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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:RANGAP1-DESI1 (FusionGDB2 ID:71658)

Fusion Gene Summary for RANGAP1-DESI1

check button Fusion gene summary
Fusion gene informationFusion gene name: RANGAP1-DESI1
Fusion gene ID: 71658
HgeneTgene
Gene symbol

RANGAP1

DESI1

Gene ID

5905

51029

Gene nameRan GTPase activating protein 1desumoylating isopeptidase 2
SynonymsFug1|RANGAP|SDC1orf121|CGI-146|DESI|DESI1|DeSI-2|FAM152A|PNAS-4|PPPDE1
Cytomap

22q13.2

1q44

Type of geneprotein-codingprotein-coding
Descriptionran GTPase-activating protein 1segregation distorter homologsegregation distortiondeubiquitinase DESI2PPPDE peptidase domain-containing protein 1desumoylating isopeptidase 1family with sequence similarity 152, member A
Modification date2020031320200313
UniProtAcc.

Q6ICB0

Ensembl transtripts involved in fusion geneENST00000405486, ENST00000356244, 
ENST00000455915, ENST00000407260, 
ENST00000263256, ENST00000463886, 
Fusion gene scores* DoF score16 X 14 X 7=15685 X 3 X 3=45
# samples 185
** MAII scorelog2(18/1568*10)=-3.12285674778553
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/45*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: RANGAP1 [Title/Abstract] AND DESI1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointRANGAP1(41676937)-DESI1(42003865), # samples:2
Anticipated loss of major functional domain due to fusion event.RANGAP1-DESI1 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
HgeneRANGAP1

GO:0046826

negative regulation of protein export from nucleus

16449645

HgeneRANGAP1

GO:0090630

activation of GTPase activity

16428860


check buttonFusion gene breakpoints across RANGAP1 (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 DESI1 (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
ChimerDB4OVTCGA-04-1356-01ARANGAP1chr22

41676937

-DESI1chr22

42003865

-
ChimerDB4OVTCGA-04-1356-01ARANGAP1chr22

41676937

-DESI1chr22

42003865

-
ChimerDB4OVTCGA-04-1356-01ARANGAP1chr22

41681990

-DESI1chr22

42003865

-


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Fusion Gene ORF analysis for RANGAP1-DESI1

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-shiftENST00000405486ENST00000263256RANGAP1chr22

41676937

-DESI1chr22

42003865

-
5CDS-intronENST00000405486ENST00000463886RANGAP1chr22

41676937

-DESI1chr22

42003865

-
Frame-shiftENST00000356244ENST00000263256RANGAP1chr22

41676937

-DESI1chr22

42003865

-
5CDS-intronENST00000356244ENST00000463886RANGAP1chr22

41676937

-DESI1chr22

42003865

-
Frame-shiftENST00000455915ENST00000263256RANGAP1chr22

41676937

-DESI1chr22

42003865

-
5CDS-intronENST00000455915ENST00000463886RANGAP1chr22

41676937

-DESI1chr22

42003865

-
intron-3CDSENST00000407260ENST00000263256RANGAP1chr22

41676937

-DESI1chr22

42003865

-
intron-intronENST00000407260ENST00000463886RANGAP1chr22

41676937

-DESI1chr22

42003865

-
intron-3CDSENST00000405486ENST00000263256RANGAP1chr22

41681990

-DESI1chr22

42003865

-
intron-intronENST00000405486ENST00000463886RANGAP1chr22

41681990

-DESI1chr22

42003865

-
5UTR-3CDSENST00000356244ENST00000263256RANGAP1chr22

41681990

-DESI1chr22

42003865

-
5UTR-intronENST00000356244ENST00000463886RANGAP1chr22

41681990

-DESI1chr22

42003865

-
intron-3CDSENST00000455915ENST00000263256RANGAP1chr22

41681990

-DESI1chr22

42003865

-
intron-intronENST00000455915ENST00000463886RANGAP1chr22

41681990

-DESI1chr22

42003865

-
intron-3CDSENST00000407260ENST00000263256RANGAP1chr22

41681990

-DESI1chr22

42003865

-
intron-intronENST00000407260ENST00000463886RANGAP1chr22

41681990

-DESI1chr22

42003865

-

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 RANGAP1-DESI1


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 RANGAP1-DESI1


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
.DESI1

Q6ICB0

FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: Protease which deconjugates SUMO1, SUMO2 and SUMO3 from some substrate proteins. Has isopeptidase but not SUMO-processing activity (By similarity). Desumoylates ZBTB46 (By similarity). Collaborates with UBQLN4 in the export of ubiquitinated proteins from the nucleus to the cytoplasm (PubMed:29666234). {ECO:0000250|UniProtKB:Q9CQT7, ECO:0000269|PubMed:29666234}.

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 RANGAP1-DESI1


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 RANGAP1-DESI1


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 RANGAP1-DESI1


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 RANGAP1-DESI1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneRANGAP1C0079744Diffuse Large B-Cell Lymphoma1CTD_human