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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:COL8A1-COL8A1 (FusionGDB2 ID:18462)

Fusion Gene Summary for COL8A1-COL8A1

check button Fusion gene summary
Fusion gene informationFusion gene name: COL8A1-COL8A1
Fusion gene ID: 18462
HgeneTgene
Gene symbol

COL8A1

COL8A1

Gene ID

1295

1295

Gene namecollagen type VIII alpha 1 chaincollagen type VIII alpha 1 chain
SynonymsC3orf7C3orf7
Cytomap

3q12.1

3q12.1

Type of geneprotein-codingprotein-coding
Descriptioncollagen alpha-1(VIII) chaincell proliferation-inducing protein 41collagen VIII, alpha-1 polypeptidecollagen, type VIII, alpha 1endothelial collagensmag-64smooth muscle cell-expressed and macrophage conditioned medium-induced protein smag-64collagen alpha-1(VIII) chaincell proliferation-inducing protein 41collagen VIII, alpha-1 polypeptidecollagen, type VIII, alpha 1endothelial collagensmag-64smooth muscle cell-expressed and macrophage conditioned medium-induced protein smag-64
Modification date2020032720200327
UniProtAcc

P27658

P27658

Ensembl transtripts involved in fusion geneENST00000261037, ENST00000273342, 
ENST00000463753, 
ENST00000463753, 
ENST00000273342, ENST00000261037, 
Fusion gene scores* DoF score5 X 5 X 3=757 X 5 X 5=175
# samples 57
** MAII scorelog2(5/75*10)=-0.584962500721156
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/175*10)=-1.32192809488736
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: COL8A1 [Title/Abstract] AND COL8A1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCOL8A1(99514637)-COL8A1(99514745), # samples:1
Anticipated loss of major functional domain due to fusion event.
* 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 buttonFusion gene breakpoints across COL8A1 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across COL8A1 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

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
ChiTaRS5.0N/ABG938623COL8A1chr3

99514637

-COL8A1chr3

99514745

+


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Fusion Gene ORF analysis for COL8A1-COL8A1

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
5CDS-intronENST00000261037ENST00000463753COL8A1chr3

99514637

-COL8A1chr3

99514745

+
5CDS-intronENST00000273342ENST00000463753COL8A1chr3

99514637

-COL8A1chr3

99514745

+
Frame-shiftENST00000261037ENST00000273342COL8A1chr3

99514637

-COL8A1chr3

99514745

+
Frame-shiftENST00000273342ENST00000261037COL8A1chr3

99514637

-COL8A1chr3

99514745

+
Frame-shiftENST00000273342ENST00000273342COL8A1chr3

99514637

-COL8A1chr3

99514745

+
In-frameENST00000261037ENST00000261037COL8A1chr3

99514637

-COL8A1chr3

99514745

+
intron-3CDSENST00000463753ENST00000261037COL8A1chr3

99514637

-COL8A1chr3

99514745

+
intron-3CDSENST00000463753ENST00000273342COL8A1chr3

99514637

-COL8A1chr3

99514745

+
intron-intronENST00000463753ENST00000463753COL8A1chr3

99514637

-COL8A1chr3

99514745

+

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 COL8A1-COL8A1


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)

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.
genomic feature

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.

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Fusion Protein Features for COL8A1-COL8A1


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/chr3:99514637/chr3:99514745)
- 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
COL8A1

P27658

COL8A1

P27658

FUNCTION: Macromolecular component of the subendothelium. Major component of the Descemet's membrane (basement membrane) of corneal endothelial cells. Also component of the endothelia of blood vessels. Necessary for migration and proliferation of vascular smooth muscle cells and thus, has a potential role in the maintenance of vessel wall integrity and structure, in particular in atherogenesis. {ECO:0000269|PubMed:11708810}.; FUNCTION: Vastatin, the C-terminal fragment comprising the NC1 domain, inhibits aortic endothelial cell proliferation and causes cell apoptosis. {ECO:0000269|PubMed:11708810}.FUNCTION: Macromolecular component of the subendothelium. Major component of the Descemet's membrane (basement membrane) of corneal endothelial cells. Also component of the endothelia of blood vessels. Necessary for migration and proliferation of vascular smooth muscle cells and thus, has a potential role in the maintenance of vessel wall integrity and structure, in particular in atherogenesis. {ECO:0000269|PubMed:11708810}.; FUNCTION: Vastatin, the C-terminal fragment comprising the NC1 domain, inhibits aortic endothelial cell proliferation and causes cell apoptosis. {ECO:0000269|PubMed:11708810}.

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
TgeneCOL8A1chr3:99514637chr3:99514745ENST0000026103705611_7440745.0DomainC1q
TgeneCOL8A1chr3:99514637chr3:99514745ENST0000027334204611_7440745.0DomainC1q
TgeneCOL8A1chr3:99514637chr3:99514745ENST0000026103705118_5710745.0RegionNote=Triple-helical region (COL1)
TgeneCOL8A1chr3:99514637chr3:99514745ENST000002610370529_1170745.0RegionNote=Nonhelical region (NC2)
TgeneCOL8A1chr3:99514637chr3:99514745ENST0000026103705572_7440745.0RegionNote=Nonhelical region (NC1)
TgeneCOL8A1chr3:99514637chr3:99514745ENST0000027334204118_5710745.0RegionNote=Triple-helical region (COL1)
TgeneCOL8A1chr3:99514637chr3:99514745ENST000002733420429_1170745.0RegionNote=Nonhelical region (NC2)
TgeneCOL8A1chr3:99514637chr3:99514745ENST0000027334204572_7440745.0RegionNote=Nonhelical region (NC1)

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneCOL8A1chr3:99514637chr3:99514745ENST00000261037-15611_7440745.0DomainC1q
HgeneCOL8A1chr3:99514637chr3:99514745ENST00000273342-14611_7440745.0DomainC1q
HgeneCOL8A1chr3:99514637chr3:99514745ENST00000261037-15118_5710745.0RegionNote=Triple-helical region (COL1)
HgeneCOL8A1chr3:99514637chr3:99514745ENST00000261037-1529_1170745.0RegionNote=Nonhelical region (NC2)
HgeneCOL8A1chr3:99514637chr3:99514745ENST00000261037-15572_7440745.0RegionNote=Nonhelical region (NC1)
HgeneCOL8A1chr3:99514637chr3:99514745ENST00000273342-14118_5710745.0RegionNote=Triple-helical region (COL1)
HgeneCOL8A1chr3:99514637chr3:99514745ENST00000273342-1429_1170745.0RegionNote=Nonhelical region (NC2)
HgeneCOL8A1chr3:99514637chr3:99514745ENST00000273342-14572_7440745.0RegionNote=Nonhelical region (NC1)


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Fusion Gene Sequence for COL8A1-COL8A1


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 COL8A1-COL8A1


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 COL8A1-COL8A1


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 COL8A1-COL8A1


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