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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:NCF1-GTF2IRD1 (FusionGDB2 ID:57588)

Fusion Gene Summary for NCF1-GTF2IRD1

check button Fusion gene summary
Fusion gene informationFusion gene name: NCF1-GTF2IRD1
Fusion gene ID: 57588
HgeneTgene
Gene symbol

NCF1

GTF2IRD1

Gene ID

653361

9569

Gene nameneutrophil cytosolic factor 1GTF2I repeat domain containing 1
SynonymsNCF1A|NOXO2|SH3PXD1A|p47phoxBEN|CREAM1|GTF3|MUSTRD1|RBAP2|WBS|WBSCR11|WBSCR12|hMusTRD1alpha1
Cytomap

7q11.23

7q11.23

Type of geneprotein-codingprotein-coding
Descriptionneutrophil cytosol factor 147 kDa autosomal chronic granulomatous disease protein47 kDa neutrophil oxidase factorNADPH oxidase organizer 2NCF-1NCF-47KSH3 and PX domain-containing protein 1Aneutrophil NADPH oxidase factor 1neutrophil cytosolic factgeneral transcription factor II-I repeat domain-containing protein 1USE B1-binding proteinWilliams-Beuren syndrome chromosome region 11binding factor for early enhancergeneral transcription factor 3general transcription factor IIImuscle TFII-I repea
Modification date2020031320200313
UniProtAcc

P14598

Q9UHL9

Ensembl transtripts involved in fusion geneENST00000443956, ENST00000289473, 
ENST00000265755, ENST00000424337, 
ENST00000455841, ENST00000476977, 
ENST00000489094, 
Fusion gene scores* DoF score1 X 1 X 1=112 X 10 X 9=1080
# samples 112
** MAII scorelog2(1/1*10)=3.32192809488736log2(12/1080*10)=-3.16992500144231
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: NCF1 [Title/Abstract] AND GTF2IRD1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointNCF1(74193768)-GTF2IRD1(73922404), # 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
HgeneNCF1

GO:0006612

protein targeting to membrane

12356722

HgeneNCF1

GO:0034614

cellular response to reactive oxygen species

26514923

HgeneNCF1

GO:0071276

cellular response to cadmium ion

26514923


check buttonFusion gene breakpoints across NCF1 (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 GTF2IRD1 (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-HU-A4HDNCF1chr7

74193768

+GTF2IRD1chr7

73922404

+


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Fusion Gene ORF analysis for NCF1-GTF2IRD1

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
3UTR-5UTRENST00000443956ENST00000265755NCF1chr7

74193768

+GTF2IRD1chr7

73922404

+
3UTR-5UTRENST00000443956ENST00000424337NCF1chr7

74193768

+GTF2IRD1chr7

73922404

+
3UTR-5UTRENST00000443956ENST00000455841NCF1chr7

74193768

+GTF2IRD1chr7

73922404

+
3UTR-5UTRENST00000443956ENST00000476977NCF1chr7

74193768

+GTF2IRD1chr7

73922404

+
3UTR-5UTRENST00000443956ENST00000489094NCF1chr7

74193768

+GTF2IRD1chr7

73922404

+
5CDS-5UTRENST00000289473ENST00000265755NCF1chr7

74193768

+GTF2IRD1chr7

73922404

+
5CDS-5UTRENST00000289473ENST00000424337NCF1chr7

74193768

+GTF2IRD1chr7

73922404

+
5CDS-5UTRENST00000289473ENST00000455841NCF1chr7

74193768

+GTF2IRD1chr7

73922404

+
5CDS-5UTRENST00000289473ENST00000476977NCF1chr7

74193768

+GTF2IRD1chr7

73922404

+
5CDS-5UTRENST00000289473ENST00000489094NCF1chr7

74193768

+GTF2IRD1chr7

73922404

+

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 NCF1-GTF2IRD1


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)
NCF1chr774193768+GTF2IRD1chr773922404+1.34E-070.9999999
NCF1chr774193768+GTF2IRD1chr773922404+1.34E-070.9999999

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 NCF1-GTF2IRD1


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/:74193768/:73922404)
- 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
NCF1

P14598

GTF2IRD1

Q9UHL9

FUNCTION: NCF2, NCF1, and a membrane bound cytochrome b558 are required for activation of the latent NADPH oxidase (necessary for superoxide production). {ECO:0000269|PubMed:19801500, ECO:0000269|PubMed:2547247, ECO:0000269|PubMed:2550933}.FUNCTION: May be a transcription regulator involved in cell-cycle progression and skeletal muscle differentiation. May repress GTF2I transcriptional functions, by preventing its nuclear residency, or by inhibiting its transcriptional activation. May contribute to slow-twitch fiber type specificity during myogenesis and in regenerating muscles. Binds troponin I slow-muscle fiber enhancer (USE B1). Binds specifically and with high affinity to the EFG sequences derived from the early enhancer of HOXC8 (By similarity). {ECO:0000250, ECO:0000269|PubMed:11438732}.

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 NCF1-GTF2IRD1


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 NCF1-GTF2IRD1


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 NCF1-GTF2IRD1


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 NCF1-GTF2IRD1


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