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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:ING4-A2ML1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ING4-A2ML1
FusionPDB ID: 39745
FusionGDB2.0 ID: 39745
HgeneTgene
Gene symbol

ING4

A2ML1

Gene ID

51147

144568

Gene nameinhibitor of growth family member 4alpha-2-macroglobulin like 1
Synonymsmy036|p29ING4CPAMD9|OMS|p170
Cytomap

12p13.31

12p13.31

Type of geneprotein-codingprotein-coding
Descriptioninhibitor of growth protein 4brain my036 proteincandidate tumor suppressor p33 ING1 homologalpha-2-macroglobulin-like protein 1C3 and PZP-like, alpha-2-macroglobulin domain containing 9
Modification date2020032220200313
UniProtAcc

Q9UNL4

Main function of 5'-partner protein: FUNCTION: Component of HBO1 complexes, which specifically mediate acetylation of histone H3 at 'Lys-14' (H3K14ac), and have reduced activity toward histone H4 (PubMed:16387653). Through chromatin acetylation it may function in DNA replication (PubMed:16387653). May inhibit tumor progression by modulating the transcriptional output of signaling pathways which regulate cell proliferation (PubMed:15251430, PubMed:15528276). Can suppress brain tumor angiogenesis through transcriptional repression of RELA/NFKB3 target genes when complexed with RELA (PubMed:15029197). May also specifically suppress loss of contact inhibition elicited by activated oncogenes such as MYC (PubMed:15029197). Represses hypoxia inducible factor's (HIF) activity by interacting with HIF prolyl hydroxylase 2 (EGLN1) (PubMed:15897452). Can enhance apoptosis induced by serum starvation in mammary epithelial cell line HC11 (By similarity). {ECO:0000250|UniProtKB:Q8C0D7, ECO:0000269|PubMed:15029197, ECO:0000269|PubMed:15251430, ECO:0000269|PubMed:15528276, ECO:0000269|PubMed:15897452, ECO:0000269|PubMed:16387653}.

A8K2U0

Main function of 5'-partner protein: FUNCTION: Is able to inhibit all four classes of proteinases by a unique 'trapping' mechanism. This protein has a peptide stretch, called the 'bait region' which contains specific cleavage sites for different proteinases. When a proteinase cleaves the bait region, a conformational change is induced in the protein which traps the proteinase. The entrapped enzyme remains active against low molecular weight substrates (activity against high molecular weight substrates is greatly reduced). Following cleavage in the bait region a thioester bond is hydrolyzed and mediates the covalent binding of the protein to the proteinase (By similarity). Displays inhibitory activity against chymotrypsin, papain, thermolysin, subtilisin A and, to a lesser extent, elastase but not trypsin. May play an important role during desquamation by inhibiting extracellular proteases. {ECO:0000250|UniProtKB:P01023, ECO:0000269|PubMed:16298998}.
Ensembl transtripts involved in fusion geneENST idsENST00000341550, ENST00000396807, 
ENST00000412586, ENST00000423703, 
ENST00000444704, ENST00000446105, 
ENST00000486287, 
ENST00000540049, 
ENST00000299698, ENST00000539547, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score3 X 3 X 3=277 X 6 X 4=168
# samples 36
** MAII scorelog2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(6/168*10)=-1.48542682717024
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: ING4 [Title/Abstract] AND A2ML1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: ING4 [Title/Abstract] AND A2ML1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ING4(6772231)-A2ML1(9027021), # samples:3
Anticipated loss of major functional domain due to fusion event.ING4-A2ML1 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.
ING4-A2ML1 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
HgeneING4

GO:0006260

DNA replication

16387653

HgeneING4

GO:0006473

protein acetylation

12750254

HgeneING4

GO:0006915

apoptotic process

15251430

HgeneING4

GO:0006978

DNA damage response, signal transduction by p53 class mediator resulting in transcription of p21 class mediator

