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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:STIM1-WT1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: STIM1-WT1
FusionPDB ID: 87410
FusionGDB2.0 ID: 87410
HgeneTgene
Gene symbol

STIM1

WT1

Gene ID

6786

7490

Gene namestromal interaction molecule 1WT1 transcription factor
SynonymsD11S4896E|GOK|IMD10|STRMK|TAM|TAM1AWT1|GUD|NPHS4|WAGR|WIT-2|WT33
Cytomap

11p15.4

11p13

Type of geneprotein-codingprotein-coding
Descriptionstromal interaction molecule 1Wilms tumor proteinWilms tumor 1
Modification date2020032920200320
UniProtAcc.

P19544

Main function of 5'-partner protein: FUNCTION: Transcription factor that plays an important role in cellular development and cell survival (PubMed:7862533). Recognizes and binds to the DNA sequence 5'-GCG(T/G)GGGCG-3' (PubMed:7862533, PubMed:17716689, PubMed:25258363). Regulates the expression of numerous target genes, including EPO. Plays an essential role for development of the urogenital system. It has a tumor suppressor as well as an oncogenic role in tumor formation. Function may be isoform-specific: isoforms lacking the KTS motif may act as transcription factors (PubMed:15520190). Isoforms containing the KTS motif may bind mRNA and play a role in mRNA metabolism or splicing (PubMed:16934801). Isoform 1 has lower affinity for DNA, and can bind RNA (PubMed:19123921). {ECO:0000269|PubMed:15520190, ECO:0000269|PubMed:16934801, ECO:0000269|PubMed:17716689, ECO:0000269|PubMed:19123921, ECO:0000269|PubMed:19416806, ECO:0000269|PubMed:25258363, ECO:0000269|PubMed:7862533}.
Ensembl transtripts involved in fusion geneENST idsENST00000527484, ENST00000300737, 
ENST00000527651, ENST00000533977, 
ENST00000332351, ENST00000379079, 
ENST00000448076, ENST00000530998, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score21 X 13 X 12=32763 X 6 X 5=90
# samples 234
** MAII scorelog2(23/3276*10)=-3.83222959069663
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/90*10)=-1.16992500144231
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: STIM1 [Title/Abstract] AND WT1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: STIM1 [Title/Abstract] AND WT1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)STIM1(4076867)-WT1(32421590), # samples:1
Anticipated loss of major functional domain due to fusion event.STIM1-WT1 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.
STIM1-WT1 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.
STIM1-WT1 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.
STIM1-WT1 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
HgeneSTIM1

