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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:BAHD1-KNSTRN (FusionGDB2 ID:8896)

Fusion Gene Summary for BAHD1-KNSTRN

check button Fusion gene summary
Fusion gene informationFusion gene name: BAHD1-KNSTRN
Fusion gene ID: 8896
HgeneTgene
Gene symbol

BAHD1

KNSTRN

Gene ID

22893

90417

Gene namebromo adjacent homology domain containing 1kinetochore localized astrin (SPAG5) binding protein
Synonyms-C15orf23|HSD11|SKAP|TRAF4AF1
Cytomap

15q15.1

15q15.1

Type of geneprotein-codingprotein-coding
Descriptionbromo adjacent homology domain-containing 1 proteinBAH domain-containing protein 1small kinetochore-associated proteinTRAF4 associated factor 1kinastrinkinetochore-localized astrin-binding proteinputative TRAF4-associated factor 1small kinetochore associated proteinsmall kinetochore-associated protein, kinetochore-localized astri
Modification date2020031320200313
UniProtAcc

Q8TBE0

Q9Y448

Ensembl transtripts involved in fusion geneENST00000416165, ENST00000560846, 
ENST00000561234, 
ENST00000249776, 
ENST00000416151, ENST00000448395, 
ENST00000608100, 
Fusion gene scores* DoF score2 X 2 X 2=81 X 2 X 1=2
# samples 32
** MAII scorelog2(3/8*10)=1.90689059560852log2(2/2*10)=3.32192809488736
Context

PubMed: BAHD1 [Title/Abstract] AND KNSTRN [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointBAHD1(40733467)-KNSTRN(40678563), # samples:2
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 buttonFusion gene breakpoints across BAHD1 (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 KNSTRN (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
ChimerDB4LIHCTCGA-2Y-A9H0-01ABAHD1chr15

40733467

+KNSTRNchr15

40678563

+
ChimerDB4LIHCTCGA-2Y-A9H0BAHD1chr15

40733467

+KNSTRNchr15

40675429

+
ChimerDB4LIHCTCGA-2Y-A9H0BAHD1chr15

40733467

+KNSTRNchr15

40678563

+


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Fusion Gene ORF analysis for BAHD1-KNSTRN

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-3CDSENST00000416165ENST00000249776BAHD1chr15

