UTHEALTH HOME    ABOUT SBMI    A-Z    WEBMAIL    INSIDE THE UNIVERSITY
FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Terms of Use

Center for Computational Systems Medicine level2
leaf

Fusion Gene Summary

leaf

Fusion Gene Sample Information

leaf

Fusion ORF Analysis

leaf

Fusion Amino Acid Sequences

leaf

Fusion Protein Functional Features

leaf

Fusion Protein Structure

leaf

pLDDT scores

leaf

Ramachandran Plot of Fusion Protein Structure

leaf

Fusion Protein-Protein Interaction

leaf

Related drugs with this fusion protein

leaf

Related disease with this fusion protein

Fusion Protein:EPC1-AKR1E2

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: EPC1-AKR1E2
FusionPDB ID: 26883
FusionGDB2.0 ID: 26883
HgeneTgene
Gene symbol

EPC1

AKR1E2

Gene ID

80314

83592

Gene nameenhancer of polycomb homolog 1aldo-keto reductase family 1 member E2
SynonymsEpl1AKR1CL2|AKRDC1|LoopADR|TAKR|hTSP|htAKR
Cytomap

10p11.22

10p15.1

Type of geneprotein-codingprotein-coding
Descriptionenhancer of polycomb homolog 11,5-anhydro-D-fructose reductaseAF reductasealdo-keto reductase family 1 member C-like protein 2aldo-keto reductase family 1, member C-like 2aldo-keto reductase loopADRtestis aldo-keto reductasetestis-specific protein
Modification date2020031320200313
UniProtAcc

Q9H2F5

Q96JD6

Ensembl transtripts involved in fusion geneENST idsENST00000263062, ENST00000319778, 
ENST00000375110, ENST00000480402, 
ENST00000334019, ENST00000345253, 
ENST00000525281, ENST00000532248, 
ENST00000298375, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score17 X 14 X 8=19046 X 3 X 6=108
# samples 208
** MAII scorelog2(20/1904*10)=-3.25096157353322
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/108*10)=-0.432959407276106
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: EPC1 [Title/Abstract] AND AKR1E2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)EPC1(32635691)-AKR1E2(4872867), # samples:3
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
HgeneEPC1

GO:0000122

negative regulation of transcription by RNA polymerase II

10976108

HgeneEPC1

GO:0043967

histone H4 acetylation

14966270

HgeneEPC1

GO:0043968

histone H2A acetylation

14966270

HgeneEPC1

GO:0045814

negative regulation of gene expression, epigenetic

10976108

HgeneEPC1

GO:0045892

negative regulation of transcription, DNA-templated

10976108

HgeneEPC1

GO:0045944

positive regulation of transcription by RNA polymerase II

10976108

TgeneAKR1E2

GO:0055114

oxidation-reduction process

15118078


check buttonFusion gene breakpoints across EPC1 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across AKR1E2 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


Top

Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
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
ChimerDB4ESCATCGA-IG-A8O2-01AEPC1chr10

32635691

-AKR1E2chr10

4872867

+
ChimerDB4ESCATCGA-IG-A8O2EPC1chr10

32635690

-AKR1E2chr10

4872866

+
ChimerDB4ESCATCGA-IG-A8O2EPC1chr10

32635691

-AKR1E2chr10

4872867

+
ChimerDB4ESCATCGA-IG-A8O2EPC1chr10

32667419

-AKR1E2chr10

4872867

+


Top

Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000319778EPC1chr1032635691-ENST00000298375AKR1E2chr104872867+19124563031379358
ENST00000263062EPC1chr1032635691-ENST00000298375AKR1E2chr104872867+18794232701346358
ENST00000319778EPC1chr1032635690-ENST00000298375AKR1E2chr104872866+19124563031379358
ENST00000263062EPC1chr1032635690-ENST00000298375AKR1E2chr104872866+18794232701346358
ENST00000375110EPC1chr1032667419-ENST00000298375AKR1E2chr104872867+17643082811231316

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
ENST00000319778ENST00000298375EPC1chr1032635691-AKR1E2chr104872867+0.0011625110.99883753
ENST00000263062ENST00000298375EPC1chr1032635691-AKR1E2chr104872867+0.0011579910.99884206
ENST00000319778ENST00000298375EPC1chr1032635690-AKR1E2chr104872866+0.0011625110.99883753
ENST00000263062ENST00000298375EPC1chr1032635690-AKR1E2chr104872866+0.0011579910.99884206
ENST00000375110ENST00000298375EPC1chr1032667419-AKR1E2chr104872867+0.0010621180.9989379

