDS-intronENST00000540804ENST00000396369MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
5UTR-3UTRENST00000308259ENST00000484949MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
5UTR-3UTRENST00000535664ENST00000484949MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
5UTR-5UTRENST00000308259ENST00000586576MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
5UTR-5UTRENST00000308259ENST00000589718MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
5UTR-5UTRENST00000535664ENST00000586576MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
5UTR-5UTRENST00000535664ENST00000589718MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
5UTR-intronENST00000308259ENST00000266434MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
5UTR-intronENST00000308259ENST00000308721MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
5UTR-intronENST00000308259ENST00000396367MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
5UTR-intronENST00000308259ENST00000396369MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
5UTR-intronENST00000535664ENST00000266434MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
5UTR-intronENST00000535664ENST00000308721MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
5UTR-intronENST00000535664ENST00000396367MSRB3chr12

65672645

-BCL2L14chr12

12204730

+
5UTR-intronENST00000535664ENST00000396369MSRB3chr12

65672645

-BCL2L14chr12

12204730

+

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 MSRB3-BCL2L14


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)


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Fusion Protein Features for MSRB3-BCL2L14


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/:65672645/:12204730)
- 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
..
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: 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}.

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 MSRB3-BCL2L14


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 MSRB3-BCL2L14


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 MSRB3-BCL2L14


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 MSRB3-BCL2L14


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneMSRB3C3711374Nonsyndromic Deafness3CLINGEN
HgeneMSRB3C1384666hearing impairment2CTD_human;GENOMICS_ENGLAND
HgeneMSRB3C2239351DEAFNESS, AUTOSOMAL RECESSIVE 742CTD_human;GENOMICS_ENGLAND;UNIPROT