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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:CSTF1-BLM (FusionGDB2 ID:20001)

Fusion Gene Summary for CSTF1-BLM

check button Fusion gene summary
Fusion gene informationFusion gene name: CSTF1-BLM
Fusion gene ID: 20001
HgeneTgene
Gene symbol

CSTF1

BLM

Gene ID

1477

641

Gene namecleavage stimulation factor subunit 1BLM RecQ like helicase
SynonymsCstF-50|CstFp50BS|MGRISCE1|RECQ2|RECQL2|RECQL3
Cytomap

20q13.2-q13.31

15q26.1

Type of geneprotein-codingprotein-coding
Descriptioncleavage stimulation factor subunit 1CF-1 50 kDa subunitCSTF 50 kDa subunitcleavage stimulation factor 50 kDa subunitcleavage stimulation factor, 3' pre-RNA, subunit 1, 50kDcleavage stimulation factor, 3' pre-RNA, subunit 1, 50kDaBloom syndrome proteinBloom syndrome RecQ like helicaseBloom syndrome, RecQ helicase-likeDNA helicase, RecQ-like type 2recQ protein-like 3
Modification date2020031320200313
UniProtAcc.

Q13867

Ensembl transtripts involved in fusion geneENST00000493039, ENST00000217109, 
ENST00000355112, ENST00000560509, 
ENST00000560136, 
Fusion gene scores* DoF score4 X 6 X 4=967 X 13 X 3=273
# samples 48
** MAII scorelog2(4/96*10)=-1.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/273*10)=-1.77082904603249
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CSTF1 [Title/Abstract] AND BLM [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCSTF1(54967769)-BLM(91352367), # samples:3
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
TgeneBLM

GO:0000729

DNA double-strand break processing

21325134

TgeneBLM

GO:0006974

cellular response to DNA damage stimulus

23509288

TgeneBLM

GO:0007095

mitotic G2 DNA damage checkpoint

11309417

TgeneBLM

GO:0010165

response to X-ray

11309417

TgeneBLM

GO:0031297

replication fork processing

17115688

TgeneBLM

GO:0032508

DNA duplex unwinding

11735402|24816114|25901030

TgeneBLM

GO:0044806

G-quadruplex DNA unwinding

11735402

TgeneBLM

GO:0045893

positive regulation of transcription, DNA-templated

11781842

TgeneBLM

GO:0051259

protein complex oligomerization

28228481

TgeneBLM

GO:0051260

protein homooligomerization

28228481

TgeneBLM

GO:0061820

telomeric D-loop disassembly

19734539

TgeneBLM

GO:0071479

cellular response to ionizing radiation

23509288

TgeneBLM

GO:0072711

cellular response to hydroxyurea

23509288

TgeneBLM

GO:0072757

cellular response to camptothecin

23509288


check buttonFusion gene breakpoints across CSTF1 (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 BLM (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
ChimerDB4SKCMTCGA-ER-A196-01ACSTF1chr20

54967594

+BLMchr15

91352367

+
ChimerDB4SKCMTCGA-ER-A196-01ACSTF1chr20

54967769

-BLMchr15

91352367

+
ChimerDB4SKCMTCGA-ER-A196-01ACSTF1chr20

54967769

+BLMchr15

91352367

+
ChimerDB4SKCMTCGA-ER-A196-01ACSTF1chr20

54967871

+BLMchr15

91352367

+


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Fusion Gene ORF analysis for CSTF1-BLM

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-3CDSENST00000493039ENST00000355112CSTF1chr20

54967769

+BLMchr15

91352367

+
3UTR-3CDSENST00000493039ENST00000355112CSTF1chr20

54967871

+BLMchr15

91352367

+
3UTR-3CDSENST00000493039ENST00000560509CSTF1chr20

54967769

+BLMchr15

91352367

+
3UTR-3CDSENST00000493039ENST00000560509CSTF1chr20

54967871

+BLMchr15

91352367

+
3UTR-3UTRENST00000493039ENST00000560136CSTF1chr20

54967769

+BLMchr15

91352367

+
3UTR-3UTRENST00000493039ENST00000560136CSTF1chr20

54967871

+BLMchr15

91352367

+
5UTR-3CDSENST00000217109ENST00000355112CSTF1chr20

54967594

+BLMchr15

91352367

+
5UTR-3CDSENST00000217109ENST00000355112CSTF1chr20

54967769

+BLMchr15

91352367

+
5UTR-3CDSENST00000217109ENST00000560509CSTF1chr20

54967594

+BLMchr15

91352367

+
5UTR-3CDSENST00000217109ENST00000560509CSTF1chr20

54967769

+BLMchr15

91352367

+
5UTR-3UTRENST00000217109ENST00000560136CSTF1chr20

54967594

+BLMchr15

91352367

+
5UTR-3UTRENST00000217109ENST00000560136CSTF1chr20

54967769

+BLMchr15

91352367

+
intron-3CDSENST00000217109ENST00000355112CSTF1chr20

54967871

+BLMchr15

91352367

+
intron-3CDSENST00000217109ENST00000560509CSTF1chr20

54967871

+BLMchr15

91352367

+
intron-3CDSENST00000493039ENST00000355112CSTF1chr20

54967594

+BLMchr15

91352367

+
intron-3CDSENST00000493039ENST00000560509CSTF1chr20

54967594

+BLMchr15

91352367

+
intron-3UTRENST00000217109ENST00000560136CSTF1chr20

54967871

+BLMchr15

91352367

+
intron-3UTRENST00000493039ENST00000560136CSTF1chr20

54967594

+BLMchr15

91352367

+

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 CSTF1-BLM


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)
CSTF1chr2054967871+BLMchr1591352366+0.0109994780.98900044
CSTF1chr2054967769+BLMchr1591352366+0.0018851040.99811494
CSTF1chr2054967871+BLMchr1591352366+0.0109994780.98900044
CSTF1chr2054967769+BLMchr1591352366+0.0018851040.99811494

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 CSTF1-BLM


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/:54967769/:91352367)
- 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
.BLM

Q13867

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: The normal physiological role of BLM hydrolase is unknown, but it catalyzes the inactivation of the antitumor drug BLM (a glycopeptide) by hydrolyzing the carboxamide bond of its B-aminoalaninamide moiety thus protecting normal and malignant cells from BLM toxicity. {ECO:0000250}.

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 CSTF1-BLM


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 CSTF1-BLM


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 CSTF1-BLM


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 CSTF1-BLM


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