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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:CHCHD3-APBB2 (FusionGDB2 ID:HG54927TG323)

Fusion Gene Summary for CHCHD3-APBB2

check button Fusion gene summary
Fusion gene informationFusion gene name: CHCHD3-APBB2
Fusion gene ID: hg54927tg323
HgeneTgene
Gene symbol

CHCHD3

APBB2

Gene ID

54927

323

Gene namecoiled-coil-helix-coiled-coil-helix domain containing 3amyloid beta precursor protein binding family B member 2
SynonymsMICOS19|MINOS3|Mic19|PPP1R22FE65L|FE65L1
Cytomap('CHCHD3')('APBB2')

7q32.3-q33

4p14-p13

Type of geneprotein-codingprotein-coding
DescriptionMICOS complex subunit MIC19coiled-coil-helix-coiled-coil-helix domain-containing protein 3, mitochondrialmitochondrial contact site and cristae organizing system subunit 19mitochondrial inner membrane organizing system 3protein phosphatase 1, regulatoamyloid-beta A4 precursor protein-binding family B member 2Fe65-like 1protein Fe65-like 1
Modification date2020032720200327
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000262570, ENST00000448878, 
ENST00000542753, ENST00000476546, 
Fusion gene scores* DoF score23 X 25 X 10=575012 X 12 X 9=1296
# samples 3117
** MAII scorelog2(31/5750*10)=-4.21322183544486
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(17/1296*10)=-2.93045906674692
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CHCHD3 [Title/Abstract] AND APBB2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCHCHD3(132766617)-APBB2(40832594), # samples:1
Anticipated loss of major functional domain due to fusion event.CHCHD3-APBB2 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
CHCHD3-APBB2 seems lost the major protein functional domain in Hgene partner, which is a transcription factor 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
HgeneCHCHD3

GO:0000122

negative regulation of transcription by RNA polymerase II

22567091



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
ChimerDB4Non-CancerTCGA-BR-7851-11ACHCHD3chr7

132766617

-APBB2chr4

40832594

-


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Fusion Gene ORF analysis for CHCHD3-APBB2

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-5UTRENST00000262570ENST00000502841CHCHD3chr7

132766617

-APBB2chr4

40832594

-
5CDS-5UTRENST00000262570ENST00000504305CHCHD3chr7

132766617

-APBB2chr4

40832594

-
5CDS-5UTRENST00000262570ENST00000543538CHCHD3chr7

132766617

-APBB2chr4

40832594

-
5CDS-5UTRENST00000448878ENST00000502841CHCHD3chr7

132766617

-APBB2chr4

40832594

-
5CDS-5UTRENST00000448878ENST00000504305CHCHD3chr7

132766617

-APBB2chr4

40832594

-
5CDS-5UTRENST00000448878ENST00000543538CHCHD3chr7

132766617

-APBB2chr4

40832594

-
5CDS-5UTRENST00000542753ENST00000502841CHCHD3chr7

132766617

-APBB2chr4

40832594

-
5CDS-5UTRENST00000542753ENST00000504305CHCHD3chr7

132766617

-APBB2chr4

40832594

-
5CDS-5UTRENST00000542753ENST00000543538CHCHD3chr7

132766617

-APBB2chr4

40832594

-
5CDS-intronENST00000262570ENST00000511572CHCHD3chr7

132766617

-APBB2chr4

40832594

-
5CDS-intronENST00000448878ENST00000511572CHCHD3chr7

132766617

-APBB2chr4

40832594

-
5CDS-intronENST00000542753ENST00000511572CHCHD3chr7

132766617

-APBB2chr4

40832594

-
5UTR-3CDSENST00000476546ENST00000295974CHCHD3chr7

132766617

-APBB2chr4

40832594

-
5UTR-3CDSENST00000476546ENST00000506352CHCHD3chr7

132766617

-APBB2chr4

40832594

-
5UTR-3CDSENST00000476546ENST00000508593CHCHD3chr7

132766617

-APBB2chr4

40832594

-
5UTR-3CDSENST00000476546ENST00000513140CHCHD3chr7

132766617

-APBB2chr4

40832594

-
5UTR-5UTRENST00000476546ENST00000502841CHCHD3chr7

132766617

-APBB2chr4

40832594

-
5UTR-5UTRENST00000476546ENST00000504305CHCHD3chr7

132766617

-APBB2chr4

40832594

-
5UTR-5UTRENST00000476546ENST00000543538CHCHD3chr7

132766617

-APBB2chr4

40832594

-
5UTR-intronENST00000476546ENST00000511572CHCHD3chr7

132766617

-APBB2chr4

40832594

-
Frame-shiftENST00000262570ENST00000295974CHCHD3chr7

132766617

-APBB2chr4

40832594

-
Frame-shiftENST00000262570ENST00000506352CHCHD3chr7

132766617

-APBB2chr4

40832594

-
Frame-shiftENST00000262570ENST00000508593CHCHD3chr7

132766617

-APBB2chr4

40832594

-
Frame-shiftENST00000262570ENST00000513140CHCHD3chr7

132766617

-APBB2chr4

40832594

-
Frame-shiftENST00000448878ENST00000295974CHCHD3chr7

132766617

-APBB2chr4

40832594

-
Frame-shiftENST00000448878ENST00000506352CHCHD3chr7

132766617

-APBB2chr4

40832594

-
Frame-shiftENST00000448878ENST00000508593CHCHD3chr7

132766617

-APBB2chr4

40832594

-
Frame-shiftENST00000448878ENST00000513140CHCHD3chr7

132766617

-APBB2chr4

40832594

-
Frame-shiftENST00000542753ENST00000295974CHCHD3chr7

132766617

-APBB2chr4

40832594

-
Frame-shiftENST00000542753ENST00000506352CHCHD3chr7

132766617

-APBB2chr4

40832594

-
Frame-shiftENST00000542753ENST00000508593CHCHD3chr7

132766617

-APBB2chr4

40832594

-
Frame-shiftENST00000542753ENST00000513140CHCHD3chr7

132766617

-APBB2chr4

40832594

-

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 CHCHD3-APBB2


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 CHCHD3-APBB2


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/:132766617/:40832594)
- 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 CHCHD3-APBB2


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 CHCHD3-APBB2


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 CHCHD3-APBB2


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 CHCHD3-APBB2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCHCHD3C0013146Drug abuse1CTD_human
HgeneCHCHD3C0013170Drug habituation1CTD_human
HgeneCHCHD3C0013222Drug Use Disorders1CTD_human
HgeneCHCHD3C0029231Organic Mental Disorders, Substance-Induced1CTD_human
HgeneCHCHD3C0038580Substance Dependence1CTD_human
HgeneCHCHD3C0038586Substance Use Disorders1CTD_human
HgeneCHCHD3C0236969Substance-Related Disorders1CTD_human
HgeneCHCHD3C0740858Substance abuse problem1CTD_human
HgeneCHCHD3C1510472Drug Dependence1CTD_human
HgeneCHCHD3C4316881Prescription Drug Abuse1CTD_human
TgeneC0043094Weight Gain1CTD_human