FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

Fusion Gene Summary

leaf

Fusion Gene ORF analysis

leaf

Fusion Genomic Features

leaf

Fusion Protein Features

leaf

Fusion Gene Sequence

leaf

Fusion Gene PPI analysis

leaf

Related Drugs

leaf

Related Diseases

Fusion gene:TCEA1-MTSS1 (FusionGDB2 ID:89649)

Fusion Gene Summary for TCEA1-MTSS1

check button Fusion gene summary
Fusion gene informationFusion gene name: TCEA1-MTSS1
Fusion gene ID: 89649
HgeneTgene
Gene symbol

TCEA1

MTSS1

Gene ID

6917

9788

Gene nametranscription elongation factor A1MTSS I-BAR domain containing 1
SynonymsGTF2S|SII|TCEA|TF2S|TFIISMIM|MIMA|MIMB
Cytomap

8q11.23

8q24.13

Type of geneprotein-codingprotein-coding
Descriptiontranscription elongation factor A protein 1epididymis secretory sperm binding proteintranscription elongation factor A (SII), 1transcription elongation factor S-II protein 1transcription elongation factor TFIIS.otranscription factor IISprotein MTSS 1MTSS1, I-BAR domain containingmetastasis suppressor 1metastasis suppressor YGL-1metastasis suppressor protein 1missing in metastasis protein
Modification date2020031320200313
UniProtAcc.

O43312

Ensembl transtripts involved in fusion geneENST00000396401, ENST00000521604, 
ENST00000521086, ENST00000518784, 
ENST00000520534, ENST00000522635, 
ENST00000354184, ENST00000325064, 
ENST00000395508, ENST00000431961, 
ENST00000523587, ENST00000524090, 
ENST00000378017, ENST00000518547, 
Fusion gene scores* DoF score8 X 7 X 6=3367 X 7 X 4=196
# samples 77
** MAII scorelog2(7/336*10)=-2.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/196*10)=-1.48542682717024
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: TCEA1 [Title/Abstract] AND MTSS1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointTCEA1(54906228)-MTSS1(125716432), # samples:1
Anticipated loss of major functional domain due to fusion event.TCEA1-MTSS1 seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
TCEA1-MTSS1 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
TCEA1-MTSS1 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
TCEA1-MTSS1 seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor 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

check buttonFusion gene breakpoints across TCEA1 (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 MTSS1 (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
ChimerDB4CESCTCGA-R2-A69V-01ATCEA1chr8

54906228

-MTSS1chr8

125716432

-


Top

Fusion Gene ORF analysis for TCEA1-MTSS1

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
5CDS-5UTRENST00000396401ENST00000354184TCEA1chr8

54906228

-MTSS1chr8

125716432

-
5CDS-5UTRENST00000521604ENST00000354184TCEA1chr8

54906228

-MTSS1chr8

125716432

-
5CDS-intronENST00000396401ENST00000325064TCEA1chr8

54906228

-MTSS1chr8

125716432

-
5CDS-intronENST00000396401ENST00000395508TCEA1chr8

54906228

-MTSS1chr8

125716432

-
5CDS-intronENST00000396401ENST00000431961TCEA1chr8

54906228

-MTSS1chr8

125716432

-
5CDS-intronENST00000396401ENST00000523587TCEA1chr8

54906228

-MTSS1chr8

125716432

-
5CDS-intronENST00000396401ENST00000524090TCEA1chr8

54906228

-MTSS1chr8

125716432

-
5CDS-intronENST00000521604ENST00000325064TCEA1chr8

54906228

-MTSS1chr8

125716432

-
5CDS-intronENST00000521604ENST00000395508TCEA1chr8

54906228

-MTSS1chr8

125716432

-
5CDS-intronENST00000521604ENST00000431961TCEA1chr8

54906228

-MTSS1chr8

125716432

-
5CDS-intronENST00000521604ENST00000523587TCEA1chr8

54906228

-MTSS1chr8

125716432

-
5CDS-intronENST00000521604ENST00000524090TCEA1chr8

54906228

-MTSS1chr8

125716432

-
5UTR-3CDSENST00000521086ENST00000378017TCEA1chr8

54906228

-MTSS1chr8

125716432

-
5UTR-3CDSENST00000521086ENST00000518547TCEA1chr8

54906228

-MTSS1chr8

125716432

-
5UTR-5UTRENST00000521086ENST00000354184TCEA1chr8

54906228

-MTSS1chr8

125716432

-
5UTR-intronENST00000521086ENST00000325064TCEA1chr8

54906228

-MTSS1chr8

125716432

-
5UTR-intronENST00000521086ENST00000395508TCEA1chr8

54906228

-MTSS1chr8

125716432

-
5UTR-intronENST00000521086ENST00000431961TCEA1chr8

54906228

-MTSS1chr8

125716432

-
5UTR-intronENST00000521086ENST00000523587TCEA1chr8

54906228

-MTSS1chr8

125716432

-
5UTR-intronENST00000521086ENST00000524090TCEA1chr8

54906228

-MTSS1chr8

125716432

-
Frame-shiftENST00000396401ENST00000378017TCEA1chr8

54906228

-MTSS1chr8

125716432

-
Frame-shiftENST00000396401ENST00000518547TCEA1chr8

54906228

-MTSS1chr8

125716432

-
Frame-shiftENST00000521604ENST00000378017TCEA1chr8

54906228

-MTSS1chr8

125716432

-
Frame-shiftENST00000521604ENST00000518547TCEA1chr8

54906228

-MTSS1chr8

125716432

-
intron-3CDSENST00000518784ENST00000378017TCEA1chr8

54906228

-MTSS1chr8

125716432

-
intron-3CDSENST00000518784ENST00000518547TCEA1chr8

54906228

-MTSS1chr8

125716432

-
intron-3CDSENST00000520534ENST00000378017TCEA1chr8

54906228

-MTSS1chr8

125716432

-
intron-3CDSENST00000520534ENST00000518547TCEA1chr8

54906228

-MTSS1chr8

125716432

-
intron-3CDSENST00000522635ENST00000378017TCEA1chr8

54906228

-MTSS1chr8

125716432

-
intron-3CDSENST00000522635ENST00000518547TCEA1chr8

54906228

-MTSS1chr8

125716432

-
intron-5UTRENST00000518784ENST00000354184TCEA1chr8

54906228

-MTSS1chr8

125716432

-
intron-5UTRENST00000520534ENST00000354184TCEA1chr8

54906228

-MTSS1chr8

125716432

-
intron-5UTRENST00000522635ENST00000354184TCEA1chr8

54906228

-MTSS1chr8

125716432

-
intron-intronENST00000518784ENST00000325064TCEA1chr8

54906228

-MTSS1chr8

125716432

-
intron-intronENST00000518784ENST00000395508TCEA1chr8

54906228

-MTSS1chr8

125716432

-
intron-intronENST00000518784ENST00000431961TCEA1chr8

54906228

-MTSS1chr8

125716432

-
intron-intronENST00000518784ENST00000523587TCEA1chr8

54906228

-MTSS1chr8

125716432

-
intron-intronENST00000518784ENST00000524090TCEA1chr8

54906228

-MTSS1chr8

125716432

-
intron-intronENST00000520534ENST00000325064TCEA1chr8

54906228

-MTSS1chr8

125716432

-
intron-intronENST00000520534ENST00000395508TCEA1chr8

54906228

-MTSS1chr8

125716432

-
intron-intronENST00000520534ENST00000431961TCEA1chr8

54906228

-MTSS1chr8

125716432

-
intron-intronENST00000520534ENST00000523587TCEA1chr8

54906228

-MTSS1chr8

125716432

-
intron-intronENST00000520534ENST00000524090TCEA1chr8

54906228

-MTSS1chr8

125716432

-
intron-intronENST00000522635ENST00000325064TCEA1chr8

54906228

-MTSS1chr8

125716432

-
intron-intronENST00000522635ENST00000395508TCEA1chr8

54906228

-MTSS1chr8

125716432

-
intron-intronENST00000522635ENST00000431961TCEA1chr8

54906228

-MTSS1chr8

125716432

-
intron-intronENST00000522635ENST00000523587TCEA1chr8

54906228

-MTSS1chr8

125716432

-
intron-intronENST00000522635ENST00000524090TCEA1chr8

54906228

-MTSS1chr8

125716432

-

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

Top

Fusion Genomic Features for TCEA1-MTSS1


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.

Top

Fusion Protein Features for TCEA1-MTSS1


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/:54906228/:125716432)
- 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
.MTSS1

O43312

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: May be related to cancer progression or tumor metastasis in a variety of organ sites, most likely through an interaction with the actin cytoskeleton.

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


Top

Fusion Gene Sequence for TCEA1-MTSS1


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.

Top

Fusion Gene PPI Analysis for TCEA1-MTSS1


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


Top

Related Drugs for TCEA1-MTSS1


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

Top

Related Diseases for TCEA1-MTSS1


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