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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:ATXN3-THSD7A (FusionGDB2 ID:8523)

Fusion Gene Summary for ATXN3-THSD7A

check button Fusion gene summary
Fusion gene informationFusion gene name: ATXN3-THSD7A
Fusion gene ID: 8523
HgeneTgene
Gene symbol

ATXN3

THSD7A

Gene ID

4287

221981

Gene nameataxin 3thrombospondin type 1 domain containing 7A
SynonymsAT3|ATX3|JOS|MJD|MJD1|SCA3-
Cytomap

14q32.12

7p21.3

Type of geneprotein-codingprotein-coding
Descriptionataxin-3Machado-Joseph disease protein 1josephinolivopontocerebellar ataxia 3spinocerebellar ataxia type 3 proteinthrombospondin type-1 domain-containing protein 7Athrombospondin, type I, domain containing 7A
Modification date2020031320200322
UniProtAcc

P54252

.
Ensembl transtripts involved in fusion geneENST00000545170, ENST00000429774, 
ENST00000393287, ENST00000502250, 
ENST00000503767, ENST00000340660, 
ENST00000532032, ENST00000554491, 
ENST00000423059, ENST00000480061, 
Fusion gene scores* DoF score4 X 5 X 5=1007 X 7 X 5=245
# samples 57
** MAII scorelog2(5/100*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/245*10)=-1.8073549220576
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ATXN3 [Title/Abstract] AND THSD7A [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointATXN3(92537366)-THSD7A(11676452), # 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
HgeneATXN3

GO:0070536

protein K63-linked deubiquitination

22970133

HgeneATXN3

GO:0071108

protein K48-linked deubiquitination

22970133


check buttonFusion gene breakpoints across ATXN3 (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 THSD7A (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/AAI357266ATXN3chr14

92537366

+THSD7Achr7

11676452

+


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Fusion Gene ORF analysis for ATXN3-THSD7A

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-3CDSENST00000545170ENST00000423059ATXN3chr14

92537366

+THSD7Achr7

11676452

+
intron-5UTRENST00000545170ENST00000480061ATXN3chr14

92537366

+THSD7Achr7

11676452

+
intron-3CDSENST00000429774ENST00000423059ATXN3chr14

92537366

+THSD7Achr7

11676452

+
intron-5UTRENST00000429774ENST00000480061ATXN3chr14

92537366

+THSD7Achr7

11676452

+
intron-3CDSENST00000393287ENST00000423059ATXN3chr14

92537366

+THSD7Achr7

11676452

+
intron-5UTRENST00000393287ENST00000480061ATXN3chr14

92537366

+THSD7Achr7

11676452

+
intron-3CDSENST00000502250ENST00000423059ATXN3chr14

92537366

+THSD7Achr7

11676452

+
intron-5UTRENST00000502250ENST00000480061ATXN3chr14

92537366

+THSD7Achr7

11676452

+
intron-3CDSENST00000503767ENST00000423059ATXN3chr14

92537366

+THSD7Achr7

11676452

+
intron-5UTRENST00000503767ENST00000480061ATXN3chr14

92537366

+THSD7Achr7

11676452

+
intron-3CDSENST00000340660ENST00000423059ATXN3chr14

92537366

+THSD7Achr7

11676452

+
intron-5UTRENST00000340660ENST00000480061ATXN3chr14

92537366

+THSD7Achr7

11676452

+
intron-3CDSENST00000532032ENST00000423059ATXN3chr14

92537366

+THSD7Achr7

11676452

+
intron-5UTRENST00000532032ENST00000480061ATXN3chr14

92537366

+THSD7Achr7

11676452

+
intron-3CDSENST00000554491ENST00000423059ATXN3chr14

92537366

+THSD7Achr7

11676452

+
intron-5UTRENST00000554491ENST00000480061ATXN3chr14

92537366

+THSD7Achr7

11676452

+

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 ATXN3-THSD7A


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 ATXN3-THSD7A


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
ATXN3

P54252

.
FUNCTION: Deubiquitinating enzyme involved in protein homeostasis maintenance, transcription, cytoskeleton regulation, myogenesis and degradation of misfolded chaperone substrates (PubMed:12297501, PubMed:17696782, PubMed:23625928, PubMed:28445460, PubMed:16118278). Binds long polyubiquitin chains and trims them, while it has weak or no activity against chains of 4 or less ubiquitins (PubMed:17696782). Involved in degradation of misfolded chaperone substrates via its interaction with STUB1/CHIP: recruited to monoubiquitinated STUB1/CHIP, and restricts the length of ubiquitin chain attached to STUB1/CHIP substrates and preventing further chain extension (By similarity). Interacts with key regulators of transcription and represses transcription: acts as a histone-binding protein that regulates transcription (PubMed:12297501). Regulates autophagy via the deubiquitination of 'Lys-402' of BECN1 leading to the stabilization of BECN1 (PubMed:28445460). {ECO:0000250|UniProtKB:Q9CVD2, ECO:0000269|PubMed:12297501, ECO:0000269|PubMed:16118278, ECO:0000269|PubMed:17696782, ECO:0000269|PubMed:23625928, ECO:0000269|PubMed:28445460}.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.

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 ATXN3-THSD7A


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 ATXN3-THSD7A


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 ATXN3-THSD7A


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 ATXN3-THSD7A


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneATXN3C0011570Mental Depression5PSYGENET
HgeneATXN3C0011581Depressive disorder5PSYGENET
HgeneATXN3C0027746Nerve Degeneration1CTD_human
TgeneTHSD7AC0005586Bipolar Disorder1CTD_human
TgeneTHSD7AC0005587Depression, Bipolar1CTD_human
TgeneTHSD7AC0024713Manic Disorder1CTD_human
TgeneTHSD7AC0338831Manic1CTD_human