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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:IRF6-IRF6 (FusionGDB2 ID:40091)

Fusion Gene Summary for IRF6-IRF6

check button Fusion gene summary
Fusion gene informationFusion gene name: IRF6-IRF6
Fusion gene ID: 40091
HgeneTgene
Gene symbol

IRF6

IRF6

Gene ID

3664

3664

Gene nameinterferon regulatory factor 6interferon regulatory factor 6
SynonymsLPS|OFC6|PIT|PPS|PPS1|VWS|VWS1LPS|OFC6|PIT|PPS|PPS1|VWS|VWS1
Cytomap

1q32.2

1q32.2

Type of geneprotein-codingprotein-coding
Descriptioninterferon regulatory factor 6interferon regulatory factor 6
Modification date2020031320200313
UniProtAcc.

O14896

Ensembl transtripts involved in fusion geneENST00000367021, ENST00000542854, 
ENST00000367021, ENST00000542854, 
Fusion gene scores* DoF score6 X 6 X 5=1804 X 4 X 3=48
# samples 74
** MAII scorelog2(7/180*10)=-1.36257007938471
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/48*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: IRF6 [Title/Abstract] AND IRF6 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointIRF6(209964165)-IRF6(209963900), # 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
HgeneIRF6

GO:0007050

cell cycle arrest

18212048

HgeneIRF6

GO:0008285

negative regulation of cell proliferation

18212048

HgeneIRF6

GO:0045944

positive regulation of transcription by RNA polymerase II

21807998

TgeneIRF6

GO:0007050

cell cycle arrest

18212048

TgeneIRF6

GO:0008285

negative regulation of cell proliferation

18212048

TgeneIRF6

GO:0045944

positive regulation of transcription by RNA polymerase II

21807998


check buttonFusion gene breakpoints across IRF6 (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 IRF6 (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/ABF769897IRF6chr1

209964165

-IRF6chr1

209963900

+


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Fusion Gene ORF analysis for IRF6-IRF6

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-3CDSENST00000367021ENST00000367021IRF6chr1

209964165

-IRF6chr1

209963900

+
intron-3CDSENST00000367021ENST00000542854IRF6chr1

209964165

-IRF6chr1

209963900

+
intron-3CDSENST00000542854ENST00000367021IRF6chr1

209964165

-IRF6chr1

209963900

+
intron-3CDSENST00000542854ENST00000542854IRF6chr1

209964165

-IRF6chr1

209963900

+

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 IRF6-IRF6


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 IRF6-IRF6


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
.IRF6

O14896

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: Probable DNA-binding transcriptional activator. Key determinant of the keratinocyte proliferation-differentiation switch involved in appropriate epidermal development (By similarity). Plays a role in regulating mammary epithelial cell proliferation (By similarity). May regulate WDR65 transcription (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 IRF6-IRF6


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 IRF6-IRF6


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 IRF6-IRF6


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 IRF6-IRF6


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneIRF6C4551864VAN DER WOUDE SYNDROME 19GENOMICS_ENGLAND;UNIPROT
HgeneIRF6C0008924Cleft upper lip4CTD_human;ORPHANET
HgeneIRF6C0265259Popliteal pterygium syndrome4CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneIRF6C0175697Van der Woude syndrome3CTD_human;GENOMICS_ENGLAND;ORPHANET
HgeneIRF6C1837213OROFACIAL CLEFT 6, SUSCEPTIBILITY TO2CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneIRF6C0008925Cleft Palate1CTD_human;GENOMICS_ENGLAND
HgeneIRF6C0037268Skin Abnormalities1CTD_human
HgeneIRF6C0158646Cleft palate with cleft lip1ORPHANET
HgeneIRF6C0206762Limb Deformities, Congenital1CTD_human
HgeneIRF6C0376634Craniofacial Abnormalities1CTD_human
HgeneIRF6C1298692Cleft lip and alveolus1ORPHANET
HgeneIRF6C1837218Cleft palate, isolated1CTD_human
TgeneIRF6C4551864VAN DER WOUDE SYNDROME 19GENOMICS_ENGLAND;UNIPROT
TgeneIRF6C0008924Cleft upper lip4CTD_human;ORPHANET
TgeneIRF6C0265259Popliteal pterygium syndrome4CTD_human;GENOMICS_ENGLAND;UNIPROT
TgeneIRF6C0175697Van der Woude syndrome3CTD_human;GENOMICS_ENGLAND;ORPHANET
TgeneIRF6C1837213OROFACIAL CLEFT 6, SUSCEPTIBILITY TO2CTD_human;GENOMICS_ENGLAND;UNIPROT
TgeneIRF6C0008925Cleft Palate1CTD_human;GENOMICS_ENGLAND
TgeneIRF6C0037268Skin Abnormalities1CTD_human
TgeneIRF6C0158646Cleft palate with cleft lip1ORPHANET
TgeneIRF6C0206762Limb Deformities, Congenital1CTD_human
TgeneIRF6C0376634Craniofacial Abnormalities1CTD_human
TgeneIRF6C1298692Cleft lip and alveolus1ORPHANET
TgeneIRF6C1837218Cleft palate, isolated1CTD_human