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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:TCF7L2-C10orf76 (FusionGDB2 ID:89192)

Fusion Gene Summary for TCF7L2-C10orf76

check button Fusion gene summary
Fusion gene informationFusion gene name: TCF7L2-C10orf76
Fusion gene ID: 89192
HgeneTgene
Gene symbol

TCF7L2

C10orf76

Gene ID

6934

79591

Gene nametranscription factor 7 like 2armadillo like helical domain containing 3
SynonymsTCF-4|TCF4C10orf76
Cytomap

10q25.2-q25.3

10q24.32

Type of geneprotein-codingprotein-coding
Descriptiontranscription 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)armadillo-like helical domain-containing protein 3UPF0668 protein C10orf76
Modification date2020031520200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000534894, ENST00000536810, 
ENST00000545257, ENST00000355995, 
ENST00000543371, ENST00000355717, 
ENST00000538897, ENST00000349937, 
ENST00000369397, ENST00000352065, 
ENST00000369395, ENST00000542695, 
ENST00000369389, ENST00000369386, 
ENST00000466338, 		ENST00000370033, 
ENST00000311122, ENST00000495001, 
Fusion gene scores* DoF score16 X 11 X 11=19368 X 6 X 5=240
# samples 239
** MAII scorelog2(23/1936*10)=-3.07337318633022
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0		log2(9/240*10)=-1.41503749927884
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: TCF7L2 [Title/Abstract] AND C10orf76 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointTCF7L2(114711366)-C10orf76(103649247), # samples:1
Anticipated loss of major functional domain due to fusion event.TCF7L2-C10orf76 seems lost the major protein functional domain in Hgene partner, which is a transcription factor due to the frame-shifted ORF.
TCF7L2-C10orf76 seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
TCF7L2-C10orf76 seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
TCF7L2-C10orf76 seems lost the major protein functional domain in Tgene 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
HgeneTCF7L2

GO:0000122

negative regulation of transcription by RNA polymerase II

12799378

HgeneTCF7L2

GO:0006357

regulation of transcription by RNA polymerase II

9727977

HgeneTCF7L2

GO:0032092

positive regulation of protein binding

12799378

HgeneTCF7L2

GO:0032350

regulation of hormone metabolic process

15525634

HgeneTCF7L2

GO:0042593

glucose homeostasis

15525634

HgeneTCF7L2

GO:0043433

negative regulation of DNA-binding transcription factor activity

12799378

HgeneTCF7L2

GO:0045444

fat cell differentiation

10937998

HgeneTCF7L2

GO:0045892

negative regulation of transcription, DNA-templated

12799378|15525634

HgeneTCF7L2

GO:0045944

positive regulation of transcription by RNA polymerase II

9065401|19168596

HgeneTCF7L2

GO:0048625

myoblast fate commitment

10937998


check buttonFusion gene breakpoints across TCF7L2 (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 C10orf76 (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
ChimerDB4STADTCGA-BR-A4IZTCF7L2chr10

114711366

+C10orf76chr10

103649247

-


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Fusion Gene ORF analysis for TCF7L2-C10orf76

