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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:ITGB1BP1-COL5A1 (FusionGDB2 ID:HG9270TG1289)

Fusion Gene Summary for ITGB1BP1-COL5A1

check button Fusion gene summary
Fusion gene informationFusion gene name: ITGB1BP1-COL5A1
Fusion gene ID: hg9270tg1289
HgeneTgene
Gene symbol

ITGB1BP1

COL5A1

Gene ID

9270

1289

Gene nameintegrin subunit beta 1 binding protein 1collagen type V alpha 1 chain
SynonymsICAP-1A|ICAP-1B|ICAP-1alpha|ICAP1|ICAP1A|ICAP1BEDSC|EDSCL1
Cytomap('ITGB1BP1')('COL5A1')

2p25.1

9q34.3

Type of geneprotein-codingprotein-coding
Descriptionintegrin beta-1-binding protein 1bodeninintegrin cytoplasmic domain-associated protein 1integrin cytoplasmic domain-associated protein 1-alphaintegrin cytoplasmic domain-associated protein 1-betacollagen alpha-1(V) chaincollagen, type V, alpha 1
Modification date2020031320200313
UniProtAcc.

P20908

Ensembl transtripts involved in fusion geneENST00000238091, ENST00000355346, 
ENST00000456913, ENST00000488451, 
ENST00000490426, ENST00000359712, 
ENST00000360635, 
Fusion gene scores* DoF score3 X 4 X 5=6010 X 10 X 7=700
# samples 512
** MAII scorelog2(5/60*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(12/700*10)=-2.54432051622381
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ITGB1BP1 [Title/Abstract] AND COL5A1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointITGB1BP1(9563502)-COL5A1(137658846), # 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
HgeneITGB1BP1

GO:0002043

blood vessel endothelial cell proliferation involved in sprouting angiogenesis

20616313

HgeneITGB1BP1

GO:0006469

negative regulation of protein kinase activity

20616313

HgeneITGB1BP1

GO:0007160

cell-matrix adhesion

9281591

HgeneITGB1BP1

GO:0007229

integrin-mediated signaling pathway

11919189|15703214

HgeneITGB1BP1

GO:0008284

positive regulation of cell proliferation

15703214

HgeneITGB1BP1

GO:0008285

negative regulation of cell proliferation

20616313

HgeneITGB1BP1

GO:0010595

positive regulation of endothelial cell migration

20616313

HgeneITGB1BP1

GO:0032091

negative regulation of protein binding

12473654

HgeneITGB1BP1

GO:0032148

activation of protein kinase B activity

20616313

HgeneITGB1BP1

GO:0035148

tube formation

20616313

HgeneITGB1BP1

GO:0035924

cellular response to vascular endothelial growth factor stimulus

20616313

HgeneITGB1BP1

GO:0043087

regulation of GTPase activity

11807099

HgeneITGB1BP1

GO:0044344

cellular response to fibroblast growth factor stimulus

20616313

HgeneITGB1BP1

GO:0045747

positive regulation of Notch signaling pathway

20616313

HgeneITGB1BP1

GO:0045944

positive regulation of transcription by RNA polymerase II

15703214|20616313

HgeneITGB1BP1

GO:0051895

negative regulation of focal adhesion assembly

12473654

HgeneITGB1BP1

GO:0051897

positive regulation of protein kinase B signaling

20616313

HgeneITGB1BP1

GO:0070373

negative regulation of ERK1 and ERK2 cascade

20616313

HgeneITGB1BP1

GO:0072659

protein localization to plasma membrane

17916086

HgeneITGB1BP1

GO:0090051

negative regulation of cell migration involved in sprouting angiogenesis

20616313

HgeneITGB1BP1

GO:0090315

negative regulation of protein targeting to membrane

11807099

HgeneITGB1BP1

GO:0097746

regulation of blood vessel diameter

20616313

HgeneITGB1BP1

GO:1900025

negative regulation of substrate adhesion-dependent cell spreading

11807099

TgeneCOL5A1

GO:1903225

negative regulation of endodermal cell differentiation

23154389



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
ChimerDB4LUSCTCGA-66-2789-01AITGB1BP1chr2

9563502

-COL5A1chr9

137658846

+


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Fusion Gene ORF analysis for ITGB1BP1-COL5A1

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
5UTR-3CDSENST00000238091ENST00000371817ITGB1BP1chr2

