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Fusion Protein:STIM1-WT1 |
Fusion Gene and Fusion Protein Summary |
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Fusion partner gene information | Fusion gene name: STIM1-WT1 | FusionPDB ID: 87410 | FusionGDB2.0 ID: 87410 | Hgene | Tgene | Gene symbol | STIM1 | WT1 | Gene ID | 6786 | 7490 |
Gene name | stromal interaction molecule 1 | WT1 transcription factor | |
Synonyms | D11S4896E|GOK|IMD10|STRMK|TAM|TAM1 | AWT1|GUD|NPHS4|WAGR|WIT-2|WT33 | |
Cytomap | 11p15.4 | 11p13 | |
Type of gene | protein-coding | protein-coding | |
Description | stromal interaction molecule 1 | Wilms tumor proteinWilms tumor 1 | |
Modification date | 20200329 | 20200320 | |
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 gene | ENST ids | ENST00000527484, ENST00000300737, ENST00000527651, ENST00000533977, | ENST00000332351, ENST00000379079, ENST00000448076, ENST00000530998, |
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0) | * DoF score | 21 X 13 X 12=3276 | 3 X 6 X 5=90 |
# samples | 23 | 4 | |
** MAII score | log2(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) |
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Partner | Gene | GO ID | GO term | PubMed ID |
Hgene | STIM1 | GO:0002115 | store-operated calcium entry | 28219928 |
Hgene | STIM1 | GO:0005513 | detection of calcium ion | 16005298 |
Hgene | STIM1 | GO:0032237 | activation of store-operated calcium channel activity | 16005298|26322679|28219928 |
Hgene | STIM1 | GO:0045762 | positive regulation of adenylate cyclase activity | 19171672 |
Hgene | STIM1 | GO:0051924 | regulation of calcium ion transport | 16005298 |
Tgene | WT1 | GO:0000122 | negative regulation of transcription by RNA polymerase II | 7585606 |
Tgene | WT1 | GO:0007530 | sex determination | 9815658 |
Tgene | WT1 | GO:0008285 | negative regulation of cell proliferation | 9553041|9765217 |
Tgene | WT1 | GO:0030308 | negative regulation of cell growth | 9553041|9765217 |
Tgene | WT1 | GO:0045892 | negative regulation of transcription, DNA-templated | 1332065|7585606|7720589|8119964|12802290|14701728|19050011 |
Tgene | WT1 | GO:0045893 | positive regulation of transcription, DNA-templated | 8132626|9178767|9553041|9765217|12802290|14701728|16467207|21390327 |
Tgene | WT1 | GO:0045944 | positive regulation of transcription by RNA polymerase II | 23042785 |
Tgene | WT1 | GO:0071371 | cellular response to gonadotropin stimulus | 15961562 |
![]() 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. |
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![]() * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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![]() * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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Fusion Amino Acid Sequences |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | Seq length (transcript) | BP loci (transcript) | Predicted start (transcript) | Predicted stop (transcript) | Seq length (amino acids) |
ENST00000300737 | STIM1 | chr11 | 4076867 | + | ENST00000379079 | WT1 | chr11 | 32421590 | - | 2893 | 1066 | 554 | 1609 | 351 |
ENST00000300737 | STIM1 | chr11 | 4076867 | + | ENST00000332351 | WT1 | chr11 | 32421590 | - | 2902 | 1066 | 554 | 1618 | 354 |
ENST00000300737 | STIM1 | chr11 | 4076867 | + | ENST00000530998 | WT1 | chr11 | 32421590 | - | 2899 | 1066 | 554 | 1618 | 354 |
ENST00000300737 | STIM1 | chr11 | 4076867 | + | ENST00000448076 | WT1 | chr11 | 32421590 | - | 1989 | 1066 | 554 | 1609 | 351 |
ENST00000527651 | STIM1 | chr11 | 4076867 | + | ENST00000379079 | WT1 | chr11 | 32421590 | - | 2413 | 586 | 74 | 1129 | 351 |
ENST00000527651 | STIM1 | chr11 | 4076867 | + | ENST00000332351 | WT1 | chr11 | 32421590 | - | 2422 | 586 | 74 | 1138 | 354 |
