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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-ARRDC1 (FusionGDB2 ID:HG79813TG92714)

Fusion Gene Summary for EHMT1-ARRDC1

check button Fusion gene summary
Fusion gene informationFusion gene name: EHMT1-ARRDC1
Fusion gene ID: hg79813tg92714
HgeneTgene
Gene symbol

EHMT1

ARRDC1

Gene ID

79813

92714

Gene nameeuchromatic histone lysine methyltransferase 1arrestin domain containing 1
SynonymsEHMT1-IT1|EUHMTASE1|Eu-HMTase1|FP13812|GLP|GLP1|KLEFS1|KMT1D-
Cytomap('EHMT1')('ARRDC1')

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-marrestin domain-containing protein 1alpha-arrestin 1
Modification date2020031320200320
UniProtAcc.

Q8N5I2

Ensembl transtripts involved in fusion geneENST00000371394, ENST00000460843, 
ENST00000462484, ENST00000334856, 
ENST00000462484, ENST00000371394, 
ENST00000334856, ENST00000460843, 
Fusion gene scores* DoF score15 X 9 X 8=10805 X 5 X 3=75
# samples 206
** MAII scorelog2(20/1080*10)=-2.43295940727611
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/75*10)=-0.321928094887362
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: EHMT1 [Title/Abstract] AND ARRDC1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointEHMT1(140513501)-ARRDC1(140507348), # samples:4
Anticipated loss of major functional domain due to fusion event.ARRDC1-EHMT1 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
ARRDC1-EHMT1 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
ARRDC1-EHMT1 seems lost the major protein functional domain in Tgene partner, which is a epigenetic factor due to the frame-shifted ORF.
ARRDC1-EHMT1 seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
EHMT1-ARRDC1 seems lost the major protein functional domain in Hgene partner, which is a epigenetic factor due to the frame-shifted ORF.
EHMT1-ARRDC1 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
* 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 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
ChimerDB4BLCATCGA-HQ-A2OE-01AEHMT1chr9

140513501

+ARRDC1chr9

140507348

+
ChimerDB4BLCATCGA-HQ-A2OEEHMT1chr9

140513501

+ARRDC1chr9

140507347

+
ChimerDB4BRCATCGA-PL-A8LZ-01AEHMT1chr9

140513501

-ARRDC1chr9

140507348

+
ChimerDB4BRCATCGA-PL-A8LZ-01AEHMT1chr9

140513501

+ARRDC1chr9

140507348

+
ChimerDB4BRCATCGA-PL-A8LZEHMT1chr9

140513501

+ARRDC1chr9

140507347

+
ChimerDB4STADTCGA-CD-8530-01AEHMT1chr9

140513501

+ARRDC1chr9

140507348

+


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Fusion Gene ORF analysis for EHMT1-ARRDC1

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-3CDSENST00000371394ENST00000371421EHMT1chr9

140513501

+ARRDC1chr9

140507348

+
3UTR-3CDSENST00000371394ENST00000371421EHMT1chr9

140513501

+ARRDC1chr9

140507347

+
3UTR-3UTRENST00000371394ENST00000491911EHMT1chr9

140513501

+ARRDC1chr9

140507348

+
3UTR-3UTRENST00000371394ENST00000491911EHMT1chr9

140513501

+ARRDC1chr9

140507347

+
5CDS-3UTRENST00000460843ENST00000491911EHMT1chr9

140513501

+ARRDC1chr9

140507348

+
5CDS-3UTRENST00000460843ENST00000491911EHMT1chr9

140513501

+ARRDC1chr9

140507347

+
5CDS-3UTRENST00000462484ENST00000491911EHMT1chr9

140513501

+ARRDC1chr9

140507348

+
5CDS-3UTRENST00000462484ENST00000491911EHMT1chr9

140513501

+ARRDC1chr9

140507347

+
5UTR-3CDSENST00000334856ENST00000371421EHMT1chr9

140513501

+ARRDC1chr9

140507348

+
5UTR-3CDSENST00000334856ENST00000371421EHMT1chr9

140513501

+ARRDC1chr9

140507347

+
5UTR-3UTRENST00000334856ENST00000491911EHMT1chr9

140513501

+ARRDC1chr9

140507348

+
5UTR-3UTRENST00000334856ENST00000491911EHMT1chr9

140513501

+ARRDC1chr9

140507347

+
Frame-shiftENST00000460843ENST00000371421EHMT1chr9

140513501

+ARRDC1chr9

140507348

+
Frame-shiftENST00000460843ENST00000371421EHMT1chr9

140513501

+ARRDC1chr9

140507347

+
Frame-shiftENST00000462484ENST00000371421EHMT1chr9

140513501

+ARRDC1chr9

140507348

+
Frame-shiftENST00000462484ENST00000371421EHMT1chr9

140513501

+ARRDC1chr9

140507347

+

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-ARRDC1


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+ARRDC1chr9140507347+8.47E-091
EHMT1chr9140513501+ARRDC1chr9140507347+8.47E-091
EHMT1chr9140513501+ARRDC1chr9140507347+8.47E-091
EHMT1chr9140513501+ARRDC1chr9140507347+8.47E-091
EHMT1chr9140513501+ARRDC1chr9140507347+8.47E-091
EHMT1chr9140513501+ARRDC1chr9140507347+8.47E-091
EHMT1chr9140513501+ARRDC1chr9140507347+8.47E-091
EHMT1chr9140513501+ARRDC1chr9140507347+8.47E-091


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-ARRDC1


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/:140507348)
- 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
.ARRDC1

Q8N5I2

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: Functions as an adapter recruiting ubiquitin-protein ligases to their specific substrates (PubMed:23886940, PubMed:27462458). Through an ubiquitination-dependent mechanism plays for instance a role in the incorporation of SLC11A2 into extracellular vesicles (PubMed:27462458). More generally, plays a role in the extracellular transport of proteins between cells through the release in the extracellular space of microvesicles (PubMed:22315426). By participating in the ITCH-mediated ubiquitination and subsequent degradation of NOTCH1, negatively regulates the NOTCH signaling pathway (PubMed:23886940). {ECO:0000269|PubMed:22315426, ECO:0000269|PubMed:23886940, ECO:0000269|PubMed:27462458}.

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-ARRDC1


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-ARRDC1


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-ARRDC1


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-ARRDC1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneEHMT1C0795833KLEEFSTRA SYNDROME 111CLINGEN;CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneEHMT1C0025149Medulloblastoma1CTD_human
HgeneEHMT1C0205833Medullomyoblastoma1CTD_human
HgeneEHMT1C0278510Childhood Medulloblastoma1CTD_human
HgeneEHMT1C0278876Adult Medulloblastoma1CTD_human
HgeneEHMT1C0751291Desmoplastic Medulloblastoma1CTD_human
HgeneEHMT1C1275668Melanotic medulloblastoma1CTD_human