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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:EPS8L2-AGPAT2 (FusionGDB2 ID:27076)

Fusion Gene Summary for EPS8L2-AGPAT2

check button Fusion gene summary
Fusion gene informationFusion gene name: EPS8L2-AGPAT2
Fusion gene ID: 27076
HgeneTgene
Gene symbol

EPS8L2

AGPAT2

Gene ID

64787

10555

Gene nameEPS8 like 21-acylglycerol-3-phosphate O-acyltransferase 2
SynonymsDFNB106|EPS8R21-AGPAT2|BSCL|BSCL1|LPAAB|LPAAT-beta
Cytomap

11p15.5

9q34.3

Type of geneprotein-codingprotein-coding
Descriptionepidermal growth factor receptor kinase substrate 8-like protein 2EPS8-related protein 2epidermal growth factor receptor pathway substrate 8-related protein 21-acyl-sn-glycerol-3-phosphate acyltransferase beta1-AGP acyltransferase 21-AGPAT 21-acylglycerol-3-phosphate O-acyltransferase 2 (lysophosphatidic acid acyltransferase, beta)lysophosphatidic acid acyltransferase-betatesticular tissue protein Li 143
Modification date2020031320200313
UniProtAcc

Q9H6S3

O15120

Ensembl transtripts involved in fusion geneENST00000318562, ENST00000533256, 
ENST00000530636, ENST00000526198, 
ENST00000534449, 
ENST00000371694, 
ENST00000371696, ENST00000538402, 
Fusion gene scores* DoF score6 X 5 X 5=1505 X 4 X 4=80
# samples 76
** MAII scorelog2(7/150*10)=-1.09953567355091
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/80*10)=-0.415037499278844
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: EPS8L2 [Title/Abstract] AND AGPAT2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointEPS8L2(709608)-AGPAT2(139569259), # samples:4
Anticipated loss of major functional domain due to fusion event.EPS8L2-AGPAT2 seems lost the major protein functional domain in Tgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
EPS8L2-AGPAT2 seems lost the major protein functional domain in Tgene partner, which is a essential gene 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
HgeneEPS8L2

GO:0007266

Rho protein signal transduction

14565974

HgeneEPS8L2

GO:0035023

regulation of Rho protein signal transduction

14565974


check buttonFusion gene breakpoints across EPS8L2 (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 AGPAT2 (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
ChimerDB4HNSCTCGA-CQ-5333-01AEPS8L2chr11

709608

+AGPAT2chr9

139569259

-
ChimerDB4HNSCTCGA-CQ-5333EPS8L2chr11

709608

+AGPAT2chr9

139569259

-
ChimerDB4HNSCTCGA-CQ-5333EPS8L2chr11

706288

+AGPAT2chr9

139569259

-
ChimerDB4HNSCTCGA-CQ-5333EPS8L2chr11

709608

+AGPAT2chr9

139569259

-
ChimerDB4HNSCTCGA-CQ-5333EPS8L2chr11

706288

+AGPAT2chr9

139569259

-
ChimerDB4HNSCTCGA-CQ-5333-01AEPS8L2chr11

709608

-AGPAT2chr9

139569259

-


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Fusion Gene ORF analysis for EPS8L2-AGPAT2

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
Frame-shiftENST00000318562ENST00000371694EPS8L2chr11

