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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 24202

FusionGeneSummary for NFE2L3_POU6F2

check button Fusion gene summary
Fusion gene informationFusion gene name: NFE2L3_POU6F2
Fusion gene ID: 24202
HgeneTgene
Gene symbol

NFE2L3

POU6F2

Gene ID

9603

11281

Gene namenuclear factor, erythroid 2 like 3POU class 6 homeobox 2
SynonymsNRF3RPF-1|WT5|WTSL
Cytomap

7p15.2

7p14.1

Type of geneprotein-codingprotein-coding
Descriptionnuclear factor erythroid 2-related factor 3NF-E2-related factor 3NFE2-related factor 3nuclear factor, erythroid derived 2, like 3nuclear factor-erythroid 2 p45-related factor 3POU domain, class 6, transcription factor 2Wilms tumor suppressor locusretina-derived POU-domain factor-1
Modification date2018052320180403
UniProtAcc

Q9Y4A8

P78424

Ensembl transtripts involved in fusion geneENST00000056233, ENST00000403058, 
ENST00000518318, ENST00000517348, 
ENST00000559001, ENST00000464276, 
Fusion gene scores* DoF score3 X 3 X 3=275 X 5 X 7=175
# samples 39
** MAII scorelog2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(9/175*10)=-0.959358015502654
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: NFE2L3 [Title/Abstract] AND POU6F2 [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotation
* 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 button Fusion gene information from three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* 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.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
TCGALDSARCTCGA-RN-AAAQ-01ANFE2L3chr7

26217742

+POU6F2chr7

39379241

+
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

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-shiftENST00000056233ENST00000403058NFE2L3chr7

26217742

+POU6F2chr7

39379241

+
Frame-shiftENST00000056233ENST00000518318NFE2L3chr7

26217742

+POU6F2chr7

39379241

+
5CDS-3UTRENST00000056233ENST00000517348NFE2L3chr7

26217742

+POU6F2chr7

39379241

+
5CDS-3UTRENST00000056233ENST00000559001NFE2L3chr7

26217742

+POU6F2chr7

39379241

+
5CDS-intronENST00000056233ENST00000464276NFE2L3chr7

26217742

+POU6F2chr7

39379241

+

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FusionProtFeatures for NFE2L3_POU6F2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
NFE2L3

Q9Y4A8

POU6F2

P78424

Activates erythroid-specific, globin gene expression. Probable transcription factor likely to be involved inearly steps in the differentiation of amacrine and ganglion cells.Recognizes and binds to the DNA sequence 5'-ATGCAAAT-3'. Isoform 1does not bind DNA.

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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FusionGeneSequence for NFE2L3_POU6F2


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

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FusionGenePPI for NFE2L3_POU6F2


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
NFE2L3MAFK, BACH2, NFE2L3, NFE2L2, NFE2L1, NFE2, MAFG, MAFF, CREB3, PPARG, FBXW7, GSK3B, HCFC2, HCFC1POU6F2


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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RelatedDrugs for NFE2L3_POU6F2


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for NFE2L3_POU6F2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgenePOU6F2C0004352Autistic Disorder1CTD_human
TgenePOU6F2C1832099Wilms tumor and radial bilateral aplasia1CTD_human;UNIPROT