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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:IGF1R-ARID1B

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: IGF1R-ARID1B
FusionPDB ID: 38471
FusionGDB2.0 ID: 38471
HgeneTgene
Gene symbol

IGF1R

ARID1B

Gene ID

3480

57492

Gene nameinsulin like growth factor 1 receptorAT-rich interaction domain 1B
SynonymsCD221|IGFIR|IGFR|JTK136A3-5|BAF250B|BRIGHT|CSS1|DAN15|ELD/OSA1|MRD12|OSA2|P250R
Cytomap

15q26.3

6q25.3

Type of geneprotein-codingprotein-coding
Descriptioninsulin-like growth factor 1 receptorIGF-I receptorsoluble IGF1R variant 1soluble IGF1R variant 2AT-rich interactive domain-containing protein 1BARID domain-containing protein 1BAT rich interactive domain 1B (SWI1-like)BRG1-associated factor 250bBRG1-binding protein ELD/OSA1ELD (eyelid)/OSA protein
Modification date2020032920200320
UniProtAcc

P08069

Main function of 5'-partner protein: FUNCTION: Receptor tyrosine kinase which mediates actions of insulin-like growth factor 1 (IGF1). Binds IGF1 with high affinity and IGF2 and insulin (INS) with a lower affinity. The activated IGF1R is involved in cell growth and survival control. IGF1R is crucial for tumor transformation and survival of malignant cell. Ligand binding activates the receptor kinase, leading to receptor autophosphorylation, and tyrosines phosphorylation of multiple substrates, that function as signaling adapter proteins including, the insulin-receptor substrates (IRS1/2), Shc and 14-3-3 proteins. Phosphorylation of IRSs proteins lead to the activation of two main signaling pathways: the PI3K-AKT/PKB pathway and the Ras-MAPK pathway. The result of activating the MAPK pathway is increased cellular proliferation, whereas activating the PI3K pathway inhibits apoptosis and stimulates protein synthesis. Phosphorylated IRS1 can activate the 85 kDa regulatory subunit of PI3K (PIK3R1), leading to activation of several downstream substrates, including protein AKT/PKB. AKT phosphorylation, in turn, enhances protein synthesis through mTOR activation and triggers the antiapoptotic effects of IGFIR through phosphorylation and inactivation of BAD. In parallel to PI3K-driven signaling, recruitment of Grb2/SOS by phosphorylated IRS1 or Shc leads to recruitment of Ras and activation of the ras-MAPK pathway. In addition to these two main signaling pathways IGF1R signals also through the Janus kinase/signal transducer and activator of transcription pathway (JAK/STAT). Phosphorylation of JAK proteins can lead to phosphorylation/activation of signal transducers and activators of transcription (STAT) proteins. In particular activation of STAT3, may be essential for the transforming activity of IGF1R. The JAK/STAT pathway activates gene transcription and may be responsible for the transforming activity. JNK kinases can also be activated by the IGF1R. IGF1 exerts inhibiting activities on JNK activation via phosphorylation and inhibition of MAP3K5/ASK1, which is able to directly associate with the IGF1R.; FUNCTION: When present in a hybrid receptor with INSR, binds IGF1. PubMed:12138094 shows that hybrid receptors composed of IGF1R and INSR isoform Long are activated with a high affinity by IGF1, with low affinity by IGF2 and not significantly activated by insulin, and that hybrid receptors composed of IGF1R and INSR isoform Short are activated by IGF1, IGF2 and insulin. In contrast, PubMed:16831875 shows that hybrid receptors composed of IGF1R and INSR isoform Long and hybrid receptors composed of IGF1R and INSR isoform Short have similar binding characteristics, both bind IGF1 and have a low affinity for insulin.

