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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:ASPSCR1-HGS (FusionGDB2 ID:7318)

Fusion Gene Summary for ASPSCR1-HGS

check button Fusion gene summary
Fusion gene informationFusion gene name: ASPSCR1-HGS
Fusion gene ID: 7318
HgeneTgene
Gene symbol

ASPSCR1

HGS

Gene ID

79058

9146

Gene nameASPSCR1 tether for SLC2A4, UBX domain containinghepatocyte growth factor-regulated tyrosine kinase substrate
SynonymsASPCR1|ASPL|ASPS|RCC17|TUG|UBXD9|UBXN9HRS
Cytomap

17q25.3

17q25.3

Type of geneprotein-codingprotein-coding
Descriptiontether containing UBX domain for GLUT4ASPSCR1, UBX domain containing tether for SLC2A4UBX domain protein 9UBX domain-containing protein 9alveolar soft part sarcoma chromosomal region candidate gene 1 proteinalveolar soft part sarcoma chromosome regiohepatocyte growth factor-regulated tyrosine kinase substratehuman growth factor-regulated tyrosine kinase substrateprotein pp110
Modification date2020031320200327
UniProtAcc

Q9BZE9

Q68CP4

Ensembl transtripts involved in fusion geneENST00000306729, ENST00000306739, 
ENST00000580534, ENST00000581647, 
ENST00000582404, 
ENST00000329138, 
Fusion gene scores* DoF score9 X 6 X 8=4327 X 6 X 5=210
# samples 128
** MAII scorelog2(12/432*10)=-1.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/210*10)=-1.39231742277876
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ASPSCR1 [Title/Abstract] AND HGS [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointASPSCR1(79943483)-HGS(79667497), # samples:2
Anticipated loss of major functional domain due to fusion event.ASPSCR1-HGS seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
ASPSCR1-HGS 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
TgeneHGS

GO:0046426

negative regulation of JAK-STAT cascade

12444102


check buttonFusion gene breakpoints across ASPSCR1 (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 HGS (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
ChimerDB4ACCTCGA-OR-A5J7-01AASPSCR1chr17

79943483

+HGSchr17

79667497

+
ChimerDB4ACCTCGA-OR-A5J7ASPSCR1chr17

79943483

+HGSchr17

79667496

+
ChimerDB4ACCTCGA-OR-A5J7-01AASPSCR1chr17

79943483

+HGSchr17

79667497

+


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Fusion Gene ORF analysis for ASPSCR1-HGS

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-shiftENST00000306729ENST00000329138ASPSCR1chr17

79943483

+HGSchr17

79667497

+
Frame-shiftENST00000306739ENST00000329138ASPSCR1chr17

79943483

+HGSchr17

79667497

+
Frame-shiftENST00000580534ENST00000329138ASPSCR1chr17

79943483

+HGSchr17

79667497

+
Frame-shiftENST00000581647ENST00000329138ASPSCR1chr17

79943483

+HGSchr17

79667497

+
intron-3CDSENST00000582404ENST00000329138ASPSCR1chr17

79943483

+HGSchr17

79667497

+
Frame-shiftENST00000306729ENST00000329138ASPSCR1chr17

79943483

+HGSchr17

79667496

+
Frame-shiftENST00000306739ENST00000329138ASPSCR1chr17

79943483

+HGSchr17

79667496

+
Frame-shiftENST00000580534ENST00000329138ASPSCR1chr17

79943483

+HGSchr17

79667496

+
Frame-shiftENST00000581647ENST00000329138ASPSCR1chr17

79943483

+HGSchr17

79667496

+
intron-3CDSENST00000582404ENST00000329138ASPSCR1chr17

79943483

+HGSchr17

79667496

+

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 ASPSCR1-HGS


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)
ASPSCR1chr1779943483+HGSchr1779667496+4.83E-070.9999995
ASPSCR1chr1779943483+HGSchr1779667496+4.83E-070.9999995
ASPSCR1chr1779943483+HGSchr1779667496+4.83E-070.9999995
ASPSCR1chr1779943483+HGSchr1779667496+4.83E-070.9999995

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 ASPSCR1-HGS


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
ASPSCR1

Q9BZE9

HGS

Q68CP4

FUNCTION: Tethering protein that sequesters GLUT4-containing vesicles in the cytoplasm in the absence of insulin. Modulates the amount of GLUT4 that is available at the cell surface (By similarity). Enhances VCP methylation catalyzed by VCPKMT. {ECO:0000250, ECO:0000269|PubMed:23349634}.FUNCTION: Lysosomal acetyltransferase that acetylates the non-reducing terminal alpha-glucosamine residue of intralysosomal heparin or heparan sulfate, converting it into a substrate for luminal alpha-N-acetyl glucosaminidase. {ECO:0000269|PubMed:16960811, ECO:0000269|PubMed:17033958, ECO:0000269|PubMed:19823584, ECO:0000269|PubMed:20650889}.

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 ASPSCR1-HGS


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 ASPSCR1-HGS


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 ASPSCR1-HGS


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 ASPSCR1-HGS


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneASPSCR1C4518356MiT family translocation renal cell carcinoma3ORPHANET
HgeneASPSCR1C0206657Alveolar Soft Part Sarcoma1CTD_human;ORPHANET