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Center for Computational Systems Medicine
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Fusion Gene and Fusion Protein Summary

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Fusion Amino Acid Sequences (multiple BPs and multiple gene isoforms)

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Fusion Protein Breakpoint Sequences - (for the Screening of the FusionNeoAntigens)

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Potential FusionNeoAntigens in HLA I - (netMHCpan v4.1 + deepHLApan v1.1)

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Potential FusionNeoAntigens in HLA II - (netMHCIIpan v4.1)

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Fusion Breakpoint 14 AA Peptide Structure - (RoseTTAFold)

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D - (Glide)

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Vaccine Design for the FusionNeoAntigens (RNA/protein sequences)

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Potential target of CAR-T therapy development

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Information on the samples that have these potential fusion neoantigens

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Fusion Protein Targeting Drugs - (Manual Curation)

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Fusion Protein Related diseases - (Manual Curation)

Fusion Protein:CYP2E1-GLUL

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CYP2E1-GLUL
FusionPDB ID: 21058
FusionGDB2.0 ID: 21058
HgeneTgene
Gene symbol

CYP2E1

GLUL

Gene ID

1571

2752

Gene namecytochrome P450 family 2 subfamily E member 1glutamate-ammonia ligase
SynonymsCPE1|CYP2E|P450-J|P450C2EGLNS|GS|PIG43|PIG59
Cytomap

10q26.3

1q25.3

Type of geneprotein-codingprotein-coding
Descriptioncytochrome P450 2E14-nitrophenol 2-hydroxylaseCYPIIE1cytochrome P450, family 2, subfamily E, polypeptide 1cytochrome P450, subfamily IIE (ethanol-inducible), polypeptide 1cytochrome P450-Jflavoprotein-linked monooxygenasemicrosomal monooxygenasexeglutamine synthetasecell proliferation-inducing protein 59glutamate decarboxylaseglutamine synthasepalmitoyltransferase GLULproliferation-inducing protein 43
Modification date2020031520200313
UniProtAcc

P05181

Main function of 5'-partner protein: FUNCTION: A cytochrome P450 monooxygenase involved in the metabolism of fatty acids (PubMed:10553002, PubMed:18577768). Mechanistically, uses molecular oxygen inserting one oxygen atom into a substrate, and reducing the second into a water molecule, with two electrons provided by NADPH via cytochrome P450 reductase (NADPH--hemoprotein reductase) (PubMed:10553002, PubMed:18577768). Catalyzes the hydroxylation of carbon-hydrogen bonds. Hydroxylates fatty acids specifically at the omega-1 position displaying the highest catalytic activity for saturated fatty acids (PubMed:10553002, PubMed:18577768). May be involved in the oxidative metabolism of xenobiotics (Probable). {ECO:0000269|PubMed:10553002, ECO:0000269|PubMed:18577768, ECO:0000305|PubMed:9348445}.

P15104

Main function of 5'-partner protein: FUNCTION: Glutamine synthetase that catalyzes the ATP-dependent conversion of glutamate and ammonia to glutamine (PubMed:30158707, PubMed:16267323). Its role depends on tissue localization: in the brain, it regulates the levels of toxic ammonia and converts neurotoxic glutamate to harmless glutamine, whereas in the liver, it is one of the enzymes responsible for the removal of ammonia (By similarity). Essential for proliferation of fetal skin fibroblasts (PubMed:18662667). Independently of its glutamine synthetase activity, required for endothelial cell migration during vascular development: acts by regulating membrane localization and activation of the GTPase RHOJ, possibly by promoting RHOJ palmitoylation (PubMed:30158707). May act as a palmitoyltransferase for RHOJ: able to autopalmitoylate and then transfer the palmitoyl group to RHOJ (PubMed:30158707). Plays a role in ribosomal 40S subunit biogenesis (PubMed:26711351). {ECO:0000250|UniProtKB:P15105, ECO:0000269|PubMed:16267323, ECO:0000269|PubMed:18662667, ECO:0000269|PubMed:26711351, ECO:0000269|PubMed:30158707}.
Ensembl transtripts involved in fusion geneENST idsENST00000252945, ENST00000463117, 
ENST00000480558, 
ENST00000339526, 
ENST00000491322, ENST00000311223, 
ENST00000331872, ENST00000417584, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score8 X 5 X 3=12018 X 16 X 6=1728
# samples 820
** MAII scorelog2(8/120*10)=-0.584962500721156
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(20/1728*10)=-3.11103131238874
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: CYP2E1 [Title/Abstract] AND GLUL [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: CYP2E1 [Title/Abstract] AND GLUL [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CYP2E1(135345788)-GLUL(182354691), # samples:1
Anticipated loss of major functional domain due to fusion event.CYP2E1-GLUL 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.
CYP2E1-GLUL 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.
CYP2E1-GLUL 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.
CYP2E1-GLUL 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.
* 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
HgeneCYP2E1

