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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:FAT1-ELF2

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: FAT1-ELF2
FusionPDB ID: 29454
FusionGDB2.0 ID: 29454
HgeneTgene
Gene symbol

FAT1

ELF2

Gene ID

2195

1998

Gene nameFAT atypical cadherin 1E74 like ETS transcription factor 2
SynonymsCDHF7|CDHR8|FAT|ME5|hFat1EU32|NERF|NERF-1A|NERF-1B|NERF-1a,b|NERF-2
Cytomap

4q35.2

4q31.1

Type of geneprotein-codingprotein-coding
Descriptionprotocadherin Fat 1FAT tumor suppressor 1cadherin ME5cadherin family member 7cadherin-related family member 8cadherin-related tumor suppressor homologprotein fat homologETS-related transcription factor Elf-2E74-like factor 2 (ets domain transcription factor)ets family transcription factor ELF2Cnew Ets-related factor
Modification date2020031320200313
UniProtAcc

Q14517

Main function of 5'-partner protein: FUNCTION: [Protocadherin Fat 1]: Plays an essential role for cellular polarization, directed cell migration and modulating cell-cell contact. {ECO:0000250}.

Q15723

Main function of 5'-partner protein: FUNCTION: Isoform 1 transcriptionally activates the LYN and BLK promoters and acts synergistically with RUNX1 to transactivate the BLK promoter.; FUNCTION: Isoform 2 may function in repression of RUNX1-mediated transactivation.
Ensembl transtripts involved in fusion geneENST idsENST00000441802, ENST00000512347, 
ENST00000515489, ENST00000265495, 
ENST00000358635, ENST00000379549, 
ENST00000379550, ENST00000394235, 
ENST00000510408, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score16 X 17 X 8=21769 X 8 X 4=288
# samples 209
** MAII scorelog2(20/2176*10)=-3.44360665147561
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(9/288*10)=-1.67807190511264
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: FAT1 [Title/Abstract] AND ELF2 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: FAT1 [Title/Abstract] AND ELF2 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)FAT1(187627716)-ELF2(139994721), # samples:1
Anticipated loss of major functional domain due to fusion event.FAT1-ELF2 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.
FAT1-ELF2 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.
FAT1-ELF2 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.
FAT1-ELF2 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
TgeneELF2

GO:0006357

regulation of transcription by RNA polymerase II

8756667

TgeneELF2

GO:0045893

positive regulation of transcription, DNA-templated

8756667



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/chr4:187627716/chr4:139994721)
- 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 FAT1 (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 ELF2 (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)
ENST00000441802FAT1chr4187627716-ENST00000394235ELF2chr4139994721-6746347521049821590
ENST00000441802FAT1chr4187627716-ENST00000379549ELF2chr4139994721-6198347521049311573
ENST00000441802FAT1chr4187627716-ENST00000379550ELF2chr4139994721-6285347521050181602
ENST00000441802FAT1chr4187627716-ENST00000265495ELF2chr4139994721-6249347521049821590
ENST00000441802FAT1chr4187627716-ENST00000358635ELF2chr4139994721-6147347521050181602
ENST00000441802FAT1chr4187627716-ENST00000510408ELF2chr4139994721-5247347521049821590

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
ENST00000441802ENST00000394235FAT1chr4187627716-ELF2chr4139994721-0.0001356980.99986434
ENST00000441802ENST00000379549FAT1chr4187627716-ELF2chr4139994721-0.0002651860.9997348
ENST00000441802ENST00000379550FAT1chr4187627716-ELF2chr4139994721-0.0002480180.999752
ENST00000441802ENST00000265495FAT1chr4187627716-ELF2chr4139994721-0.0001837970.99981624
ENST00000441802ENST00000358635FAT1chr4187627716-ELF2chr4139994721-0.000281550.9997185
ENST00000441802ENST00000510408FAT1chr4187627716-ELF2chr4139994721-0.0003294070.9996706

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 FAT1-ELF2

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
FAT1chr4187627716ELF2chr413999472134751088GSGVGVFKIGEETVEASVHSSNAHCT

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Potential FusionNeoAntigen Information of FAT1-ELF2 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.
FAT1-ELF2_187627716_139994721.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)
FAT1-ELF2chr4187627716chr41399947213475HLA-B45:01GEETVEASV0.99660.9258918
FAT1-ELF2chr4187627716chr41399947213475HLA-B50:02GEETVEASV0.98960.8023918
FAT1-ELF2chr4187627716chr41399947213475HLA-B40:01GEETVEASV0.98290.8044918
FAT1-ELF2chr4187627716chr41399947213475HLA-B18:01EETVEASVH0.93360.94241019
FAT1-ELF2chr4187627716chr41399947213475HLA-B41:01GEETVEASV0.42470.9742918
FAT1-ELF2chr4187627716chr41399947213475HLA-B39:13GEETVEASV0.08670.9942918
FAT1-ELF2chr4187627716chr41399947213475HLA-B40:06GEETVEASV0.99690.9075918
FAT1-ELF2chr4187627716chr41399947213475HLA-B39:08GEETVEASV0.34330.9702918
FAT1-ELF2chr4187627716chr41399947213475HLA-B40:04GEETVEASV0.99150.8786918
FAT1-ELF2chr4187627716chr41399947213475HLA-B40:36GEETVEASV0.98470.823918
FAT1-ELF2chr4187627716chr41399947213475HLA-B40:49GEETVEASV0.97650.7996918
FAT1-ELF2chr4187627716chr41399947213475HLA-B18:05EETVEASVH0.93360.94241019
FAT1-ELF2chr4187627716chr41399947213475HLA-A68:02ETVEASVHS0.92830.6391120
FAT1-ELF2chr4187627716chr41399947213475HLA-B18:06EETVEASVH0.92190.95591019
FAT1-ELF2chr4187627716chr41399947213475HLA-B18:11EETVEASVH0.69440.92531019
FAT1-ELF2chr4187627716chr41399947213475HLA-B41:03GEETVEASV0.5020.8093918

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Potential FusionNeoAntigen Information of FAT1-ELF2 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.
FAT1-ELF2_187627716_139994721.msa

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)
FAT1-ELF2chr4187627716chr41399947213475DRB1-1503GVGVFKIGEETVEAS217
FAT1-ELF2chr4187627716chr41399947213475DRB1-1503SGVGVFKIGEETVEA116
FAT1-ELF2chr4187627716chr41399947213475DRB1-1523GVGVFKIGEETVEAS217
FAT1-ELF2chr4187627716chr41399947213475DRB1-1523SGVGVFKIGEETVEA116

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Fusion breakpoint peptide structures of FAT1-ELF2

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
2431FKIGEETVEASVHSFAT1ELF2chr4187627716chr41399947213475

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of FAT1-ELF2

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-B14:023BVN2431FKIGEETVEASVHS-7.15543-7.26883
HLA-B14:023BVN2431FKIGEETVEASVHS-4.77435-5.80965
HLA-B52:013W392431FKIGEETVEASVHS-6.80875-6.92215
HLA-B52:013W392431FKIGEETVEASVHS-4.20386-5.23916
HLA-A11:014UQ22431FKIGEETVEASVHS-7.5194-8.5547
HLA-A11:014UQ22431FKIGEETVEASVHS-6.9601-7.0735
HLA-A24:025HGA2431FKIGEETVEASVHS-7.52403-7.63743
HLA-A24:025HGA2431FKIGEETVEASVHS-5.82433-6.85963
HLA-B27:056PYJ2431FKIGEETVEASVHS-3.28285-4.31815
HLA-B44:053DX82431FKIGEETVEASVHS-5.91172-6.94702
HLA-B44:053DX82431FKIGEETVEASVHS-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of FAT1-ELF2

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
FAT1-ELF2chr4187627716chr41399947211019EETVEASVHAAGAGACAGTGGAAGCATCAGTTCACA
FAT1-ELF2chr4187627716chr41399947211120ETVEASVHSAGACAGTGGAAGCATCAGTTCACAGCA
FAT1-ELF2chr4187627716chr4139994721918GEETVEASVGTGAAGAGACAGTGGAAGCATCAGTTC

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
FAT1-ELF2chr4187627716chr4139994721116SGVGVFKIGEETVEACTGGCGTTGGTGTTTTCAAAATAGGTGAAGAGACAGTGGAAGCAT
FAT1-ELF2chr4187627716chr4139994721217GVGVFKIGEETVEASGCGTTGGTGTTTTCAAAATAGGTGAAGAGACAGTGGAAGCATCAG

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Information of the samples that have these potential fusion neoantigens of FAT1-ELF2

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
STADFAT1-ELF2chr4187627716ENST00000441802chr4139994721ENST00000265495TCGA-D7-A4YY

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Potential target of CAR-T therapy development for FAT1-ELF2

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 FAT1-ELF2

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 FAT1-ELF2

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