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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:BET1L-LMF1 (FusionGDB2 ID:HG51272TG64788)

Fusion Gene Summary for BET1L-LMF1

check button Fusion gene summary
Fusion gene informationFusion gene name: BET1L-LMF1
Fusion gene ID: hg51272tg64788
HgeneTgene
Gene symbol

BET1L

LMF1

Gene ID

51272

64788

Gene nameBet1 golgi vesicular membrane trafficking protein likelipase maturation factor 1
SynonymsBET1L1|GOLIM3|GS15|HSPC197C16orf26|HMFN1876|JFP11|TMEM112|TMEM112A
Cytomap('BET1L')('LMF1')

11p15.5

16p13.3

Type of geneprotein-codingprotein-coding
DescriptionBET1-like proteinGOS-15blocked early in transport 1 homolog-likegolgi SNARE 15 kDa proteingolgi SNARE with a size of 15 kDagolgi integral membrane protein 3vesicle transport protein GOS15lipase maturation factor 1transmembrane protein 112
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000410108, ENST00000325147, 
ENST00000332865, ENST00000382762, 
ENST00000486280, ENST00000529614, 
Fusion gene scores* DoF score4 X 4 X 4=648 X 6 X 5=240
# samples 47
** MAII scorelog2(4/64*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/240*10)=-1.77760757866355
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: BET1L [Title/Abstract] AND LMF1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointBET1L(168943)-LMF1(1004666), # 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
HgeneBET1L

GO:0042147

retrograde transport, endosome to Golgi

15215310



check button Fusion gene information
* 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
ChimerDB4BRCATCGA-E9-A1R4-01ABET1Lchr11

168943

-LMF1chr16

1004666

-


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Fusion Gene ORF analysis for BET1L-LMF1

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-3CDSENST00000410108ENST00000262301BET1Lchr11

168943

-LMF1chr16

1004666

-
3UTR-3CDSENST00000410108ENST00000399843BET1Lchr11

168943

-LMF1chr16

1004666

-
3UTR-5UTRENST00000410108ENST00000568897BET1Lchr11

168943

-LMF1chr16

1004666

-
3UTR-intronENST00000410108ENST00000539379BET1Lchr11

168943

-LMF1chr16

1004666

-
3UTR-intronENST00000410108ENST00000543238BET1Lchr11

168943

-LMF1chr16

1004666

-
3UTR-intronENST00000410108ENST00000568268BET1Lchr11

168943

-LMF1chr16

1004666

-
intron-3CDSENST00000325147ENST00000262301BET1Lchr11

168943

-LMF1chr16

1004666

-
intron-3CDSENST00000325147ENST00000399843BET1Lchr11

168943

-LMF1chr16

1004666

-
intron-3CDSENST00000332865ENST00000262301BET1Lchr11

168943

-LMF1chr16

1004666

-
intron-3CDSENST00000332865ENST00000399843BET1Lchr11

168943

-LMF1chr16

1004666

-
intron-3CDSENST00000382762ENST00000262301BET1Lchr11

168943

-LMF1chr16

1004666

-
intron-3CDSENST00000382762ENST00000399843BET1Lchr11

168943

-LMF1chr16

1004666

-
intron-3CDSENST00000486280ENST00000262301BET1Lchr11

168943

-LMF1chr16

1004666

-
intron-3CDSENST00000486280ENST00000399843BET1Lchr11

168943

-LMF1chr16

1004666

-
intron-3CDSENST00000529614ENST00000262301BET1Lchr11

168943

-LMF1chr16

1004666

-
intron-3CDSENST00000529614ENST00000399843BET1Lchr11

168943

-LMF1chr16

1004666

-
intron-5UTRENST00000325147ENST00000568897BET1Lchr11

168943

-LMF1chr16

1004666

-
intron-5UTRENST00000332865ENST00000568897BET1Lchr11

168943

-LMF1chr16

1004666

-
intron-5UTRENST00000382762ENST00000568897BET1Lchr11

168943

-LMF1chr16

1004666

-
intron-5UTRENST00000486280ENST00000568897BET1Lchr11

168943

-LMF1chr16

1004666

-
intron-5UTRENST00000529614ENST00000568897BET1Lchr11

168943

-LMF1chr16

1004666

-
intron-intronENST00000325147ENST00000539379BET1Lchr11

168943

-LMF1chr16

1004666

-
intron-intronENST00000325147ENST00000543238BET1Lchr11

168943

-LMF1chr16

1004666

-
intron-intronENST00000325147ENST00000568268BET1Lchr11

168943

-LMF1chr16

1004666

-
intron-intronENST00000332865ENST00000539379BET1Lchr11

168943

-LMF1chr16

1004666

-
intron-intronENST00000332865ENST00000543238BET1Lchr11

168943

-LMF1chr16

1004666

-
intron-intronENST00000332865ENST00000568268BET1Lchr11

168943

-LMF1chr16

1004666

-
intron-intronENST00000382762ENST00000539379BET1Lchr11

168943

-LMF1chr16

1004666

-
intron-intronENST00000382762ENST00000543238BET1Lchr11

168943

-LMF1chr16

1004666

-
intron-intronENST00000382762ENST00000568268BET1Lchr11

168943

-LMF1chr16

1004666

-
intron-intronENST00000486280ENST00000539379BET1Lchr11

168943

-LMF1chr16

1004666

-
intron-intronENST00000486280ENST00000543238BET1Lchr11

168943

-LMF1chr16

1004666

-
intron-intronENST00000486280ENST00000568268BET1Lchr11

168943

-LMF1chr16

1004666

-
intron-intronENST00000529614ENST00000539379BET1Lchr11

168943

-LMF1chr16

1004666

-
intron-intronENST00000529614ENST00000543238BET1Lchr11

168943

-LMF1chr16

1004666

-
intron-intronENST00000529614ENST00000568268BET1Lchr11

168943

-LMF1chr16

1004666

-

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 BET1L-LMF1


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 BET1L-LMF1


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/:168943/:1004666)
- 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 BET1L-LMF1


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 BET1L-LMF1


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 BET1L-LMF1


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 BET1L-LMF1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneC1855498Lipase deficiency combined3CTD_human;GENOMICS_ENGLAND;ORPHANET
TgeneC0020557Hypertriglyceridemia1CTD_human