GO:0002115

store-operated calcium entry

28219928

HgeneSTIM1

GO:0005513

detection of calcium ion

16005298

HgeneSTIM1

GO:0032237

activation of store-operated calcium channel activity

16005298|26322679|28219928

HgeneSTIM1

GO:0045762

positive regulation of adenylate cyclase activity

19171672

HgeneSTIM1

GO:0051924

regulation of calcium ion transport

16005298

TgeneWT1

GO:0000122

negative regulation of transcription by RNA polymerase II

7585606

TgeneWT1

GO:0007530

sex determination

9815658

TgeneWT1

GO:0008285

negative regulation of cell proliferation

9553041|9765217

TgeneWT1

GO:0030308

negative regulation of cell growth

9553041|9765217

TgeneWT1

GO:0045892

negative regulation of transcription, DNA-templated

1332065|7585606|7720589|8119964|12802290|14701728|19050011

TgeneWT1

GO:0045893

positive regulation of transcription, DNA-templated

8132626|9178767|9553041|9765217|12802290|14701728|16467207|21390327

TgeneWT1

GO:0045944

positive regulation of transcription by RNA polymerase II

23042785

TgeneWT1

GO:0071371

cellular response to gonadotropin stimulus

15961562



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/chr11:4076867/chr11:32421590)
- 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 STIM1 (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 WT1 (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)
ENST00000300737STIM1chr114076867+ENST00000379079WT1chr1132421590-289310665541609351
ENST00000300737STIM1chr114076867+ENST00000332351WT1chr1132421590-290210665541618354
ENST00000300737STIM1chr114076867+ENST00000530998WT1chr1132421590-289910665541618354
ENST00000300737STIM1chr114076867+ENST00000448076WT1chr1132421590-198910665541609351
ENST00000527651STIM1chr114076867+ENST00000379079WT1chr1132421590-2413586741129351
ENST00000527651STIM1chr114076867+ENST00000332351WT1chr1132421590-2422586741138354
ENST00000527651STIM1chr114076867+ENST00000530998WT1chr1132421590-2419586741138354
ENST00000527651STIM1chr114076867+ENST00000448076WT1chr1132421590-1509586741129351

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
ENST00000300737ENST00000379079STIM1chr114076867+WT1chr1132421590-0.002818950.99718106
ENST00000300737ENST00000332351STIM1chr114076867+WT1chr1132421590-0.0025800130.99741995
ENST00000300737ENST00000530998STIM1chr114076867+WT1chr1132421590-0.0026143670.9973857
ENST00000300737ENST00000448076STIM1chr114076867+WT1chr1132421590-0.0232392420.97676075
ENST00000527651ENST00000379079STIM1chr114076867+WT1chr1132421590-0.0013813080.9986187
ENST00000527651ENST00000332351STIM1chr114076867+WT1chr1132421590-0.0013047960.9986952
ENST00000527651ENST00000530998STIM1chr114076867+WT1chr1132421590-0.0013091070.9986909
ENST00000527651ENST00000448076STIM1chr114076867+WT1chr1132421590-0.0086016010.99139833

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 STIM1-WT1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
STIM1chr114076867WT1chr11324215901066170TFRKLQLSGHAMPSHSTGYESDNHTT
STIM1chr114076867WT1chr1132421590586170TFRKLQLSGHAMPSHSTGYESDNHTT

