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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:FKTN-RPL39 (FusionGDB2 ID:HG2218TG6170)

Fusion Gene Summary for FKTN-RPL39

check button Fusion gene summary
Fusion gene informationFusion gene name: FKTN-RPL39
Fusion gene ID: hg2218tg6170
HgeneTgene
Gene symbol

FKTN

RPL39

Gene ID

2218

6170

Gene namefukutinribosomal protein L39
SynonymsCMD1X|FCMD|LGMD2M|LGMDR13|MDDGA4|MDDGB4|MDDGC4L39|RPL39P42|RPL39_23_1806
Cytomap('FKTN')('RPL39')

9q31.2

Xq24

Type of geneprotein-codingprotein-coding
DescriptionfukutinFukuyama type congenital muscular dystrophy proteinpatient fukutinribitol-5-phosphate transferase60S ribosomal protein L39large ribosomal subunit protein eL39
Modification date2020032820200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000223528, ENST00000357998, 
ENST00000448551, ENST00000490134, 
ENST00000540160, ENST00000602661, 
Fusion gene scores* DoF score3 X 3 X 3=273 X 2 X 4=24
# samples 34
** MAII scorelog2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(4/24*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: FKTN [Title/Abstract] AND RPL39 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointFKTN(108401945)-RPL39(118920621), # 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
TgeneRPL39

GO:0002181

cytoplasmic translation

25957688

TgeneRPL39

GO:0002227

innate immune response in mucosa

12860195

TgeneRPL39

GO:0019731

antibacterial humoral response

12860195

TgeneRPL39

GO:0050830

defense response to Gram-positive bacterium

12860195

TgeneRPL39

GO:0061844

antimicrobial humoral immune response mediated by antimicrobial peptide

12860195



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/ABF848943FKTNchr9

108401945

-RPL39chrX

118920621

-


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Fusion Gene ORF analysis for FKTN-RPL39

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-3UTRENST00000223528ENST00000361575FKTNchr9

108401945

-RPL39chrX

118920621

-
3UTR-5UTRENST00000223528ENST00000468844FKTNchr9

108401945

-RPL39chrX

118920621

-
intron-3UTRENST00000357998ENST00000361575FKTNchr9

108401945

-RPL39chrX

118920621

-
intron-3UTRENST00000448551ENST00000361575FKTNchr9

108401945

-RPL39chrX

118920621

-
intron-3UTRENST00000490134ENST00000361575FKTNchr9

108401945

-RPL39chrX

118920621

-
intron-3UTRENST00000540160ENST00000361575FKTNchr9

108401945

-RPL39chrX

118920621

-
intron-3UTRENST00000602661ENST00000361575FKTNchr9

108401945

-RPL39chrX

118920621

-
intron-5UTRENST00000357998ENST00000468844FKTNchr9

108401945

-RPL39chrX

118920621

-
intron-5UTRENST00000448551ENST00000468844FKTNchr9

108401945

-RPL39chrX

118920621

-
intron-5UTRENST00000490134ENST00000468844FKTNchr9

108401945

-RPL39chrX

118920621

-
intron-5UTRENST00000540160ENST00000468844FKTNchr9

108401945

-RPL39chrX

118920621

-
intron-5UTRENST00000602661ENST00000468844FKTNchr9

108401945

-RPL39chrX

118920621

-

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 FKTN-RPL39


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)


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Fusion Protein Features for FKTN-RPL39


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/:108401945/:118920621)
- 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
..
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: 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}.

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 FKTN-RPL39


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 FKTN-RPL39


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 FKTN-RPL39


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 FKTN-RPL39


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneFKTNC0410174Fukuyama Type Congenital Muscular Dystrophy13CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneFKTNC2751052MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 47CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneFKTNC1969040MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2M5CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneFKTNC1969024CARDIOMYOPATHY, DILATED, 1X3CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneFKTNC0265221Walker-Warburg congenital muscular dystrophy2CTD_human;ORPHANET
HgeneFKTNC0026850Muscular Dystrophy1CTD_human
HgeneFKTNC0036572Seizures1GENOMICS_ENGLAND
HgeneFKTNC0340427Familial dilated cardiomyopathy1ORPHANET
HgeneFKTNC0457133Muscle eye brain disease1CTD_human;ORPHANET