ENST00000527651 | STIM1 | chr11 | 4076867 | + | ENST00000530998 | WT1 | chr11 | 32421590 | - | 2419 | 586 | 74 | 1138 | 354 |
ENST00000527651 | STIM1 | chr11 | 4076867 | + | ENST00000448076 | WT1 | chr11 | 32421590 | - | 1509 | 586 | 74 | 1129 | 351 |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
ENST00000300737 | ENST00000379079 | STIM1 | chr11 | 4076867 | + | WT1 | chr11 | 32421590 | - | 0.00281895 | 0.99718106 |
ENST00000300737 | ENST00000332351 | STIM1 | chr11 | 4076867 | + | WT1 | chr11 | 32421590 | - | 0.002580013 | 0.99741995 |
ENST00000300737 | ENST00000530998 | STIM1 | chr11 | 4076867 | + | WT1 | chr11 | 32421590 | - | 0.002614367 | 0.9973857 |
ENST00000300737 | ENST00000448076 | STIM1 | chr11 | 4076867 | + | WT1 | chr11 | 32421590 | - | 0.023239242 | 0.97676075 |
ENST00000527651 | ENST00000379079 | STIM1 | chr11 | 4076867 | + | WT1 | chr11 | 32421590 | - | 0.001381308 | 0.9986187 |
ENST00000527651 | ENST00000332351 | STIM1 | chr11 | 4076867 | + | WT1 | chr11 | 32421590 | - | 0.001304796 | 0.9986952 |
ENST00000527651 | ENST00000530998 | STIM1 | chr11 | 4076867 | + | WT1 | chr11 | 32421590 | - | 0.001309107 | 0.9986909 |
ENST00000527651 | ENST00000448076 | STIM1 | chr11 | 4076867 | + | WT1 | chr11 | 32421590 | - | 0.008601601 | 0.99139833 |
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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 |
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Hgene | Hchr | Hbp | Tgene | Tchr | Tbp | Length(fusion protein) | BP in fusion protein | Peptide |
STIM1 | chr11 | 4076867 | WT1 | chr11 | 32421590 | 1066 | 170 | TFRKLQLSGHAMPSHSTGYESDNHTT |
STIM1 | chr11 | 4076867 | WT1 | chr11 | 32421590 | 586 | 170 | TFRKLQLSGHAMPSHSTGYESDNHTT |
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Potential FusionNeoAntigen Information of STIM1-WT1 in HLA I |
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STIM1-WT1_4076867_32421590.msa |
![]() * We used NetMHCpan v4.1 (%rank<0.5) and deepHLApan v1.1 (immunogenic score>0.5) |
Fusion gene | Hchr | Hbp | Tgene | Tchr | Tbp | HLA I | FusionNeoAntigen peptide | Binding score | Immunogenic score | Neoantigen start (at BP 13) | Neoantigen end (at BP 13) |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B35:01 | MPSHSTGY | 0.9936 | 0.9185 | 11 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B35:08 | MPSHSTGY | 0.9835 | 0.9426 | 11 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B35:05 | MPSHSTGY | 0.9451 | 0.5636 | 11 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:01 | AMPSHSTGY | 0.9986 | 0.8738 | 10 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:25 | AMPSHSTGY | 0.9775 | 0.8937 | 10 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:02 | AMPSHSTGY | 0.9624 | 0.9076 | 10 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B39:01 | GHAMPSHST | 0.9308 | 0.9645 | 8 | 17 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B39:06 | GHAMPSHST | 0.9223 | 0.9234 | 8 | 17 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:10 | GHAMPSHST | 0.5462 | 0.6593 | 8 | 17 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:03 | AMPSHSTGY | 0.3719 | 0.7572 | 10 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:01 | HAMPSHSTGY | 0.9997 | 0.8702 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:25 | HAMPSHSTGY | 0.9996 | 0.892 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:02 | HAMPSHSTGY | 0.9991 | 0.9028 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B35:08 | HAMPSHSTGY | 0.9983 | 0.8913 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:17 | HAMPSHSTGY | 0.9977 | 0.85 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B35:01 | HAMPSHSTGY | 0.9962 | 0.8965 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B35:05 | HAMPSHSTGY | 0.9852 | 0.5584 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:03 | HAMPSHSTGY | 0.9847 | 0.7404 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:16 | HAMPSHSTGY | 0.9735 | 0.8105 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B39:06 | SGHAMPSHST | 0.4129 | 0.8941 | 7 | 17 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:18 | GHAMPSHSTGY | 0.9111 | 0.7509 | 8 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:07 | AMPSHSTGY | 0.9909 | 0.6454 | 10 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:21 | AMPSHSTGY | 0.9641 | 0.893 | 10 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B39:05 | GHAMPSHST | 0.8883 | 0.9581 | 8 | 17 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:05 | AMPSHSTGY | 0.882 | 0.9094 | 10 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:31 | AMPSHSTGY | 0.8627 | 0.9164 | 10 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:04 | AMPSHSTGY | 0.8142 | 0.8871 | 10 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:07 | HAMPSHSTGY | 0.9993 | 0.6654 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:21 | HAMPSHSTGY | 0.9991 | 0.8809 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:05 | HAMPSHSTGY | 0.9983 | 0.8713 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-C15:04 | HAMPSHSTGY | 0.9967 | 0.9307 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:31 | HAMPSHSTGY | 0.9965 | 0.8789 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:04 | HAMPSHSTGY | 0.981 | 0.8975 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-C03:14 | HAMPSHSTGY | 0.9633 | 0.9814 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-C12:12 | HAMPSHSTGY | 0.9491 | 0.8878 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-C12:04 | HAMPSHSTGY | 0.934 | 0.9933 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-C06:03 | HAMPSHSTGY | 0.9297 | 0.9885 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B35:23 | MPSHSTGY | 0.9937 | 0.9011 | 11 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B35:77 | MPSHSTGY | 0.9936 | 0.9185 | 11 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B35:11 | MPSHSTGY | 0.9857 | 0.9036 | 11 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B35:24 | MPSHSTGY | 0.979 | 0.8703 | 11 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B35:30 | MPSHSTGY | 0.9733 | 0.7855 | 11 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B35:17 | MPSHSTGY | 0.9733 | 0.7855 | 11 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:08 | MPSHSTGY | 0.9459 | 0.8105 | 11 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:11 | MPSHSTGY | 0.945 | 0.8004 | 11 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B35:43 | MPSHSTGY | 0.9349 | 0.815 | 11 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B18:07 | MPSHSTGY | 0.7074 | 0.859 | 11 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:27 | AMPSHSTGY | 0.9986 | 0.8927 | 10 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:33 | AMPSHSTGY | 0.9986 | 0.8738 | 10 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:34 | AMPSHSTGY | 0.9986 | 0.8738 | 10 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:125 | AMPSHSTGY | 0.9986 | 0.8738 | 10 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:50 | AMPSHSTGY | 0.9986 | 0.9143 | 10 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:135 | AMPSHSTGY | 0.9985 | 0.8848 | 10 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:12 | AMPSHSTGY | 0.996 | 0.8978 | 10 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:53 | AMPSHSTGY | 0.9936 | 0.8654 | 10 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:35 | AMPSHSTGY | 0.9926 | 0.8603 | 10 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:39 | AMPSHSTGY | 0.9758 | 0.8099 | 10 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:20 | AMPSHSTGY | 0.8848 | 0.9389 | 10 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:54 | AMPSHSTGY | 0.8499 | 0.8412 | 10 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B35:28 | AMPSHSTGY | 0.8291 | 0.9389 | 10 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:09 | GHAMPSHST | 0.5873 | 0.9373 | 8 | 17 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B39:11 | GHAMPSHST | 0.4205 | 0.9367 | 8 | 17 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:68 | AMPSHSTGY | 0.3286 | 0.6125 | 10 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-C14:02 | AMPSHSTGY | 0.0125 | 0.9724 | 10 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-C14:03 | AMPSHSTGY | 0.0125 | 0.9724 | 10 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:33 | HAMPSHSTGY | 0.9997 | 0.8702 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:34 | HAMPSHSTGY | 0.9997 | 0.8702 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:125 | HAMPSHSTGY | 0.9997 | 0.8702 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:27 | HAMPSHSTGY | 0.9997 | 0.9037 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:135 | HAMPSHSTGY | 0.9997 | 0.8867 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:08 | HAMPSHSTGY | 0.9996 | 0.833 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:53 | HAMPSHSTGY | 0.9996 | 0.8586 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:11 | HAMPSHSTGY | 0.9996 | 0.8362 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B35:43 | HAMPSHSTGY | 0.9995 | 0.8321 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:39 | HAMPSHSTGY | 0.9995 | 0.8091 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:50 | HAMPSHSTGY | 0.9994 | 0.904 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B35:11 | HAMPSHSTGY | 0.9992 | 0.871 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:35 | HAMPSHSTGY | 0.9991 | 0.8875 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:24 | HAMPSHSTGY | 0.9987 | 0.931 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:12 | HAMPSHSTGY | 0.9985 | 0.7752 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:20 | HAMPSHSTGY | 0.9984 | 0.9214 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B57:04 | HAMPSHSTGY | 0.998 | 0.9013 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-C03:02 | HAMPSHSTGY | 0.9973 | 0.9674 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B35:28 | HAMPSHSTGY | 0.9971 | 0.9244 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-C15:09 | HAMPSHSTGY | 0.9967 | 0.9307 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B35:77 | HAMPSHSTGY | 0.9962 | 0.8965 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B35:20 | HAMPSHSTGY | 0.9961 | 0.9275 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B35:23 | HAMPSHSTGY | 0.9957 | 0.913 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B35:17 | HAMPSHSTGY | 0.9926 | 0.7802 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B35:30 | HAMPSHSTGY | 0.9926 | 0.7802 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B58:06 | HAMPSHSTGY | 0.9911 | 0.9191 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:13 | HAMPSHSTGY | 0.9902 | 0.7223 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B15:54 | HAMPSHSTGY | 0.9895 | 0.8321 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-C12:02 | HAMPSHSTGY | 0.9753 | 0.9696 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-C16:04 | HAMPSHSTGY | 0.9751 | 0.9743 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-C02:02 | HAMPSHSTGY | 0.962 | 0.9855 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-C02:10 | HAMPSHSTGY | 0.962 | 0.9855 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B35:24 | HAMPSHSTGY | 0.9542 | 0.895 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-A25:01 | HAMPSHSTGY | 0.9529 | 0.9316 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-C12:03 | HAMPSHSTGY | 0.9414 | 0.9672 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-C16:01 | HAMPSHSTGY | 0.9065 | 0.9811 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-C16:02 | HAMPSHSTGY | 0.8964 | 0.9939 | 9 | 19 |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 | HLA-B18:04 | HAMPSHSTGY | 0.6356 | 0.9238 | 9 | 19 |
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Potential FusionNeoAntigen Information of STIM1-WT1 in HLA II |
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![]() * We used NetMHCIIpan v4.1 (%rank<0.5). |
Fusion gene | Hchr | Hbp | Tgene | Tchr | Tbp | HLA II | FusionNeoAntigen peptide | Neoantigen start (at BP 13) | Neoantigen end (at BP 13) |
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Fusion breakpoint peptide structures of STIM1-WT1 |
![]() * 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 name | BPseq | Hgene | Tgene | Hchr | Hbp | Tchr | Tbp | AAlen |
5624 | LSGHAMPSHSTGYE | STIM1 | WT1 | chr11 | 4076867 | chr11 | 32421590 | 1066 |
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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of STIM1-WT1 |
![]() * We used Glide to predict the interaction between HLAs and neoantigens. |
HLA allele | PDB ID | File name | BPseq | Docking score | Glide score |
HLA-B14:02 | 3BVN | 5624 | LSGHAMPSHSTGYE | -6.66111 | -6.77451 |
HLA-B14:02 | 3BVN | 5624 | LSGHAMPSHSTGYE | -6.49216 | -7.52746 |
HLA-B52:01 | 3W39 | 5624 | LSGHAMPSHSTGYE | -5.57342 | -5.68682 |
HLA-B52:01 | 3W39 | 5624 | LSGHAMPSHSTGYE | -3.59959 | -4.63489 |
HLA-A11:01 | 4UQ2 | 5624 | LSGHAMPSHSTGYE | -3.54213 | -3.65553 |
HLA-A24:02 | 5HGA | 5624 | LSGHAMPSHSTGYE | -7.6647 | -7.7781 |
HLA-A24:02 | 5HGA | 5624 | LSGHAMPSHSTGYE | -4.05482 | -5.09012 |
HLA-B44:05 | 3DX8 | 5624 | LSGHAMPSHSTGYE | -5.24587 | -5.35927 |
HLA-B44:05 | 3DX8 | 5624 | LSGHAMPSHSTGYE | -4.91507 | -5.95037 |
HLA-A02:01 | 6TDR | 5624 | LSGHAMPSHSTGYE | -3.67735 | -4.71265 |
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Vaccine Design for the FusionNeoAntigens of STIM1-WT1 |
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Fusion gene | Hchr | Hbp | Tchr | Tbp | Start in +/-13AA | End in +/-13AA | FusionNeoAntigen peptide sequence | FusionNeoAntigen RNA sequence |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 10 | 19 | AMPSHSTGY | CATGCCAAGCCACAGCACAGGGTACGA |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 11 | 19 | MPSHSTGY | GCCAAGCCACAGCACAGGGTACGA |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 7 | 17 | SGHAMPSHST | TGGCCATGCCATGCCAAGCCACAGCACAGG |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 8 | 17 | GHAMPSHST | CCATGCCATGCCAAGCCACAGCACAGG |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 8 | 19 | GHAMPSHSTGY | CCATGCCATGCCAAGCCACAGCACAGGGTACGA |
STIM1-WT1 | chr11 | 4076867 | chr11 | 32421590 | 9 | 19 | HAMPSHSTGY | TGCCATGCCAAGCCACAGCACAGGGTACGA |
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Fusion gene | Hchr | Hbp | Tchr | Tbp | Start in +/-13AA | End in +/-13AA | FusionNeoAntigen peptide | FusionNEoAntigen RNA sequence |
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Information of the samples that have these potential fusion neoantigens of STIM1-WT1 |
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Cancer type | Fusion gene | Hchr | Hbp | Henst | Tchr | Tbp | Tenst | Sample |
OV | STIM1-WT1 | chr11 | 4076867 | ENST00000300737 | chr11 | 32421590 | ENST00000332351 | TCGA-23-1028 |
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Potential target of CAR-T therapy development for STIM1-WT1 |
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![]() * Minus value of BPloci means that the break point is located before the CDS. |
- In-frame and retained 'Transmembrane'. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
![]() * 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. |
Hgene | Hchr | Hbp | Henst | Tgene | Tchr | Tbp | Tenst | DeepLoc result |
