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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:PAX5-NOL4L (FusionGDB2 ID:HG5079TG140688)

Fusion Gene Summary for PAX5-NOL4L

check button Fusion gene summary
Fusion gene informationFusion gene name: PAX5-NOL4L
Fusion gene ID: hg5079tg140688
HgeneTgene
Gene symbol

PAX5

NOL4L

Gene ID

5079

140688

Gene namepaired box 5nucleolar protein 4 like
SynonymsALL3|BSAPC20orf112|C20orf113
Cytomap('PAX5','PAX5')('C20orf112','NOL4L')

9p13.2

20q11.21

Type of geneprotein-codingprotein-coding
Descriptionpaired box protein Pax-5B-cell lineage specific activatorpaired box homeotic gene 5paired domain gene 5transcription factor PAX 5nucleolar protein 4-like
Modification date2020031320200313
UniProtAcc

Q02548

.
Ensembl transtripts involved in fusion geneENST00000358127, ENST00000377847, 
ENST00000377852, ENST00000377853, 
ENST00000414447, ENST00000446742, 
ENST00000520154, ENST00000520281, 
ENST00000522003, ENST00000523145, 
ENST00000523241, 
Fusion gene scores* DoF score15 X 15 X 7=15755 X 5 X 4=100
# samples 105
** MAII scorelog2(10/1575*10)=-3.97727992349992
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/100*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PAX5 [Title/Abstract] AND NOL4L [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointPAX5(37002696)-C20orf112(31035587), # samples:1
PAX5(37002644)-NOL4L(31035621), # samples:1
PAX5(36882001)-NOL4L(31044199), # 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 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
ChimerDB4acute lymphoblastic leukemiaEU784147PAX5chr9

37002696

C20orf112chr20

31035587

ChiTaRS5.0N/AEU784147PAX5chr9

37002644

-NOL4Lchr20

31035621

-
ChiTaRS5.0N/AEU784148PAX5chr9

36882001

-NOL4Lchr20

31044199

-


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Fusion Gene ORF analysis for PAX5-NOL4L

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-3CDSENST00000358127ENST00000359676PAX5chr9

37002696

C20orf112chr20

31035587

intron-3CDSENST00000377847ENST00000359676PAX5chr9

37002696

C20orf112chr20

31035587

intron-3CDSENST00000377852ENST00000359676PAX5chr9

37002696

C20orf112chr20

31035587

intron-3CDSENST00000377853ENST00000359676PAX5chr9

37002696

C20orf112chr20

31035587

intron-3CDSENST00000414447ENST00000359676PAX5chr9

37002696

C20orf112chr20

31035587

intron-3CDSENST00000446742ENST00000359676PAX5chr9

37002696

C20orf112chr20

31035587

intron-3CDSENST00000520154ENST00000359676PAX5chr9

37002696

C20orf112chr20

31035587

intron-3CDSENST00000520281ENST00000359676PAX5chr9

37002696

C20orf112chr20

31035587

intron-3CDSENST00000522003ENST00000359676PAX5chr9

37002696

C20orf112chr20

31035587

intron-3CDSENST00000523145ENST00000359676PAX5chr9

37002696

C20orf112chr20

31035587

intron-3CDSENST00000523241ENST00000359676PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000358127ENST00000201961PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000358127ENST00000326071PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000358127ENST00000375677PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000358127ENST00000375678PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000358127ENST00000475781PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000377847ENST00000201961PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000377847ENST00000326071PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000377847ENST00000375677PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000377847ENST00000375678PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000377847ENST00000475781PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000377852ENST00000201961PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000377852ENST00000326071PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000377852ENST00000375677PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000377852ENST00000375678PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000377852ENST00000475781PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000377853ENST00000201961PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000377853ENST00000326071PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000377853ENST00000375677PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000377853ENST00000375678PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000377853ENST00000475781PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000414447ENST00000201961PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000414447ENST00000326071PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000414447ENST00000375677PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000414447ENST00000375678PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000414447ENST00000475781PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000446742ENST00000201961PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000446742ENST00000326071PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000446742ENST00000375677PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000446742ENST00000375678PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000446742ENST00000475781PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000520154ENST00000201961PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000520154ENST00000326071PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000520154ENST00000375677PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000520154ENST00000375678PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000520154ENST00000475781PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000520281ENST00000201961PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000520281ENST00000326071PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000520281ENST00000375677PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000520281ENST00000375678PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000520281ENST00000475781PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000522003ENST00000201961PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000522003ENST00000326071PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000522003ENST00000375677PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000522003ENST00000375678PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000522003ENST00000475781PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000523145ENST00000201961PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000523145ENST00000326071PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000523145ENST00000375677PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000523145ENST00000375678PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000523145ENST00000475781PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000523241ENST00000201961PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000523241ENST00000326071PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000523241ENST00000375677PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000523241ENST00000375678PAX5chr9

37002696

C20orf112chr20

31035587

intron-intronENST00000523241ENST00000475781PAX5chr9

37002696

C20orf112chr20

31035587


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 PAX5-NOL4L


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 PAX5-NOL4L


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/:37002696/:31035587)
- 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
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}.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 PAX5-NOL4L


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 PAX5-NOL4L


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 PAX5-NOL4L


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 PAX5-NOL4L


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePAX5C0006413Burkitt Lymphoma4ORPHANET
HgenePAX5C1292769Precursor B-cell lymphoblastic leukemia4ORPHANET
HgenePAX5C0023485Precursor B-Cell Lymphoblastic Leukemia-Lymphoma2CTD_human
HgenePAX5C1961102Precursor Cell Lymphoblastic Leukemia Lymphoma2CGI;CTD_human;UNIPROT
HgenePAX5C0023452Childhood Acute Lymphoblastic Leukemia1CTD_human
HgenePAX5C0023453L2 Acute Lymphoblastic Leukemia1CTD_human
HgenePAX5C1535926Neurodevelopmental Disorders1CTD_human