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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:NFX1-NFX1 (FusionGDB2 ID:59013)

Fusion Gene Summary for NFX1-NFX1

check button Fusion gene summary
Fusion gene informationFusion gene name: NFX1-NFX1
Fusion gene ID: 59013
HgeneTgene
Gene symbol

NFX1

NFX1

Gene ID

4799

4799

Gene namenuclear transcription factor, X-box binding 1nuclear transcription factor, X-box binding 1
SynonymsNFX2|TEG-42|Tex42NFX2|TEG-42|Tex42
Cytomap

9p13.3

9p13.3

Type of geneprotein-codingprotein-coding
Descriptiontranscriptional repressor NF-X1nuclear transcription factor, X box-binding protein 1transcriptional repressor NF-X1nuclear transcription factor, X box-binding protein 1
Modification date2020031320200313
UniProtAcc

Q12986

ZNFX1

Ensembl transtripts involved in fusion geneENST00000379521, ENST00000379540, 
ENST00000318524, ENST00000463421, 
ENST00000318524, ENST00000379521, 
ENST00000379540, ENST00000463421, 
Fusion gene scores* DoF score16 X 12 X 11=211214 X 12 X 9=1512
# samples 2215
** MAII scorelog2(22/2112*10)=-3.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(15/1512*10)=-3.33342373372519
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: NFX1 [Title/Abstract] AND NFX1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointNFX1(33290538)-NFX1(33294534), # 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
HgeneNFX1

GO:0000122

negative regulation of transcription by RNA polymerase II

7964459

HgeneNFX1

GO:0051865

protein autoubiquitination

10500182

TgeneNFX1

GO:0000122

negative regulation of transcription by RNA polymerase II

7964459

TgeneNFX1

GO:0051865

protein autoubiquitination

10500182


check buttonFusion gene breakpoints across NFX1 (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 NFX1 (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/AU15306NFX1chr9

33290538

-NFX1chr9

33294534

+


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Fusion Gene ORF analysis for NFX1-NFX1

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-3CDSENST00000379521ENST00000318524NFX1chr9

33290538

-NFX1chr9

33294534

+
5UTR-3CDSENST00000379521ENST00000379521NFX1chr9

33290538

-NFX1chr9

33294534

+
5UTR-3CDSENST00000379521ENST00000379540NFX1chr9

33290538

-NFX1chr9

33294534

+
5UTR-3CDSENST00000379540ENST00000318524NFX1chr9

33290538

-NFX1chr9

33294534

+
5UTR-3CDSENST00000379540ENST00000379521NFX1chr9

33290538

-NFX1chr9

33294534

+
5UTR-3CDSENST00000379540ENST00000379540NFX1chr9

33290538

-NFX1chr9

33294534

+
5UTR-intronENST00000379521ENST00000463421NFX1chr9

33290538

-NFX1chr9

33294534

+
5UTR-intronENST00000379540ENST00000463421NFX1chr9

33290538

-NFX1chr9

33294534

+
intron-3CDSENST00000318524ENST00000318524NFX1chr9

33290538

-NFX1chr9

33294534

+
intron-3CDSENST00000318524ENST00000379521NFX1chr9

33290538

-NFX1chr9

33294534

+
intron-3CDSENST00000318524ENST00000379540NFX1chr9

33290538

-NFX1chr9

33294534

+
intron-3CDSENST00000463421ENST00000318524NFX1chr9

33290538

-NFX1chr9

33294534

+
intron-3CDSENST00000463421ENST00000379521NFX1chr9

33290538

-NFX1chr9

33294534

+
intron-3CDSENST00000463421ENST00000379540NFX1chr9

33290538

-NFX1chr9

33294534

+
intron-intronENST00000318524ENST00000463421NFX1chr9

33290538

-NFX1chr9

33294534

+
intron-intronENST00000463421ENST00000463421NFX1chr9

33290538

-NFX1chr9

33294534

+

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 NFX1-NFX1


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 NFX1-NFX1


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/:33290538/:33294534)
- 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
NFX1

Q12986

NFX1

ZNFX1

FUNCTION: Binds to the X-box motif of MHC class II genes and represses their expression. May play an important role in regulating the duration of an inflammatory response by limiting the period in which MHC class II molecules are induced by interferon-gamma. Isoform 3 binds to the X-box motif of TERT promoter and represses its expression. Together with PABPC1 or PABPC4, isoform 1 acts as a coactivator for TERT expression. Mediates E2-dependent ubiquitination. {ECO:0000269|PubMed:10500182, ECO:0000269|PubMed:15371341, ECO:0000269|PubMed:17267499}.1918

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 NFX1-NFX1


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 NFX1-NFX1


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 NFX1-NFX1


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 NFX1-NFX1


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