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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:GATA6-TBL1Y (FusionGDB2 ID:HG2627TG90665)

Fusion Gene Summary for GATA6-TBL1Y

check button Fusion gene summary
Fusion gene informationFusion gene name: GATA6-TBL1Y
Fusion gene ID: hg2627tg90665
HgeneTgene
Gene symbol

GATA6

TBL1Y

Gene ID

2627

90665

Gene nameGATA binding protein 6transducin beta like 1 Y-linked
Synonyms-DFNY2|TBL1
Cytomap('GATA6')('TBL1Y')

18q11.2

Yp11.2

Type of geneprotein-codingprotein-coding
Descriptiontranscription factor GATA-6GATA-binding factor 6F-box-like/WD repeat-containing protein TBL1Ytransducin beta-like 1transducin beta-like protein 1Ytransducin-beta-like protein 1, Y-linked
Modification date2020031320200313
UniProtAcc

Q92908

.
Ensembl transtripts involved in fusion geneENST00000269216, ENST00000581694, 
Fusion gene scores* DoF score7 X 7 X 4=1962 X 2 X 2=8
# samples 72
** MAII scorelog2(7/196*10)=-1.48542682717024
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/8*10)=1.32192809488736
Context

PubMed: GATA6 [Title/Abstract] AND TBL1Y [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointGATA6(19756624)-TBL1Y(6887815), # 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
HgeneGATA6

GO:0000122

negative regulation of transcription by RNA polymerase II

18177748

HgeneGATA6

GO:0006366

transcription by RNA polymerase II

19666519

HgeneGATA6

GO:0045766

positive regulation of angiogenesis

21127043

HgeneGATA6

GO:0045892

negative regulation of transcription, DNA-templated

18177748

HgeneGATA6

GO:0060575

intestinal epithelial cell differentiation

9566909

HgeneGATA6

GO:0070848

response to growth factor

21127043

HgeneGATA6

GO:0071158

positive regulation of cell cycle arrest

9593712

HgeneGATA6

GO:0071456

cellular response to hypoxia

21127043

HgeneGATA6

GO:0110024

positive regulation of cardiac muscle myoblast proliferation

25068583



check button Fusion gene information
* 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


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Fusion Gene ORF analysis for GATA6-TBL1Y

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

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 GATA6-TBL1Y


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)


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Fusion Protein Features for GATA6-TBL1Y


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/:19756624/:6887815)
- 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
GATA6

Q92908

.
FUNCTION: Transcriptional activator (PubMed:19666519, PubMed:27756709, PubMed:22750565, PubMed:22824924). Regulates SEMA3C and PLXNA2 (PubMed:19666519). Involved in gene regulation specifically in the gastric epithelium (PubMed:9315713). May regulate genes that protect epithelial cells from bacterial infection (PubMed:16968778). Involved in bone morphogenetic protein (BMP)-mediated cardiac-specific gene expression (By similarity). Binds to BMP response element (BMPRE) DNA sequences within cardiac activating regions (By similarity). In human skin, controls several physiological processes contributing to homeostasis of the upper pilosebaceous unit. Triggers ductal and sebaceous differentiation as well as limits cell proliferation and lipid production to prevent hyperseborrhoea. Mediates the effects of retinoic acid on sebocyte proliferation, differentiation and lipid production. Also contributes to immune regulation of sebocytes and antimicrobial responses by modulating the expression of anti-inflammatory genes such as IL10 and pro-inflammatory genes such as IL6, TLR2, TLR4, and IFNG. Activates TGFB1 signaling which controls the interfollicular epidermis fate (PubMed:33082341). {ECO:0000250|UniProtKB:Q61169, ECO:0000269|PubMed:16968778, ECO:0000269|PubMed:19666519, ECO:0000269|PubMed:22750565, ECO:0000269|PubMed:22824924, ECO:0000269|PubMed:27756709, ECO:0000269|PubMed:33082341, ECO:0000269|PubMed:9315713}.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}.

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 GATA6-TBL1Y


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 GATA6-TBL1Y


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 GATA6-TBL1Y


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 GATA6-TBL1Y


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneGATA6C1843687ATRIAL FIBRILLATION, FAMILIAL, 1 (disorder)3ORPHANET
HgeneGATA6C3888085PANCREATIC AGENESIS AND CONGENITAL HEART DEFECTS3GENOMICS_ENGLAND
HgeneGATA6C4012454HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES3CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneGATA6C0039685Tetralogy of Fallot2CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgeneGATA6C1857586CONOTRUNCAL HEART MALFORMATIONS (disorder)2CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneGATA6C2931296Yorifuji Okuno syndrome2ORPHANET
HgeneGATA6C3280939ATRIOVENTRICULAR SEPTAL DEFECT 52GENOMICS_ENGLAND;UNIPROT
HgeneGATA6C0019284Diaphragmatic Hernia1CTD_human
HgeneGATA6C0024121Lung Neoplasms1CTD_human
HgeneGATA6C0158981Neonatal diabetes mellitus1GENOMICS_ENGLAND
HgeneGATA6C0235833Congenital diaphragmatic hernia1ORPHANET
HgeneGATA6C0242379Malignant neoplasm of lung1CTD_human
HgeneGATA6C0344724Ostium secundum atrial septal defect1ORPHANET
HgeneGATA6C0344735Partial atrioventricular canal1ORPHANET
HgeneGATA6C3280943ATRIAL SEPTAL DEFECT 91CTD_human;GENOMICS_ENGLAND;UNIPROT