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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:SPIDR-COX6B1 (FusionGDB2 ID:85784)

Fusion Gene Summary for SPIDR-COX6B1

check button Fusion gene summary
Fusion gene informationFusion gene name: SPIDR-COX6B1
Fusion gene ID: 85784
HgeneTgene
Gene symbol

SPIDR

COX6B1

Gene ID

23514

1340

Gene namescaffold protein involved in DNA repaircytochrome c oxidase subunit 6B1
SynonymsKIAA0146COX6B|COXG|COXVIb1
Cytomap

8q11.21

19q13.12

Type of geneprotein-codingprotein-coding
DescriptionDNA repair-scaffolding proteinscaffolding protein involved in DNA repaircytochrome c oxidase subunit 6B1COX VIb-1cytochrome c oxidase subunit VIb polypeptide 1 (ubiquitous)
Modification date2020032020200313
UniProtAcc

Q14159

P14854

Ensembl transtripts involved in fusion geneENST00000521214, ENST00000297423, 
ENST00000517693, ENST00000518074, 
ENST00000541342, ENST00000518060, 
ENST00000246554, ENST00000392201, 
ENST00000592141, 
Fusion gene scores* DoF score24 X 12 X 15=43209 X 7 X 5=315
# samples 2710
** MAII scorelog2(27/4320*10)=-4
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(10/315*10)=-1.65535182861255
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SPIDR [Title/Abstract] AND COX6B1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointSPIDR(48613052)-COX6B1(36149496), # samples:1
Anticipated loss of major functional domain due to fusion event.SPIDR-COX6B1 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
SPIDR-COX6B1 seems lost the major protein functional domain in Tgene partner, which is a essential gene 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
HgeneSPIDR

GO:0006974

cellular response to DNA damage stimulus

23509288

HgeneSPIDR

GO:0010569

regulation of double-strand break repair via homologous recombination

23754376

HgeneSPIDR

GO:0031334

positive regulation of protein complex assembly

23509288

HgeneSPIDR

GO:0070202

regulation of establishment of protein localization to chromosome

23509288

HgeneSPIDR

GO:0071479

cellular response to ionizing radiation

23509288|23754376

HgeneSPIDR

GO:0072711

cellular response to hydroxyurea

23509288

HgeneSPIDR

GO:0072757

cellular response to camptothecin

23509288


check buttonFusion gene breakpoints across SPIDR (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 COX6B1 (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
ChimerDB4LGGTCGA-FG-5965SPIDRchr8

48613052

+COX6B1chr19

36149496

+


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Fusion Gene ORF analysis for SPIDR-COX6B1

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
3UTR-3CDSENST00000521214ENST00000246554SPIDRchr8

48613052

+COX6B1chr19

36149496

+
3UTR-3CDSENST00000521214ENST00000392201SPIDRchr8

48613052

+COX6B1chr19

36149496

+
3UTR-3CDSENST00000521214ENST00000592141SPIDRchr8

48613052

+COX6B1chr19

36149496

+
Frame-shiftENST00000297423ENST00000246554SPIDRchr8

48613052

+COX6B1chr19

36149496

+
Frame-shiftENST00000297423ENST00000392201SPIDRchr8

48613052

+COX6B1chr19

36149496

+
Frame-shiftENST00000297423ENST00000592141SPIDRchr8

48613052

+COX6B1chr19

36149496

+
Frame-shiftENST00000517693ENST00000246554SPIDRchr8

48613052

+COX6B1chr19

36149496

+
Frame-shiftENST00000517693ENST00000392201SPIDRchr8

48613052

+COX6B1chr19

36149496

+
Frame-shiftENST00000517693ENST00000592141SPIDRchr8

48613052

+COX6B1chr19

36149496

+
Frame-shiftENST00000518074ENST00000246554SPIDRchr8

48613052

+COX6B1chr19

36149496

+
Frame-shiftENST00000518074ENST00000392201SPIDRchr8

48613052

+COX6B1chr19

36149496

+
Frame-shiftENST00000518074ENST00000592141SPIDRchr8

48613052

+COX6B1chr19

36149496

+
Frame-shiftENST00000541342ENST00000246554SPIDRchr8

48613052

+COX6B1chr19

36149496

+
Frame-shiftENST00000541342ENST00000392201SPIDRchr8

48613052

+COX6B1chr19

36149496

+
Frame-shiftENST00000541342ENST00000592141SPIDRchr8

48613052

+COX6B1chr19

36149496

+
intron-3CDSENST00000518060ENST00000246554SPIDRchr8

48613052

+COX6B1chr19

36149496

+
intron-3CDSENST00000518060ENST00000392201SPIDRchr8

48613052

+COX6B1chr19

36149496

+
intron-3CDSENST00000518060ENST00000592141SPIDRchr8

48613052

+COX6B1chr19

36149496

+

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 SPIDR-COX6B1


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)
SPIDRchr848613052+COX6B1chr1936149495+0.950974940.049025085
SPIDRchr848613052+COX6B1chr1936149495+0.950974940.049025085

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.
genomic feature of top 1%

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Fusion Protein Features for SPIDR-COX6B1


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:48613052/:36149496)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

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

Q14159

COX6B1

P14854

FUNCTION: Plays a role in DNA double-strand break (DBS) repair via homologous recombination (HR). Serves as a scaffolding protein that helps to promote the recruitment of DNA-processing enzymes like the helicase BLM and recombinase RAD51 to site of DNA damage, and hence contributes to maintain genomic integrity. {ECO:0000269|PubMed:23509288, ECO:0000269|PubMed:23754376}.FUNCTION: Component of the cytochrome c oxidase, the last enzyme in the mitochondrial electron transport chain which drives oxidative phosphorylation. The respiratory chain contains 3 multisubunit complexes succinate dehydrogenase (complex II, CII), ubiquinol-cytochrome c oxidoreductase (cytochrome b-c1 complex, complex III, CIII) and cytochrome c oxidase (complex IV, CIV), that cooperate to transfer electrons derived from NADH and succinate to molecular oxygen, creating an electrochemical gradient over the inner membrane that drives transmembrane transport and the ATP synthase. Cytochrome c oxidase is the component of the respiratory chain that catalyzes the reduction of oxygen to water. Electrons originating from reduced cytochrome c in the intermembrane space (IMS) are transferred via the dinuclear copper A center (CU(A)) of subunit 2 and heme A of subunit 1 to the active site in subunit 1, a binuclear center (BNC) formed by heme A3 and copper B (CU(B)). The BNC reduces molecular oxygen to 2 water molecules using 4 electrons from cytochrome c in the IMS and 4 protons from the mitochondrial matrix. {ECO:0000250|UniProtKB:Q01519}.

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 SPIDR-COX6B1


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 SPIDR-COX6B1


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 SPIDR-COX6B1


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 SPIDR-COX6B1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource