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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:ATG13-GGA2 (FusionGDB2 ID:7521)

Fusion Gene Summary for ATG13-GGA2

check button Fusion gene summary
Fusion gene informationFusion gene name: ATG13-GGA2
Fusion gene ID: 7521
HgeneTgene
Gene symbol

ATG13

GGA2

Gene ID

9776

23062

Gene nameautophagy related 13golgi associated, gamma adaptin ear containing, ARF binding protein 2
SynonymsKIAA0652|PARATARG8VEAR
Cytomap

11p11.2

16p12.2

Type of geneprotein-codingprotein-coding
Descriptionautophagy-related protein 13ATG13 autophagy related 13 homologADP-ribosylation factor-binding protein GGA2VHS domain and ear domain of gamma-adaptinVHS domain and ear domain-containing proteingamma-adaptin-related protein 2golgi-localized, gamma ear-containing, ARF-binding protein 2
Modification date2020032720200313
UniProtAcc

O75143

Q9UJY4

Ensembl transtripts involved in fusion geneENST00000312040, ENST00000359513, 
ENST00000434074, ENST00000451945, 
ENST00000524625, ENST00000526508, 
ENST00000528494, ENST00000529655, 
ENST00000530500, ENST00000526485, 
ENST00000309859, ENST00000569182, 
ENST00000567468, 
Fusion gene scores* DoF score11 X 10 X 5=5507 X 7 X 2=98
# samples 147
** MAII scorelog2(14/550*10)=-1.97400479146706
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/98*10)=-0.485426827170242
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ATG13 [Title/Abstract] AND GGA2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointATG13(46693991)-GGA2(23486301), # 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
TgeneGGA2

GO:0034394

protein localization to cell surface

27901063

TgeneGGA2

GO:0043001

Golgi to plasma membrane protein transport

27901063


check buttonFusion gene breakpoints across ATG13 (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 GGA2 (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/AAX260489ATG13chr11

46693991

-GGA2chr16

23486301

+


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Fusion Gene ORF analysis for ATG13-GGA2

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
3UTR-3CDSENST00000312040ENST00000309859ATG13chr11

46693991

-GGA2chr16

23486301

+
3UTR-3CDSENST00000359513ENST00000309859ATG13chr11

46693991

-GGA2chr16

23486301

+
3UTR-3CDSENST00000434074ENST00000309859ATG13chr11

46693991

-GGA2chr16

23486301

+
3UTR-3CDSENST00000451945ENST00000309859ATG13chr11

46693991

-GGA2chr16

23486301

+
3UTR-3CDSENST00000524625ENST00000309859ATG13chr11

46693991

-GGA2chr16

23486301

+
3UTR-3CDSENST00000526508ENST00000309859ATG13chr11

46693991

-GGA2chr16

23486301

+
3UTR-3CDSENST00000528494ENST00000309859ATG13chr11

46693991

-GGA2chr16

23486301

+
3UTR-3CDSENST00000529655ENST00000309859ATG13chr11

46693991

-GGA2chr16

23486301

+
3UTR-3CDSENST00000530500ENST00000309859ATG13chr11

46693991

-GGA2chr16

23486301

+
3UTR-5UTRENST00000312040ENST00000569182ATG13chr11

46693991

-GGA2chr16

23486301

+
3UTR-5UTRENST00000359513ENST00000569182ATG13chr11

46693991

-GGA2chr16

23486301

+
3UTR-5UTRENST00000434074ENST00000569182ATG13chr11

46693991

-GGA2chr16

23486301

+
3UTR-5UTRENST00000451945ENST00000569182ATG13chr11

46693991

-GGA2chr16

23486301

+
3UTR-5UTRENST00000524625ENST00000569182ATG13chr11

46693991

-GGA2chr16

23486301

+
3UTR-5UTRENST00000526508ENST00000569182ATG13chr11

46693991

-GGA2chr16

23486301

+
3UTR-5UTRENST00000528494ENST00000569182ATG13chr11

46693991

-GGA2chr16

23486301

+
3UTR-5UTRENST00000529655ENST00000569182ATG13chr11

46693991

-GGA2chr16

23486301

+
3UTR-5UTRENST00000530500ENST00000569182ATG13chr11

46693991

-GGA2chr16

23486301

+
3UTR-intronENST00000312040ENST00000567468ATG13chr11

46693991

-GGA2chr16

23486301

+
3UTR-intronENST00000359513ENST00000567468ATG13chr11

46693991

-GGA2chr16

23486301

+
3UTR-intronENST00000434074ENST00000567468ATG13chr11

46693991

-GGA2chr16

23486301

+
3UTR-intronENST00000451945ENST00000567468ATG13chr11

46693991

-GGA2chr16

23486301

+
3UTR-intronENST00000524625ENST00000567468ATG13chr11

46693991

-GGA2chr16

23486301

+
3UTR-intronENST00000526508ENST00000567468ATG13chr11

46693991

-GGA2chr16

23486301

+
3UTR-intronENST00000528494ENST00000567468ATG13chr11

46693991

-GGA2chr16

23486301

+
3UTR-intronENST00000529655ENST00000567468ATG13chr11

46693991

-GGA2chr16

23486301

+
3UTR-intronENST00000530500ENST00000567468ATG13chr11

46693991

-GGA2chr16

23486301

+
intron-3CDSENST00000526485ENST00000309859ATG13chr11

46693991

-GGA2chr16

23486301

+
intron-5UTRENST00000526485ENST00000569182ATG13chr11

46693991

-GGA2chr16

23486301

+
intron-intronENST00000526485ENST00000567468ATG13chr11

46693991

-GGA2chr16

23486301

+

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 ATG13-GGA2


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 ATG13-GGA2


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/:46693991/:23486301)
- 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
ATG13

O75143

GGA2

Q9UJY4

FUNCTION: Autophagy factor required for autophagosome formation and mitophagy. Target of the TOR kinase signaling pathway that regulates autophagy through the control of the phosphorylation status of ATG13 and ULK1, and the regulation of the ATG13-ULK1-RB1CC1 complex. Through its regulation of ULK1 activity, plays a role in the regulation of the kinase activity of mTORC1 and cell proliferation. {ECO:0000269|PubMed:18936157, ECO:0000269|PubMed:19211835, ECO:0000269|PubMed:19225151, ECO:0000269|PubMed:19287211, ECO:0000269|PubMed:21795849, ECO:0000269|PubMed:21855797}.FUNCTION: Plays a role in protein sorting and trafficking between the trans-Golgi network (TGN) and endosomes. Mediates the ARF-dependent recruitment of clathrin to the TGN and binds ubiquitinated proteins and membrane cargo molecules with a cytosolic acidic cluster-dileucine (DXXLL) motif (PubMed:10747088). Mediates export of the GPCR receptor ADRA2B to the cell surface (PubMed:27901063). Regulates retrograde transport of phosphorylated form of BACE1 from endosomes to the trans-Golgi network (PubMed:15615712). {ECO:0000269|PubMed:10747088, ECO:0000269|PubMed:15615712, ECO:0000269|PubMed:27901063}.

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 ATG13-GGA2


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 ATG13-GGA2


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 ATG13-GGA2


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 ATG13-GGA2


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