9563502

-COL5A1chr9

137658846

+
5UTR-3CDSENST00000355346ENST00000371817ITGB1BP1chr2

9563502

-COL5A1chr9

137658846

+
5UTR-3CDSENST00000456913ENST00000371817ITGB1BP1chr2

9563502

-COL5A1chr9

137658846

+
5UTR-3CDSENST00000488451ENST00000371817ITGB1BP1chr2

9563502

-COL5A1chr9

137658846

+
5UTR-3CDSENST00000490426ENST00000371817ITGB1BP1chr2

9563502

-COL5A1chr9

137658846

+
5UTR-intronENST00000238091ENST00000464187ITGB1BP1chr2

9563502

-COL5A1chr9

137658846

+
5UTR-intronENST00000355346ENST00000464187ITGB1BP1chr2

9563502

-COL5A1chr9

137658846

+
5UTR-intronENST00000456913ENST00000464187ITGB1BP1chr2

9563502

-COL5A1chr9

137658846

+
5UTR-intronENST00000488451ENST00000464187ITGB1BP1chr2

9563502

-COL5A1chr9

137658846

+
5UTR-intronENST00000490426ENST00000464187ITGB1BP1chr2

9563502

-COL5A1chr9

137658846

+
intron-3CDSENST00000359712ENST00000371817ITGB1BP1chr2

9563502

-COL5A1chr9

137658846

+
intron-3CDSENST00000360635ENST00000371817ITGB1BP1chr2

9563502

-COL5A1chr9

137658846

+
intron-intronENST00000359712ENST00000464187ITGB1BP1chr2

9563502

-COL5A1chr9

137658846

+
intron-intronENST00000360635ENST00000464187ITGB1BP1chr2

9563502

-COL5A1chr9

137658846

+

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 ITGB1BP1-COL5A1


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)
ITGB1BP1chr29563501-COL5A1chr9137658845+0.0002503820.9997496
ITGB1BP1chr29563501-COL5A1chr9137658845+0.0002503820.9997496


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 ITGB1BP1-COL5A1


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/:9563502/:137658846)
- 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
.COL5A1

P20908

FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}.FUNCTION: Type V collagen is a member of group I collagen (fibrillar forming collagen). It is a minor connective tissue component of nearly ubiquitous distribution. Type V collagen binds to DNA, heparan sulfate, thrombospondin, heparin, and insulin.

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 ITGB1BP1-COL5A1


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 ITGB1BP1-COL5A1


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 ITGB1BP1-COL5A1


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 ITGB1BP1-COL5A1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneITGB1BP1C0005941Bone Diseases, Developmental1CTD_human
HgeneITGB1BP1C0376634Craniofacial Abnormalities1CTD_human
TgeneC4552122EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 17GENOMICS_ENGLAND;UNIPROT
TgeneC0268335Ehlers-Danlos syndrome type 13CTD_human;GENOMICS_ENGLAND
TgeneC0220679Ehlers-Danlos Syndrome, Autosomal Dominant, Type Unspecified2ORPHANET
TgeneC0268336Ehlers-Danlos syndrome type 22CTD_human;GENOMICS_ENGLAND
TgeneC0000786Spontaneous abortion1CTD_human
TgeneC0000822Abortion, Tubal1CTD_human
TgeneC0005779Blood Coagulation Disorders1GENOMICS_ENGLAND
TgeneC0007097Carcinoma1CTD_human
TgeneC0022548Keloid1CTD_human
TgeneC0023893Liver Cirrhosis, Experimental1CTD_human
TgeneC0024667Animal Mammary Neoplasms1CTD_human
TgeneC0024668Mammary Neoplasms, Experimental1CTD_human
TgeneC0033578Prostatic Neoplasms1CTD_human
TgeneC0205696Anaplastic carcinoma1CTD_human
TgeneC0205697Carcinoma, Spindle-Cell1CTD_human
TgeneC0205698Undifferentiated carcinoma1CTD_human
TgeneC0205699Carcinomatosis1CTD_human
TgeneC0376358Malignant neoplasm of prostate1CTD_human
TgeneC1257925Mammary Carcinoma, Animal1CTD_human
TgeneC1458140Bleeding tendency1GENOMICS_ENGLAND
TgeneC1846545Autoimmune Lymphoproliferative Syndrome Type 2B1GENOMICS_ENGLAND
TgeneC3830362Early Pregnancy Loss1CTD_human
TgeneC4225429Ehlers-Danlos syndrome classic type1GENOMICS_ENGLAND
TgeneC4552766Miscarriage1CTD_human