16387653

HgeneING4

GO:0007050

cell cycle arrest

15251430

HgeneING4

GO:0008285

negative regulation of cell proliferation

12750254|15251430

HgeneING4

GO:0043065

positive regulation of apoptotic process

16387653

HgeneING4

GO:0043966

histone H3 acetylation

16387653

HgeneING4

GO:0043981

histone H4-K5 acetylation

16387653

HgeneING4

GO:0043982

histone H4-K8 acetylation

16387653

HgeneING4

GO:0043983

histone H4-K12 acetylation

16387653

HgeneING4

GO:0043984

histone H4-K16 acetylation

16387653

HgeneING4

GO:0045892

negative regulation of transcription, DNA-templated

15029197

HgeneING4

GO:0045926

negative regulation of growth

12750254

TgeneA2ML1

GO:0052548

regulation of endopeptidase activity

16298998



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/chr12:6772231/chr12:9027021)
- 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 ING4 (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 A2ML1 (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)
ENST00000341550ING4chr126772231-ENST00000299698A2ML1chr129027021+9578478649696
ENST00000341550ING4chr126772231-ENST00000539547A2ML1chr129027021+628842722766
ENST00000396807ING4chr126772231-ENST00000299698A2ML1chr129027021+9497677848896
ENST00000396807ING4chr126772231-ENST00000539547A2ML1chr129027021+620761921966
ENST00000446105ING4chr126772231-ENST00000299698A2ML1chr129027021+9517878049096
ENST00000446105ING4chr126772231-ENST00000539547A2ML1chr129027021+622782122166
ENST00000444704ING4chr126772231-ENST00000299698A2ML1chr129027021+9103773944996
ENST00000444704ING4chr126772231-ENST00000539547A2ML1chr129027021+58137418058
ENST00000423703ING4chr126772231-ENST00000299698A2ML1chr129027021+9103773944996
ENST00000423703ING4chr126772231-ENST00000539547A2ML1chr129027021+58137418058
ENST00000412586ING4chr126772231-ENST00000299698A2ML1chr129027021+9103773944996
ENST00000412586ING4chr126772231-ENST00000539547A2ML1chr129027021+58137418058

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
ENST00000341550ENST00000299698ING4chr126772231-A2ML1chr129027021+0.925113860.07488609
ENST00000341550ENST00000539547ING4chr126772231-A2ML1chr129027021+0.326354440.67364556
ENST00000396807ENST00000299698ING4chr126772231-A2ML1chr129027021+0.891014930.108985096
ENST00000396807ENST00000539547ING4chr126772231-A2ML1chr129027021+0.218175140.7818249
ENST00000446105ENST00000299698ING4chr126772231-A2ML1chr129027021+0.90723650.09276349
ENST00000446105ENST00000539547ING4chr126772231-A2ML1chr129027021+0.242142470.7578575
ENST00000444704ENST00000299698ING4chr126772231-A2ML1chr129027021+0.850879970.14912003
ENST00000444704ENST00000539547ING4chr126772231-A2ML1chr129027021+0.136172560.8638274
ENST00000423703ENST00000299698ING4chr126772231-A2ML1chr129027021+0.850879970.14912003
ENST00000423703ENST00000539547ING4chr126772231-A2ML1chr129027021+0.136172560.8638274
ENST00000412586ENST00000299698ING4chr126772231-A2ML1chr129027021+0.850879970.14912003
ENST00000412586ENST00000539547ING4chr126772231-A2ML1chr129027021+0.136172560.8638274

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 ING4-A2ML1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
ING4chr126772231A2ML1chr1290270217619RWLRGCIWNIIWTLIKNTQTYTFTIS
ING4chr126772231A2ML1chr1290270217819RWLRGCIWNIIWTLIKNTQTYTFTIS
ING4chr126772231A2ML1chr1290270218419RWLRGCIWNIIWTLIKNTQTYTFTIS

