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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:HSFY1-PAX5 (FusionGDB2 ID:37731)

Fusion Gene Summary for HSFY1-PAX5

check button Fusion gene summary
Fusion gene informationFusion gene name: HSFY1-PAX5
Fusion gene ID: 37731
HgeneTgene
Gene symbol

HSFY1

PAX5

Gene ID

86614

5079

Gene nameheat shock transcription factor Y-linked 1paired box 5
SynonymsHSF2L|HSFYALL3|BSAP
Cytomap

Yq11.222

9p13.2

Type of geneprotein-codingprotein-coding
Descriptionheat shock transcription factor, Y-linkedheat shock transcription factor 2-like proteinpaired box protein Pax-5B-cell lineage specific activatorpaired box homeotic gene 5paired domain gene 5transcription factor PAX 5
Modification date2020032720200313
UniProtAcc

Q96LI6

Q02548

Ensembl transtripts involved in fusion geneENST00000307393, ENST00000309834, 
ENST00000382856, 
ENST00000358127, 
ENST00000377847, ENST00000377852, 
ENST00000377853, ENST00000414447, 
ENST00000446742, ENST00000520154, 
ENST00000520281, ENST00000522003, 
ENST00000523145, ENST00000523241, 
Fusion gene scores* DoF score4 X 4 X 1=168 X 7 X 6=336
# samples 49
** MAII scorelog2(4/16*10)=1.32192809488736
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(9/336*10)=-1.90046432644909
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: HSFY1 [Title/Abstract] AND PAX5 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointHSFY1(20693941)-PAX5(37010441), # 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 buttonFusion gene breakpoints across HSFY1 (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 PAX5 (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
ChiTaRS5.0N/AFN103507HSFY1chrY

20693941

-PAX5chr9

37010441

-


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Fusion Gene ORF analysis for HSFY1-PAX5

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
intron-intronENST00000307393ENST00000358127HSFY1chrY

20693941

-PAX5chr9

37010441

-
intron-intronENST00000307393ENST00000377847HSFY1chrY

20693941

-PAX5chr9

37010441

-
intron-intronENST00000307393ENST00000377852HSFY1chrY

20693941

-PAX5chr9

37010441

-
intron-intronENST00000307393ENST00000377853HSFY1chrY

20693941

-PAX5chr9

37010441

-
intron-intronENST00000307393ENST00000414447HSFY1chrY

20693941

-PAX5chr9

37010441

-
intron-intronENST00000307393ENST00000446742HSFY1chrY

20693941

-PAX5chr9

37010441

-
intron-intronENST00000307393ENST00000520154HSFY1chrY

20693941

-PAX5chr9

37010441

-
intron-intronENST00000307393ENST00000520281HSFY1chrY

20693941

-PAX5chr9

37010441

-
intron-intronENST00000307393ENST00000522003HSFY1chrY

20693941

-PAX5chr9

37010441

-
intron-intronENST00000307393ENST00000523145HSFY1chrY

20693941

-PAX5chr9

37010441

-
intron-intronENST00000307393ENST00000523241HSFY1chrY

20693941

-PAX5chr9

37010441

-
intron-intronENST00000309834ENST00000358127HSFY1chrY

20693941

-PAX5chr9

37010441

-
intron-intronENST00000309834ENST00000377847HSFY1chrY

20693941

-PAX5chr9

37010441

-
intron-intronENST00000309834ENST00000377852HSFY1chrY

20693941

-PAX5chr9

37010441

-
intron-intronENST00000309834ENST00000377853HSFY1chrY

20693941

-PAX5chr9

37010441

-
intron-intronENST00000309834ENST00000414447HSFY1chrY

20693941

-PAX5chr9

37010441

-
intron-intronENST00000309834ENST00000446742HSFY1chrY

20693941

-PAX5chr9

37010441

-
intron-intronENST00000309834ENST00000520154HSFY1chrY

20693941

-PAX5chr9

37010441

-
intron-intronENST00000309834ENST00000520281HSFY1chrY

20693941

-PAX5chr9

37010441

-
intron-intronENST00000309834ENST00000522003HSFY1chrY

20693941

-PAX5chr9

37010441

-
intron-intronENST00000309834ENST00000523145HSFY1chrY

20693941

-PAX5chr9

37010441

-
intron-intronENST00000309834ENST00000523241HSFY1chrY

20693941

-PAX5chr9

37010441

-
intron-intronENST00000382856ENST00000358127HSFY1chrY

20693941

-PAX5chr9

37010441

-
intron-intronENST00000382856ENST00000377847HSFY1chrY

20693941

-PAX5chr9

37010441

-
intron-intronENST00000382856ENST00000377852HSFY1chrY

20693941

-PAX5chr9

37010441

-
intron-intronENST00000382856ENST00000377853HSFY1chrY

20693941

-PAX5chr9

37010441

-
intron-intronENST00000382856ENST00000414447HSFY1chrY

20693941

-PAX5chr9

37010441

-
intron-intronENST00000382856ENST00000446742HSFY1chrY

20693941

-PAX5chr9

37010441

-
intron-intronENST00000382856ENST00000520154HSFY1chrY

20693941

-PAX5chr9

37010441

-
intron-intronENST00000382856ENST00000520281HSFY1chrY

20693941

-PAX5chr9

37010441

-
intron-intronENST00000382856ENST00000522003HSFY1chrY

20693941

-PAX5chr9

37010441

-
intron-intronENST00000382856ENST00000523145HSFY1chrY

20693941

-PAX5chr9

37010441

-
intron-intronENST00000382856ENST00000523241HSFY1chrY

20693941

-PAX5chr9

37010441

-

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 HSFY1-PAX5


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)

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.

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Fusion Protein Features for HSFY1-PAX5


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/:20693941/:37010441)
- 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
HSFY1

Q96LI6

PAX5

Q02548

FUNCTION: Transcription factor that plays an essential role in commitment of lymphoid progenitors to the B-lymphocyte lineage (PubMed:10811620, PubMed:27181361). Fulfills a dual role by repressing B-lineage inappropriate genes and simultaneously activating B-lineage-specific genes (PubMed:10811620, PubMed:27181361). In turn, regulates cell adhesion and migration, induces V(H)-to-D(H)J(H) recombination, facilitates pre-B-cell receptor signaling and promotes development to the mature B-cell stage (PubMed:32612238). Repression of the cohesin-release factor WAPL causes global changes of the chromosomal architecture in pro-B cells to facilitate the generation of a diverse antibody repertoire (PubMed:32612238). {ECO:0000269|PubMed:10811620, ECO:0000269|PubMed:27181361, ECO:0000269|PubMed:32612238}.; FUNCTION: (Microbial infection) Plays an essential role in the maintenance of Epstein-Barr virus genome copy number within the host cell by promoting EBNA1/oriP-dependent binding and transcription (PubMed:31941781). Participates also in the inhibition of lytic EBV reactivation by modulating viral BZLF1 activity (PubMed:23678172). {ECO:0000269|PubMed:23678172, ECO:0000269|PubMed:31941781}.

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 HSFY1-PAX5


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 HSFY1-PAX5


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 HSFY1-PAX5


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 HSFY1-PAX5


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