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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:DPP10-NAGA (FusionGDB2 ID:HG57628TG4668)

Fusion Gene Summary for DPP10-NAGA

check button Fusion gene summary
Fusion gene informationFusion gene name: DPP10-NAGA
Fusion gene ID: hg57628tg4668
HgeneTgene
Gene symbol

DPP10

NAGA

Gene ID

57628

4668

Gene namedipeptidyl peptidase like 10alpha-N-acetylgalactosaminidase
SynonymsDPL2|DPPY|DPRP-3|DPRP3D22S674|GALB
Cytomap('DPP10')('NAGA')

2q14.1

22q13.2

Type of geneprotein-codingprotein-coding
Descriptioninactive dipeptidyl peptidase 10DPP Xdipeptidyl peptidase 10dipeptidyl peptidase IV-related protein 3dipeptidyl peptidase Xdipeptidyl peptidase-like protein 2dipeptidyl-peptidase 10 (inactive)dipeptidyl-peptidase 10 (non-functional)alpha-N-acetylgalactosaminidaseAcetylgalactosaminidase, alpha-N- (alpha-galactosidase B)N-acetylgalactosaminidase, alpha-alpha-galactosidase B
Modification date2020031320200313
UniProtAcc.

P17050

Ensembl transtripts involved in fusion geneENST00000310323, ENST00000393147, 
ENST00000409163, ENST00000410059, 
ENST00000488208, 
Fusion gene scores* DoF score13 X 13 X 1=1692 X 2 X 1=4
# samples 132
** MAII scorelog2(13/169*10)=-0.37851162325373
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/4*10)=2.32192809488736
Context

PubMed: DPP10 [Title/Abstract] AND NAGA [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointDPP10(116464974)-NAGA(42455359), # 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
HgeneDPP10

GO:1903078

positive regulation of protein localization to plasma membrane

15671030

TgeneNAGA

GO:0016052

carbohydrate catabolic process

19683538



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/AEC562587DPP10chr2

116464974

-NAGAchr22

42455359

-


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Fusion Gene ORF analysis for DPP10-NAGA

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-3UTRENST00000310323ENST00000396398DPP10chr2

116464974

-NAGAchr22

42455359

-
intron-3UTRENST00000393147ENST00000396398DPP10chr2

116464974

-NAGAchr22

42455359

-
intron-3UTRENST00000409163ENST00000396398DPP10chr2

116464974

-NAGAchr22

42455359

-
intron-3UTRENST00000410059ENST00000396398DPP10chr2

116464974

-NAGAchr22

42455359

-
intron-3UTRENST00000488208ENST00000396398DPP10chr2

116464974

-NAGAchr22

42455359

-
intron-intronENST00000310323ENST00000402937DPP10chr2

116464974

-NAGAchr22

42455359

-
intron-intronENST00000310323ENST00000403363DPP10chr2

116464974

-NAGAchr22

42455359

-
intron-intronENST00000393147ENST00000402937DPP10chr2

116464974

-NAGAchr22

42455359

-
intron-intronENST00000393147ENST00000403363DPP10chr2

116464974

-NAGAchr22

42455359

-
intron-intronENST00000409163ENST00000402937DPP10chr2

116464974

-NAGAchr22

42455359

-
intron-intronENST00000409163ENST00000403363DPP10chr2

116464974

-NAGAchr22

42455359

-
intron-intronENST00000410059ENST00000402937DPP10chr2

116464974

-NAGAchr22

42455359

-
intron-intronENST00000410059ENST00000403363DPP10chr2

116464974

-NAGAchr22

42455359

-
intron-intronENST00000488208ENST00000402937DPP10chr2

116464974

-NAGAchr22

42455359

-
intron-intronENST00000488208ENST00000403363DPP10chr2

116464974

-NAGAchr22

42455359

-

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 DPP10-NAGA


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)


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Fusion Protein Features for DPP10-NAGA


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/:116464974/:42455359)
- 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
.NAGA

P17050

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: Removes terminal alpha-N-acetylgalactosamine residues from glycolipids and glycopeptides. Required for the breakdown of glycolipids. {ECO:0000269|PubMed:9741689}.

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 DPP10-NAGA


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 DPP10-NAGA


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 DPP10-NAGA


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneNAGAP17050DB09462GlycerinSmall moleculeApproved|Investigational

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Related Diseases for DPP10-NAGA


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneDPP10C0023903Liver neoplasms1CTD_human
HgeneDPP10C0032927Precancerous Conditions1CTD_human
HgeneDPP10C0282313Condition, Preneoplastic1CTD_human
HgeneDPP10C0345904Malignant neoplasm of liver1CTD_human
HgeneDPP10C1510586Autism Spectrum Disorders1CTD_human
TgeneC1836522Schindler Disease, Type II7CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
TgeneC1836544Schindler Disease, Type I5CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
TgeneC1836545Schindler Disease, Type III2CTD_human;ORPHANET
TgeneC0036572Seizures1GENOMICS_ENGLAND
TgeneC0270724Infantile Neuroaxonal Dystrophy1CTD_human
TgeneC0338473Neuroaxonal Dystrophies1CTD_human
TgeneC0751716Adult Neuroaxonal Dystrophy1CTD_human
TgeneC0751717Juvenile Neuroaxonal Dystrophy1CTD_human
TgeneC0751718Late Infantile Neuroaxonal Dystrophy1CTD_human