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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:ING3-CHMP1A

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ING3-CHMP1A
FusionPDB ID: 39740
FusionGDB2.0 ID: 39740
HgeneTgene
Gene symbol

ING3

CHMP1A

Gene ID

54556

5119

Gene nameinhibitor of growth family member 3charged multivesicular body protein 1A
SynonymsEaf4|ING2|MEAF4|p47ING3CHMP1|PCH8|PCOLN3|PRSM1|VPS46-1|VPS46A
Cytomap

7q31.31

16q24.3

Type of geneprotein-codingprotein-coding
Descriptioninhibitor of growth protein 3charged multivesicular body protein 1acharged multivesicular body protein 1/chromatin modifying protein 1chromatin modifying protein 1Aprocollagen (type III) N-endopeptidaseprotease, metallo, 1, 33kDvacuolar protein sorting-associated protein 46-1
Modification date2020031320200313
UniProtAcc

Q9NXR8

Main function of 5'-partner protein: 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. Component of a SWR1-like complex that specifically mediates the removal of histone H2A.Z/H2AZ1 from the nucleosome. {ECO:0000269|PubMed:12545155, ECO:0000269|PubMed:14966270, ECO:0000269|PubMed:24463511}.

Q9HD42

Main function of 5'-partner protein: FUNCTION: Probable peripherally associated component of the endosomal sorting required for transport complex III (ESCRT-III) which is involved in multivesicular bodies (MVBs) formation and sorting of endosomal cargo proteins into MVBs. MVBs contain intraluminal vesicles (ILVs) that are generated by invagination and scission from the limiting membrane of the endosome and mostly are delivered to lysosomes enabling degradation of membrane proteins, such as stimulated growth factor receptors, lysosomal enzymes and lipids. The MVB pathway appears to require the sequential function of ESCRT-O, -I,-II and -III complexes. ESCRT-III proteins mostly dissociate from the invaginating membrane before the ILV is released. The ESCRT machinery also functions in topologically equivalent membrane fission events, such as the terminal stages of cytokinesis and the budding of enveloped viruses (HIV-1 and other lentiviruses). ESCRT-III proteins are believed to mediate the necessary vesicle extrusion and/or membrane fission activities, possibly in conjunction with the AAA ATPase VPS4. Involved in cytokinesis. Involved in recruiting VPS4A and/or VPS4B to the midbody of dividing cells. May also be involved in chromosome condensation. Targets the Polycomb group (PcG) protein BMI1/PCGF4 to regions of condensed chromatin. May play a role in stable cell cycle progression and in PcG gene silencing. {ECO:0000269|PubMed:11559747, ECO:0000269|PubMed:11559748, ECO:0000269|PubMed:19129479, ECO:0000269|PubMed:23045692}.
Ensembl transtripts involved in fusion geneENST idsENST00000315870, ENST00000339121, 
ENST00000431467, ENST00000445699, 
ENST00000547614, ENST00000253475, 
ENST00000397901, ENST00000535997, 
ENST00000550102, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score6 X 1 X 3=1845 X 11 X 21=10395
# samples 648
** MAII scorelog2(6/18*10)=1.73696559416621
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(48/10395*10)=-4.43671154213721
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: ING3 [Title/Abstract] AND CHMP1A [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: ING3 [Title/Abstract] AND CHMP1A [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ING3(120595678)-CHMP1A(89713739), # samples:1
Anticipated loss of major functional domain due to fusion event.ING3-CHMP1A 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.
ING3-CHMP1A 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.
ING3-CHMP1A 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.
ING3-CHMP1A 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.
ING3-CHMP1A seems lost the major protein functional domain in Hgene partner, which is a epigenetic factor due to the frame-shifted ORF.
ING3-CHMP1A seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
ING3-CHMP1A seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor 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
HgeneING3

GO:0043065

positive regulation of apoptotic process

16387653

HgeneING3

GO:0043967

histone H4 acetylation

14966270|16387653

HgeneING3

GO:0043968

histone H2A acetylation

14966270|16387653

TgeneCHMP1A

GO:0007076

mitotic chromosome condensation

11559747

TgeneCHMP1A

GO:0016192

vesicle-mediated transport

11559748

TgeneCHMP1A

GO:0016458

gene silencing

11559747

TgeneCHMP1A

GO:0045892

negative regulation of transcription, DNA-templated

11559747



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/chr7:120595678/chr16:89713739)
- 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 ING3 (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 CHMP1A (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)
ENST00000315870ING3chr7120595678+ENST00000397901CHMP1Achr1689713739-2389415112753213
ENST00000315870ING3chr7120595678+ENST00000535997CHMP1Achr1689713739-2357415112753213
ENST00000315870ING3chr7120595678+ENST00000550102CHMP1Achr1689713739-931415112753213
ENST00000339121ING3chr7120595678+ENST00000397901CHMP1Achr1689713739-237540198739213
ENST00000339121ING3chr7120595678+ENST00000535997CHMP1Achr1689713739-234340198739213
ENST00000339121ING3chr7120595678+ENST00000550102CHMP1Achr1689713739-91740198739213
ENST00000445699ING3chr7120595678+ENST00000253475CHMP1Achr1689713739-3624165724702961163
ENST00000431467ING3chr7120595678+ENST00000397901CHMP1Achr1689713739-226128741625194
ENST00000431467ING3chr7120595678+ENST00000535997CHMP1Achr1689713739-222928741625194
ENST00000431467ING3chr7120595678+ENST00000550102CHMP1Achr1689713739-80328741625194

