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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:DPYSL2-FSTL5 (FusionGDB2 ID:24096)

Fusion Gene Summary for DPYSL2-FSTL5

check button Fusion gene summary
Fusion gene informationFusion gene name: DPYSL2-FSTL5
Fusion gene ID: 24096
HgeneTgene
Gene symbol

DPYSL2

FSTL5

Gene ID

1808

56884

Gene namedihydropyrimidinase like 2follistatin like 5
SynonymsCRMP-2|CRMP2|DHPRP2|DRP-2|DRP2|N2A3|ULIP-2|ULIP2-
Cytomap

8p21.2

4q32.2

Type of geneprotein-codingprotein-coding
Descriptiondihydropyrimidinase-related protein 2collapsin response mediator protein hCRMP-2unc-33-like phosphoprotein 2follistatin-related protein 5follistatin-like protein 5
Modification date2020032720200313
UniProtAcc

Q16555

Q8N475

Ensembl transtripts involved in fusion geneENST00000521913, ENST00000311151, 
ENST00000523027, ENST00000521983, 
ENST00000306100, ENST00000379164, 
ENST00000536695, ENST00000427802, 
ENST00000511170, 
Fusion gene scores* DoF score17 X 15 X 7=17854 X 3 X 3=36
# samples 163
** MAII scorelog2(16/1785*10)=-3.4797802640291
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/36*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: DPYSL2 [Title/Abstract] AND FSTL5 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointDPYSL2(26441499)-FSTL5(162508727), # samples:2
Anticipated loss of major functional domain due to fusion event.DPYSL2-FSTL5 seems lost the major protein functional domain in Hgene partner, which is a essential gene 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

check buttonFusion gene breakpoints across DPYSL2 (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 FSTL5 (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
ChimerDB4SARCTCGA-DX-AB2O-01ADPYSL2chr8

26441499

+FSTL5chr4

162508727

-
ChimerDB4SARCTCGA-DX-AB2O-01ADPYSL2chr8

26441499

-FSTL5chr4

162508727

-


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Fusion Gene ORF analysis for DPYSL2-FSTL5

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
Frame-shiftENST00000521913ENST00000306100DPYSL2chr8

26441499

+FSTL5chr4

162508727

-
Frame-shiftENST00000521913ENST00000379164DPYSL2chr8

26441499

+FSTL5chr4

162508727

-
Frame-shiftENST00000521913ENST00000536695DPYSL2chr8

26441499

+FSTL5chr4

162508727

-
Frame-shiftENST00000521913ENST00000427802DPYSL2chr8

26441499

+FSTL5chr4

162508727

-
5CDS-5UTRENST00000521913ENST00000511170DPYSL2chr8

26441499

+FSTL5chr4

162508727

-
Frame-shiftENST00000311151ENST00000306100DPYSL2chr8

26441499

+FSTL5chr4

162508727

-
Frame-shiftENST00000311151ENST00000379164DPYSL2chr8

26441499

+FSTL5chr4

162508727

-
Frame-shiftENST00000311151ENST00000536695DPYSL2chr8

26441499

+FSTL5chr4

162508727

-
Frame-shiftENST00000311151ENST00000427802DPYSL2chr8

26441499

+FSTL5chr4

162508727

-
5CDS-5UTRENST00000311151ENST00000511170DPYSL2chr8

26441499

+FSTL5chr4

162508727

-
Frame-shiftENST00000523027ENST00000306100DPYSL2chr8

26441499

+FSTL5chr4

162508727

-
Frame-shiftENST00000523027ENST00000379164DPYSL2chr8

26441499

+FSTL5chr4

162508727

-
Frame-shiftENST00000523027ENST00000536695DPYSL2chr8

26441499

+FSTL5chr4

162508727

-
Frame-shiftENST00000523027ENST00000427802DPYSL2chr8

26441499

+FSTL5chr4

162508727

-
5CDS-5UTRENST00000523027ENST00000511170DPYSL2chr8

26441499

+FSTL5chr4

162508727

-
intron-3CDSENST00000521983ENST00000306100DPYSL2chr8

26441499

+FSTL5chr4

162508727

-
intron-3CDSENST00000521983ENST00000379164DPYSL2chr8

26441499

+FSTL5chr4

162508727

-
intron-3CDSENST00000521983ENST00000536695DPYSL2chr8

26441499

+FSTL5chr4

162508727

-
intron-3CDSENST00000521983ENST00000427802DPYSL2chr8

26441499

+FSTL5chr4

162508727

-
intron-5UTRENST00000521983ENST00000511170DPYSL2chr8

26441499

+FSTL5chr4

162508727

-

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 DPYSL2-FSTL5


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 DPYSL2-FSTL5


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
DPYSL2

Q16555

FSTL5

Q8N475

FUNCTION: Plays a role in neuronal development and polarity, as well as in axon growth and guidance, neuronal growth cone collapse and cell migration. Necessary for signaling by class 3 semaphorins and subsequent remodeling of the cytoskeleton. May play a role in endocytosis. {ECO:0000269|PubMed:11477421, ECO:0000269|PubMed:15466863, ECO:0000269|PubMed:20801876}.

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 DPYSL2-FSTL5


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 DPYSL2-FSTL5


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 DPYSL2-FSTL5


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 DPYSL2-FSTL5


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneDPYSL2C0005586Bipolar Disorder4PSYGENET
HgeneDPYSL2C0001973Alcoholic Intoxication, Chronic1PSYGENET
HgeneDPYSL2C0002395Alzheimer's Disease1CTD_human
HgeneDPYSL2C0011251Delusional disorder1CTD_human
HgeneDPYSL2C0011265Presenile dementia1CTD_human
HgeneDPYSL2C0011570Mental Depression1PSYGENET
HgeneDPYSL2C0011581Depressive disorder1PSYGENET
HgeneDPYSL2C0029408Degenerative polyarthritis1CTD_human
HgeneDPYSL2C0036349Paranoid Schizophrenia1CTD_human
HgeneDPYSL2C0086743Osteoarthrosis Deformans1CTD_human
HgeneDPYSL2C0276496Familial Alzheimer Disease (FAD)1CTD_human
HgeneDPYSL2C0494463Alzheimer Disease, Late Onset1CTD_human
HgeneDPYSL2C0546126Acute Confusional Senile Dementia1CTD_human
HgeneDPYSL2C0750900Alzheimer's Disease, Focal Onset1CTD_human
HgeneDPYSL2C0750901Alzheimer Disease, Early Onset1CTD_human
TgeneFSTL5C0005586Bipolar Disorder1CTD_human
TgeneFSTL5C0005587Depression, Bipolar1CTD_human
TgeneFSTL5C0024713Manic Disorder1CTD_human
TgeneFSTL5C0338831Manic1CTD_human