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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:FMN1-KANSL1 (FusionGDB2 ID:30723)

Fusion Gene Summary for FMN1-KANSL1

check button Fusion gene summary
Fusion gene informationFusion gene name: FMN1-KANSL1
Fusion gene ID: 30723
HgeneTgene
Gene symbol

FMN1

KANSL1

Gene ID

342184

284058

Gene nameformin 1KAT8 regulatory NSL complex subunit 1
SynonymsFMN|LDCENP-36|KDVS|KIAA1267|MSL1v1|NSL1|hMSL1v1
Cytomap

15q13.3

17q21.31

Type of geneprotein-codingprotein-coding
Descriptionformin-1formin (limb deformity)limb deformity protein homologKAT8 regulatory NSL complex subunit 1MLL1/MLL complex subunit KANSL1MSL1 homolog 1NSL complex protein NSL1centromere protein 36male-specific lethal 1 homolognon-specific lethal 1 homolog
Modification date2020031320200327
UniProtAcc

Q68DA7

A0AUZ9

Ensembl transtripts involved in fusion geneENST00000334528, ENST00000559047, 
ENST00000320930, ENST00000558197, 
ENST00000559150, ENST00000561249, 
ENST00000262419, ENST00000393476, 
ENST00000432791, ENST00000572904, 
ENST00000574590, ENST00000575318, 
ENST00000576248, 
Fusion gene scores* DoF score11 X 9 X 5=49517 X 18 X 11=3366
# samples 1228
** MAII scorelog2(12/495*10)=-2.04439411935845
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(28/3366*10)=-3.58753644438498
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: FMN1 [Title/Abstract] AND KANSL1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointFMN1(33357158)-KANSL1(44249598), # samples:2
KANSL1(44270189)-FMN1(33384404), # samples:2
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
TgeneKANSL1

GO:0043981

histone H4-K5 acetylation

20018852

TgeneKANSL1

GO:0043982

histone H4-K8 acetylation

20018852

TgeneKANSL1

GO:0043984

histone H4-K16 acetylation

20018852


check buttonFusion gene breakpoints across FMN1 (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 KANSL1 (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
ChimerDB4SKCMTCGA-FS-A1Z4-06AFMN1chr15

33357158

-KANSL1chr17

44249598

-


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Fusion Gene ORF analysis for FMN1-KANSL1

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
5CDS-5UTRENST00000334528ENST00000262419FMN1chr15

