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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:EHMT1-RABL6 (FusionGDB2 ID:25587)

Fusion Gene Summary for EHMT1-RABL6

check button Fusion gene summary
Fusion gene informationFusion gene name: EHMT1-RABL6
Fusion gene ID: 25587
HgeneTgene
Gene symbol

EHMT1

RABL6

Gene ID

79813

55684

Gene nameeuchromatic histone lysine methyltransferase 1RAB, member RAS oncogene family like 6
SynonymsEHMT1-IT1|EUHMTASE1|Eu-HMTase1|FP13812|GLP|GLP1|KLEFS1|KMT1DC9orf86|PARF|RBEL1|pp8875
Cytomap

9q34.3

9q34.3

Type of geneprotein-codingprotein-coding
Descriptionhistone-lysine N-methyltransferase EHMT1EHMT1 intronic transcript 1G9a-like protein 1H3-K9-HMTase 5euchromatic histone-lysine N-methyltransferase 1histone H3-K9 methyltransferase 5histone-lysine N-methyltransferase, H3 lysine-9 specific 5lysine N-mrab-like protein 6Rab-like GTP-binding protein 1Cpartner of ARFputative GTP-binding protein Parf
Modification date2020031320200313
UniProtAcc

Q9H9B1

Q3YEC7

Ensembl transtripts involved in fusion geneENST00000371394, ENST00000460843, 
ENST00000462484, ENST00000334856, 
ENST00000466096, ENST00000311502, 
ENST00000357466, ENST00000371663, 
ENST00000371671, ENST00000371675, 
ENST00000432842, 
Fusion gene scores* DoF score15 X 9 X 8=10804 X 5 X 3=60
# samples 205
** MAII scorelog2(20/1080*10)=-2.43295940727611
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/60*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: EHMT1 [Title/Abstract] AND RABL6 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointEHMT1(140513501)-RABL6(139730194), # 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
HgeneEHMT1

GO:0006325

chromatin organization

12004135

HgeneEHMT1

GO:0016571

histone methylation

12004135

HgeneEHMT1

GO:0018027

peptidyl-lysine dimethylation

20118233


check buttonFusion gene breakpoints across EHMT1 (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 RABL6 (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-EJ-A46GEHMT1chr9

140513501

+RABL6chr9

139730194

+


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Fusion Gene ORF analysis for EHMT1-RABL6

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-3UTRENST00000371394ENST00000466096EHMT1chr9

140513501

+RABL6chr9

139730194

+
3UTR-intronENST00000371394ENST00000311502EHMT1chr9

140513501

+RABL6chr9

139730194

+
3UTR-intronENST00000371394ENST00000357466EHMT1chr9

140513501

+RABL6chr9

139730194

+
3UTR-intronENST00000371394ENST00000371663EHMT1chr9

140513501

+RABL6chr9

139730194

+
3UTR-intronENST00000371394ENST00000371671EHMT1chr9

140513501

+RABL6chr9

139730194

+
3UTR-intronENST00000371394ENST00000371675EHMT1chr9

140513501

+RABL6chr9

139730194

+
3UTR-intronENST00000371394ENST00000432842EHMT1chr9

140513501

+RABL6chr9

139730194

+
5CDS-3UTRENST00000460843ENST00000466096EHMT1chr9

140513501

+RABL6chr9

139730194

+
5CDS-3UTRENST00000462484ENST00000466096EHMT1chr9

140513501

+RABL6chr9

139730194

+
5CDS-intronENST00000460843ENST00000311502EHMT1chr9

140513501

+RABL6chr9

139730194

+
5CDS-intronENST00000460843ENST00000357466EHMT1chr9

140513501

+RABL6chr9

139730194

+
5CDS-intronENST00000460843ENST00000371663EHMT1chr9

140513501

+RABL6chr9

139730194

+
5CDS-intronENST00000460843ENST00000371671EHMT1chr9

140513501

+RABL6chr9

139730194

+
5CDS-intronENST00000460843ENST00000371675EHMT1chr9

140513501

+RABL6chr9

139730194

+
5CDS-intronENST00000460843ENST00000432842EHMT1chr9

140513501

+RABL6chr9

139730194

+
5CDS-intronENST00000462484ENST00000311502EHMT1chr9

140513501

+RABL6chr9

139730194

+
5CDS-intronENST00000462484ENST00000357466EHMT1chr9

140513501

+RABL6chr9

139730194

+
5CDS-intronENST00000462484ENST00000371663EHMT1chr9

140513501

+RABL6chr9

139730194

+
5CDS-intronENST00000462484ENST00000371671EHMT1chr9

140513501

+RABL6chr9

139730194

+
5CDS-intronENST00000462484ENST00000371675EHMT1chr9

140513501

+RABL6chr9

139730194

+
5CDS-intronENST00000462484ENST00000432842EHMT1chr9

140513501

+RABL6chr9

139730194

+
5UTR-3UTRENST00000334856ENST00000466096EHMT1chr9

140513501

+RABL6chr9

139730194

+
5UTR-intronENST00000334856ENST00000311502EHMT1chr9

140513501

+RABL6chr9

139730194

+
5UTR-intronENST00000334856ENST00000357466EHMT1chr9

140513501

+RABL6chr9

139730194

+
5UTR-intronENST00000334856ENST00000371663EHMT1chr9

140513501

+RABL6chr9

139730194

+
5UTR-intronENST00000334856ENST00000371671EHMT1chr9

140513501

+RABL6chr9

139730194

+
5UTR-intronENST00000334856ENST00000371675EHMT1chr9

140513501

+RABL6chr9

139730194

+
5UTR-intronENST00000334856ENST00000432842EHMT1chr9

140513501

+RABL6chr9

139730194

+

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 EHMT1-RABL6


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)
EHMT1chr9140513501+RABL6chr9139730193+3.80E-161
EHMT1chr9140513501+RABL6chr9139730193+3.80E-161

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.
genomic feature

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 EHMT1-RABL6


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/:140513501/:139730194)
- 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
EHMT1

Q9H9B1

RABL6

Q3YEC7

FUNCTION: Histone methyltransferase that specifically mono- and dimethylates 'Lys-9' of histone H3 (H3K9me1 and H3K9me2, respectively) in euchromatin. H3K9me represents a specific tag for epigenetic transcriptional repression by recruiting HP1 proteins to methylated histones. Also weakly methylates 'Lys-27' of histone H3 (H3K27me). Also required for DNA methylation, the histone methyltransferase activity is not required for DNA methylation, suggesting that these 2 activities function independently. Probably targeted to histone H3 by different DNA-binding proteins like E2F6, MGA, MAX and/or DP1. During G0 phase, it probably contributes to silencing of MYC- and E2F-responsive genes, suggesting a role in G0/G1 transition in cell cycle. In addition to the histone methyltransferase activity, also methylates non-histone proteins: mediates dimethylation of 'Lys-373' of p53/TP53. Represses the expression of mitochondrial function-related genes, perhaps by occupying their promoter regions, working in concert with probable chromatin reader BAZ2B (By similarity). {ECO:0000250|UniProtKB:Q5DW34, ECO:0000269|PubMed:12004135, ECO:0000269|PubMed:20118233}.FUNCTION: May enhance cellular proliferation. May reduce growth inhibitory activity of CDKN2A. {ECO:0000269|PubMed:16582619}.

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 EHMT1-RABL6


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 EHMT1-RABL6


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 EHMT1-RABL6


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 EHMT1-RABL6


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