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Potential FusionNeoAntigen Information of ING4-A2ML1 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.
ING4-A2ML1_6772231_9027021.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)
ING4-A2ML1chr126772231chr12902702184HLA-B15:01TLIKNTQTY0.99980.78241221
ING4-A2ML1chr126772231chr12902702184HLA-B15:25TLIKNTQTY0.99810.76881221
ING4-A2ML1chr126772231chr12902702184HLA-B15:02TLIKNTQTY0.99360.79481221
ING4-A2ML1chr126772231chr12902702184HLA-B35:08TLIKNTQTY0.94210.69621221
ING4-A2ML1chr126772231chr12902702184HLA-B35:01TLIKNTQTY0.85040.75421221
ING4-A2ML1chr126772231chr12902702184HLA-B15:03TLIKNTQTY0.82290.57341221
ING4-A2ML1chr126772231chr12902702184HLA-B15:18TLIKNTQTY0.68740.51611221
ING4-A2ML1chr126772231chr12902702184HLA-A32:13TLIKNTQTY0.19760.79141221
ING4-A2ML1chr126772231chr12902702184HLA-B15:01WTLIKNTQTY0.99860.86431121
ING4-A2ML1chr126772231chr12902702184HLA-B15:25WTLIKNTQTY0.99730.88691121
ING4-A2ML1chr126772231chr12902702184HLA-B15:02WTLIKNTQTY0.99260.90631121
ING4-A2ML1chr126772231chr12902702184HLA-B15:01IWTLIKNTQTY0.99120.89111021
ING4-A2ML1chr126772231chr12902702184HLA-B15:25IWTLIKNTQTY0.95070.83791021
ING4-A2ML1chr126772231chr12902702184HLA-B15:07TLIKNTQTY0.99860.56241221
ING4-A2ML1chr126772231chr12902702184HLA-B15:21TLIKNTQTY0.99350.78471221
ING4-A2ML1chr126772231chr12902702184HLA-B15:05TLIKNTQTY0.94280.70361221
ING4-A2ML1chr126772231chr12902702184HLA-B15:04TLIKNTQTY0.91290.7551221
ING4-A2ML1chr126772231chr12902702184HLA-B15:31TLIKNTQTY0.88320.71481221
ING4-A2ML1chr126772231chr12902702184HLA-C12:16TLIKNTQTY0.81360.96941221
ING4-A2ML1chr126772231chr12902702184HLA-C07:10TLIKNTQTY0.53510.91961221
ING4-A2ML1chr126772231chr12902702184HLA-C03:14TLIKNTQTY0.13440.95971221
ING4-A2ML1chr126772231chr12902702184HLA-B15:21WTLIKNTQTY0.99160.88331121
ING4-A2ML1chr126772231chr12902702184HLA-B15:05WTLIKNTQTY0.98420.7951121
ING4-A2ML1chr126772231chr12902702184HLA-B15:31WTLIKNTQTY0.96780.80481121
ING4-A2ML1chr126772231chr12902702184HLA-B15:07IWTLIKNTQTY0.99310.61991021
ING4-A2ML1chr126772231chr12902702184HLA-B15:05IWTLIKNTQTY0.90170.81611021
ING4-A2ML1chr126772231chr12902702184HLA-B15:34TLIKNTQTY0.99980.78241221
ING4-A2ML1chr126772231chr12902702184HLA-B15:33TLIKNTQTY0.99980.78241221
ING4-A2ML1chr126772231chr12902702184HLA-B15:125TLIKNTQTY0.99980.78241221
ING4-A2ML1chr126772231chr12902702184HLA-B15:135TLIKNTQTY0.99980.77081221
ING4-A2ML1chr126772231chr12902702184HLA-B15:27TLIKNTQTY0.99980.79841221
ING4-A2ML1chr126772231chr12902702184HLA-B15:50TLIKNTQTY0.99970.9361221
ING4-A2ML1chr126772231chr12902702184HLA-B15:11TLIKNTQTY0.99950.73991221
ING4-A2ML1chr126772231chr12902702184HLA-B15:08TLIKNTQTY0.99940.76461221
ING4-A2ML1chr126772231chr12902702184HLA-B35:43TLIKNTQTY0.99910.75561221
ING4-A2ML1chr126772231chr12902702184HLA-B15:24TLIKNTQTY0.99910.70961221
ING4-A2ML1chr126772231chr12902702184HLA-B15:53TLIKNTQTY0.9990.75011221
ING4-A2ML1chr126772231chr12902702184HLA-B15:12TLIKNTQTY0.9990.74031221
ING4-A2ML1chr126772231chr12902702184HLA-B15:35TLIKNTQTY0.99870.75041221
ING4-A2ML1chr126772231chr12902702184HLA-B15:39TLIKNTQTY0.99810.64071221
ING4-A2ML1chr126772231chr12902702184HLA-B35:11TLIKNTQTY0.99040.77921221
ING4-A2ML1chr126772231chr12902702184HLA-B15:54TLIKNTQTY0.96490.72751221
ING4-A2ML1chr126772231chr12902702184HLA-B15:20TLIKNTQTY0.94480.75411221
ING4-A2ML1chr126772231chr12902702184HLA-B35:28TLIKNTQTY0.91850.74961221
ING4-A2ML1chr126772231chr12902702184HLA-B35:20TLIKNTQTY0.88290.76151221
ING4-A2ML1chr126772231chr12902702184HLA-B35:23TLIKNTQTY0.86440.74681221
ING4-A2ML1chr126772231chr12902702184HLA-B35:77TLIKNTQTY0.85040.75421221
ING4-A2ML1chr126772231chr12902702184HLA-B35:17TLIKNTQTY0.76420.6291221
ING4-A2ML1chr126772231chr12902702184HLA-B35:30TLIKNTQTY0.76420.6291221
ING4-A2ML1chr126772231chr12902702184HLA-C12:02TLIKNTQTY0.76120.97621221
ING4-A2ML1chr126772231chr12902702184HLA-C03:02TLIKNTQTY0.69970.93631221
ING4-A2ML1chr126772231chr12902702184HLA-A25:01TLIKNTQTY0.66450.821221
ING4-A2ML1chr126772231chr12902702184HLA-B35:24TLIKNTQTY0.6070.82481221
ING4-A2ML1chr126772231chr12902702184HLA-B15:68TLIKNTQTY0.59830.50631221
ING4-A2ML1chr126772231chr12902702184HLA-C07:17TLIKNTQTY0.58560.96311221
ING4-A2ML1chr126772231chr12902702184HLA-B15:73TLIKNTQTY0.57970.64621221
ING4-A2ML1chr126772231chr12902702184HLA-B15:30TLIKNTQTY0.46310.75061221
ING4-A2ML1chr126772231chr12902702184HLA-A32:01TLIKNTQTY0.45090.86111221
ING4-A2ML1chr126772231chr12902702184HLA-B48:02TLIKNTQTY0.36170.73061221
ING4-A2ML1chr126772231chr12902702184HLA-B18:04TLIKNTQTY0.31620.85771221
ING4-A2ML1chr126772231chr12902702184HLA-B18:07TLIKNTQTY0.12570.81891221
ING4-A2ML1chr126772231chr12902702184HLA-B18:08TLIKNTQTY0.09410.59291221
ING4-A2ML1chr126772231chr12902702184HLA-C02:02TLIKNTQTY0.07980.95631221
ING4-A2ML1chr126772231chr12902702184HLA-C02:10TLIKNTQTY0.07980.95631221
ING4-A2ML1chr126772231chr12902702184HLA-B15:33WTLIKNTQTY0.99860.86431121
ING4-A2ML1chr126772231chr12902702184HLA-B15:34WTLIKNTQTY0.99860.86431121
ING4-A2ML1chr126772231chr12902702184HLA-B15:125WTLIKNTQTY0.99860.86431121
ING4-A2ML1chr126772231chr12902702184HLA-B15:135WTLIKNTQTY0.99850.85941121
ING4-A2ML1chr126772231chr12902702184HLA-B15:27WTLIKNTQTY0.99840.88241121
ING4-A2ML1chr126772231chr12902702184HLA-B15:39WTLIKNTQTY0.99730.80041121
ING4-A2ML1chr126772231chr12902702184HLA-B15:20WTLIKNTQTY0.98510.85441121
ING4-A2ML1chr126772231chr12902702184HLA-A25:01WTLIKNTQTY0.73360.85571121
ING4-A2ML1chr126772231chr12902702184HLA-B15:35IWTLIKNTQTY0.99140.85241021
ING4-A2ML1chr126772231chr12902702184HLA-B15:33IWTLIKNTQTY0.99120.89111021
ING4-A2ML1chr126772231chr12902702184HLA-B15:34IWTLIKNTQTY0.99120.89111021
ING4-A2ML1chr126772231chr12902702184HLA-B15:125IWTLIKNTQTY0.99120.89111021
ING4-A2ML1chr126772231chr12902702184HLA-B15:27IWTLIKNTQTY0.99110.88991021
ING4-A2ML1chr126772231chr12902702184HLA-B15:135IWTLIKNTQTY0.98850.87881021
ING4-A2ML1chr126772231chr12902702184HLA-B15:39IWTLIKNTQTY0.95650.68531021
ING4-A2ML1chr126772231chr12902702184HLA-B15:20IWTLIKNTQTY0.90410.87121021

