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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:MYBL1-KDM2B (FusionGDB2 ID:56170)

Fusion Gene Summary for MYBL1-KDM2B

check button Fusion gene summary
Fusion gene informationFusion gene name: MYBL1-KDM2B
Fusion gene ID: 56170
HgeneTgene
Gene symbol

MYBL1

KDM2B

Gene ID

4603

84678

Gene nameMYB proto-oncogene like 1lysine demethylase 2B
SynonymsA-MYB|AMYBCXXC2|FBXL10|Fbl10|JHDM1B|PCCX2
Cytomap

8q13.1

12q24.31

Type of geneprotein-codingprotein-coding
Descriptionmyb-related protein Amyb-like protein 1v-myb avian myeloblastosis viral oncogene homolog-like 1lysine-specific demethylase 2BCXXC-type zinc finger protein 2F-box and leucine-rich repeat protein 10F-box protein FBL10F-box/LRR-repeat protein 10JEMMA (Jumonji domain, EMSY-interactor, methyltransferase motif) protein[Histone-H3]-lysine-36 demethy
Modification date2020031320200313
UniProtAcc

P10243

Q8NHM5

Ensembl transtripts involved in fusion geneENST00000517885, ENST00000522419, 
ENST00000522677, ENST00000524176, 
ENST00000377069, ENST00000377071, 
ENST00000536437, ENST00000538046, 
ENST00000542973, ENST00000543852, 
Fusion gene scores* DoF score5 X 8 X 4=1608 X 13 X 8=832
# samples 418
** MAII scorelog2(4/160*10)=-2
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(18/832*10)=-2.20858662181142
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: MYBL1 [Title/Abstract] AND KDM2B [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointMYBL1(67484576)-KDM2B(121993836), # 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
HgeneMYBL1

GO:0045944

positive regulation of transcription by RNA polymerase II

7987850

TgeneKDM2B

GO:0035518

histone H2A monoubiquitination

16943429

TgeneKDM2B

GO:0070544

histone H3-K36 demethylation

26237645


check buttonFusion gene breakpoints across MYBL1 (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 KDM2B (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/AEC549669MYBL1chr8

67484576

+KDM2Bchr12

121993836

-


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Fusion Gene ORF analysis for MYBL1-KDM2B

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-intronENST00000517885ENST00000377069MYBL1chr8

67484576

+KDM2Bchr12

121993836

-
intron-intronENST00000517885ENST00000377071MYBL1chr8

67484576

+KDM2Bchr12

121993836

-
intron-intronENST00000517885ENST00000536437MYBL1chr8

67484576

+KDM2Bchr12

121993836

-
intron-intronENST00000517885ENST00000538046MYBL1chr8

67484576

+KDM2Bchr12

121993836

-
intron-intronENST00000517885ENST00000542973MYBL1chr8

67484576

+KDM2Bchr12

121993836

-
intron-intronENST00000517885ENST00000543852MYBL1chr8

67484576

+KDM2Bchr12

121993836

-
intron-intronENST00000522419ENST00000377069MYBL1chr8

67484576

+KDM2Bchr12

121993836

-
intron-intronENST00000522419ENST00000377071MYBL1chr8

67484576

+KDM2Bchr12

121993836

-
intron-intronENST00000522419ENST00000536437MYBL1chr8

67484576

+KDM2Bchr12

121993836

-
intron-intronENST00000522419ENST00000538046MYBL1chr8

67484576

+KDM2Bchr12

121993836

-
intron-intronENST00000522419ENST00000542973MYBL1chr8

67484576

+KDM2Bchr12

121993836

-
intron-intronENST00000522419ENST00000543852MYBL1chr8

67484576

+KDM2Bchr12

121993836

-
intron-intronENST00000522677ENST00000377069MYBL1chr8

67484576

+KDM2Bchr12

121993836

-
intron-intronENST00000522677ENST00000377071MYBL1chr8

67484576

+KDM2Bchr12

121993836

-
intron-intronENST00000522677ENST00000536437MYBL1chr8

67484576

+KDM2Bchr12

121993836

-
intron-intronENST00000522677ENST00000538046MYBL1chr8

67484576

+KDM2Bchr12

121993836

-
intron-intronENST00000522677ENST00000542973MYBL1chr8

67484576

+KDM2Bchr12

121993836

-
intron-intronENST00000522677ENST00000543852MYBL1chr8

67484576

+KDM2Bchr12

121993836

-
intron-intronENST00000524176ENST00000377069MYBL1chr8

67484576

+KDM2Bchr12

121993836

-
intron-intronENST00000524176ENST00000377071MYBL1chr8

67484576

+KDM2Bchr12

121993836

-
intron-intronENST00000524176ENST00000536437MYBL1chr8

67484576

+KDM2Bchr12

121993836

-
intron-intronENST00000524176ENST00000538046MYBL1chr8

67484576

+KDM2Bchr12

121993836

-
intron-intronENST00000524176ENST00000542973MYBL1chr8

67484576

+KDM2Bchr12

121993836

-
intron-intronENST00000524176ENST00000543852MYBL1chr8

67484576

+KDM2Bchr12

121993836

-

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 MYBL1-KDM2B


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 MYBL1-KDM2B


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/:67484576/:121993836)
- 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
MYBL1

P10243

KDM2B

Q8NHM5

FUNCTION: Transcription factor that specifically recognizes the sequence 5'-YAAC[GT]G-3' (PubMed:8058310, PubMed:7987850). Acts as a master regulator of male meiosis by promoting expression of piRNAs: activates expression of both piRNA precursor RNAs and expression of protein-coding genes involved in piRNA metabolism (By similarity). The piRNA metabolic process mediates the repression of transposable elements during meiosis by forming complexes composed of piRNAs and Piwi proteins and governs the methylation and subsequent repression of transposons, which is essential for the germline integrity (By similarity). Transcriptional activator of SOX30 (By similarity). {ECO:0000250|UniProtKB:P51960, ECO:0000269|PubMed:7987850, ECO:0000269|PubMed:8058310}.FUNCTION: Histone demethylase that demethylates 'Lys-4' and 'Lys-36' of histone H3, thereby playing a central role in histone code (PubMed:16362057, PubMed:17994099, PubMed:26237645). Preferentially demethylates trimethylated H3 'Lys-4' and dimethylated H3 'Lys-36' residue while it has weak or no activity for mono- and tri-methylated H3 'Lys-36' (PubMed:16362057, PubMed:17994099, PubMed:26237645). Preferentially binds the transcribed region of ribosomal RNA and represses the transcription of ribosomal RNA genes which inhibits cell growth and proliferation (PubMed:16362057, PubMed:17994099). May also serve as a substrate-recognition component of the SCF (SKP1-CUL1-F-box protein)-type E3 ubiquitin ligase complex (Probable). {ECO:0000269|PubMed:16362057, ECO:0000269|PubMed:17994099, ECO:0000269|PubMed:26237645, ECO:0000305}.

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 MYBL1-KDM2B


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 MYBL1-KDM2B


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 MYBL1-KDM2B


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 MYBL1-KDM2B


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