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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:XPR1-NCF2 (FusionGDB2 ID:99063)

Fusion Gene Summary for XPR1-NCF2

check button Fusion gene summary
Fusion gene informationFusion gene name: XPR1-NCF2
Fusion gene ID: 99063
HgeneTgene
Gene symbol

XPR1

NCF2

Gene ID

9213

4688

Gene namexenotropic and polytropic retrovirus receptor 1neutrophil cytosolic factor 2
SynonymsIBGC6|SLC53A1|SYG1|X3NCF-2|NOXA2|P67-PHOX|P67PHOX
Cytomap

1q25.3

1q25.3

Type of geneprotein-codingprotein-coding
Descriptionxenotropic and polytropic retrovirus receptor 1X-receptorprotein SYG1 homologsolute carrier family 53 (phosphate exporter), member 1xenotropic and polytropic murine leukemia virus receptor X3neutrophil cytosol factor 267 kDa neutrophil oxidase factorNADPH oxidase activator 2chronic granulomatous disease, autosomal 2neutrophil NADPH oxidase factor 2neutrophil cytosolic factor 2 (65kD, chronic granulomatous disease, autosomal 2)
Modification date2020031320200313
UniProtAcc.

P19878

Ensembl transtripts involved in fusion geneENST00000367590, ENST00000367589, 
ENST00000467345, 
ENST00000418089, 
ENST00000413720, ENST00000367536, 
ENST00000367535, ENST00000469280, 
Fusion gene scores* DoF score24 X 7 X 12=20163 X 2 X 3=18
# samples 274
** MAII scorelog2(27/2016*10)=-2.90046432644909
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/18*10)=1.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: XPR1 [Title/Abstract] AND NCF2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointXPR1(180651547)-NCF2(183546842), # samples:1
Anticipated loss of major functional domain due to fusion event.XPR1-NCF2 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
XPR1-NCF2 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
* 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

check buttonFusion gene breakpoints across XPR1 (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 NCF2 (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
ChimerDB4SKCMTCGA-FS-A1ZD-06AXPR1chr1

180651547

-NCF2chr1

183546842

-


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Fusion Gene ORF analysis for XPR1-NCF2

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
Frame-shiftENST00000367590ENST00000418089XPR1chr1

180651547

-NCF2chr1

183546842

-
Frame-shiftENST00000367590ENST00000413720XPR1chr1

180651547

-NCF2chr1

183546842

-
Frame-shiftENST00000367590ENST00000367536XPR1chr1

180651547

-NCF2chr1

183546842

-
Frame-shiftENST00000367590ENST00000367535XPR1chr1

180651547

-NCF2chr1

183546842

-
5CDS-intronENST00000367590ENST00000469280XPR1chr1

180651547

-NCF2chr1

183546842

-
Frame-shiftENST00000367589ENST00000418089XPR1chr1

180651547

-NCF2chr1

183546842

-
Frame-shiftENST00000367589ENST00000413720XPR1chr1

180651547

-NCF2chr1

183546842

-
Frame-shiftENST00000367589ENST00000367536XPR1chr1

180651547

-NCF2chr1

183546842

-
Frame-shiftENST00000367589ENST00000367535XPR1chr1

180651547

-NCF2chr1

183546842

-
5CDS-intronENST00000367589ENST00000469280XPR1chr1

180651547

-NCF2chr1

183546842

-
intron-3CDSENST00000467345ENST00000418089XPR1chr1

180651547

-NCF2chr1

183546842

-
intron-3CDSENST00000467345ENST00000413720XPR1chr1

180651547

-NCF2chr1

183546842

-
intron-3CDSENST00000467345ENST00000367536XPR1chr1

180651547

-NCF2chr1

183546842

-
intron-3CDSENST00000467345ENST00000367535XPR1chr1

180651547

-NCF2chr1

183546842

-
intron-intronENST00000467345ENST00000469280XPR1chr1

180651547

-NCF2chr1

183546842

-

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 XPR1-NCF2


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 XPR1-NCF2


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
.NCF2

P19878

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: NCF2, NCF1, and a membrane bound cytochrome b558 are required for activation of the latent NADPH oxidase (necessary for superoxide production). {ECO:0000269|PubMed:12207919}.

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 XPR1-NCF2


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 XPR1-NCF2


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 XPR1-NCF2


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 XPR1-NCF2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneXPR1C4225335BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 62CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneXPR1C0004782Basal Ganglia Diseases1CTD_human
HgeneXPR1C0006663Calcinosis1CTD_human
HgeneXPR1C0015371Extrapyramidal Disorders1CTD_human
HgeneXPR1C0015624Fanconi Syndrome1GENOMICS_ENGLAND
HgeneXPR1C0263628Tumoral calcinosis1CTD_human
HgeneXPR1C0393590Fahr's syndrome (disorder)1ORPHANET
HgeneXPR1C0521174Microcalcification1CTD_human
HgeneXPR1C0750951Lenticulostriate Disorders1CTD_human
TgeneNCF2C1856245Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II10CTD_human;GENOMICS_ENGLAND;UNIPROT
TgeneNCF2C0003873Rheumatoid Arthritis1CTD_human