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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:FBN3-TCOF1 (FusionGDB2 ID:29491)

Fusion Gene Summary for FBN3-TCOF1

check button Fusion gene summary
Fusion gene informationFusion gene name: FBN3-TCOF1
Fusion gene ID: 29491
HgeneTgene
Gene symbol

FBN3

TCOF1

Gene ID

84467

6949

Gene namefibrillin 3treacle ribosome biogenesis factor 1
Synonyms-MFD1|TCS|TCS1|treacle
Cytomap

19p13.2

5q32-q33.1

Type of geneprotein-codingprotein-coding
Descriptionfibrillin-3treacle proteinTreacher Collins syndrome proteinTreacher Collins-Franceschetti syndrome 1nucleolar trafficking phosphoprotein
Modification date2020032020200313
UniProtAcc

Q75N90

.
Ensembl transtripts involved in fusion geneENST00000600128, ENST00000270509, 
ENST00000601739, 
ENST00000451292, 
ENST00000377797, ENST00000445265, 
ENST00000323668, ENST00000439160, 
ENST00000394269, ENST00000504761, 
ENST00000513346, ENST00000506063, 
Fusion gene scores* DoF score3 X 3 X 1=913 X 11 X 9=1287
# samples 315
** MAII scorelog2(3/9*10)=1.73696559416621
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(15/1287*10)=-3.10097764772482
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: FBN3 [Title/Abstract] AND TCOF1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointFBN3(8132030)-TCOF1(149777995), # 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 FBN3 (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 TCOF1 (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
ChiTaRS5.0N/ADL058591FBN3chr19

8132030

+TCOF1chr5

149777995

-


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Fusion Gene ORF analysis for FBN3-TCOF1

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-3CDSENST00000600128ENST00000451292FBN3chr19

8132030

+TCOF1chr5

149777995

-
intron-3CDSENST00000600128ENST00000377797FBN3chr19

8132030

+TCOF1chr5

149777995

-
intron-3CDSENST00000600128ENST00000445265FBN3chr19

8132030

+TCOF1chr5

149777995

-
intron-3CDSENST00000600128ENST00000323668FBN3chr19

8132030

+TCOF1chr5

149777995

-
intron-3CDSENST00000600128ENST00000439160FBN3chr19

8132030

+TCOF1chr5

149777995

-
intron-intronENST00000600128ENST00000394269FBN3chr19

8132030

+TCOF1chr5

149777995

-
intron-intronENST00000600128ENST00000504761FBN3chr19

8132030

+TCOF1chr5

149777995

-
intron-intronENST00000600128ENST00000513346FBN3chr19

8132030

+TCOF1chr5

149777995

-
intron-intronENST00000600128ENST00000506063FBN3chr19

8132030

+TCOF1chr5

149777995

-
intron-3CDSENST00000270509ENST00000451292FBN3chr19

8132030

+TCOF1chr5

149777995

-
intron-3CDSENST00000270509ENST00000377797FBN3chr19

8132030

+TCOF1chr5

149777995

-
intron-3CDSENST00000270509ENST00000445265FBN3chr19

8132030

+TCOF1chr5

149777995

-
intron-3CDSENST00000270509ENST00000323668FBN3chr19

8132030

+TCOF1chr5

149777995

-
intron-3CDSENST00000270509ENST00000439160FBN3chr19

8132030

+TCOF1chr5

149777995

-
intron-intronENST00000270509ENST00000394269FBN3chr19

8132030

+TCOF1chr5

149777995

-
intron-intronENST00000270509ENST00000504761FBN3chr19

8132030

+TCOF1chr5

149777995

-
intron-intronENST00000270509ENST00000513346FBN3chr19

8132030

+TCOF1chr5

149777995

-
intron-intronENST00000270509ENST00000506063FBN3chr19

8132030

+TCOF1chr5

149777995

-
intron-3CDSENST00000601739ENST00000451292FBN3chr19

8132030

+TCOF1chr5

149777995

-
intron-3CDSENST00000601739ENST00000377797FBN3chr19

8132030

+TCOF1chr5

149777995

-
intron-3CDSENST00000601739ENST00000445265FBN3chr19

8132030

+TCOF1chr5

149777995

-
intron-3CDSENST00000601739ENST00000323668FBN3chr19

8132030

+TCOF1chr5

149777995

-
intron-3CDSENST00000601739ENST00000439160FBN3chr19

8132030

+TCOF1chr5

149777995

-
intron-intronENST00000601739ENST00000394269FBN3chr19

8132030

+TCOF1chr5

149777995

-
intron-intronENST00000601739ENST00000504761FBN3chr19

8132030

+TCOF1chr5

149777995

-
intron-intronENST00000601739ENST00000513346FBN3chr19

8132030

+TCOF1chr5

149777995

-
intron-intronENST00000601739ENST00000506063FBN3chr19

8132030

+TCOF1chr5

149777995

-

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 FBN3-TCOF1


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.

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 FBN3-TCOF1


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
FBN3

Q75N90

.
FUNCTION: [Fibrillin-3]: Fibrillins are structural components of 10-12 nm extracellular calcium-binding microfibrils, which occur either in association with elastin or in elastin-free bundles. Fibrillin-containing microfibrils provide long-term force bearing structural support. {ECO:0000269|PubMed:14962672}.FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.

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 FBN3-TCOF1


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 FBN3-TCOF1


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 FBN3-TCOF1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneFBN3Q75N90DB11348Calcium PhosphateLigandSmall moleculeApproved
HgeneFBN3Q75N90DB11348Calcium PhosphateLigandSmall moleculeApproved
HgeneFBN3Q75N90DB14481Calcium phosphate dihydrateSmall moleculeApproved
HgeneFBN3Q75N90DB14481Calcium phosphate dihydrateSmall moleculeApproved
HgeneFBN3Q75N90DB11093Calcium citrateLigandSmall moleculeApproved|Investigational
HgeneFBN3Q75N90DB11093Calcium citrateLigandSmall moleculeApproved|Investigational

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Related Diseases for FBN3-TCOF1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneTCOF1C0265241Franceschetti-Klein syndrome7CLINGEN
TgeneTCOF1C0242387Mandibulofacial Dysostosis5CTD_human;GENOMICS_ENGLAND;UNIPROT
TgeneTCOF1C0152423Congenital small ears1GENOMICS_ENGLAND
TgeneTCOF1C0376634Craniofacial Abnormalities1CTD_human