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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:SLIT2-HMG20B (FusionGDB2 ID:83667)

Fusion Gene Summary for SLIT2-HMG20B

check button Fusion gene summary
Fusion gene informationFusion gene name: SLIT2-HMG20B
Fusion gene ID: 83667
HgeneTgene
Gene symbol

SLIT2

HMG20B

Gene ID

9353

10362

Gene nameslit guidance ligand 2high mobility group 20B
SynonymsSLIL3|Slit-2BRAF25|BRAF35|HMGX2|HMGXB2|PP7706|SMARCE1r|SOXL|pp8857
Cytomap

4p15.31

19p13.3

Type of geneprotein-codingprotein-coding
Descriptionslit homolog 2 proteinSWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1-relatedBRCA2-associated factor 35HMG box domain containing 2HMG box-containing protein 20BHMG domain-containing protein 2HMG domain-containing protein HMGX2
Modification date2020031320200327
UniProtAcc.

Q9P0W2

Ensembl transtripts involved in fusion geneENST00000273739, ENST00000503823, 
ENST00000503837, ENST00000504154, 
ENST00000509394, 
ENST00000333651, 
ENST00000585741, 
Fusion gene scores* DoF score5 X 5 X 2=508 X 6 X 3=144
# samples 68
** MAII scorelog2(6/50*10)=0.263034405833794
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(8/144*10)=-0.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SLIT2 [Title/Abstract] AND HMG20B [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointSLIT2(20479196)-HMG20B(3579079), # 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
HgeneSLIT2

GO:0001933

negative regulation of protein phosphorylation

18345009

HgeneSLIT2

GO:0002689

negative regulation of leukocyte chemotaxis

11309622

HgeneSLIT2

GO:0007411

axon guidance

11748139

HgeneSLIT2

GO:0008045

motor neuron axon guidance

10102268

HgeneSLIT2

GO:0010593

negative regulation of lamellipodium assembly

16439689

HgeneSLIT2

GO:0010596

negative regulation of endothelial cell migration

18345009

HgeneSLIT2

GO:0014912

negative regulation of smooth muscle cell migration

16439689

HgeneSLIT2

GO:0021834

chemorepulsion involved in embryonic olfactory bulb interneuron precursor migration

11748139

HgeneSLIT2

GO:0021836

chemorepulsion involved in postnatal olfactory bulb interneuron migration

15207848

HgeneSLIT2

GO:0030336

negative regulation of cell migration

19005219

HgeneSLIT2

GO:0030837

negative regulation of actin filament polymerization

19759280

HgeneSLIT2

GO:0031290

retinal ganglion cell axon guidance

10864954|19498462

HgeneSLIT2

GO:0043116

negative regulation of vascular permeability

18345009

HgeneSLIT2

GO:0048754

branching morphogenesis of an epithelial tube

18345009

HgeneSLIT2

GO:0048846

axon extension involved in axon guidance

16840550

HgeneSLIT2

GO:0050919

negative chemotaxis

11748139

HgeneSLIT2

GO:0050929

induction of negative chemotaxis

10197527

HgeneSLIT2

GO:0051058

negative regulation of small GTPase mediated signal transduction

16439689

HgeneSLIT2

GO:0071504

cellular response to heparin

17062560

HgeneSLIT2

GO:0071672

negative regulation of smooth muscle cell chemotaxis

16439689

HgeneSLIT2

GO:0071676

negative regulation of mononuclear cell migration

16439689

HgeneSLIT2

GO:0090024

negative regulation of neutrophil chemotaxis

19759280

HgeneSLIT2

GO:0090260

negative regulation of retinal ganglion cell axon guidance

17062560

HgeneSLIT2

GO:0090288

negative regulation of cellular response to growth factor stimulus

16439689


check buttonFusion gene breakpoints across SLIT2 (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 HMG20B (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/AEC582533SLIT2chr4

20479196

+HMG20Bchr19

3579079

-


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Fusion Gene ORF analysis for SLIT2-HMG20B

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-3UTRENST00000273739ENST00000333651SLIT2chr4

20479196

+HMG20Bchr19

3579079

-
intron-3UTRENST00000503823ENST00000333651SLIT2chr4

20479196

+HMG20Bchr19

3579079

-
intron-3UTRENST00000503837ENST00000333651SLIT2chr4

20479196

+HMG20Bchr19

3579079

-
intron-3UTRENST00000504154ENST00000333651SLIT2chr4

20479196

+HMG20Bchr19

3579079

-
intron-3UTRENST00000509394ENST00000333651SLIT2chr4

20479196

+HMG20Bchr19

3579079

-
intron-intronENST00000273739ENST00000585741SLIT2chr4

20479196

+HMG20Bchr19

3579079

-
intron-intronENST00000503823ENST00000585741SLIT2chr4

20479196

+HMG20Bchr19

3579079

-
intron-intronENST00000503837ENST00000585741SLIT2chr4

20479196

+HMG20Bchr19

3579079

-
intron-intronENST00000504154ENST00000585741SLIT2chr4

20479196

+HMG20Bchr19

3579079

-
intron-intronENST00000509394ENST00000585741SLIT2chr4

20479196

+HMG20Bchr19

3579079

-

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 SLIT2-HMG20B


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 SLIT2-HMG20B


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/:20479196/:3579079)
- 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
.HMG20B

Q9P0W2

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}.FUNCTION: Required for correct progression through G2 phase of the cell cycle and entry into mitosis. Required for RCOR1/CoREST mediated repression of neuronal specific gene promoters.

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 SLIT2-HMG20B


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 SLIT2-HMG20B


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 SLIT2-HMG20B


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 SLIT2-HMG20B


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