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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:FYTTD1-IFIT1 (FusionGDB2 ID:31942)

Fusion Gene Summary for FYTTD1-IFIT1

check button Fusion gene summary
Fusion gene informationFusion gene name: FYTTD1-IFIT1
Fusion gene ID: 31942
HgeneTgene
Gene symbol

FYTTD1

IFIT1

Gene ID

84248

3434

Gene nameforty-two-three domain containing 1interferon induced protein with tetratricopeptide repeats 1
SynonymsUIFC56|G10P1|IFI-56|IFI-56K|IFI56|IFIT-1|IFNAI1|ISG56|P56|RNM561
Cytomap

3q29

10q23.31

Type of geneprotein-codingprotein-coding
DescriptionUAP56-interacting factorforty-two-three domain-containing protein 1protein 40-2-3interferon-induced protein with tetratricopeptide repeats 1interferon, alpha-inducible protein (MW 56kD)interferon-induced 56 kDa proteininterferon-inducible mRNA 561
Modification date2020031320200313
UniProtAcc

Q96QD9

Q5T764

Ensembl transtripts involved in fusion geneENST00000241502, ENST00000415708, 
ENST00000424384, ENST00000428395, 
ENST00000492360, 
ENST00000546318, 
ENST00000371804, 
Fusion gene scores* DoF score7 X 7 X 6=2944 X 2 X 3=24
# samples 74
** MAII scorelog2(7/294*10)=-2.0703893278914
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/24*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: FYTTD1 [Title/Abstract] AND IFIT1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointFYTTD1(197476945)-IFIT1(91162038), # samples:3
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
TgeneIFIT1

GO:0009615

response to virus

19416887

TgeneIFIT1

GO:0019060

intracellular transport of viral protein in host cell

19008854

TgeneIFIT1

GO:0032091

negative regulation of protein binding

19416887

TgeneIFIT1

GO:0045070

positive regulation of viral genome replication

19416887

TgeneIFIT1

GO:0051097

negative regulation of helicase activity

19008854

TgeneIFIT1

GO:0071357

cellular response to type I interferon

19008854

TgeneIFIT1

GO:0071360

cellular response to exogenous dsRNA

19008854


check buttonFusion gene breakpoints across FYTTD1 (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 IFIT1 (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
ChimerDB4PRADTCGA-G9-6364-01AFYTTD1chr3

197476945

-IFIT1chr10

91162038

+
ChimerDB4PRADTCGA-G9-6364-01AFYTTD1chr3

197476945

+IFIT1chr10

91162038

+
ChimerDB4PRADTCGA-G9-6364FYTTD1chr3

197476945

+IFIT1chr10

91162038

+


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Fusion Gene ORF analysis for FYTTD1-IFIT1

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-5UTRENST00000241502ENST00000546318FYTTD1chr3

197476945

+IFIT1chr10

91162038

+
Frame-shiftENST00000241502ENST00000371804FYTTD1chr3

197476945

+IFIT1chr10

91162038

+
intron-3CDSENST00000415708ENST00000371804FYTTD1chr3

197476945

+IFIT1chr10

91162038

+
intron-3CDSENST00000424384ENST00000371804FYTTD1chr3

197476945

+IFIT1chr10

91162038

+
intron-3CDSENST00000428395ENST00000371804FYTTD1chr3

197476945

+IFIT1chr10

91162038

+
intron-3CDSENST00000492360ENST00000371804FYTTD1chr3

197476945

+IFIT1chr10

91162038

+
intron-5UTRENST00000415708ENST00000546318FYTTD1chr3

197476945

+IFIT1chr10

91162038

+
intron-5UTRENST00000424384ENST00000546318FYTTD1chr3

197476945

+IFIT1chr10

91162038

+
intron-5UTRENST00000428395ENST00000546318FYTTD1chr3

197476945

+IFIT1chr10

91162038

+
intron-5UTRENST00000492360ENST00000546318FYTTD1chr3

197476945

+IFIT1chr10

91162038

+

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 FYTTD1-IFIT1


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)
FYTTD1chr3197476945+IFIT1chr1091162037+4.38E-131
FYTTD1chr3197476945+IFIT1chr1091162037+4.38E-131
FYTTD1chr3197476945+IFIT1chr1091162037+4.38E-131
FYTTD1chr3197476945+IFIT1chr1091162037+4.38E-131

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 FYTTD1-IFIT1


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/:197476945/:91162038)
- 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
FYTTD1

Q96QD9

IFIT1

Q5T764

FUNCTION: Required for mRNA export from the nucleus to the cytoplasm. Acts as an adapter that uses the DDX39B/UAP56-NFX1 pathway to ensure efficient mRNA export and delivering to the nuclear pore. Associates with spliced and unspliced mRNAs simultaneously with ALYREF/THOC4. {ECO:0000269|PubMed:19836239}.

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 FYTTD1-IFIT1


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 FYTTD1-IFIT1


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 FYTTD1-IFIT1


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 FYTTD1-IFIT1


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