33357158

-KANSL1chr17

44249598

-
5CDS-5UTRENST00000334528ENST00000393476FMN1chr15

33357158

-KANSL1chr17

44249598

-
5CDS-5UTRENST00000334528ENST00000432791FMN1chr15

33357158

-KANSL1chr17

44249598

-
5CDS-5UTRENST00000334528ENST00000572904FMN1chr15

33357158

-KANSL1chr17

44249598

-
5CDS-5UTRENST00000334528ENST00000574590FMN1chr15

33357158

-KANSL1chr17

44249598

-
5CDS-5UTRENST00000559047ENST00000262419FMN1chr15

33357158

-KANSL1chr17

44249598

-
5CDS-5UTRENST00000559047ENST00000393476FMN1chr15

33357158

-KANSL1chr17

44249598

-
5CDS-5UTRENST00000559047ENST00000432791FMN1chr15

33357158

-KANSL1chr17

44249598

-
5CDS-5UTRENST00000559047ENST00000572904FMN1chr15

33357158

-KANSL1chr17

44249598

-
5CDS-5UTRENST00000559047ENST00000574590FMN1chr15

33357158

-KANSL1chr17

44249598

-
5CDS-intronENST00000334528ENST00000575318FMN1chr15

33357158

-KANSL1chr17

44249598

-
5CDS-intronENST00000334528ENST00000576248FMN1chr15

33357158

-KANSL1chr17

44249598

-
5CDS-intronENST00000559047ENST00000575318FMN1chr15

33357158

-KANSL1chr17

44249598

-
5CDS-intronENST00000559047ENST00000576248FMN1chr15

33357158

-KANSL1chr17

44249598

-
intron-5UTRENST00000320930ENST00000262419FMN1chr15

33357158

-KANSL1chr17

44249598

-
intron-5UTRENST00000320930ENST00000393476FMN1chr15

33357158

-KANSL1chr17

44249598

-
intron-5UTRENST00000320930ENST00000432791FMN1chr15

33357158

-KANSL1chr17

44249598

-
intron-5UTRENST00000320930ENST00000572904FMN1chr15

33357158

-KANSL1chr17

44249598

-
intron-5UTRENST00000320930ENST00000574590FMN1chr15

33357158

-KANSL1chr17

44249598

-
intron-5UTRENST00000558197ENST00000262419FMN1chr15

33357158

-KANSL1chr17

44249598

-
intron-5UTRENST00000558197ENST00000393476FMN1chr15

33357158

-KANSL1chr17

44249598

-
intron-5UTRENST00000558197ENST00000432791FMN1chr15

33357158

-KANSL1chr17

44249598

-
intron-5UTRENST00000558197ENST00000572904FMN1chr15

33357158

-KANSL1chr17

44249598

-
intron-5UTRENST00000558197ENST00000574590FMN1chr15

33357158

-KANSL1chr17

44249598

-
intron-5UTRENST00000559150ENST00000262419FMN1chr15

33357158

-KANSL1chr17

44249598

-
intron-5UTRENST00000559150ENST00000393476FMN1chr15

33357158

-KANSL1chr17

44249598

-
intron-5UTRENST00000559150ENST00000432791FMN1chr15

33357158

-KANSL1chr17

44249598

-
intron-5UTRENST00000559150ENST00000572904FMN1chr15

33357158

-KANSL1chr17

44249598

-
intron-5UTRENST00000559150ENST00000574590FMN1chr15

33357158

-KANSL1chr17

44249598

-
intron-5UTRENST00000561249ENST00000262419FMN1chr15

33357158

-KANSL1chr17

44249598

-
intron-5UTRENST00000561249ENST00000393476FMN1chr15

33357158

-KANSL1chr17

44249598

-
intron-5UTRENST00000561249ENST00000432791FMN1chr15

33357158

-KANSL1chr17

44249598

-
intron-5UTRENST00000561249ENST00000572904FMN1chr15

33357158

-KANSL1chr17

44249598

-
intron-5UTRENST00000561249ENST00000574590FMN1chr15

33357158

-KANSL1chr17

44249598

-
intron-intronENST00000320930ENST00000575318FMN1chr15

33357158

-KANSL1chr17

44249598

-
intron-intronENST00000320930ENST00000576248FMN1chr15

33357158

-KANSL1chr17

44249598

-
intron-intronENST00000558197ENST00000575318FMN1chr15

33357158

-KANSL1chr17

44249598

-
intron-intronENST00000558197ENST00000576248FMN1chr15

33357158

-KANSL1chr17

44249598

-
intron-intronENST00000559150ENST00000575318FMN1chr15

33357158

-KANSL1chr17

44249598

-
intron-intronENST00000559150ENST00000576248FMN1chr15

33357158

-KANSL1chr17

44249598

-
intron-intronENST00000561249ENST00000575318FMN1chr15

33357158

-KANSL1chr17

44249598

-
intron-intronENST00000561249ENST00000576248FMN1chr15

33357158

-KANSL1chr17

44249598

-

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 FMN1-KANSL1


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 FMN1-KANSL1


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/:33357158/:44249598)
- 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
FMN1

Q68DA7

KANSL1

A0AUZ9

FUNCTION: Plays a role in the formation of adherens junction and the polymerization of linear actin cables. {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 FMN1-KANSL1


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 FMN1-KANSL1


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 FMN1-KANSL1


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 FMN1-KANSL1


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