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Potential FusionNeoAntigen Information of STIM1-WT1 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.
STIM1-WT1_4076867_32421590.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)
STIM1-WT1chr114076867chr11324215901066HLA-B35:01MPSHSTGY0.99360.91851119
STIM1-WT1chr114076867chr11324215901066HLA-B35:08MPSHSTGY0.98350.94261119
STIM1-WT1chr114076867chr11324215901066HLA-B35:05MPSHSTGY0.94510.56361119
STIM1-WT1chr114076867chr11324215901066HLA-B15:01AMPSHSTGY0.99860.87381019
STIM1-WT1chr114076867chr11324215901066HLA-B15:25AMPSHSTGY0.97750.89371019
STIM1-WT1chr114076867chr11324215901066HLA-B15:02AMPSHSTGY0.96240.90761019
STIM1-WT1chr114076867chr11324215901066HLA-B39:01GHAMPSHST0.93080.9645817
STIM1-WT1chr114076867chr11324215901066HLA-B39:06GHAMPSHST0.92230.9234817
STIM1-WT1chr114076867chr11324215901066HLA-B15:10GHAMPSHST0.54620.6593817
STIM1-WT1chr114076867chr11324215901066HLA-B15:03AMPSHSTGY0.37190.75721019
STIM1-WT1chr114076867chr11324215901066HLA-B15:01HAMPSHSTGY0.99970.8702919
STIM1-WT1chr114076867chr11324215901066HLA-B15:25HAMPSHSTGY0.99960.892919
STIM1-WT1chr114076867chr11324215901066HLA-B15:02HAMPSHSTGY0.99910.9028919
STIM1-WT1chr114076867chr11324215901066HLA-B35:08HAMPSHSTGY0.99830.8913919
STIM1-WT1chr114076867chr11324215901066HLA-B15:17HAMPSHSTGY0.99770.85919
STIM1-WT1chr114076867chr11324215901066HLA-B35:01HAMPSHSTGY0.99620.8965919
STIM1-WT1chr114076867chr11324215901066HLA-B35:05HAMPSHSTGY0.98520.5584919
STIM1-WT1chr114076867chr11324215901066HLA-B15:03HAMPSHSTGY0.98470.7404919
STIM1-WT1chr114076867chr11324215901066HLA-B15:16HAMPSHSTGY0.97350.8105919
STIM1-WT1chr114076867chr11324215901066HLA-B39:06SGHAMPSHST0.41290.8941717
STIM1-WT1chr114076867chr11324215901066HLA-B15:18GHAMPSHSTGY0.91110.7509819
STIM1-WT1chr114076867chr11324215901066HLA-B15:07AMPSHSTGY0.99090.64541019
STIM1-WT1chr114076867chr11324215901066HLA-B15:21AMPSHSTGY0.96410.8931019
STIM1-WT1chr114076867chr11324215901066HLA-B39:05GHAMPSHST0.88830.9581817
STIM1-WT1chr114076867chr11324215901066HLA-B15:05AMPSHSTGY0.8820.90941019
STIM1-WT1chr114076867chr11324215901066HLA-B15:31AMPSHSTGY0.86270.91641019
STIM1-WT1chr114076867chr11324215901066HLA-B15:04AMPSHSTGY0.81420.88711019
STIM1-WT1chr114076867chr11324215901066HLA-B15:07HAMPSHSTGY0.99930.6654919
STIM1-WT1chr114076867chr11324215901066HLA-B15:21HAMPSHSTGY0.99910.8809919
STIM1-WT1chr114076867chr11324215901066HLA-B15:05HAMPSHSTGY0.99830.8713919
STIM1-WT1chr114076867chr11324215901066HLA-C15:04HAMPSHSTGY0.99670.9307919
STIM1-WT1chr114076867chr11324215901066HLA-B15:31HAMPSHSTGY0.99650.8789919
STIM1-WT1chr114076867chr11324215901066HLA-B15:04HAMPSHSTGY0.9810.8975919
STIM1-WT1chr114076867chr11324215901066HLA-C03:14HAMPSHSTGY0.96330.9814919
STIM1-WT1chr114076867chr11324215901066HLA-C12:12HAMPSHSTGY0.94910.8878919
STIM1-WT1chr114076867chr11324215901066HLA-C12:04HAMPSHSTGY0.9340.9933919
STIM1-WT1chr114076867chr11324215901066HLA-C06:03HAMPSHSTGY0.92970.9885919
STIM1-WT1chr114076867chr11324215901066HLA-B35:23MPSHSTGY0.99370.90111119
STIM1-WT1chr114076867chr11324215901066HLA-B35:77MPSHSTGY0.99360.91851119
STIM1-WT1chr114076867chr11324215901066HLA-B35:11MPSHSTGY0.98570.90361119
STIM1-WT1chr114076867chr11324215901066HLA-B35:24MPSHSTGY0.9790.87031119
STIM1-WT1chr114076867chr11324215901066HLA-B35:30MPSHSTGY0.97330.78551119
STIM1-WT1chr114076867chr11324215901066HLA-B35:17MPSHSTGY0.97330.78551119
STIM1-WT1chr114076867chr11324215901066HLA-B15:08MPSHSTGY0.94590.81051119
STIM1-WT1chr114076867chr11324215901066HLA-B15:11MPSHSTGY0.9450.80041119
STIM1-WT1chr114076867chr11324215901066HLA-B35:43MPSHSTGY0.93490.8151119
STIM1-WT1chr114076867chr11324215901066HLA-B18:07MPSHSTGY0.70740.8591119
STIM1-WT1chr114076867chr11324215901066HLA-B15:27AMPSHSTGY0.99860.89271019
STIM1-WT1chr114076867chr11324215901066HLA-B15:33AMPSHSTGY0.99860.87381019
STIM1-WT1chr114076867chr11324215901066HLA-B15:34AMPSHSTGY0.99860.87381019