GO:0002933

lipid hydroxylation

10553002

HgeneCYP2E1

GO:0016098

monoterpenoid metabolic process

16401082

HgeneCYP2E1

GO:0017144

drug metabolic process

19219744

HgeneCYP2E1

GO:0018960

4-nitrophenol metabolic process

9348445

HgeneCYP2E1

GO:0046483

heterocycle metabolic process

19651758

HgeneCYP2E1

GO:0055114

oxidation-reduction process

16401082|19219744

TgeneGLUL

GO:0008283

cell proliferation

18662667

TgeneGLUL

GO:0010594

regulation of endothelial cell migration

30158707

TgeneGLUL

GO:0018345

protein palmitoylation

30158707

TgeneGLUL

GO:1903670

regulation of sprouting angiogenesis

30158707



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/chr10:135345788/chr1:182354691)
- 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 buttonRetention analysis results 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, are available here.

check buttonFusion gene breakpoints across CYP2E1 (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 GLUL (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Amino Acid Sequences


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)
ENST00000463117CYP2E1chr10135345788+ENST00000331872GLULchr1182354691-41409202001438412
ENST00000463117CYP2E1chr10135345788+ENST00000417584GLULchr1182354691-41399202001438412
ENST00000463117CYP2E1chr10135345788+ENST00000311223GLULchr1182354691-41399202001438412
ENST00000252945CYP2E1chr10135345788+ENST00000331872GLULchr1182354691-3901681331199388
ENST00000252945CYP2E1chr10135345788+ENST00000417584GLULchr1182354691-3900681331199388
ENST00000252945CYP2E1chr10135345788+ENST00000311223GLULchr1182354691-3900681331199388

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
ENST00000463117ENST00000331872CYP2E1chr10135345788+GLULchr1182354691-0.0002726750.9997273
ENST00000463117ENST00000417584CYP2E1chr10135345788+GLULchr1182354691-0.0002719830.999728
ENST00000463117ENST00000311223CYP2E1chr10135345788+GLULchr1182354691-0.0002719830.999728
ENST00000252945ENST00000331872CYP2E1chr10135345788+GLULchr1182354691-0.0002554180.9997446
ENST00000252945ENST00000417584CYP2E1chr10135345788+GLULchr1182354691-0.0002550140.99974495
ENST00000252945ENST00000311223CYP2E1chr10135345788+GLULchr1182354691-0.0002550140.99974495

check button Predicted full-length fusion amino acid sequences. For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among all the predicted ones.

Get the fusion protein sequences from here.

Fusion protein sequence information is available in the fasta format.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

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Fusion Protein Breakpoint Sequences for CYP2E1-GLUL

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
CYP2E1chr10135345788GLULchr1182354691681198RKHFDYNDEKFLRLMYLFNENFHLLS
CYP2E1chr10135345788GLULchr1182354691920222RKHFDYNDEKFLRLMYLFNENFHLLS

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Potential FusionNeoAntigen Information of CYP2E1-GLUL in HLA I

check button Multiple sequence alignments of the potential FusionNeoAntigens per fusion breakpoints. If the MSA is empty, then it means that there were predicted fusion neoantigens in this fusion breakpoint, but those predicted fusion neoantigens were not across the breakpoint, which is not fusion-specific.
CYP2E1-GLUL_135345788_182354691.msa