709608

+AGPAT2chr9

139569259

-
Frame-shiftENST00000318562ENST00000371696EPS8L2chr11

709608

+AGPAT2chr9

139569259

-
Frame-shiftENST00000318562ENST00000538402EPS8L2chr11

709608

+AGPAT2chr9

139569259

-
Frame-shiftENST00000533256ENST00000371694EPS8L2chr11

709608

+AGPAT2chr9

139569259

-
Frame-shiftENST00000533256ENST00000371696EPS8L2chr11

709608

+AGPAT2chr9

139569259

-
Frame-shiftENST00000533256ENST00000538402EPS8L2chr11

709608

+AGPAT2chr9

139569259

-
Frame-shiftENST00000530636ENST00000371694EPS8L2chr11

709608

+AGPAT2chr9

139569259

-
Frame-shiftENST00000530636ENST00000371696EPS8L2chr11

709608

+AGPAT2chr9

139569259

-
Frame-shiftENST00000530636ENST00000538402EPS8L2chr11

709608

+AGPAT2chr9

139569259

-
Frame-shiftENST00000526198ENST00000371694EPS8L2chr11

709608

+AGPAT2chr9

139569259

-
Frame-shiftENST00000526198ENST00000371696EPS8L2chr11

709608

+AGPAT2chr9

139569259

-
Frame-shiftENST00000526198ENST00000538402EPS8L2chr11

709608

+AGPAT2chr9

139569259

-
intron-3CDSENST00000534449ENST00000371694EPS8L2chr11

709608

+AGPAT2chr9

139569259

-
intron-3CDSENST00000534449ENST00000371696EPS8L2chr11

709608

+AGPAT2chr9

139569259

-
intron-3CDSENST00000534449ENST00000538402EPS8L2chr11

709608

+AGPAT2chr9

139569259

-
5UTR-3CDSENST00000318562ENST00000371694EPS8L2chr11

706288

+AGPAT2chr9

139569259

-
5UTR-3CDSENST00000318562ENST00000371696EPS8L2chr11

706288

+AGPAT2chr9

139569259

-
5UTR-3CDSENST00000318562ENST00000538402EPS8L2chr11

706288

+AGPAT2chr9

139569259

-
5UTR-3CDSENST00000533256ENST00000371694EPS8L2chr11

706288

+AGPAT2chr9

139569259

-
5UTR-3CDSENST00000533256ENST00000371696EPS8L2chr11

706288

+AGPAT2chr9

139569259

-
5UTR-3CDSENST00000533256ENST00000538402EPS8L2chr11

706288

+AGPAT2chr9

139569259

-
intron-3CDSENST00000530636ENST00000371694EPS8L2chr11

706288

+AGPAT2chr9

139569259

-
intron-3CDSENST00000530636ENST00000371696EPS8L2chr11

706288

+AGPAT2chr9

139569259

-
intron-3CDSENST00000530636ENST00000538402EPS8L2chr11

706288

+AGPAT2chr9

139569259

-
intron-3CDSENST00000526198ENST00000371694EPS8L2chr11

706288

+AGPAT2chr9

139569259

-
intron-3CDSENST00000526198ENST00000371696EPS8L2chr11

706288

+AGPAT2chr9

139569259

-
intron-3CDSENST00000526198ENST00000538402EPS8L2chr11

706288

+AGPAT2chr9

139569259

-
intron-3CDSENST00000534449ENST00000371694EPS8L2chr11

706288

+AGPAT2chr9

139569259

-
intron-3CDSENST00000534449ENST00000371696EPS8L2chr11

706288

+AGPAT2chr9

139569259

-
intron-3CDSENST00000534449ENST00000538402EPS8L2chr11

706288

+AGPAT2chr9

139569259

-

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 EPS8L2-AGPAT2


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 EPS8L2-AGPAT2


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
EPS8L2

Q9H6S3

AGPAT2

O15120

FUNCTION: Stimulates guanine exchange activity of SOS1. May play a role in membrane ruffling and remodeling of the actin cytoskeleton. In the cochlea, is required for stereocilia maintenance in adult hair cells (By similarity). {ECO:0000250|UniProtKB:Q99K30, ECO:0000269|PubMed:14565974}.FUNCTION: Converts 1-acyl-sn-glycerol-3-phosphate (lysophosphatidic acid or LPA) into 1,2-diacyl-sn-glycerol-3-phosphate (phosphatidic acid or PA) by incorporating an acyl moiety at the sn-2 position of the glycerol backbone. {ECO:0000269|PubMed:15629135, ECO:0000269|PubMed:19075029, ECO:0000269|PubMed:21873652, ECO:0000269|PubMed:9242711}.

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 EPS8L2-AGPAT2


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 EPS8L2-AGPAT2


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 EPS8L2-AGPAT2


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 EPS8L2-AGPAT2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneEPS8L2C3711374Nonsyndromic Deafness3CLINGEN
HgeneEPS8L2C4539954DEAFNESS, AUTOSOMAL RECESSIVE 1061GENOMICS_ENGLAND
TgeneAGPAT2C1720862Congenital Generalized Lipodystrophy Type 13CTD_human;GENOMICS_ENGLAND;UNIPROT
TgeneAGPAT2C0023787Lipodystrophy2GENOMICS_ENGLAND