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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:ARHGAP21-MSRB2 (FusionGDB2 ID:5990)

Fusion Gene Summary for ARHGAP21-MSRB2

check button Fusion gene summary
Fusion gene informationFusion gene name: ARHGAP21-MSRB2
Fusion gene ID: 5990
HgeneTgene
Gene symbol

ARHGAP21

MSRB2

Gene ID

57584

22921

Gene nameRho GTPase activating protein 21methionine sulfoxide reductase B2
SynonymsARHGAP10CBS-1|CBS1|CGI-131|MSRB|PILB
Cytomap

10p12.1|10p12.3

10p12.2

Type of geneprotein-codingprotein-coding
Descriptionrho GTPase-activating protein 21Rho-GTPase activating protein 10rho GTPase-activating protein 10rho-type GTPase-activating protein 21methionine-R-sulfoxide reductase B2, mitochondrialpilin-like transcription factor
Modification date2020032020200313
UniProtAcc

Q5T5U3

Q9Y3D2

Ensembl transtripts involved in fusion geneENST00000396432, ENST00000320481, 
ENST00000493154, 
ENST00000468633, 
ENST00000376510, 
Fusion gene scores* DoF score10 X 9 X 6=5404 X 4 X 4=64
# samples 125
** MAII scorelog2(12/540*10)=-2.16992500144231
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/64*10)=-0.356143810225275
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ARHGAP21 [Title/Abstract] AND MSRB2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointARHGAP21(25010766)-MSRB2(23399171), # samples:3
Anticipated loss of major functional domain due to fusion event.ARHGAP21-MSRB2 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
HgeneARHGAP21

GO:0051683

establishment of Golgi localization

20525016


check buttonFusion gene breakpoints across ARHGAP21 (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 MSRB2 (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
ChimerDB4STADTCGA-R5-A7O7-01AARHGAP21chr10

25010766

-MSRB2chr10

23399171

+
ChimerDB4STADTCGA-R5-A7O7ARHGAP21chr10

25010765

-MSRB2chr10

23399170

+


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Fusion Gene ORF analysis for ARHGAP21-MSRB2

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
5CDS-intronENST00000396432ENST00000468633ARHGAP21chr10

25010766

-MSRB2chr10

23399171

+
5CDS-intronENST00000396432ENST00000468633ARHGAP21chr10

25010765

-MSRB2chr10

23399170

+
Frame-shiftENST00000396432ENST00000376510ARHGAP21chr10

25010766

-MSRB2chr10

23399171

+
Frame-shiftENST00000396432ENST00000376510ARHGAP21chr10

25010765

-MSRB2chr10

23399170

+
intron-3CDSENST00000320481ENST00000376510ARHGAP21chr10

25010766

-MSRB2chr10

23399171

+
intron-3CDSENST00000320481ENST00000376510ARHGAP21chr10

25010765

-MSRB2chr10

23399170

+
intron-3CDSENST00000493154ENST00000376510ARHGAP21chr10

25010766

-MSRB2chr10

23399171

+
intron-3CDSENST00000493154ENST00000376510ARHGAP21chr10

25010765

-MSRB2chr10

23399170

+
intron-intronENST00000320481ENST00000468633ARHGAP21chr10

25010766

-MSRB2chr10

23399171

+
intron-intronENST00000320481ENST00000468633ARHGAP21chr10

25010765

-MSRB2chr10

23399170

+
intron-intronENST00000493154ENST00000468633ARHGAP21chr10

25010766

-MSRB2chr10

23399171

+
intron-intronENST00000493154ENST00000468633ARHGAP21chr10

25010765

-MSRB2chr10

23399170

+

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 ARHGAP21-MSRB2


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)
ARHGAP21chr1025010765-MSRB2chr1023399170+0.0011010250.998899
ARHGAP21chr1025010765-MSRB2chr1023399170+0.0011010250.998899
ARHGAP21chr1025010765-MSRB2chr1023399170+0.0011010250.998899
ARHGAP21chr1025010765-MSRB2chr1023399170+0.0011010250.998899

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 ARHGAP21-MSRB2


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/:25010766/:23399171)
- 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
ARHGAP21

Q5T5U3

MSRB2

Q9Y3D2

FUNCTION: Functions as a GTPase-activating protein (GAP) for RHOA and CDC42. Downstream partner of ARF1 which may control Golgi apparatus structure and function. Also required for CTNNA1 recruitment to adherens junctions. {ECO:0000269|PubMed:15793564, ECO:0000269|PubMed:16184169}.FUNCTION: Methionine-sulfoxide reductase that specifically reduces methionine (R)-sulfoxide back to methionine. While in many cases, methionine oxidation is the result of random oxidation following oxidative stress, methionine oxidation is also a post-translational modification that takes place on specific residue. Upon oxidative stress, may play a role in the preservation of mitochondrial integrity by decreasing the intracellular reactive oxygen species build-up through its scavenging role, hence contributing to cell survival and protein maintenance. {ECO:0000269|PubMed:18424444}.

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 ARHGAP21-MSRB2


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 ARHGAP21-MSRB2


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 ARHGAP21-MSRB2


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 ARHGAP21-MSRB2


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