check button Potential FusionNeoAntigen Information
* We used NetMHCpan v4.1 (%rank<0.5) and deepHLApan v1.1 (immunogenic score>0.5)
Fusion geneHchrHbpTgeneTchrTbpHLA IFusionNeoAntigen peptideBinding scoreImmunogenic scoreNeoantigen start (at BP 13)Neoantigen end (at BP 13)
CYP2E1-GLULchr10135345788chr1182354691681HLA-B18:01DEKFLRLM0.99930.9555715
CYP2E1-GLULchr10135345788chr1182354691681HLA-B18:01DEKFLRLMY0.99820.9486716
CYP2E1-GLULchr10135345788chr1182354691681HLA-B44:03DEKFLRLMY0.99160.9542716
CYP2E1-GLULchr10135345788chr1182354691681HLA-B14:02EKFLRLMYL0.99040.5611817
CYP2E1-GLULchr10135345788chr1182354691681HLA-B14:01EKFLRLMYL0.99040.5611817
CYP2E1-GLULchr10135345788chr1182354691681HLA-B39:01YNDEKFLRL0.97060.9459514
CYP2E1-GLULchr10135345788chr1182354691681HLA-A32:13KFLRLMYLF0.94160.9414918
CYP2E1-GLULchr10135345788chr1182354691681HLA-B08:01EKFLRLMYL0.90690.6243817
CYP2E1-GLULchr10135345788chr1182354691681HLA-B14:01YNDEKFLRL0.89710.744514
CYP2E1-GLULchr10135345788chr1182354691681HLA-B14:02YNDEKFLRL0.89710.744514
CYP2E1-GLULchr10135345788chr1182354691681HLA-B39:13YNDEKFLRL0.88630.9195514
CYP2E1-GLULchr10135345788chr1182354691681HLA-B08:09EKFLRLMYL0.82860.6288817
CYP2E1-GLULchr10135345788chr1182354691681HLA-C04:10YNDEKFLRL0.99990.6259514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C08:15YNDEKFLRL0.99990.9372514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C04:07YNDEKFLRL0.99990.6189514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C05:09YNDEKFLRL0.99990.9092514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C01:17YNDEKFLRL0.99970.921514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C04:06YNDEKFLRL0.99740.8542514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C03:07YNDEKFLRL0.99580.9787514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C15:06YNDEKFLRL0.99530.931514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C03:19YNDEKFLRL0.99480.9862514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C01:30YNDEKFLRL0.99450.9419514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C08:13YNDEKFLRL0.99180.9351514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C08:04YNDEKFLRL0.99180.9351514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C08:03YNDEKFLRL0.9830.9828514
CYP2E1-GLULchr10135345788chr1182354691681HLA-B39:09YNDEKFLRL0.9830.5311514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C07:10YNDEKFLRL0.96690.9538514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C07:13YNDEKFLRL0.96680.9076514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C07:67YNDEKFLRL0.96350.9246514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C07:80YNDEKFLRL0.96350.9246514
CYP2E1-GLULchr10135345788chr1182354691681HLA-B39:12YNDEKFLRL0.96260.9497514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C07:29YNDEKFLRL0.95950.9571514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C07:27YNDEKFLRL0.95720.9581514
CYP2E1-GLULchr10135345788chr1182354691681HLA-B39:12EKFLRLMYL0.95720.9417817
CYP2E1-GLULchr10135345788chr1182354691681HLA-C07:95YNDEKFLRL0.95040.7161514
CYP2E1-GLULchr10135345788chr1182354691681HLA-B39:08YNDEKFLRL0.94990.6396514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C07:19YNDEKFLRL0.93930.6888514
CYP2E1-GLULchr10135345788chr1182354691681HLA-B39:05YNDEKFLRL0.91420.9351514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C04:14YNDEKFLRL0.90660.7178514
CYP2E1-GLULchr10135345788chr1182354691681HLA-A02:07YNDEKFLRL0.8390.6166514
CYP2E1-GLULchr10135345788chr1182354691681HLA-B14:03YNDEKFLRL0.72950.7993514
CYP2E1-GLULchr10135345788chr1182354691681HLA-B14:03EKFLRLMYL0.28530.8034817
CYP2E1-GLULchr10135345788chr1182354691681HLA-C02:06YNDEKFLRL0.2850.9246514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C04:10DYNDEKFLRL0.99510.6363414
CYP2E1-GLULchr10135345788chr1182354691681HLA-C04:07DYNDEKFLRL0.99430.6413414
CYP2E1-GLULchr10135345788chr1182354691681HLA-B18:05DEKFLRLM0.99930.9555715
CYP2E1-GLULchr10135345788chr1182354691681HLA-B18:06DEKFLRLM0.99930.9615715
CYP2E1-GLULchr10135345788chr1182354691681HLA-B18:08DEKFLRLM0.99910.9152715
CYP2E1-GLULchr10135345788chr1182354691681HLA-B18:03DEKFLRLM0.9990.9527715
CYP2E1-GLULchr10135345788chr1182354691681HLA-B18:11DEKFLRLM0.9910.8965715
CYP2E1-GLULchr10135345788chr1182354691681HLA-C01:03YNDEKFLRL0.99990.9062514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C05:01YNDEKFLRL0.99990.9092514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C04:01YNDEKFLRL0.99990.6189514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C04:03YNDEKFLRL0.99990.6442514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C18:01YNDEKFLRL0.99990.625514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C08:02YNDEKFLRL0.99990.9372514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C01:02YNDEKFLRL0.99980.9161514
CYP2E1-GLULchr10135345788chr1182354691681HLA-B18:04DEKFLRLMY0.99870.9551716
CYP2E1-GLULchr10135345788chr1182354691681HLA-B18:08DEKFLRLMY0.99860.8894716
CYP2E1-GLULchr10135345788chr1182354691681HLA-B18:07DEKFLRLMY0.99850.9204716
CYP2E1-GLULchr10135345788chr1182354691681HLA-B18:05DEKFLRLMY0.99820.9486716
CYP2E1-GLULchr10135345788chr1182354691681HLA-B18:03DEKFLRLMY0.99770.9459716
CYP2E1-GLULchr10135345788chr1182354691681HLA-B18:06DEKFLRLMY0.99760.9548716
CYP2E1-GLULchr10135345788chr1182354691681HLA-C04:04YNDEKFLRL0.9960.8278514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C15:05YNDEKFLRL0.99530.9323514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C15:02YNDEKFLRL0.99280.9196514
CYP2E1-GLULchr10135345788chr1182354691681HLA-B44:26DEKFLRLMY0.99160.9542716
CYP2E1-GLULchr10135345788chr1182354691681HLA-B44:13DEKFLRLMY0.99160.9542716
CYP2E1-GLULchr10135345788chr1182354691681HLA-B44:07DEKFLRLMY0.99160.9542716
CYP2E1-GLULchr10135345788chr1182354691681HLA-C03:67YNDEKFLRL0.98660.9779514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C03:06YNDEKFLRL0.98520.9877514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C08:01YNDEKFLRL0.9830.9828514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C06:06YNDEKFLRL0.98230.9838514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C03:04YNDEKFLRL0.98170.9876514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C03:03YNDEKFLRL0.98170.9876514
CYP2E1-GLULchr10135345788chr1182354691681HLA-B39:02YNDEKFLRL0.97430.9288514
CYP2E1-GLULchr10135345788chr1182354691681HLA-B39:31YNDEKFLRL0.97320.9473514
CYP2E1-GLULchr10135345788chr1182354691681HLA-B39:11YNDEKFLRL0.9680.6056514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C07:02YNDEKFLRL0.96350.9246514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C07:17YNDEKFLRL0.96310.9724514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C07:01YNDEKFLRL0.93720.6929514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C07:04YNDEKFLRL0.92190.8859514
CYP2E1-GLULchr10135345788chr1182354691681HLA-B08:18EKFLRLMYL0.90690.6243817
CYP2E1-GLULchr10135345788chr1182354691681HLA-B18:11DEKFLRLMY0.87670.8949716
CYP2E1-GLULchr10135345788chr1182354691681HLA-C17:01YNDEKFLRL0.8070.7685514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C06:17EKFLRLMYL0.1410.9923817
CYP2E1-GLULchr10135345788chr1182354691681HLA-C06:02EKFLRLMYL0.1410.9923817
CYP2E1-GLULchr10135345788chr1182354691681HLA-B07:13YNDEKFLRL0.01690.7447514
CYP2E1-GLULchr10135345788chr1182354691681HLA-C18:01DYNDEKFLRL0.99450.6425414
CYP2E1-GLULchr10135345788chr1182354691681HLA-C04:01DYNDEKFLRL0.99430.6413414
CYP2E1-GLULchr10135345788chr1182354691681HLA-A32:01RLMYLFNENF0.99050.93081222
CYP2E1-GLULchr10135345788chr1182354691681HLA-B18:03DEKFLRLMYLF0.99320.9073718

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Potential FusionNeoAntigen Information of CYP2E1-GLUL in HLA II

check button Multiple sequence alignments of the potential FusionNeoAntigens per fusion breakpoints. If the MSA is empty, then it means that there were predicted fusion neoantigens in this fusion breakpoint, but those predicted fusion neoantigens were not across the breakpoint, which is not fusion-specific.

check button Potential FusionNeoAntigen Information
* We used NetMHCIIpan v4.1 (%rank<0.5).
Fusion geneHchrHbpTgeneTchrTbpHLA IIFusionNeoAntigen peptideNeoantigen start (at BP 13)Neoantigen end (at BP 13)

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Fusion breakpoint peptide structures of CYP2E1-GLUL

check button3D structures of the fusion breakpoint peptide of 14AA sequence that have potential fusion neoantigens
* The minimum length of the amino acid sequence in RoseTTAFold is 14AA. Here, we predicted the 14AA fusion protein breakpoint sequence not the fusion neoantigen peptide, which is shorter than 14 AA.
File nameBPseqHgeneTgeneHchrHbpTchrTbpAAlen
6109NDEKFLRLMYLFNECYP2E1GLULchr10135345788chr1182354691681

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of CYP2E1-GLUL

check buttonVirtual screening between 25 HLAs (from PDB) and FusionNeoAntigens
* We used Glide to predict the interaction between HLAs and neoantigens.
HLA allelePDB IDFile nameBPseqDocking scoreGlide score
HLA-B14:023BVN6109NDEKFLRLMYLFNE-7.9962-8.1096
HLA-B14:023BVN6109NDEKFLRLMYLFNE-5.70842-6.74372
HLA-B52:013W396109NDEKFLRLMYLFNE-6.83737-6.95077
HLA-B52:013W396109NDEKFLRLMYLFNE-4.4836-5.5189
HLA-A11:014UQ26109NDEKFLRLMYLFNE-10.0067-10.1201
HLA-A11:014UQ26109NDEKFLRLMYLFNE-9.03915-10.0745
HLA-A24:025HGA6109NDEKFLRLMYLFNE-6.56204-6.67544
HLA-A24:025HGA6109NDEKFLRLMYLFNE-5.42271-6.45801
HLA-B44:053DX86109NDEKFLRLMYLFNE-7.85648-8.89178
HLA-B44:053DX86109NDEKFLRLMYLFNE-5.3978-5.5112
HLA-A02:016TDR6109NDEKFLRLMYLFNE-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of CYP2E1-GLUL

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-Is.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptide sequenceFusionNeoAntigen RNA sequence
CYP2E1-GLULchr10135345788chr11823546911222RLMYLFNENFCAGTGGGAATTTCAGATTGGACCTTGTGAA
CYP2E1-GLULchr10135345788chr1182354691414DYNDEKFLRLCACCTACTCAGCACTCCCTGGCTCCAGTGG
CYP2E1-GLULchr10135345788chr1182354691514YNDEKFLRLCTACTCAGCACTCCCTGGCTCCAGTGG
CYP2E1-GLULchr10135345788chr1182354691715DEKFLRLMAGCACTCCCTGGCTCCAGTGGGAA
CYP2E1-GLULchr10135345788chr1182354691716DEKFLRLMYAGCACTCCCTGGCTCCAGTGGGAATTT
CYP2E1-GLULchr10135345788chr1182354691718DEKFLRLMYLFAGCACTCCCTGGCTCCAGTGGGAATTTCAGATT
CYP2E1-GLULchr10135345788chr1182354691817EKFLRLMYLACTCCCTGGCTCCAGTGGGAATTTCAG
CYP2E1-GLULchr10135345788chr1182354691918KFLRLMYLFCCCTGGCTCCAGTGGGAATTTCAGATT

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence

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Information of the samples that have these potential fusion neoantigens of CYP2E1-GLUL

check button These samples were reported as having these fusion breakpoints. For individual breakpoints, we checked the open reading frames considering multiple gene isoforms and chose the in-frame fusion genes only. Then, we made fusion protein sequences and predicted the fusion neoantigens. These fusion-positive samples may have these potential fusion neoantigens.
Cancer typeFusion geneHchrHbpHenstTchrTbpTenstSample
LIHCCYP2E1-GLULchr10135345788ENST00000252945chr1182354691ENST00000311223TCGA-UB-A7MC-01A

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Potential target of CAR-T therapy development for CYP2E1-GLUL

check button Predicted 3D structure. We used RoseTTAFold.

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, to provide the retention of the transmembrane domain, we only show the protein feature retention information of those transmembrane features


* Minus value of BPloci means that the break point is located before the CDS.
- In-frame and retained 'Transmembrane'.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

check button Subcellular localization prediction of the transmembrane domain retained fusion proteins
* We used DeepLoc 1.0. The order of the X-axis of the barplot is as follows: Entry_ID, Localization, Type, Nucleus, Cytoplasm, Extracellular, Mitochondrion, Cell_membrane, Endoplasmic_reticulum, Plastid, Golgi.apparatus, Lysosome.Vacuole, Peroxisome. Y-axis is the output score of DeepLoc. Clicking the image will open a new tab with a large image.
HgeneHchrHbpHenstTgeneTchrTbpTenstDeepLoc result

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Related Drugs to CYP2E1-GLUL

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

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Related Diseases to CYP2E1-GLUL

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