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
ENST00000315870ENST00000397901ING3chr7120595678+CHMP1Achr1689713739-0.0015956670.9984043
ENST00000315870ENST00000535997ING3chr7120595678+CHMP1Achr1689713739-0.0015237120.9984763
ENST00000315870ENST00000550102ING3chr7120595678+CHMP1Achr1689713739-0.0012618530.9987381
ENST00000339121ENST00000397901ING3chr7120595678+CHMP1Achr1689713739-0.0016313670.9983687
ENST00000339121ENST00000535997ING3chr7120595678+CHMP1Achr1689713739-0.0017022370.99829775
ENST00000339121ENST00000550102ING3chr7120595678+CHMP1Achr1689713739-0.0010861130.9989139
ENST00000445699ENST00000253475ING3chr7120595678+CHMP1Achr1689713739-0.86934280.13065717
ENST00000431467ENST00000397901ING3chr7120595678+CHMP1Achr1689713739-0.0026991970.9973008
ENST00000431467ENST00000535997ING3chr7120595678+CHMP1Achr1689713739-0.0025726140.9974274
ENST00000431467ENST00000550102ING3chr7120595678+CHMP1Achr1689713739-0.0011199960.99887997

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 ING3-CHMP1A

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
ING3chr7120595678CHMP1Achr168971373928782DEKVQLANQIYDLVTKNMAQVTKALD
ING3chr7120595678CHMP1Achr1689713739401101DEKVQLANQIYDLVTKNMAQVTKALD
ING3chr7120595678CHMP1Achr1689713739415101DEKVQLANQIYDLVTKNMAQVTKALD

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Potential FusionNeoAntigen Information of ING3-CHMP1A 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.
ING3-CHMP1A_120595678_89713739.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)
ING3-CHMP1Achr7120595678chr1689713739415HLA-C04:10IYDLVTKNM0.99950.5848918
ING3-CHMP1Achr7120595678chr1689713739415HLA-C04:07IYDLVTKNM0.99940.6239918
ING3-CHMP1Achr7120595678chr1689713739415HLA-C07:05IYDLVTKNM0.98570.9433918
ING3-CHMP1Achr7120595678chr1689713739415HLA-C07:27IYDLVTKNM0.98390.9116918
ING3-CHMP1Achr7120595678chr1689713739415HLA-C07:29IYDLVTKNM0.98290.8851918
ING3-CHMP1Achr7120595678chr1689713739415HLA-C07:13IYDLVTKNM0.98050.8167918
ING3-CHMP1Achr7120595678chr1689713739415HLA-C07:10IYDLVTKNM0.97450.914918
ING3-CHMP1Achr7120595678chr1689713739415HLA-C07:80IYDLVTKNM0.97350.8384918
ING3-CHMP1Achr7120595678chr1689713739415HLA-C07:67IYDLVTKNM0.97350.8384918
ING3-CHMP1Achr7120595678chr1689713739415HLA-C07:46IYDLVTKNM0.95940.6638918
ING3-CHMP1Achr7120595678chr1689713739415HLA-C04:06IYDLVTKNM0.9540.7088918
ING3-CHMP1Achr7120595678chr1689713739415HLA-C04:14IYDLVTKNM0.70130.5903918
ING3-CHMP1Achr7120595678chr1689713739415HLA-C12:16IYDLVTKNM0.3870.9408918
ING3-CHMP1Achr7120595678chr1689713739415HLA-C04:03IYDLVTKNM0.99950.6768918
ING3-CHMP1Achr7120595678chr1689713739415HLA-C04:01IYDLVTKNM0.99940.6239918
ING3-CHMP1Achr7120595678chr1689713739415HLA-C18:01IYDLVTKNM0.99930.6349918
ING3-CHMP1Achr7120595678chr1689713739415HLA-C03:67IYDLVTKNM0.9910.9694918
ING3-CHMP1Achr7120595678chr1689713739415HLA-C14:02IYDLVTKNM0.98780.9488918
ING3-CHMP1Achr7120595678chr1689713739415HLA-C14:03IYDLVTKNM0.98780.9488918
ING3-CHMP1Achr7120595678chr1689713739415HLA-C07:17IYDLVTKNM0.97550.9427918
ING3-CHMP1Achr7120595678chr1689713739415HLA-C07:02IYDLVTKNM0.97350.8384918
ING3-CHMP1Achr7120595678chr1689713739415HLA-C07:04IYDLVTKNM0.9560.9084918
ING3-CHMP1Achr7120595678chr1689713739415HLA-C06:06IYDLVTKNM0.94090.979918
ING3-CHMP1Achr7120595678chr1689713739415HLA-C04:04IYDLVTKNM0.92340.68918

