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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:BCL2L12-FLT3LG (FusionGDB2 ID:9346)

Fusion Gene Summary for BCL2L12-FLT3LG

check button Fusion gene summary
Fusion gene informationFusion gene name: BCL2L12-FLT3LG
Fusion gene ID: 9346
HgeneTgene
Gene symbol

BCL2L12

FLT3LG

Gene ID

83596

2323

Gene nameBCL2 like 12fms related receptor tyrosine kinase 3 ligand
Synonyms-FL|FLG3L|FLT3L
Cytomap

19q13.33

19q13.33

Type of geneprotein-codingprotein-coding
Descriptionbcl-2-like protein 12BCL2-like 12 (proline rich)Bcl-2 related proline-rich proteinfms-related tyrosine kinase 3 ligandflt3 ligandfms related tyrosine kinase 3 ligand
Modification date2020031320200313
UniProtAcc

Q9HB09

P49771

Ensembl transtripts involved in fusion geneENST00000246784, ENST00000246785, 
ENST00000441864, ENST00000594793, 
ENST00000204637, ENST00000594009, 
ENST00000596435, ENST00000597551, 
ENST00000600429, ENST00000344019, 
ENST00000595510, 
Fusion gene scores* DoF score2 X 2 X 2=87 X 8 X 7=392
# samples 210
** MAII scorelog2(2/8*10)=1.32192809488736log2(10/392*10)=-1.97085365434048
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: BCL2L12 [Title/Abstract] AND FLT3LG [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointBCL2L12(50173745)-FLT3LG(49989272), # 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
HgeneBCL2L12

GO:0045944

positive regulation of transcription by RNA polymerase II

22262180

HgeneBCL2L12

GO:1990001

inhibition of cysteine-type endopeptidase activity involved in apoptotic process

22262180

TgeneFLT3LG

GO:0008284

positive regulation of cell proliferation

8180375

TgeneFLT3LG

GO:0035162

embryonic hemopoiesis

21149635


check buttonFusion gene breakpoints across BCL2L12 (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 FLT3LG (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
ChimerDB4PRADTCGA-ZG-A9LN-01ABCL2L12chr19

50173745

-FLT3LGchr19

49989272

+
ChimerDB4PRADTCGA-ZG-A9LN-01ABCL2L12chr19

50173745

+FLT3LGchr19

49989272

+
ChimerDB4PRADTCGA-ZG-A9LNBCL2L12chr19

50173745

+FLT3LGchr19

49989272

+


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Fusion Gene ORF analysis for BCL2L12-FLT3LG

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-3UTRENST00000246784ENST00000204637BCL2L12chr19

50173745

+FLT3LGchr19

49989272

+
3UTR-3UTRENST00000246784ENST00000594009BCL2L12chr19

50173745

+FLT3LGchr19

49989272

+
3UTR-3UTRENST00000246784ENST00000596435BCL2L12chr19

50173745

+FLT3LGchr19

49989272

+
3UTR-3UTRENST00000246784ENST00000597551BCL2L12chr19

50173745

+FLT3LGchr19

49989272

+
3UTR-3UTRENST00000246784ENST00000600429BCL2L12chr19

50173745

+FLT3LGchr19

49989272

+
3UTR-intronENST00000246784ENST00000344019BCL2L12chr19

50173745

+FLT3LGchr19

49989272

+
3UTR-intronENST00000246784ENST00000595510BCL2L12chr19

50173745

+FLT3LGchr19

49989272

+
5CDS-3UTRENST00000246785ENST00000204637BCL2L12chr19

50173745

+FLT3LGchr19

49989272

+
5CDS-3UTRENST00000246785ENST00000594009BCL2L12chr19

50173745

+FLT3LGchr19

49989272

+
5CDS-3UTRENST00000246785ENST00000596435BCL2L12chr19

50173745

+FLT3LGchr19

49989272

+
5CDS-3UTRENST00000246785ENST00000597551BCL2L12chr19

50173745

+FLT3LGchr19

49989272

+
5CDS-3UTRENST00000246785ENST00000600429BCL2L12chr19

50173745

+FLT3LGchr19

49989272

+
5CDS-3UTRENST00000441864ENST00000204637BCL2L12chr19

50173745

+FLT3LGchr19

49989272

+
5CDS-3UTRENST00000441864ENST00000594009BCL2L12chr19

50173745

+FLT3LGchr19

49989272

+
5CDS-3UTRENST00000441864ENST00000596435BCL2L12chr19

50173745

+FLT3LGchr19

49989272

+
5CDS-3UTRENST00000441864ENST00000597551BCL2L12chr19

50173745

+FLT3LGchr19

49989272

+
5CDS-3UTRENST00000441864ENST00000600429BCL2L12chr19

50173745

+FLT3LGchr19

49989272

+
5CDS-intronENST00000246785ENST00000344019BCL2L12chr19

50173745

+FLT3LGchr19

49989272

+
5CDS-intronENST00000246785ENST00000595510BCL2L12chr19

50173745

+FLT3LGchr19

49989272

+
5CDS-intronENST00000441864ENST00000344019BCL2L12chr19

50173745

+FLT3LGchr19

49989272

+
5CDS-intronENST00000441864ENST00000595510BCL2L12chr19

50173745

+FLT3LGchr19

49989272

+
intron-3UTRENST00000594793ENST00000204637BCL2L12chr19

50173745

+FLT3LGchr19

49989272

+
intron-3UTRENST00000594793ENST00000594009BCL2L12chr19

50173745

+FLT3LGchr19

49989272

+
intron-3UTRENST00000594793ENST00000596435BCL2L12chr19

50173745

+FLT3LGchr19

49989272

+
intron-3UTRENST00000594793ENST00000597551BCL2L12chr19

50173745

+FLT3LGchr19

49989272

+
intron-3UTRENST00000594793ENST00000600429BCL2L12chr19

50173745

+FLT3LGchr19

49989272

+
intron-intronENST00000594793ENST00000344019BCL2L12chr19

50173745

+FLT3LGchr19

49989272

+
intron-intronENST00000594793ENST00000595510BCL2L12chr19

50173745

+FLT3LGchr19

49989272

+

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 BCL2L12-FLT3LG


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)
BCL2L12chr1950173745+FLT3LGchr1949989271+1.82E-060.9999982
BCL2L12chr1950173745+FLT3LGchr1949989271+1.82E-060.9999982
BCL2L12chr1950173745+FLT3LGchr1949989271+1.82E-060.9999982
BCL2L12chr1950173745+FLT3LGchr1949989271+1.82E-060.9999982

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 BCL2L12-FLT3LG


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/:50173745/:49989272)
- 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
BCL2L12

Q9HB09

FLT3LG

P49771

FUNCTION: Stimulates the proliferation of early hematopoietic cells by activating FLT3. Synergizes well with a number of other colony stimulating factors and interleukins.

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 BCL2L12-FLT3LG


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 BCL2L12-FLT3LG


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 BCL2L12-FLT3LG


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 BCL2L12-FLT3LG


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