Top

Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>26883_26883_1_EPC1-AKR1E2_EPC1_chr10_32635690_ENST00000263062_AKR1E2_chr10_4872866_ENST00000298375_length(amino acids)=358AA_BP=51
MSKLSFRARALDASKPLPVFRCEDLPDLHEYASINRAVPQMPTGMEKEEESASPGKVTEAVKEAIDAGYRHFDCAYFYHNEREVGAGIRC
KIKEGAVRREDLFIATKLWCTCHKKSLVETACRKSLKALKLNYLDLYLIHWPMGFKPPHPEWIMSCSELSFCLSHPRVQDLPLDESNMVI
PSDTDFLDTWEAMEDLVITGLVKNIGVSNFNHEQLERLLNKPGLRFKPLTNQIECHPYLTQKNLISFCQSRDVSVTAYRPLGGSCEGVDL

--------------------------------------------------------------

>26883_26883_2_EPC1-AKR1E2_EPC1_chr10_32635690_ENST00000319778_AKR1E2_chr10_4872866_ENST00000298375_length(amino acids)=358AA_BP=51
MSKLSFRARALDASKPLPVFRCEDLPDLHEYASINRAVPQMPTGMEKEEESASPGKVTEAVKEAIDAGYRHFDCAYFYHNEREVGAGIRC
KIKEGAVRREDLFIATKLWCTCHKKSLVETACRKSLKALKLNYLDLYLIHWPMGFKPPHPEWIMSCSELSFCLSHPRVQDLPLDESNMVI
PSDTDFLDTWEAMEDLVITGLVKNIGVSNFNHEQLERLLNKPGLRFKPLTNQIECHPYLTQKNLISFCQSRDVSVTAYRPLGGSCEGVDL

--------------------------------------------------------------

>26883_26883_3_EPC1-AKR1E2_EPC1_chr10_32635691_ENST00000263062_AKR1E2_chr10_4872867_ENST00000298375_length(amino acids)=358AA_BP=51
MSKLSFRARALDASKPLPVFRCEDLPDLHEYASINRAVPQMPTGMEKEEESASPGKVTEAVKEAIDAGYRHFDCAYFYHNEREVGAGIRC
KIKEGAVRREDLFIATKLWCTCHKKSLVETACRKSLKALKLNYLDLYLIHWPMGFKPPHPEWIMSCSELSFCLSHPRVQDLPLDESNMVI
PSDTDFLDTWEAMEDLVITGLVKNIGVSNFNHEQLERLLNKPGLRFKPLTNQIECHPYLTQKNLISFCQSRDVSVTAYRPLGGSCEGVDL

--------------------------------------------------------------

>26883_26883_4_EPC1-AKR1E2_EPC1_chr10_32635691_ENST00000319778_AKR1E2_chr10_4872867_ENST00000298375_length(amino acids)=358AA_BP=51
MSKLSFRARALDASKPLPVFRCEDLPDLHEYASINRAVPQMPTGMEKEEESASPGKVTEAVKEAIDAGYRHFDCAYFYHNEREVGAGIRC
KIKEGAVRREDLFIATKLWCTCHKKSLVETACRKSLKALKLNYLDLYLIHWPMGFKPPHPEWIMSCSELSFCLSHPRVQDLPLDESNMVI
PSDTDFLDTWEAMEDLVITGLVKNIGVSNFNHEQLERLLNKPGLRFKPLTNQIECHPYLTQKNLISFCQSRDVSVTAYRPLGGSCEGVDL

--------------------------------------------------------------

>26883_26883_5_EPC1-AKR1E2_EPC1_chr10_32667419_ENST00000375110_AKR1E2_chr10_4872867_ENST00000298375_length(amino acids)=316AA_BP=7
MPSSLPALMASPGKVTEAVKEAIDAGYRHFDCAYFYHNEREVGAGIRCKIKEGAVRREDLFIATKLWCTCHKKSLVETACRKSLKALKLN
YLDLYLIHWPMGFKPPHPEWIMSCSELSFCLSHPRVQDLPLDESNMVIPSDTDFLDTWEAMEDLVITGLVKNIGVSNFNHEQLERLLNKP
GLRFKPLTNQIECHPYLTQKNLISFCQSRDVSVTAYRPLGGSCEGVDLIDNPVIKRIAKEHGKSPAQILIRFQIQRNVIVIPGSITPSHI

--------------------------------------------------------------

Top

Fusion Protein Functional Features


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/chr10:32635691/chr10:4872867)
- 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
EPC1