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-shiftENST00000534894ENST00000370033TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
5CDS-intronENST00000534894ENST00000311122TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
5CDS-5UTRENST00000534894ENST00000495001TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
Frame-shiftENST00000536810ENST00000370033TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
5CDS-intronENST00000536810ENST00000311122TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
5CDS-5UTRENST00000536810ENST00000495001TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
Frame-shiftENST00000545257ENST00000370033TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
5CDS-intronENST00000545257ENST00000311122TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
5CDS-5UTRENST00000545257ENST00000495001TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
Frame-shiftENST00000355995ENST00000370033TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
5CDS-intronENST00000355995ENST00000311122TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
5CDS-5UTRENST00000355995ENST00000495001TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
Frame-shiftENST00000543371ENST00000370033TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
5CDS-intronENST00000543371ENST00000311122TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
5CDS-5UTRENST00000543371ENST00000495001TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
Frame-shiftENST00000355717ENST00000370033TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
5CDS-intronENST00000355717ENST00000311122TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
5CDS-5UTRENST00000355717ENST00000495001TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
Frame-shiftENST00000538897ENST00000370033TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
5CDS-intronENST00000538897ENST00000311122TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
5CDS-5UTRENST00000538897ENST00000495001TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
Frame-shiftENST00000349937ENST00000370033TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
5CDS-intronENST00000349937ENST00000311122TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
5CDS-5UTRENST00000349937ENST00000495001TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
Frame-shiftENST00000369397ENST00000370033TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
5CDS-intronENST00000369397ENST00000311122TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
5CDS-5UTRENST00000369397ENST00000495001TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
Frame-shiftENST00000352065ENST00000370033TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
5CDS-intronENST00000352065ENST00000311122TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
5CDS-5UTRENST00000352065ENST00000495001TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
Frame-shiftENST00000369395ENST00000370033TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
5CDS-intronENST00000369395ENST00000311122TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
5CDS-5UTRENST00000369395ENST00000495001TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
5UTR-3CDSENST00000542695ENST00000370033TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
5UTR-intronENST00000542695ENST00000311122TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
5UTR-5UTRENST00000542695ENST00000495001TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
intron-3CDSENST00000369389ENST00000370033TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
intron-intronENST00000369389ENST00000311122TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
intron-5UTRENST00000369389ENST00000495001TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
intron-3CDSENST00000369386ENST00000370033TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
intron-intronENST00000369386ENST00000311122TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
intron-5UTRENST00000369386ENST00000495001TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
intron-3CDSENST00000466338ENST00000370033TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
intron-intronENST00000466338ENST00000311122TCF7L2chr10

114711366

+C10orf76chr10

103649247

-
intron-5UTRENST00000466338ENST00000495001TCF7L2chr10

114711366

+C10orf76chr10

103649247

-

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 TCF7L2-C10orf76


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 TCF7L2-C10orf76


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
..
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: 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 TCF7L2-C10orf76


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 TCF7L2-C10orf76


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 TCF7L2-C10orf76


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 TCF7L2-C10orf76


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneTCF7L2C0036341Schizophrenia4PSYGENET
HgeneTCF7L2C0011860Diabetes Mellitus, Non-Insulin-Dependent3CTD_human
HgeneTCF7L2C0009402Colorectal Carcinoma2CTD_human;UNIPROT
HgeneTCF7L2C0009404Colorectal Neoplasms2CTD_human
HgeneTCF7L2C0001418Adenocarcinoma1CTD_human
HgeneTCF7L2C0005586Bipolar Disorder1PSYGENET
HgeneTCF7L2C0007102Malignant tumor of colon1CTD_human
HgeneTCF7L2C0007193Cardiomyopathy, Dilated1CTD_human
HgeneTCF7L2C0009375Colonic Neoplasms1CTD_human
HgeneTCF7L2C0010068Coronary heart disease1CTD_human
HgeneTCF7L2C0020507Hyperplasia1CTD_human
HgeneTCF7L2C0036337Schizoaffective Disorder1PSYGENET
HgeneTCF7L2C0087031Juvenile-Onset Still Disease1CTD_human
HgeneTCF7L2C0151744Myocardial Ischemia1CTD_human
HgeneTCF7L2C0205641Adenocarcinoma, Basal Cell1CTD_human
HgeneTCF7L2C0205642Adenocarcinoma, Oxyphilic1CTD_human
HgeneTCF7L2C0205643Carcinoma, Cribriform1CTD_human
HgeneTCF7L2C0205644Carcinoma, Granular Cell1CTD_human
HgeneTCF7L2C0205645Adenocarcinoma, Tubular1CTD_human
HgeneTCF7L2C0600519Ventricular Remodeling1CTD_human
HgeneTCF7L2C0600520Left Ventricle Remodeling1CTD_human
HgeneTCF7L2C1449563Cardiomyopathy, Familial Idiopathic1CTD_human
HgeneTCF7L2C1535926Neurodevelopmental Disorders1CTD_human
HgeneTCF7L2C2931456Prostate cancer, familial1CTD_human
HgeneTCF7L2C3495559Juvenile arthritis1CTD_human
HgeneTCF7L2C3714758Juvenile psoriatic arthritis1CTD_human
HgeneTCF7L2C4552091Polyarthritis, Juvenile, Rheumatoid Factor Negative1CTD_human
HgeneTCF7L2C4704862Polyarthritis, Juvenile, Rheumatoid Factor Positive1CTD_human
HgeneTCF7L2C4722327PROSTATE CANCER, HEREDITARY, 11CTD_human