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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: 17489

FusionGeneSummary for INO80_PDE6B

check button Fusion gene summary
Fusion gene informationFusion gene name: INO80_PDE6B
Fusion gene ID: 17489
HgeneTgene
Gene symbol

INO80

PDE6B

Gene ID

54617

5158

Gene nameINO80 complex subunitphosphodiesterase 6B
SynonymsINO80A|INOC1|hINO80CSNB3|CSNBAD2|GMP-PDEbeta|PDEB|RP40|rd1
Cytomap

15q15.1

4p16.3

Type of geneprotein-codingprotein-coding
DescriptionDNA helicase INO80INO80 complex subunit AINO80 homologhomolog of yeast INO80putative DNA helicase INO80 complex homolog 1rod cGMP-specific 3',5'-cyclic phosphodiesterase subunit betaGMP-PDE betaphosphodiesterase 6B, cGMP-specific, rod, betarod cGMP-phosphodiesterase beta-subunit
Modification date2018052320180522
UniProtAcc

Q9ULG1

P35913

Ensembl transtripts involved in fusion geneENST00000361937, ENST00000401393, 
ENST00000561244, 
ENST00000255622, 
ENST00000496514, ENST00000429163, 
Fusion gene scores* DoF score6 X 6 X 5=1803 X 3 X 3=27
# samples 63
** MAII scorelog2(6/180*10)=-1.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: INO80 [Title/Abstract] AND PDE6B [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
ChiTaRS3.1BM725061INO80chr15

41291127

-PDE6Bchr4

664297

+
* 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-3UTRENST00000361937ENST00000255622INO80chr15

41291127

-PDE6Bchr4

664297

+
intron-3UTRENST00000361937ENST00000496514INO80chr15

41291127

-PDE6Bchr4

664297

+
intron-intronENST00000361937ENST00000429163INO80chr15

41291127

-PDE6Bchr4

664297

+
intron-3UTRENST00000401393ENST00000255622INO80chr15

41291127

-PDE6Bchr4

664297

+
intron-3UTRENST00000401393ENST00000496514INO80chr15

41291127

-PDE6Bchr4

664297

+
intron-intronENST00000401393ENST00000429163INO80chr15

41291127

-PDE6Bchr4

664297

+
intron-3UTRENST00000561244ENST00000255622INO80chr15

41291127

-PDE6Bchr4

664297

+
intron-3UTRENST00000561244ENST00000496514INO80chr15

41291127

-PDE6Bchr4

664297

+
intron-intronENST00000561244ENST00000429163INO80chr15

41291127

-PDE6Bchr4

664297

+

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FusionProtFeatures for INO80_PDE6B


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
INO80

Q9ULG1

PDE6B

P35913

ATPase component of the chromatin remodeling INO80complex which is involved in transcriptional regulation, DNAreplication and DNA repair (PubMed:16230350, PubMed:16298340,PubMed:17721549, PubMed:20855601, PubMed:20237820). Binds DNA(PubMed:16298340, PubMed:21303910). As part of the INO80 complex,remodels chromatin by shifting nucleosomes (PubMed:16230350,PubMed:21303910). Regulates transcription upon recruitment by YY1to YY1-activated genes, where it acts as an essential coactivator(PubMed:17721549). Involved in UV-damage excision DNA repair(PubMed:20855601). The contribution to DNA double-strand breakrepair appears to be largely indirect through transcriptionalregulation (PubMed:20687897). Involved in DNA replication(PubMed:20237820). Required for microtubule assembly duringmitosis thereby regulating chromosome segregation cycle(PubMed:20237820). {ECO:0000269|PubMed:16230350,ECO:0000269|PubMed:16298340, ECO:0000269|PubMed:17721549,ECO:0000269|PubMed:20237820, ECO:0000269|PubMed:20687897,ECO:0000269|PubMed:20855601, ECO:0000269|PubMed:21303910}. This protein participates in processes of transmissionand amplification of the visual signal. Necessary for theformation of a functional phosphodiesterase holoenzyme.

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 INO80_PDE6B


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 INO80_PDE6B


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 INO80_PDE6B


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 INO80_PDE6B


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgenePDE6BC3151107RETINITIS PIGMENTOSA 40 (disorder)7UNIPROT
TgenePDE6BC0035304Retinal Degeneration4CTD_human
TgenePDE6BC0035334Retinitis Pigmentosa1CTD_human;HPO;ORPHANET
TgenePDE6BC0339535Night blindness, congenital stationary1CTD_human;HPO;ORPHANET
TgenePDE6BC1876182NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 21CTD_human;UNIPROT