Q9H2F5

AKR1E2

Q96JD6

FUNCTION: Component of the NuA4 histone acetyltransferase (HAT) complex which is involved in transcriptional activation of select genes principally by acetylation of nucleosomal histones H4 and H2A. This modification may both alter nucleosome - DNA interactions and promote interaction of the modified histones with other proteins which positively regulate transcription. This complex may be required for the activation of transcriptional programs associated with oncogene and proto-oncogene mediated growth induction, tumor suppressor mediated growth arrest and replicative senescence, apoptosis, and DNA repair. NuA4 may also play a direct role in DNA repair when directly recruited to sites of DNA damage. {ECO:0000269|PubMed:14966270}.FUNCTION: Catalyzes the NADPH-dependent reduction of 1,5-anhydro-D-fructose (AF) to 1,5-anhydro-D-glucitol (By similarity). Has low NADPH-dependent reductase activity towards 9,10-phenanthrenequinone (in vitro) (PubMed:12604216, PubMed:15118078). {ECO:0000250|UniProtKB:Q9DCT1, ECO:0000269|PubMed:12604216, ECO:0000269|PubMed:15118078}.

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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgeneAKR1E2chr10:32635690chr10:4872866ENST00000298375010265_27713.0321.0Nucleotide bindingNADP
TgeneAKR1E2chr10:32635690chr10:4872866ENST0000033401908265_27713.0264.0Nucleotide bindingNADP
TgeneAKR1E2chr10:32635690chr10:4872866ENST0000034525307265_27713.0223.0Nucleotide bindingNADP
TgeneAKR1E2chr10:32635690chr10:4872866ENST0000053224807265_27713.0251.0Nucleotide bindingNADP
TgeneAKR1E2chr10:32635691chr10:4872867ENST00000298375010265_27713.0321.0Nucleotide bindingNADP
TgeneAKR1E2chr10:32635691chr10:4872867ENST0000033401908265_27713.0264.0Nucleotide bindingNADP
TgeneAKR1E2chr10:32635691chr10:4872867ENST0000034525307265_27713.0223.0Nucleotide bindingNADP
TgeneAKR1E2chr10:32635691chr10:4872867ENST0000053224807265_27713.0251.0Nucleotide bindingNADP
TgeneAKR1E2chr10:32667419chr10:4872867ENST00000298375010265_27713.0321.0Nucleotide bindingNADP
TgeneAKR1E2chr10:32667419chr10:4872867ENST0000033401908265_27713.0264.0Nucleotide bindingNADP
TgeneAKR1E2chr10:32667419chr10:4872867ENST0000034525307265_27713.0223.0Nucleotide bindingNADP
TgeneAKR1E2chr10:32667419chr10:4872867ENST0000053224807265_27713.0251.0Nucleotide bindingNADP

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


Top

Fusion Protein Structures

check button PDB and CIF files of the predicted fusion proteins
* Here we show the 3D structure of the fusion proteins using Mol*. AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Model confidence is shown from the pLDDT values per residue. pLDDT corresponds to the model’s prediction of its score on the local Distance Difference Test. It is a measure of local accuracy (from AlphfaFold website). To color code individual residues, we transformed individual PDB files into CIF format.
Fusion protein PDB link (fusion AA seq ID in FusionPDB)HgeneHchrHbpHstrandTgeneTchrTbpTstrandAA seqLen(AA seq)
PDB file >>>699_EPC1_32635691_AKR1E2_4872867_ranked_0.pdbEPC13266741932635691ENST00000298375AKR1E2chr104872867+
MSKLSFRARALDASKPLPVFRCEDLPDLHEYASINRAVPQMPTGMEKEEESASPGKVTEAVKEAIDAGYRHFDCAYFYHNEREVGAGIRC
KIKEGAVRREDLFIATKLWCTCHKKSLVETACRKSLKALKLNYLDLYLIHWPMGFKPPHPEWIMSCSELSFCLSHPRVQDLPLDESNMVI
PSDTDFLDTWEAMEDLVITGLVKNIGVSNFNHEQLERLLNKPGLRFKPLTNQIECHPYLTQKNLISFCQSRDVSVTAYRPLGGSCEGVDL
358


Top

pLDDT score distribution

check button pLDDT score distribution of the predicted wild-type structures of two partner proteins from AlphaFold2
* AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100.
EPC1_pLDDT.png
all structure
all structure
AKR1E2_pLDDT.png
all structure
all structure

check button pLDDT score distribution of the predicted fusion protein structures from AlphaFold2
* AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100.
all structure


Top

Ramachandran Plot of Fusion Protein Structure


check button Ramachandran plot of the torsional angles - phi (φ)and psi (ψ) - of the residues (amino acids) contained in this fusion protein peptide.
Fusion AA seq ID in FusionPDB and their Ramachandran plots

Top

Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
EPC1
AKR1E2


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


Top

Related Drugs to EPC1-AKR1E2


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

Top

Related Diseases to EPC1-AKR1E2


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

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