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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:TIA1-HSPA13 (FusionGDB2 ID:90184)

Fusion Gene Summary for TIA1-HSPA13

check button Fusion gene summary
Fusion gene informationFusion gene name: TIA1-HSPA13
Fusion gene ID: 90184
HgeneTgene
Gene symbol

TIA1

HSPA13

Gene ID

7072

6782

Gene nameTIA1 cytotoxic granule associated RNA binding proteinheat shock protein family A (Hsp70) member 13
SynonymsTIA-1|WDMSTCH
Cytomap

2p13.3

21q11.2

Type of geneprotein-codingprotein-coding
Descriptionnucleolysin TIA-1 isoform p40nucleolysin TIA-1T-cell-restricted intracellular antigen-1p40-TIA-1 (containing p15-TIA-1)heat shock 70 kDa protein 13heat shock protein 70kDa family, member 13microsomal stress 70 protein ATPase corestress 70 protein chaperone, microsome-associated, 60kDstress 70 protein chaperone, microsome-associated, 60kDastress-70 protein chaperone m
Modification date2020031320200313
UniProtAcc.

P48723

Ensembl transtripts involved in fusion geneENST00000433529, ENST00000415783, 
ENST00000282574, ENST00000445587, 
ENST00000482876, ENST00000416149, 
ENST00000285667, ENST00000544452, 
ENST00000478035, 
Fusion gene scores* DoF score11 X 9 X 8=7923 X 3 X 2=18
# samples 133
** MAII scorelog2(13/792*10)=-2.60698880705116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: TIA1 [Title/Abstract] AND HSPA13 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointTIA1(70444115)-HSPA13(15746130), # 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
HgeneTIA1

GO:0048024

regulation of mRNA splicing, via spliceosome

11106748


check buttonFusion gene breakpoints across TIA1 (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 HSPA13 (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/AT06637TIA1chr2

70444115

+HSPA13chr21

15746130

+


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Fusion Gene ORF analysis for TIA1-HSPA13

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-3CDSENST00000433529ENST00000285667TIA1chr2

70444115

+HSPA13chr21

15746130

+
intron-3CDSENST00000433529ENST00000544452TIA1chr2

70444115

+HSPA13chr21

15746130

+
intron-intronENST00000433529ENST00000478035TIA1chr2

70444115

+HSPA13chr21

15746130

+
intron-3CDSENST00000415783ENST00000285667TIA1chr2

70444115

+HSPA13chr21

15746130

+
intron-3CDSENST00000415783ENST00000544452TIA1chr2

70444115

+HSPA13chr21

15746130

+
intron-intronENST00000415783ENST00000478035TIA1chr2

70444115

+HSPA13chr21

15746130

+
intron-3CDSENST00000282574ENST00000285667TIA1chr2

70444115

+HSPA13chr21

15746130

+
intron-3CDSENST00000282574ENST00000544452TIA1chr2

70444115

+HSPA13chr21

15746130

+
intron-intronENST00000282574ENST00000478035TIA1chr2

70444115

+HSPA13chr21

15746130

+
intron-3CDSENST00000445587ENST00000285667TIA1chr2

70444115

+HSPA13chr21

15746130

+
intron-3CDSENST00000445587ENST00000544452TIA1chr2

70444115

+HSPA13chr21

15746130

+
intron-intronENST00000445587ENST00000478035TIA1chr2

70444115

+HSPA13chr21

15746130

+
intron-3CDSENST00000482876ENST00000285667TIA1chr2

70444115

+HSPA13chr21

15746130

+
intron-3CDSENST00000482876ENST00000544452TIA1chr2

70444115

+HSPA13chr21

15746130

+
intron-intronENST00000482876ENST00000478035TIA1chr2

70444115

+HSPA13chr21

15746130

+
intron-3CDSENST00000416149ENST00000285667TIA1chr2

70444115

+HSPA13chr21

15746130

+
intron-3CDSENST00000416149ENST00000544452TIA1chr2

70444115

+HSPA13chr21

15746130

+
intron-intronENST00000416149ENST00000478035TIA1chr2

70444115

+HSPA13chr21

15746130

+

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 TIA1-HSPA13


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 TIA1-HSPA13


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
.HSPA13

P48723

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.FUNCTION: Has peptide-independent ATPase activity.

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 TIA1-HSPA13


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 TIA1-HSPA13


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 TIA1-HSPA13


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneHSPA13P48723DB09130CopperSmall moleculeApproved|Investigational
TgeneHSPA13P48723DB09130CopperSmall moleculeApproved|Investigational

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Related Diseases for TIA1-HSPA13


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneTIA1C0221054Welander Distal Myopathy3GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgeneTIA1C2931290Welander distal myopathy, Swedish type3CTD_human;ORPHANET