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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:BACH2-BIVM (FusionGDB2 ID:HG60468TG54841)

Fusion Gene Summary for BACH2-BIVM

check button Fusion gene summary
Fusion gene informationFusion gene name: BACH2-BIVM
Fusion gene ID: hg60468tg54841
HgeneTgene
Gene symbol

BACH2

BIVM

Gene ID

60468

54841

Gene nameBTB domain and CNC homolog 2basic, immunoglobulin-like variable motif containing
SynonymsBTBD25|IMD60-
Cytomap('BACH2')('BIVM')

6q15

13q33.1

Type of geneprotein-codingprotein-coding
Descriptiontranscription regulator protein BACH2BTB and CNC homolog 2BTB and CNC homology 1, basic leucine zipper transcription factor 2basic immunoglobulin-like variable motif-containing protein
Modification date2020031320200313
UniProtAcc

Q9BYV9

Q86UB2

Ensembl transtripts involved in fusion geneENST00000257749, ENST00000343122, 
ENST00000470301, ENST00000537989, 
Fusion gene scores* DoF score6 X 5 X 5=1503 X 3 X 3=27
# samples 63
** MAII scorelog2(6/150*10)=-1.32192809488736
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: BACH2 [Title/Abstract] AND BIVM [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointBACH2(90916288)-BIVM(103468778), # 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


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
ChimerDB4SARCTCGA-X6-A8C2-01ABACH2chr6

90916288

-BIVMchr13

103468778

+


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Fusion Gene ORF analysis for BACH2-BIVM

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-3CDSENST00000257749ENST00000257336BACH2chr6

90916288

-BIVMchr13

103468778

+
5UTR-3CDSENST00000343122ENST00000257336BACH2chr6

90916288

-BIVMchr13

103468778

+
5UTR-3CDSENST00000470301ENST00000257336BACH2chr6

90916288

-BIVMchr13

103468778

+
5UTR-3CDSENST00000537989ENST00000257336BACH2chr6

90916288

-BIVMchr13

103468778

+
5UTR-5UTRENST00000257749ENST00000419638BACH2chr6

90916288

-BIVMchr13

103468778

+
5UTR-5UTRENST00000257749ENST00000448849BACH2chr6

90916288

-BIVMchr13

103468778

+
5UTR-5UTRENST00000343122ENST00000419638BACH2chr6

90916288

-BIVMchr13

103468778

+
5UTR-5UTRENST00000343122ENST00000448849BACH2chr6

90916288

-BIVMchr13

103468778

+
5UTR-5UTRENST00000470301ENST00000419638BACH2chr6

90916288

-BIVMchr13

103468778

+
5UTR-5UTRENST00000470301ENST00000448849BACH2chr6

90916288

-BIVMchr13

103468778

+
5UTR-5UTRENST00000537989ENST00000419638BACH2chr6

90916288

-BIVMchr13

103468778

+
5UTR-5UTRENST00000537989ENST00000448849BACH2chr6

90916288

-BIVMchr13

103468778

+
5UTR-intronENST00000257749ENST00000491929BACH2chr6

90916288

-BIVMchr13

103468778

+
5UTR-intronENST00000343122ENST00000491929BACH2chr6

90916288

-BIVMchr13

103468778

+
5UTR-intronENST00000470301ENST00000491929BACH2chr6

90916288

-BIVMchr13

103468778

+
5UTR-intronENST00000537989ENST00000491929BACH2chr6

90916288

-BIVMchr13

103468778

+

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 BACH2-BIVM


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)
BACH2chr690916287-BIVMchr13103468777+2.42E-050.9999758
BACH2chr690916287-BIVMchr13103468777+2.42E-050.9999758


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 BACH2-BIVM


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/:90916288/:103468778)
- 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
BACH2

Q9BYV9

BIVM

Q86UB2

FUNCTION: Transcriptional regulator that acts as repressor or activator (By similarity). Binds to Maf recognition elements (MARE) (By similarity). Plays an important role in coordinating transcription activation and repression by MAFK (By similarity). Induces apoptosis in response to oxidative stress through repression of the antiapoptotic factor HMOX1 (PubMed:17018862). Positively regulates the nuclear import of actin (By similarity). Is a key regulator of adaptive immunity, crucial for the maintenance of regulatory T-cell function and B-cell maturation (PubMed:28530713). {ECO:0000250|UniProtKB:P97303, ECO:0000269|PubMed:17018862, ECO:0000269|PubMed:28530713}.

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 BACH2-BIVM


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 BACH2-BIVM


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 BACH2-BIVM


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 BACH2-BIVM


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneBACH2C0007570Celiac Disease1CTD_human
HgeneBACH2C0010346Crohn Disease1CTD_human
HgeneBACH2C0011854Diabetes Mellitus, Insulin-Dependent1CTD_human
HgeneBACH2C0023467Leukemia, Myelocytic, Acute1CTD_human
HgeneBACH2C0026998Acute Myeloid Leukemia, M11CTD_human
HgeneBACH2C0042900Vitiligo1CTD_human
HgeneBACH2C0086438Hypogammaglobulinemia1GENOMICS_ENGLAND
HgeneBACH2C0156147Crohn's disease of large bowel1CTD_human
HgeneBACH2C0205734Diabetes, Autoimmune1CTD_human
HgeneBACH2C0267380Crohn's disease of the ileum1CTD_human
HgeneBACH2C0342302Brittle diabetes1CTD_human
HgeneBACH2C0678202Regional enteritis1CTD_human
HgeneBACH2C0949272IIeocolitis1CTD_human
HgeneBACH2C1879321Acute Myeloid Leukemia (AML-M2)1CTD_human
HgeneBACH2C3837958Diabetes Mellitus, Ketosis-Prone1CTD_human
HgeneBACH2C4554117Diabetes Mellitus, Sudden-Onset1CTD_human