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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: 28064

FusionGeneSummary for POU6F2_ZNF366

check button Fusion gene summary
Fusion gene informationFusion gene name: POU6F2_ZNF366
Fusion gene ID: 28064
HgeneTgene
Gene symbol

POU6F2

ZNF366

Gene ID

11281

167465

Gene namePOU class 6 homeobox 2zinc finger protein 366
SynonymsRPF-1|WT5|WTSLDC-SCRIPT|DCSCRIPT
Cytomap

7p14.1

5q13.2|5q13.2

Type of geneprotein-codingprotein-coding
DescriptionPOU domain, class 6, transcription factor 2Wilms tumor suppressor locusretina-derived POU-domain factor-1zinc finger protein 366dendritic cell-specific transcript protein
Modification date2018040320180523
UniProtAcc

P78424

Q8N895

Ensembl transtripts involved in fusion geneENST00000403058, ENST00000518318, 
ENST00000517348, ENST00000559001, 
ENST00000464276, 
ENST00000318442, 
Fusion gene scores* DoF score3 X 3 X 2=182 X 2 X 2=8
# samples 32
** MAII scorelog2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(2/8*10)=1.32192809488736
Context

PubMed: POU6F2 [Title/Abstract] AND ZNF366 [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
TgeneZNF366

GO:0000122

negative regulation of transcription by RNA polymerase II

17085477

TgeneZNF366

GO:0033147

negative regulation of intracellular estrogen receptor signaling pathway

17085477

TgeneZNF366

GO:0043627

response to estrogen

17085477


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
ChiTaRS3.1BF996277POU6F2chr7

39368420

+ZNF366chr5

71739730

+
* 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
intron-3CDSENST00000403058ENST00000318442POU6F2chr7

39368420

+ZNF366chr5

71739730

+
intron-3CDSENST00000518318ENST00000318442POU6F2chr7

39368420

+ZNF366chr5

71739730

+
intron-3CDSENST00000517348ENST00000318442POU6F2chr7

39368420

+ZNF366chr5

71739730

+
intron-3CDSENST00000559001ENST00000318442POU6F2chr7

39368420

+ZNF366chr5

71739730

+
intron-3CDSENST00000464276ENST00000318442POU6F2chr7

39368420

+ZNF366chr5

71739730

+

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FusionProtFeatures for POU6F2_ZNF366


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
POU6F2

P78424

ZNF366

Q8N895

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. Has transcriptional repression activity. Acts ascorepressor of ESR1; the function seems to involve CTBP1 andhistone deacetylases. {ECO:0000269|PubMed:17085477}.

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 POU6F2_ZNF366


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 POU6F2_ZNF366


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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RelatedDrugs for POU6F2_ZNF366


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 POU6F2_ZNF366


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePOU6F2C0004352Autistic Disorder1CTD_human
HgenePOU6F2C1832099Wilms tumor and radial bilateral aplasia1CTD_human;UNIPROT
TgeneZNF366C0236969Substance-Related Disorders1CTD_human
TgeneZNF366C1458155Mammary Neoplasms1CTD_human