STIM1-WT1chr114076867chr11324215901066HLA-B15:125AMPSHSTGY0.99860.87381019
STIM1-WT1chr114076867chr11324215901066HLA-B15:50AMPSHSTGY0.99860.91431019
STIM1-WT1chr114076867chr11324215901066HLA-B15:135AMPSHSTGY0.99850.88481019
STIM1-WT1chr114076867chr11324215901066HLA-B15:12AMPSHSTGY0.9960.89781019
STIM1-WT1chr114076867chr11324215901066HLA-B15:53AMPSHSTGY0.99360.86541019
STIM1-WT1chr114076867chr11324215901066HLA-B15:35AMPSHSTGY0.99260.86031019
STIM1-WT1chr114076867chr11324215901066HLA-B15:39AMPSHSTGY0.97580.80991019
STIM1-WT1chr114076867chr11324215901066HLA-B15:20AMPSHSTGY0.88480.93891019
STIM1-WT1chr114076867chr11324215901066HLA-B15:54AMPSHSTGY0.84990.84121019
STIM1-WT1chr114076867chr11324215901066HLA-B35:28AMPSHSTGY0.82910.93891019
STIM1-WT1chr114076867chr11324215901066HLA-B15:09GHAMPSHST0.58730.9373817
STIM1-WT1chr114076867chr11324215901066HLA-B39:11GHAMPSHST0.42050.9367817
STIM1-WT1chr114076867chr11324215901066HLA-B15:68AMPSHSTGY0.32860.61251019
STIM1-WT1chr114076867chr11324215901066HLA-C14:02AMPSHSTGY0.01250.97241019
STIM1-WT1chr114076867chr11324215901066HLA-C14:03AMPSHSTGY0.01250.97241019
STIM1-WT1chr114076867chr11324215901066HLA-B15:33HAMPSHSTGY0.99970.8702919
STIM1-WT1chr114076867chr11324215901066HLA-B15:34HAMPSHSTGY0.99970.8702919
STIM1-WT1chr114076867chr11324215901066HLA-B15:125HAMPSHSTGY0.99970.8702919
STIM1-WT1chr114076867chr11324215901066HLA-B15:27HAMPSHSTGY0.99970.9037919
STIM1-WT1chr114076867chr11324215901066HLA-B15:135HAMPSHSTGY0.99970.8867919
STIM1-WT1chr114076867chr11324215901066HLA-B15:08HAMPSHSTGY0.99960.833919
STIM1-WT1chr114076867chr11324215901066HLA-B15:53HAMPSHSTGY0.99960.8586919
STIM1-WT1chr114076867chr11324215901066HLA-B15:11HAMPSHSTGY0.99960.8362919
STIM1-WT1chr114076867chr11324215901066HLA-B35:43HAMPSHSTGY0.99950.8321919
STIM1-WT1chr114076867chr11324215901066HLA-B15:39HAMPSHSTGY0.99950.8091919
STIM1-WT1chr114076867chr11324215901066HLA-B15:50HAMPSHSTGY0.99940.904919
STIM1-WT1chr114076867chr11324215901066HLA-B35:11HAMPSHSTGY0.99920.871919
STIM1-WT1chr114076867chr11324215901066HLA-B15:35HAMPSHSTGY0.99910.8875919
STIM1-WT1chr114076867chr11324215901066HLA-B15:24HAMPSHSTGY0.99870.931919
STIM1-WT1chr114076867chr11324215901066HLA-B15:12HAMPSHSTGY0.99850.7752919
STIM1-WT1chr114076867chr11324215901066HLA-B15:20HAMPSHSTGY0.99840.9214919
STIM1-WT1chr114076867chr11324215901066HLA-B57:04HAMPSHSTGY0.9980.9013919
STIM1-WT1chr114076867chr11324215901066HLA-C03:02HAMPSHSTGY0.99730.9674919
STIM1-WT1chr114076867chr11324215901066HLA-B35:28HAMPSHSTGY0.99710.9244919
STIM1-WT1chr114076867chr11324215901066HLA-C15:09HAMPSHSTGY0.99670.9307919
STIM1-WT1chr114076867chr11324215901066HLA-B35:77HAMPSHSTGY0.99620.8965919
STIM1-WT1chr114076867chr11324215901066HLA-B35:20HAMPSHSTGY0.99610.9275919
STIM1-WT1chr114076867chr11324215901066HLA-B35:23HAMPSHSTGY0.99570.913919
STIM1-WT1chr114076867chr11324215901066HLA-B35:17HAMPSHSTGY0.99260.7802919
STIM1-WT1chr114076867chr11324215901066HLA-B35:30HAMPSHSTGY0.99260.7802919
STIM1-WT1chr114076867chr11324215901066HLA-B58:06HAMPSHSTGY0.99110.9191919
STIM1-WT1chr114076867chr11324215901066HLA-B15:13HAMPSHSTGY0.99020.7223919
STIM1-WT1chr114076867chr11324215901066HLA-B15:54HAMPSHSTGY0.98950.8321919
STIM1-WT1chr114076867chr11324215901066HLA-C12:02HAMPSHSTGY0.97530.9696919
STIM1-WT1chr114076867chr11324215901066HLA-C16:04HAMPSHSTGY0.97510.9743919
STIM1-WT1chr114076867chr11324215901066HLA-C02:02HAMPSHSTGY0.9620.9855919
STIM1-WT1chr114076867chr11324215901066HLA-C02:10HAMPSHSTGY0.9620.9855919
STIM1-WT1chr114076867chr11324215901066HLA-B35:24HAMPSHSTGY0.95420.895919
STIM1-WT1chr114076867chr11324215901066HLA-A25:01HAMPSHSTGY0.95290.9316919
STIM1-WT1chr114076867chr11324215901066HLA-C12:03HAMPSHSTGY0.94140.9672919
STIM1-WT1chr114076867chr11324215901066HLA-C16:01HAMPSHSTGY0.90650.9811919
STIM1-WT1chr114076867chr11324215901066HLA-C16:02HAMPSHSTGY0.89640.9939919
STIM1-WT1chr114076867chr11324215901066HLA-B18:04HAMPSHSTGY0.63560.9238919

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Potential FusionNeoAntigen Information of STIM1-WT1 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 STIM1-WT1

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
5624LSGHAMPSHSTGYESTIM1WT1chr114076867chr11324215901066

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of STIM1-WT1

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-B14:023BVN5624LSGHAMPSHSTGYE-6.66111-6.77451
HLA-B14:023BVN5624LSGHAMPSHSTGYE-6.49216-7.52746
HLA-B52:013W395624LSGHAMPSHSTGYE-5.57342-5.68682
HLA-B52:013W395624LSGHAMPSHSTGYE-3.59959-4.63489
HLA-A11:014UQ25624LSGHAMPSHSTGYE-3.54213-3.65553
HLA-A24:025HGA5624LSGHAMPSHSTGYE-7.6647-7.7781
HLA-A24:025HGA5624LSGHAMPSHSTGYE-4.05482-5.09012
HLA-B44:053DX85624LSGHAMPSHSTGYE-5.24587-5.35927
HLA-B44:053DX85624LSGHAMPSHSTGYE-4.91507-5.95037
HLA-A02:016TDR5624LSGHAMPSHSTGYE-3.67735-4.71265

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Vaccine Design for the FusionNeoAntigens of STIM1-WT1

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
STIM1-WT1chr114076867chr11324215901019AMPSHSTGYCATGCCAAGCCACAGCACAGGGTACGA
STIM1-WT1chr114076867chr11324215901119MPSHSTGYGCCAAGCCACAGCACAGGGTACGA
STIM1-WT1chr114076867chr1132421590717SGHAMPSHSTTGGCCATGCCATGCCAAGCCACAGCACAGG
STIM1-WT1chr114076867chr1132421590817GHAMPSHSTCCATGCCATGCCAAGCCACAGCACAGG
STIM1-WT1chr114076867chr1132421590819GHAMPSHSTGYCCATGCCATGCCAAGCCACAGCACAGGGTACGA
STIM1-WT1chr114076867chr1132421590919HAMPSHSTGYTGCCATGCCAAGCCACAGCACAGGGTACGA

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 STIM1-WT1

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
OVSTIM1-WT1chr114076867ENST00000300737chr1132421590ENST00000332351TCGA-23-1028

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Potential target of CAR-T therapy development for STIM1-WT1

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 STIM1-WT1

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 STIM1-WT1

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
TgeneWT1C0950121Denys-Drash Syndrome20CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
TgeneWT1C0027708Nephroblastoma8CGI;CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
TgeneWT1C3151568NEPHROTIC SYNDROME, TYPE 46CTD_human;GENOMICS_ENGLAND;UNIPROT
TgeneWT1C0950122Frasier Syndrome4CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
TgeneWT1C1837026MEACHAM SYNDROME (disorder)3CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
TgeneWT1C0023467Leukemia, Myelocytic, Acute2CGI;CTD_human
TgeneWT1C0026998Acute Myeloid Leukemia, M12CTD_human
TgeneWT1C0345967Malignant mesothelioma2CTD_human;GENOMICS_ENGLAND
TgeneWT1C1879321Acute Myeloid Leukemia (AML-M2)2CTD_human
TgeneWT1C2930471Bilateral Wilms Tumor2CTD_human
TgeneWT1C0006142Malignant neoplasm of breast1CTD_human
TgeneWT1C0007102Malignant tumor of colon1CTD_human
TgeneWT1C0009375Colonic Neoplasms1CTD_human
TgeneWT1C0017636Glioblastoma1CTD_human
TgeneWT1C0017658Glomerulonephritis1CTD_human
TgeneWT1C0018054Gonadal Dysgenesis, 46,XY1ORPHANET
TgeneWT1C0019284Diaphragmatic Hernia1CTD_human
TgeneWT1C0023418leukemia1CTD_human
TgeneWT1C0023473Myeloid Leukemia, Chronic1CTD_human
TgeneWT1C0023487Acute Promyelocytic Leukemia1CTD_human
TgeneWT1C0024121Lung Neoplasms1CTD_human
TgeneWT1C0027809Neurilemmoma1CTD_human
TgeneWT1C0029463Osteosarcoma1CTD_human
TgeneWT1C0030297Pancreatic Neoplasm1CTD_human
TgeneWT1C0031149Peritoneal Neoplasms1CTD_human
TgeneWT1C0085215Ovarian Failure, Premature1CTD_human
TgeneWT1C0086367Gonadotropin-Resistant Ovary Syndrome1CTD_human
TgeneWT1C0206115WAGR Syndrome1CTD_human;GENOMICS_ENGLAND;ORPHANET
TgeneWT1C0235833Congenital diaphragmatic hernia1CTD_human
TgeneWT1C0242379Malignant neoplasm of lung1CTD_human
TgeneWT1C0265699Congenital hernia of foramen of Morgagni1CTD_human
TgeneWT1C0265700Congenital hernia of foramen of Bochdalek1CTD_human
TgeneWT1C0334588Giant Cell Glioblastoma1CTD_human
TgeneWT1C0346647Malignant neoplasm of pancreas1CTD_human
TgeneWT1C0346990Carcinomatosis of peritoneal cavity1CTD_human
TgeneWT1C0678222Breast Carcinoma1CTD_human
TgeneWT1C0751374Schwannomatosis, Plexiform1CTD_human
TgeneWT1C1257931Mammary Neoplasms, Human1CTD_human
TgeneWT1C1458155Mammary Neoplasms1CTD_human
TgeneWT1C1621958Glioblastoma Multiforme1CTD_human
TgeneWT1C1704377Bright Disease1CTD_human
TgeneWT1C1840452Hyaloideoretinal degeneration of Wagner1GENOMICS_ENGLAND
TgeneWT1C1868672NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE1ORPHANET
TgeneWT1C2931803Deletion 11p131ORPHANET
TgeneWT1C2936694Swyer Syndrome1ORPHANET
TgeneWT1C3494522Hypergonadotropic Ovarian Failure, X-Linked1CTD_human
TgeneWT1C451074446,XY partial gonadal dysgenesis1ORPHANET
TgeneWT1C4552079Premature Ovarian Failure 11CTD_human
TgeneWT1C4704874Mammary Carcinoma, Human1CTD_human