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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:ZC3H13-TCF7L2 (FusionGDB2 ID:100528)

Fusion Gene Summary for ZC3H13-TCF7L2

check button Fusion gene summary
Fusion gene informationFusion gene name: ZC3H13-TCF7L2
Fusion gene ID: 100528
HgeneTgene
Gene symbol

ZC3H13

TCF7L2

Gene ID

23091

6934

Gene namezinc finger CCCH-type containing 13transcription factor 7 like 2
SynonymsKIAA0853|XioTCF-4|TCF4
Cytomap

13q14.13

10q25.2-q25.3

Type of geneprotein-codingprotein-coding
Descriptionzinc finger CCCH domain-containing protein 13transcription factor 7-like 2HMG box transcription factor 4T-cell factor 4T-cell-specific transcription factor 4hTCF-4transcription factor 7-like 2 (T-cell specific, HMG-box)
Modification date2020031320200315
UniProtAcc.

Q9NQB0

Ensembl transtripts involved in fusion geneENST00000282007, ENST00000242848, 
ENST00000378921, ENST00000470308, 
ENST00000349937, ENST00000352065, 
ENST00000355717, ENST00000355995, 
ENST00000369395, ENST00000369397, 
ENST00000534894, ENST00000536810, 
ENST00000538897, ENST00000543371, 
ENST00000545257, ENST00000542695, 
ENST00000369386, ENST00000369389, 
ENST00000466338, 
Fusion gene scores* DoF score9 X 10 X 7=63012 X 11 X 10=1320
# samples 1117
** MAII scorelog2(11/630*10)=-2.51784830486262
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(17/1320*10)=-2.95693127810811
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ZC3H13 [Title/Abstract] AND TCF7L2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointZC3H13(46626832)-TCF7L2(114799783), # 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
TgeneTCF7L2

GO:0000122

negative regulation of transcription by RNA polymerase II

12799378

TgeneTCF7L2

GO:0006357

regulation of transcription by RNA polymerase II

9727977

TgeneTCF7L2

GO:0032092

positive regulation of protein binding

12799378

TgeneTCF7L2

GO:0032350

regulation of hormone metabolic process

15525634

TgeneTCF7L2

GO:0042593

glucose homeostasis

15525634

TgeneTCF7L2

GO:0043433

negative regulation of DNA-binding transcription factor activity

12799378

TgeneTCF7L2

GO:0045444

fat cell differentiation

10937998

TgeneTCF7L2

GO:0045892

negative regulation of transcription, DNA-templated

12799378|15525634

TgeneTCF7L2

GO:0045944

positive regulation of transcription by RNA polymerase II

9065401|19168596

TgeneTCF7L2

GO:0048625

myoblast fate commitment

10937998


check buttonFusion gene breakpoints across ZC3H13 (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 TCF7L2 (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
ChimerDB4ESCATCGA-L5-A8NMZC3H13chr13

46626832

-TCF7L2chr10

114799783

+


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Fusion Gene ORF analysis for ZC3H13-TCF7L2

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
5UTR-3CDSENST00000282007ENST00000349937ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
5UTR-3CDSENST00000282007ENST00000352065ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
5UTR-3CDSENST00000282007ENST00000355717ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
5UTR-3CDSENST00000282007ENST00000355995ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
5UTR-3CDSENST00000282007ENST00000369395ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
5UTR-3CDSENST00000282007ENST00000369397ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
5UTR-3CDSENST00000282007ENST00000534894ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
5UTR-3CDSENST00000282007ENST00000536810ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
5UTR-3CDSENST00000282007ENST00000538897ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
5UTR-3CDSENST00000282007ENST00000543371ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
5UTR-3CDSENST00000282007ENST00000545257ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
5UTR-5UTRENST00000282007ENST00000542695ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
5UTR-intronENST00000282007ENST00000369386ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
5UTR-intronENST00000282007ENST00000369389ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
5UTR-intronENST00000282007ENST00000466338ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000242848ENST00000349937ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000242848ENST00000352065ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000242848ENST00000355717ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000242848ENST00000355995ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000242848ENST00000369395ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000242848ENST00000369397ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000242848ENST00000534894ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000242848ENST00000536810ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000242848ENST00000538897ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000242848ENST00000543371ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000242848ENST00000545257ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000378921ENST00000349937ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000378921ENST00000352065ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000378921ENST00000355717ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000378921ENST00000355995ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000378921ENST00000369395ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000378921ENST00000369397ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000378921ENST00000534894ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000378921ENST00000536810ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000378921ENST00000538897ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000378921ENST00000543371ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000378921ENST00000545257ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000470308ENST00000349937ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000470308ENST00000352065ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000470308ENST00000355717ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000470308ENST00000355995ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000470308ENST00000369395ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000470308ENST00000369397ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000470308ENST00000534894ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000470308ENST00000536810ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000470308ENST00000538897ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000470308ENST00000543371ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-3CDSENST00000470308ENST00000545257ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-5UTRENST00000242848ENST00000542695ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-5UTRENST00000378921ENST00000542695ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-5UTRENST00000470308ENST00000542695ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-intronENST00000242848ENST00000369386ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-intronENST00000242848ENST00000369389ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-intronENST00000242848ENST00000466338ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-intronENST00000378921ENST00000369386ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-intronENST00000378921ENST00000369389ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-intronENST00000378921ENST00000466338ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-intronENST00000470308ENST00000369386ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-intronENST00000470308ENST00000369389ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+
intron-intronENST00000470308ENST00000466338ZC3H13chr13

46626832

-TCF7L2chr10

114799783

+

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 ZC3H13-TCF7L2


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)
ZC3H13chr1346626832-TCF7L2chr10114799783+6.37E-091
ZC3H13chr1346626832-TCF7L2chr10114799783+6.37E-091

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.
genomic feature of top 1%

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Fusion Protein Features for ZC3H13-TCF7L2


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/:46626832/:114799783)
- 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
.TCF7L2

Q9NQB0

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: Participates in the Wnt signaling pathway and modulates MYC expression by binding to its promoter in a sequence-specific manner. Acts as repressor in the absence of CTNNB1, and as activator in its presence. Activates transcription from promoters with several copies of the Tcf motif 5'-CCTTTGATC-3' in the presence of CTNNB1. TLE1, TLE2, TLE3 and TLE4 repress transactivation mediated by TCF7L2/TCF4 and CTNNB1. Expression of dominant-negative mutants results in cell-cycle arrest in G1. Necessary for the maintenance of the epithelial stem-cell compartment of the small intestine. {ECO:0000269|PubMed:12408868, ECO:0000269|PubMed:12727872, ECO:0000269|PubMed:19443654, ECO:0000269|PubMed:22699938, ECO:0000269|PubMed:9727977}.

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 ZC3H13-TCF7L2


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 ZC3H13-TCF7L2


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 ZC3H13-TCF7L2


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 ZC3H13-TCF7L2


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