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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: 36434

FusionGeneSummary for STEAP1B_POU6F2

check button Fusion gene summary
Fusion gene informationFusion gene name: STEAP1B_POU6F2
Fusion gene ID: 36434
HgeneTgene
Gene symbol

STEAP1B

POU6F2

Gene ID

256227

11281

Gene nameSTEAP family member 1BPOU class 6 homeobox 2
Synonyms-RPF-1|WT5|WTSL
Cytomap

7p15.3

7p14.1

Type of geneprotein-codingprotein-coding
DescriptionSTEAP family member 1BSTEAP family protein MGC87042POU domain, class 6, transcription factor 2Wilms tumor suppressor locusretina-derived POU-domain factor-1
Modification date2018052320180403
UniProtAcc

Q6NZ63

P78424

Ensembl transtripts involved in fusion geneENST00000406890, ENST00000404369, 
ENST00000403058, ENST00000518318, 
ENST00000517348, ENST00000559001, 
ENST00000464276, 
Fusion gene scores* DoF score1 X 1 X 1=15 X 5 X 7=175
# samples 19
** MAII scorelog2(1/1*10)=3.32192809488736log2(9/175*10)=-0.959358015502654
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: STEAP1B [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
TCGALDLUADTCGA-55-8089-01ASTEAP1Bchr7

22532184

-POU6F2chr7

39125460

+
* 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-shiftENST00000406890ENST00000403058STEAP1Bchr7

22532184

-POU6F2chr7

39125460

+
Frame-shiftENST00000406890ENST00000518318STEAP1Bchr7

22532184

-POU6F2chr7

39125460

+
5CDS-3UTRENST00000406890ENST00000517348STEAP1Bchr7

22532184

-POU6F2chr7

39125460

+
5CDS-5UTRENST00000406890ENST00000559001STEAP1Bchr7

22532184

-POU6F2chr7

39125460

+
5CDS-5UTRENST00000406890ENST00000464276STEAP1Bchr7

22532184

-POU6F2chr7

39125460

+
Frame-shiftENST00000404369ENST00000403058STEAP1Bchr7

22532184

-POU6F2chr7

39125460

+
Frame-shiftENST00000404369ENST00000518318STEAP1Bchr7

22532184

-POU6F2chr7

39125460

+
5CDS-3UTRENST00000404369ENST00000517348STEAP1Bchr7

22532184

-POU6F2chr7

39125460

+
5CDS-5UTRENST00000404369ENST00000559001STEAP1Bchr7

22532184

-POU6F2chr7

39125460

+
5CDS-5UTRENST00000404369ENST00000464276STEAP1Bchr7

22532184

-POU6F2chr7

39125460

+

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FusionProtFeatures for STEAP1B_POU6F2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
STEAP1B

Q6NZ63

POU6F2

P78424

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 STEAP1B_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 STEAP1B_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
STEAP1BSTEAP1, TRIM25POU6F2


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 STEAP1B_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 STEAP1B_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