40733467

+KNSTRNchr15

40678563

+
5UTR-3CDSENST00000416165ENST00000249776BAHD1chr15

40733467

+KNSTRNchr15

40675429

+
5UTR-3CDSENST00000416165ENST00000416151BAHD1chr15

40733467

+KNSTRNchr15

40678563

+
5UTR-3CDSENST00000416165ENST00000416151BAHD1chr15

40733467

+KNSTRNchr15

40675429

+
5UTR-3CDSENST00000416165ENST00000448395BAHD1chr15

40733467

+KNSTRNchr15

40678563

+
5UTR-3CDSENST00000416165ENST00000448395BAHD1chr15

40733467

+KNSTRNchr15

40675429

+
5UTR-3CDSENST00000416165ENST00000608100BAHD1chr15

40733467

+KNSTRNchr15

40678563

+
5UTR-5UTRENST00000416165ENST00000608100BAHD1chr15

40733467

+KNSTRNchr15

40675429

+
intron-3CDSENST00000560846ENST00000249776BAHD1chr15

40733467

+KNSTRNchr15

40678563

+
intron-3CDSENST00000560846ENST00000249776BAHD1chr15

40733467

+KNSTRNchr15

40675429

+
intron-3CDSENST00000560846ENST00000416151BAHD1chr15

40733467

+KNSTRNchr15

40678563

+
intron-3CDSENST00000560846ENST00000416151BAHD1chr15

40733467

+KNSTRNchr15

40675429

+
intron-3CDSENST00000560846ENST00000448395BAHD1chr15

40733467

+KNSTRNchr15

40678563

+
intron-3CDSENST00000560846ENST00000448395BAHD1chr15

40733467

+KNSTRNchr15

40675429

+
intron-3CDSENST00000560846ENST00000608100BAHD1chr15

40733467

+KNSTRNchr15

40678563

+
intron-3CDSENST00000561234ENST00000249776BAHD1chr15

40733467

+KNSTRNchr15

40678563

+
intron-3CDSENST00000561234ENST00000249776BAHD1chr15

40733467

+KNSTRNchr15

40675429

+
intron-3CDSENST00000561234ENST00000416151BAHD1chr15

40733467

+KNSTRNchr15

40678563

+
intron-3CDSENST00000561234ENST00000416151BAHD1chr15

40733467

+KNSTRNchr15

40675429

+
intron-3CDSENST00000561234ENST00000448395BAHD1chr15

40733467

+KNSTRNchr15

40678563

+
intron-3CDSENST00000561234ENST00000448395BAHD1chr15

40733467

+KNSTRNchr15

40675429

+
intron-3CDSENST00000561234ENST00000608100BAHD1chr15

40733467

+KNSTRNchr15

40678563

+
intron-5UTRENST00000560846ENST00000608100BAHD1chr15

40733467

+KNSTRNchr15

40675429

+
intron-5UTRENST00000561234ENST00000608100BAHD1chr15

40733467

+KNSTRNchr15

40675429

+

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 BAHD1-KNSTRN


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)
BAHD1chr1540733467+KNSTRNchr1540675428+0.457008120.5429919
BAHD1chr1540733467+KNSTRNchr1540678562+0.000196980.999803
BAHD1chr1540733467+KNSTRNchr1540678562+0.000196980.999803
BAHD1chr1540733467+KNSTRNchr1540675428+0.457008120.5429919
BAHD1chr1540733467+KNSTRNchr1540678562+0.000196980.999803
BAHD1chr1540733467+KNSTRNchr1540678562+0.000196980.999803

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.
genomic feature of top 1%

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Fusion Protein Features for BAHD1-KNSTRN


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/:40733467/:40678563)
- 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
BAHD1

Q8TBE0

KNSTRN

Q9Y448

FUNCTION: Heterochromatin protein that acts as a transcription repressor and has the ability to promote the formation of large heterochromatic domains. May act by recruiting heterochromatin proteins such as CBX5 (HP1 alpha), HDAC5 and MBD1. Represses IGF2 expression by binding to its CpG-rich P3 promoter and recruiting heterochromatin proteins. At specific stages of Listeria infection, in complex with TRIM28, corepresses interferon-stimulated genes, including IFNL1, IFNL2 and IFNL3. {ECO:0000269|PubMed:19666599, ECO:0000269|PubMed:21252314}.FUNCTION: Essential component of the mitotic spindle required for faithful chromosome segregation and progression into anaphase (PubMed:19667759). Promotes the metaphase-to-anaphase transition and is required for chromosome alignment, normal timing of sister chromatid segregation, and maintenance of spindle pole architecture (PubMed:19667759, PubMed:22110139). The astrin (SPAG5)-kinastrin (SKAP) complex promotes stable microtubule-kinetochore attachments (PubMed:21402792). Required for kinetochore oscillations and dynamics of microtubule plus-ends during live cell mitosis, possibly by forming a link between spindle microtubule plus-ends and mitotic chromosomes to achieve faithful cell division (PubMed:23035123). May be involved in UV-induced apoptosis via its interaction with PRPF19; however, these results need additional evidences (PubMed:24718257). {ECO:0000269|PubMed:19667759, ECO:0000269|PubMed:21402792, ECO:0000269|PubMed:22110139, ECO:0000269|PubMed:23035123, ECO:0000305|PubMed:24718257}.

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 BAHD1-KNSTRN


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 BAHD1-KNSTRN


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 BAHD1-KNSTRN


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 BAHD1-KNSTRN


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource