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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:ERBB2IP-ASXL1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ERBB2IP-ASXL1
FusionPDB ID: 27153
FusionGDB2.0 ID: 27153
HgeneTgene
Gene symbol

ERBB2IP

ASXL1

Gene ID

55914

171023

Gene nameerbb2 interacting proteinASXL transcriptional regulator 1
SynonymsERBB2IP|HEL-S-78|LAP2BOPS|MDS
Cytomap

5q12.3

20q11.21

Type of geneprotein-codingprotein-coding
Descriptionerbindensin-180-like proteinepididymis secretory protein Li 78protein LAP2polycomb group protein ASXL1additional sex combs like 1, transcriptional regulatoradditional sex combs like transcriptional regulator 1putative Polycomb group protein ASXL1
Modification date2020032220200313
UniProtAcc.

Q8IXJ9

Main function of 5'-partner protein: FUNCTION: Probable Polycomb group (PcG) protein involved in transcriptional regulation mediated by ligand-bound nuclear hormone receptors, such as retinoic acid receptors (RARs) and peroxisome proliferator-activated receptor gamma (PPARG) (PubMed:16606617). Acts as coactivator of RARA and RXRA through association with NCOA1 (PubMed:16606617). Acts as corepressor for PPARG and suppresses its adipocyte differentiation-inducing activity (By similarity). Non-catalytic component of the PR-DUB complex, a complex that specifically mediates deubiquitination of histone H2A monoubiquitinated at 'Lys-119' (H2AK119ub1) (PubMed:20436459). Acts as a sensor of N(6)-methyladenosine methylation on DNA (m6A): recognizes and binds m6A DNA, leading to its ubiquitination and degradation by TRIP12, thereby inactivating the PR-DUB complex and regulating Polycomb silencing (PubMed:30982744). {ECO:0000250|UniProtKB:P59598, ECO:0000269|PubMed:16606617, ECO:0000269|PubMed:20436459, ECO:0000269|PubMed:30982744}.
Ensembl transtripts involved in fusion geneENST idsENST00000284037, ENST00000380935, 
ENST00000380936, ENST00000380938, 
ENST00000380939, ENST00000380943, 
ENST00000506030, ENST00000508515, 
ENST00000511297, ENST00000416865, 
ENST00000503913, 
ENST00000470145, 
ENST00000542461, ENST00000306058, 
ENST00000375689, ENST00000375687, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score14 X 4 X 10=56010 X 7 X 6=420
# samples 2010
** MAII scorelog2(20/560*10)=-1.48542682717024
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(10/420*10)=-2.0703893278914
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: ERBB2IP [Title/Abstract] AND ASXL1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: ERBB2IP [Title/Abstract] AND ASXL1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ERBB2IP(65350779)-ASXL1(31015931), # samples:1
Anticipated loss of major functional domain due to fusion event.ERBB2IP-ASXL1 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.
ERBB2IP-ASXL1 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.
ERBB2IP-ASXL1 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.
ERBB2IP-ASXL1 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
TgeneASXL1

GO:0035522

monoubiquitinated histone H2A deubiquitination

20436459



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/chr5:65350779/chr20:31015931)
- 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 ERBB2IP (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 ASXL1 (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)
ENST00000284037ERBB2IPchr565350779-ENST00000375687ASXL1chr2031015931+10377402238983952668
ENST00000380943ERBB2IPchr565350779-ENST00000375687ASXL1chr2031015931+10296394130883142668
ENST00000380935ERBB2IPchr565350779-ENST00000375687ASXL1chr2031015931+10278392329082962668
ENST00000380939ERBB2IPchr565350779-ENST00000375687ASXL1chr2031015931+10278392329082962668
ENST00000380936ERBB2IPchr565350779-ENST00000375687ASXL1chr2031015931+10278392329082962668
ENST00000380938ERBB2IPchr565350779-ENST00000375687ASXL1chr2031015931+10242388725482602668
ENST00000511297ERBB2IPchr565350779-ENST00000375687ASXL1chr2031015931+10113375813781312664
ENST00000506030ERBB2IPchr565350779-ENST00000375687ASXL1chr2031015931+1007937249180972668
ENST00000508515ERBB2IPchr565350779-ENST00000375687ASXL1chr2031015931+1004736925980652668

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
ENST00000284037ENST00000375687ERBB2IPchr565350779-ASXL1chr2031015931+0.000918320.9990816
ENST00000380943ENST00000375687ERBB2IPchr565350779-ASXL1chr2031015931+0.0008244350.9991755
ENST00000380935ENST00000375687ERBB2IPchr565350779-ASXL1chr2031015931+0.0008072420.9991928
ENST00000380939ENST00000375687ERBB2IPchr565350779-ASXL1chr2031015931+0.0008072420.9991928
ENST00000380936ENST00000375687ERBB2IPchr565350779-ASXL1chr2031015931+0.0008072420.9991928
ENST00000380938ENST00000375687ERBB2IPchr565350779-ASXL1chr2031015931+0.0007666010.99923337
ENST00000511297ENST00000375687ERBB2IPchr565350779-ASXL1chr2031015931+0.0006798970.99932015
ENST00000506030ENST00000375687ERBB2IPchr565350779-ASXL1chr2031015931+0.0006322660.9993678
ENST00000508515ENST00000375687ERBB2IPchr565350779-ASXL1chr2031015931+0.0006137160.9993863

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 ERBB2IP-ASXL1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
ERBB2IPchr565350779ASXL1chr203101593136921211QVLRHIEAKKLEKKDALQWSRHPATV
ERBB2IPchr565350779ASXL1chr203101593137241211QVLRHIEAKKLEKKDALQWSRHPATV
ERBB2IPchr565350779ASXL1chr203101593137581207QVLRHIEAKKLEKKDALQWSRHPATV
ERBB2IPchr565350779ASXL1chr203101593138871211QVLRHIEAKKLEKKDALQWSRHPATV
ERBB2IPchr565350779ASXL1chr203101593139231211QVLRHIEAKKLEKKDALQWSRHPATV
ERBB2IPchr565350779ASXL1chr203101593139411211QVLRHIEAKKLEKKDALQWSRHPATV
ERBB2IPchr565350779ASXL1chr203101593140221211QVLRHIEAKKLEKKDALQWSRHPATV

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Potential FusionNeoAntigen Information of ERBB2IP-ASXL1 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.
ERBB2IP-ASXL1_65350779_31015931.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)
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B44:03LEKKDALQW0.99830.96021019
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B44:02LEKKDALQW0.99710.54171019
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B47:01LEKKDALQW0.98620.74371019
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B44:05LEKKDALQW0.98620.61991019
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B14:02KKLEKKDAL0.74090.6005817
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B14:01KKLEKKDAL0.74090.6005817
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B39:13KKLEKKDAL0.36840.7965817
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B57:01KLEKKDALQW0.99820.989919
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B58:01KLEKKDALQW0.97950.9812919
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-A32:13KLEKKDALQW0.82640.9741919
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B44:02KLEKKDALQW0.81780.5837919
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B44:03KLEKKDALQW0.75830.978919
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B44:05KLEKKDALQW0.74860.658919
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B44:02KKLEKKDALQW0.99450.6306819
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B44:03KKLEKKDALQW0.9930.9821819
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B44:04LEKKDALQW0.99710.53291019
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B44:08LEKKDALQW0.99610.6791019
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B44:09LEKKDALQW0.99090.68781019
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B44:10LEKKDALQW0.71770.82151019
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B14:03KKLEKKDAL0.28620.5995817
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B44:04KLEKKDALQW0.88790.613919
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B44:08KLEKKDALQW0.79730.7026919
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B44:08KKLEKKDALQW0.99140.7318819
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B44:04KKLEKKDALQW0.99120.6654819
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B44:13LEKKDALQW0.99830.96021019
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B44:07LEKKDALQW0.99830.96021019
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B44:26LEKKDALQW0.99830.96021019
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B44:22LEKKDALQW0.99710.54171019
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B39:02KKLEKKDAL0.65530.804817
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B15:24LEKKDALQW0.63960.96221019
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B15:13LEKKDALQW0.57050.94971019
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B48:02LEKKDALQW0.19670.88191019
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B57:10KLEKKDALQW0.99820.989919
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B57:04KLEKKDALQW0.99450.8505919
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B15:24KLEKKDALQW0.95670.9787919
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-A32:01KLEKKDALQW0.92390.9869919
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B44:22KLEKKDALQW0.81780.5837919
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B44:13KLEKKDALQW0.75830.978919
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B44:26KLEKKDALQW0.75830.978919
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B44:07KLEKKDALQW0.75830.978919
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B44:21KKLEKKDALQW0.99670.5054819
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B44:22KKLEKKDALQW0.99450.6306819
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B44:13KKLEKKDALQW0.9930.9821819
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B44:07KKLEKKDALQW0.9930.9821819
ERBB2IP-ASXL1chr565350779chr20310159314022HLA-B44:26KKLEKKDALQW0.9930.9821819

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Potential FusionNeoAntigen Information of ERBB2IP-ASXL1 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.
ERBB2IP-ASXL1_65350779_31015931.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)
ERBB2IP-ASXL1chr565350779chr20310159314022DRB1-0103QVLRHIEAKKLEKKD015
ERBB2IP-ASXL1chr565350779chr20310159314022DRB1-0123QVLRHIEAKKLEKKD015
ERBB2IP-ASXL1chr565350779chr20310159314022DRB1-1208QVLRHIEAKKLEKKD015
ERBB2IP-ASXL1chr565350779chr20310159314022DRB1-1221QVLRHIEAKKLEKKD015

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Fusion breakpoint peptide structures of ERBB2IP-ASXL1

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
1528EAKKLEKKDALQWSERBB2IPASXL1chr565350779chr20310159314022

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of ERBB2IP-ASXL1

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-B14:023BVN1528EAKKLEKKDALQWS-7.9962-8.1096
HLA-B14:023BVN1528EAKKLEKKDALQWS-5.70842-6.74372
HLA-B52:013W391528EAKKLEKKDALQWS-6.83737-6.95077
HLA-B52:013W391528EAKKLEKKDALQWS-4.4836-5.5189
HLA-A11:014UQ21528EAKKLEKKDALQWS-10.0067-10.1201
HLA-A11:014UQ21528EAKKLEKKDALQWS-9.03915-10.0745
HLA-A24:025HGA1528EAKKLEKKDALQWS-6.56204-6.67544
HLA-A24:025HGA1528EAKKLEKKDALQWS-5.42271-6.45801
HLA-B44:053DX81528EAKKLEKKDALQWS-7.85648-8.89178
HLA-B44:053DX81528EAKKLEKKDALQWS-5.3978-5.5112
HLA-A02:016TDR1528EAKKLEKKDALQWS-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of ERBB2IP-ASXL1

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
ERBB2IP-ASXL1chr565350779chr20310159311019LEKKDALQWTTAGAAAAGAAGGATGCCCTGCAGTGG
ERBB2IP-ASXL1chr565350779chr2031015931817KKLEKKDALAAAAAGTTAGAAAAGAAGGATGCCCTG
ERBB2IP-ASXL1chr565350779chr2031015931819KKLEKKDALQWAAAAAGTTAGAAAAGAAGGATGCCCTGCAGTGG
ERBB2IP-ASXL1chr565350779chr2031015931919KLEKKDALQWAAGTTAGAAAAGAAGGATGCCCTGCAGTGG

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
ERBB2IP-ASXL1chr565350779chr2031015931015QVLRHIEAKKLEKKDCAAGTACTTCGACATATTGAAGCCAAAAAGTTAGAAAAGAAGGAT

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Information of the samples that have these potential fusion neoantigens of ERBB2IP-ASXL1

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
LUADERBB2IP-ASXL1chr565350779ENST00000284037chr2031015931ENST00000375687TCGA-50-5944-01A

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Potential target of CAR-T therapy development for ERBB2IP-ASXL1

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 ERBB2IP-ASXL1

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 ERBB2IP-ASXL1

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