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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 10504

FusionGeneSummary for DPP9_ARHGAP1

check button Fusion gene summary
Fusion gene informationFusion gene name: DPP9_ARHGAP1
Fusion gene ID: 10504
HgeneTgene
Gene symbol

DPP9

ARHGAP1

Gene ID

91039

392

Gene namedipeptidyl peptidase 9Rho GTPase activating protein 1
SynonymsDP9|DPLP9|DPRP-2|DPRP2CDC42GAP|RHOGAP|RHOGAP1|p50rhoGAP
Cytomap

19p13.3

11p11.2

Type of geneprotein-codingprotein-coding
Descriptiondipeptidyl peptidase 9DPP IXdipeptidyl peptidase IV-related protein-2dipeptidyl peptidase IXdipeptidyl peptidase-like protein 9dipeptidylpeptidase 9rho GTPase-activating protein 1CDC42 GTPase-activating proteinGTPase-activating protein rhoGAPGTPase-activating protein rhoOGAPGTPase-activating protein, Rho, 1rho-related small GTPase protein activatorrho-type GTPase-activating protein 1
Modification date2018052020180522
UniProtAcc

Q86TI2

Q07960

Ensembl transtripts involved in fusion geneENST00000262960, ENST00000598800, 
ENST00000597849, ENST00000594671, 
ENST00000601173, 
ENST00000311956, 
Fusion gene scores* DoF score5 X 6 X 1=307 X 5 X 5=175
# samples 119
** MAII scorelog2(11/30*10)=1.87446911791614
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(9/175*10)=-0.959358015502654
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: DPP9 [Title/Abstract] AND ARHGAP1 [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotation
* 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
TgeneARHGAP1

GO:0007264

small GTPase mediated signal transduction

8253717|8288572


check button Fusion gene information from three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* 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.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS3.1AW190431DPP9chr19

4675845

+ARHGAP1chr11

46699468

+
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

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-3UTRENST00000262960ENST00000311956DPP9chr19

4675845

+ARHGAP1chr11

46699468

+
intron-3UTRENST00000598800ENST00000311956DPP9chr19

4675845

+ARHGAP1chr11

46699468

+
intron-3UTRENST00000597849ENST00000311956DPP9chr19

4675845

+ARHGAP1chr11

46699468

+
intron-3UTRENST00000594671ENST00000311956DPP9chr19

4675845

+ARHGAP1chr11

46699468

+
intron-3UTRENST00000601173ENST00000311956DPP9chr19

4675845

+ARHGAP1chr11

46699468

+

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FusionProtFeatures for DPP9_ARHGAP1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
DPP9

Q86TI2

ARHGAP1

Q07960

GTPase activator for the Rho, Rac and Cdc42 proteins,converting them to the putatively inactive GDP-bound state. Cdc42seems to be the preferred substrate.

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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FusionGeneSequence for DPP9_ARHGAP1


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

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FusionGenePPI for DPP9_ARHGAP1


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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RelatedDrugs for DPP9_ARHGAP1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for DPP9_ARHGAP1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneDPP9C1800706Idiopathic Pulmonary Fibrosis1CTD_human;ORPHANET
TgeneARHGAP1C0036341Schizophrenia1PSYGENET