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Potential FusionNeoAntigen Information of ING3-CHMP1A 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.
ING3-CHMP1A_120595678_89713739.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)
ING3-CHMP1Achr7120595678chr1689713739415DRB1-0466NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-0802NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-0802ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-0808NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-0809NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-0809ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-0811NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-0813NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-0815NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-0821NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-0821ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-0824NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-0824ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-0824LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-0830NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1101NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1101ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1101LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1105NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1105ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1108NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1108ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1109NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1109ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1109LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1110NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1110ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1110LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1112NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1112ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1112LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1115NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1115ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1115LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1119NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1119ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1124NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1124ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1124LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1127NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1127ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1128NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1128ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1128LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1129NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1129ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1129LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1130NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1131NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1131ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1132NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1132ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1133NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1133ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1133LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1137NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1137ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1137LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1139NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1139ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1139LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1149NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1149ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1149LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1151NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1151ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1151LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1153NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1153ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1161NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1161ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1161LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1162NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1162ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1162LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1166NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1166ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1166LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1169NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1172NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1173NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1173ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1174NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1174ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1174LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1175NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1175ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1175LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1180NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1180ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1181NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1181ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1181LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1187NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1187ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1190NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1190ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1190LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1191NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1191ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1193NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1193ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1194NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1194ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1194LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1195NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1195ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1195LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1196NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1196ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1196LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1305NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1305ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1305LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1307NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1307ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1307LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-13100NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-13100ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1314NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1314ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1314LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1326NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1326ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1326LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1337NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1337ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1346NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1346ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1347NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1347ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1350NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1350ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1350LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1356NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1356ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1360NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1360ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1360LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1362NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1362ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1362LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1382NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1382ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1385NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1385ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1386NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1402NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1402ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1409NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1409ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1414NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1414ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1414LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1422NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1422ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1425NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1425ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1427NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1427ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1430NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1430ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1436NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1436ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1436LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1441NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1441ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1442NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1442ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1444NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1444ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1444LANQIYDLVTKNMAQ520
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1451NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1451ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1453NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1453ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1469NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1469ANQIYDLVTKNMAQV621
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1494NQIYDLVTKNMAQVT722
ING3-CHMP1Achr7120595678chr1689713739415DRB1-1494ANQIYDLVTKNMAQV621

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Fusion breakpoint peptide structures of ING3-CHMP1A

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
466ANQIYDLVTKNMAQING3CHMP1Achr7120595678chr1689713739415

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of ING3-CHMP1A

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-B14:023BVN466ANQIYDLVTKNMAQ-7.15543-7.26883
HLA-B14:023BVN466ANQIYDLVTKNMAQ-4.77435-5.80965
HLA-B52:013W39466ANQIYDLVTKNMAQ-6.80875-6.92215
HLA-B52:013W39466ANQIYDLVTKNMAQ-4.20386-5.23916
HLA-A11:014UQ2466ANQIYDLVTKNMAQ-7.5194-8.5547
HLA-A11:014UQ2466ANQIYDLVTKNMAQ-6.9601-7.0735
HLA-A24:025HGA466ANQIYDLVTKNMAQ-7.52403-7.63743
HLA-A24:025HGA466ANQIYDLVTKNMAQ-5.82433-6.85963
HLA-B27:056PYJ466ANQIYDLVTKNMAQ-3.28285-4.31815
HLA-B44:053DX8466ANQIYDLVTKNMAQ-5.91172-6.94702
HLA-B44:053DX8466ANQIYDLVTKNMAQ-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of ING3-CHMP1A

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
ING3-CHMP1Achr7120595678chr1689713739918IYDLVTKNMATATATGACTTGGTGACCAAGAATATG

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
ING3-CHMP1Achr7120595678chr1689713739520LANQIYDLVTKNMAQTTGGCAAACCAGATATATGACTTGGTGACCAAGAATATGGCCCAG
ING3-CHMP1Achr7120595678chr1689713739621ANQIYDLVTKNMAQVGCAAACCAGATATATGACTTGGTGACCAAGAATATGGCCCAGGTG
ING3-CHMP1Achr7120595678chr1689713739722NQIYDLVTKNMAQVTAACCAGATATATGACTTGGTGACCAAGAATATGGCCCAGGTGACC

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Information of the samples that have these potential fusion neoantigens of ING3-CHMP1A

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
STADING3-CHMP1Achr7120595678ENST00000315870chr1689713739ENST00000397901TCGA-BR-7958

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Potential target of CAR-T therapy development for ING3-CHMP1A

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 ING3-CHMP1A

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 ING3-CHMP1A

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