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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:FARSB-BTBD7 (FusionGDB2 ID:29422)

Fusion Gene Summary for FARSB-BTBD7

check button Fusion gene summary
Fusion gene informationFusion gene name: FARSB-BTBD7
Fusion gene ID: 29422
HgeneTgene
Gene symbol

FARSB

BTBD7

Gene ID

10056

55727

Gene namephenylalanyl-tRNA synthetase subunit betaBTB domain containing 7
SynonymsFARSLB|FRSB|HSPC173|NEDBLLA|PheHB|PheRS|RILDBCFUP1
Cytomap

2q36.1

14q32.12

Type of geneprotein-codingprotein-coding
Descriptionphenylalanine--tRNA ligase beta subunitphenylalanine tRNA ligase 1, beta, cytoplasmicphenylalanine-tRNA ligase beta chainphenylalanine-tRNA synthetase-like, beta subunitphenylalanyl-tRNA synthetase beta chainphenylalanyl-tRNA synthetase beta subunitBTB/POZ domain-containing protein 7BTB (POZ) domain containing 7
Modification date2020031320200313
UniProtAcc

Q9NSD9

Q9P203

Ensembl transtripts involved in fusion geneENST00000281828, ENST00000536361, 
ENST00000298896, ENST00000334746, 
ENST00000393170, ENST00000554565, 
ENST00000555525, 
Fusion gene scores* DoF score5 X 6 X 3=904 X 6 X 5=120
# samples 57
** MAII scorelog2(5/90*10)=-0.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/120*10)=-0.777607578663552
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: FARSB [Title/Abstract] AND BTBD7 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointBTBD7(93749228)-FARSB(223436735), # samples:1
FARSB(223436735)-BTBD7(93749228), # 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
HgeneFARSB

GO:0006432

phenylalanyl-tRNA aminoacylation

20223217

HgeneFARSB

GO:0051290

protein heterotetramerization

20223217


check buttonFusion gene breakpoints across FARSB (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 BTBD7 (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/AAA628074FARSBchr2

223436735

+BTBD7chr14

93749228

+


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Fusion Gene ORF analysis for FARSB-BTBD7

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-intronENST00000281828ENST00000298896FARSBchr2

223436735

+BTBD7chr14

93749228

+
intron-intronENST00000281828ENST00000334746FARSBchr2

223436735

+BTBD7chr14

93749228

+
intron-intronENST00000281828ENST00000393170FARSBchr2

223436735

+BTBD7chr14

93749228

+
intron-intronENST00000281828ENST00000554565FARSBchr2

223436735

+BTBD7chr14

93749228

+
intron-intronENST00000281828ENST00000555525FARSBchr2

223436735

+BTBD7chr14

93749228

+
intron-intronENST00000536361ENST00000298896FARSBchr2

223436735

+BTBD7chr14

93749228

+
intron-intronENST00000536361ENST00000334746FARSBchr2

223436735

+BTBD7chr14

93749228

+
intron-intronENST00000536361ENST00000393170FARSBchr2

223436735

+BTBD7chr14

93749228

+
intron-intronENST00000536361ENST00000554565FARSBchr2

223436735

+BTBD7chr14

93749228

+
intron-intronENST00000536361ENST00000555525FARSBchr2

223436735

+BTBD7chr14

93749228

+

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 FARSB-BTBD7


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 FARSB-BTBD7


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/:93749228/:223436735)
- 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
FARSB

Q9NSD9

BTBD7

Q9P203

FUNCTION: Acts as a mediator of epithelial dynamics and organ branching by promoting cleft progression. Induced following accumulation of fibronectin in forming clefts, leading to local expression of the cell-scattering SNAIL2 and suppression of E-cadherin levels, thereby altering cell morphology and reducing cell-cell adhesion. This stimulates cell separation at the base of forming clefts by local, dynamic intercellular gap formation and promotes cleft progression (By similarity). {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 FARSB-BTBD7


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 FARSB-BTBD7


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 FARSB-BTBD7


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 FARSB-BTBD7


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