Q8NFD5

Main function of 5'-partner protein: FUNCTION: Involved in transcriptional activation and repression of select genes by chromatin remodeling (alteration of DNA-nucleosome topology). Component of SWI/SNF chromatin remodeling complexes that carry out key enzymatic activities, changing chromatin structure by altering DNA-histone contacts within a nucleosome in an ATP-dependent manner. Belongs to the neural progenitors-specific chromatin remodeling complex (npBAF complex) and the neuron-specific chromatin remodeling complex (nBAF complex). During neural development a switch from a stem/progenitor to a postmitotic chromatin remodeling mechanism occurs as neurons exit the cell cycle and become committed to their adult state. The transition from proliferating neural stem/progenitor cells to postmitotic neurons requires a switch in subunit composition of the npBAF and nBAF complexes. As neural progenitors exit mitosis and differentiate into neurons, npBAF complexes which contain ACTL6A/BAF53A and PHF10/BAF45A, are exchanged for homologous alternative ACTL6B/BAF53B and DPF1/BAF45B or DPF3/BAF45C subunits in neuron-specific complexes (nBAF). The npBAF complex is essential for the self-renewal/proliferative capacity of the multipotent neural stem cells. The nBAF complex along with CREST plays a role regulating the activity of genes essential for dendrite growth (By similarity). Binds DNA non-specifically (PubMed:14982958, PubMed:15170388). {ECO:0000250|UniProtKB:E9Q4N7, ECO:0000269|PubMed:14982958, ECO:0000269|PubMed:15170388, ECO:0000303|PubMed:12672490, ECO:0000303|PubMed:22952240, ECO:0000303|PubMed:26601204}.
Ensembl transtripts involved in fusion geneENST idsENST00000268035, ENST00000558762, 
ENST00000560432, 
ENST00000478761, 
ENST00000275248, ENST00000346085, 
ENST00000350026, ENST00000367148, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score24 X 15 X 6=216010 X 12 X 6=720
# samples 2512
** MAII scorelog2(25/2160*10)=-3.11103131238874
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(12/720*10)=-2.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: IGF1R [Title/Abstract] AND ARID1B [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: IGF1R [Title/Abstract] AND ARID1B [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)IGF1R(99251336)-ARID1B(157469758), # samples:3
Anticipated loss of major functional domain due to fusion event.IGF1R-ARID1B 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.
IGF1R-ARID1B 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.
IGF1R-ARID1B 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.
IGF1R-ARID1B 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
HgeneIGF1R

GO:0043066

negative regulation of apoptotic process

12556535

HgeneIGF1R

GO:0046328

regulation of JNK cascade

12556535

HgeneIGF1R

GO:0046777

protein autophosphorylation

1846292|7679099|11162456

HgeneIGF1R

GO:0048009

insulin-like growth factor receptor signaling pathway

7679099

HgeneIGF1R

GO:0048015

phosphatidylinositol-mediated signaling

7692086

HgeneIGF1R

GO:0051389

inactivation of MAPKK activity

12556535



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/chr15:99251336/chr6:157469758)
- 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 IGF1R (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 ARID1B (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)
ENST00000268035IGF1Rchr1599251336+ENST00000350026ARID1Bchr6157469758+6709125161154491612
ENST00000268035IGF1Rchr1599251336+ENST00000346085ARID1Bchr6157469758+8338125161154491612
ENST00000268035IGF1Rchr1599251336+ENST00000367148ARID1Bchr6157469758+6985125161156081665
ENST00000268035IGF1Rchr1599251336+ENST00000275248ARID1Bchr6157469758+6985125161156081665
ENST00000558762IGF1Rchr1599251336+ENST00000350026ARID1Bchr6157469758+6636117853853761612
ENST00000558762IGF1Rchr1599251336+ENST00000346085ARID1Bchr6157469758+8265117853853761612
ENST00000558762IGF1Rchr1599251336+ENST00000367148ARID1Bchr6157469758+6912117853855351665
ENST00000558762IGF1Rchr1599251336+ENST00000275248ARID1Bchr6157469758+6912117853855351665

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
ENST00000268035ENST00000350026IGF1Rchr1599251336+ARID1Bchr6157469758+0.0029610820.99703896
ENST00000268035ENST00000346085IGF1Rchr1599251336+ARID1Bchr6157469758+0.0010954240.9989046
ENST00000268035ENST00000367148IGF1Rchr1599251336+ARID1Bchr6157469758+0.0028196190.99718034
ENST00000268035ENST00000275248IGF1Rchr1599251336+ARID1Bchr6157469758+0.0028196190.99718034
ENST00000558762ENST00000350026IGF1Rchr1599251336+ARID1Bchr6157469758+0.0026916370.9973084
ENST00000558762ENST00000346085IGF1Rchr1599251336+ARID1Bchr6157469758+0.0010144890.99898547
ENST00000558762ENST00000367148IGF1Rchr1599251336+ARID1Bchr6157469758+0.0025529760.997447
ENST00000558762ENST00000275248IGF1Rchr1599251336+ARID1Bchr6157469758+0.0025529760.997447

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 IGF1R-ARID1B

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
IGF1Rchr1599251336ARID1Bchr61574697581178214NYRCWTTNRCQKSNYSRPPAYSGVPS
IGF1Rchr1599251336ARID1Bchr61574697581251214NYRCWTTNRCQKSNYSRPPAYSGVPS

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Potential FusionNeoAntigen Information of IGF1R-ARID1B 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.
IGF1R-ARID1B_99251336_157469758.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)
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B15:25SNYSRPPAY0.98770.69431221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-A30:08KSNYSRPPA0.98110.53351120
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B15:02SNYSRPPAY0.97950.70051221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B15:03SNYSRPPAY0.77950.51281221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B18:01SNYSRPPAY0.11290.77531221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B15:25KSNYSRPPAY0.99320.74811121
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B15:17KSNYSRPPAY0.98740.72361121
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-A30:08KSNYSRPPAY0.95820.54341121
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B15:03QKSNYSRPPAY0.98770.51411021
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B15:21SNYSRPPAY0.97610.67231221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B15:05SNYSRPPAY0.97530.59091221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B15:31SNYSRPPAY0.95040.59741221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-C12:16SNYSRPPAY0.80840.81121221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B15:04SNYSRPPAY0.7950.72851221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-C15:04SNYSRPPAY0.78920.62921221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-C07:67SNYSRPPAY0.78630.72141221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-C07:80SNYSRPPAY0.78630.72141221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-C07:46SNYSRPPAY0.78360.61141221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-C07:10SNYSRPPAY0.77360.77571221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-C07:27SNYSRPPAY0.71360.78651221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-C07:05SNYSRPPAY0.68680.80621221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-C03:14SNYSRPPAY0.37170.84051221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-C12:12SNYSRPPAY0.22090.76531221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-C12:04SNYSRPPAY0.20870.94441221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-C06:03SNYSRPPAY0.20140.92961221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B15:07KSNYSRPPAY0.99590.52621121
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-C15:04KSNYSRPPAY0.98820.63771121
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B15:27SNYSRPPAY0.99310.6991221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B15:50SNYSRPPAY0.99070.6361221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B15:11SNYSRPPAY0.99070.65311221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B15:39SNYSRPPAY0.98890.58361221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B35:43SNYSRPPAY0.9870.64731221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-A30:01KSNYSRPPA0.98320.66071120
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B15:20SNYSRPPAY0.97270.67851221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B35:28SNYSRPPAY0.95910.68831221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B15:35SNYSRPPAY0.95470.65871221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B15:12SNYSRPPAY0.9540.73821221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B35:20SNYSRPPAY0.9360.6981221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B15:53SNYSRPPAY0.9180.65571221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-C07:17SNYSRPPAY0.87040.80581221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-C15:09SNYSRPPAY0.78920.62921221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-C07:02SNYSRPPAY0.78630.72141221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B18:11SNYSRPPAY0.78080.65521221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-C03:02SNYSRPPAY0.73650.81271221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B15:54SNYSRPPAY0.73070.64481221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B48:02SNYSRPPAY0.6490.6631221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-C12:02SNYSRPPAY0.5690.82231221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-C16:04SNYSRPPAY0.55490.84961221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B18:04SNYSRPPAY0.4320.80021221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-C16:01SNYSRPPAY0.31970.89741221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-C16:02SNYSRPPAY0.31220.94841221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-C06:02SNYSRPPAY0.30990.93921221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-C06:17SNYSRPPAY0.30990.93921221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-C12:03SNYSRPPAY0.2750.85021221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-C06:06SNYSRPPAY0.23080.9321221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B18:07SNYSRPPAY0.15130.68821221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B18:03SNYSRPPAY0.13380.76241221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B18:06SNYSRPPAY0.1330.76971221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B18:05SNYSRPPAY0.11290.77531221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B18:08SNYSRPPAY0.10070.6431221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-C06:08SNYSRPPAY0.02070.90771221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-C02:02SNYSRPPAY0.00510.86411221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-C02:10SNYSRPPAY0.00510.86411221
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B15:35KSNYSRPPAY0.99560.71281121
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B15:39KSNYSRPPAY0.99310.65751121
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-B58:06KSNYSRPPAY0.98830.5491121
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-C15:09KSNYSRPPAY0.98820.63771121
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-A30:01KSNYSRPPAY0.95930.641121
IGF1R-ARID1Bchr1599251336chr61574697581251HLA-C16:02KSNYSRPPAY0.90130.95741121