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Potential FusionNeoAntigen Information of ING4-A2ML1 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 ING4-A2ML1

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
4068IWNIIWTLIKNTQTING4A2ML1chr126772231chr12902702184

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of ING4-A2ML1

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-B14:023BVN4068IWNIIWTLIKNTQT-7.9962-8.1096
HLA-B14:023BVN4068IWNIIWTLIKNTQT-5.70842-6.74372
HLA-B52:013W394068IWNIIWTLIKNTQT-6.83737-6.95077
HLA-B52:013W394068IWNIIWTLIKNTQT-4.4836-5.5189
HLA-A11:014UQ24068IWNIIWTLIKNTQT-10.0067-10.1201
HLA-A11:014UQ24068IWNIIWTLIKNTQT-9.03915-10.0745
HLA-A24:025HGA4068IWNIIWTLIKNTQT-6.56204-6.67544
HLA-A24:025HGA4068IWNIIWTLIKNTQT-5.42271-6.45801
HLA-B44:053DX84068IWNIIWTLIKNTQT-7.85648-8.89178
HLA-B44:053DX84068IWNIIWTLIKNTQT-5.3978-5.5112
HLA-A02:016TDR4068IWNIIWTLIKNTQT-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of ING4-A2ML1

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
ING4-A2ML1chr126772231chr1290270211021IWTLIKNTQTYATCTGGACACTCATTAAGAACACTCAGACTTAC
ING4-A2ML1chr126772231chr1290270211121WTLIKNTQTYTGGACACTCATTAAGAACACTCAGACTTAC
ING4-A2ML1chr126772231chr1290270211221TLIKNTQTYACACTCATTAAGAACACTCAGACTTAC

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 ING4-A2ML1

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
SKCMING4-A2ML1chr126772231ENST00000341550chr129027021ENST00000539547TCGA-D3-A3CC-06A

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Potential target of CAR-T therapy development for ING4-A2ML1

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 ING4-A2ML1

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 ING4-A2ML1

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