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Potential FusionNeoAntigen Information of IGF1R-ARID1B 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 IGF1R-ARID1B

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
9527TNRCQKSNYSRPPAIGF1RARID1Bchr1599251336chr61574697581251

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of IGF1R-ARID1B

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-B14:023BVN9527TNRCQKSNYSRPPA-7.15543-7.26883
HLA-B14:023BVN9527TNRCQKSNYSRPPA-4.77435-5.80965
HLA-B52:013W399527TNRCQKSNYSRPPA-6.80875-6.92215
HLA-B52:013W399527TNRCQKSNYSRPPA-4.20386-5.23916
HLA-A11:014UQ29527TNRCQKSNYSRPPA-7.5194-8.5547
HLA-A11:014UQ29527TNRCQKSNYSRPPA-6.9601-7.0735
HLA-A24:025HGA9527TNRCQKSNYSRPPA-7.52403-7.63743
HLA-A24:025HGA9527TNRCQKSNYSRPPA-5.82433-6.85963
HLA-B27:056PYJ9527TNRCQKSNYSRPPA-3.28285-4.31815
HLA-B44:053DX89527TNRCQKSNYSRPPA-5.91172-6.94702
HLA-B44:053DX89527TNRCQKSNYSRPPA-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of IGF1R-ARID1B

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
IGF1R-ARID1Bchr1599251336chr61574697581021QKSNYSRPPAYGCCAGAAAAGTAACTACTCCAGACCCCCAGCGT
IGF1R-ARID1Bchr1599251336chr61574697581120KSNYSRPPAAGAAAAGTAACTACTCCAGACCCCCAG
IGF1R-ARID1Bchr1599251336chr61574697581121KSNYSRPPAYAGAAAAGTAACTACTCCAGACCCCCAGCGT
IGF1R-ARID1Bchr1599251336chr61574697581221SNYSRPPAYAAAGTAACTACTCCAGACCCCCAGCGT

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 IGF1R-ARID1B

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
BRCAIGF1R-ARID1Bchr1599251336ENST00000268035chr6157469758ENST00000275248TCGA-E9-A1NF-01A

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Potential target of CAR-T therapy development for IGF1R-ARID1B

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 IGF1R-ARID1B

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 IGF1R-ARID1B

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