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Related Drugs to STIM1-WT1 |
![]() (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Drug | Source | PMID |
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Related Diseases to STIM1-WT1 |
![]() (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Disease | Source | PMID |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Tgene | WT1 | C0950121 | Denys-Drash Syndrome | 20 | CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT |
Tgene | WT1 | C0027708 | Nephroblastoma | 8 | CGI;CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT |
Tgene | WT1 | C3151568 | NEPHROTIC SYNDROME, TYPE 4 | 6 | CTD_human;GENOMICS_ENGLAND;UNIPROT |
Tgene | WT1 | C0950122 | Frasier Syndrome | 4 | CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT |
Tgene | WT1 | C1837026 | MEACHAM SYNDROME (disorder) | 3 | CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT |
Tgene | WT1 | C0023467 | Leukemia, Myelocytic, Acute | 2 | CGI;CTD_human |
Tgene | WT1 | C0026998 | Acute Myeloid Leukemia, M1 | 2 | CTD_human |
Tgene | WT1 | C0345967 | Malignant mesothelioma | 2 | CTD_human;GENOMICS_ENGLAND |
Tgene | WT1 | C1879321 | Acute Myeloid Leukemia (AML-M2) | 2 | CTD_human |
Tgene | WT1 | C2930471 | Bilateral Wilms Tumor | 2 | CTD_human |
Tgene | WT1 | C0006142 | Malignant neoplasm of breast | 1 | CTD_human |
Tgene | WT1 | C0007102 | Malignant tumor of colon | 1 | CTD_human |
Tgene | WT1 | C0009375 | Colonic Neoplasms | 1 | CTD_human |
Tgene | WT1 | C0017636 | Glioblastoma | 1 | CTD_human |
Tgene | WT1 | C0017658 | Glomerulonephritis | 1 | CTD_human |
Tgene | WT1 | C0018054 | Gonadal Dysgenesis, 46,XY | 1 | ORPHANET |
Tgene | WT1 | C0019284 | Diaphragmatic Hernia | 1 | CTD_human |
Tgene | WT1 | C0023418 | leukemia | 1 | CTD_human |
Tgene | WT1 | C0023473 | Myeloid Leukemia, Chronic | 1 | CTD_human |
Tgene | WT1 | C0023487 | Acute Promyelocytic Leukemia | 1 | CTD_human |
Tgene | WT1 | C0024121 | Lung Neoplasms | 1 | CTD_human |
Tgene | WT1 | C0027809 | Neurilemmoma | 1 | CTD_human |
Tgene | WT1 | C0029463 | Osteosarcoma | 1 | CTD_human |
Tgene | WT1 | C0030297 | Pancreatic Neoplasm | 1 | CTD_human |
Tgene | WT1 | C0031149 | Peritoneal Neoplasms | 1 | CTD_human |
Tgene | WT1 | C0085215 | Ovarian Failure, Premature | 1 | CTD_human |
Tgene | WT1 | C0086367 | Gonadotropin-Resistant Ovary Syndrome | 1 | CTD_human |
Tgene | WT1 | C0206115 | WAGR Syndrome | 1 | CTD_human;GENOMICS_ENGLAND;ORPHANET |
Tgene | WT1 | C0235833 | Congenital diaphragmatic hernia | 1 | CTD_human |
Tgene | WT1 | C0242379 | Malignant neoplasm of lung | 1 | CTD_human |
Tgene | WT1 | C0265699 | Congenital hernia of foramen of Morgagni | 1 | CTD_human |
Tgene | WT1 | C0265700 | Congenital hernia of foramen of Bochdalek | 1 | CTD_human |
Tgene | WT1 | C0334588 | Giant Cell Glioblastoma | 1 | CTD_human |
Tgene | WT1 | C0346647 | Malignant neoplasm of pancreas | 1 | CTD_human |
Tgene | WT1 | C0346990 | Carcinomatosis of peritoneal cavity | 1 | CTD_human |
Tgene | WT1 | C0678222 | Breast Carcinoma | 1 | CTD_human |
Tgene | WT1 | C0751374 | Schwannomatosis, Plexiform | 1 | CTD_human |
Tgene | WT1 | C1257931 | Mammary Neoplasms, Human | 1 | CTD_human |
Tgene | WT1 | C1458155 | Mammary Neoplasms | 1 | CTD_human |
Tgene | WT1 | C1621958 | Glioblastoma Multiforme | 1 | CTD_human |
Tgene | WT1 | C1704377 | Bright Disease | 1 | CTD_human |
Tgene | WT1 | C1840452 | Hyaloideoretinal degeneration of Wagner | 1 | GENOMICS_ENGLAND |
Tgene | WT1 | C1868672 | NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE | 1 | ORPHANET |
Tgene | WT1 | C2931803 | Deletion 11p13 | 1 | ORPHANET |
Tgene | WT1 | C2936694 | Swyer Syndrome | 1 | ORPHANET |
Tgene | WT1 | C3494522 | Hypergonadotropic Ovarian Failure, X-Linked | 1 | CTD_human |
Tgene | WT1 | C4510744 | 46,XY partial gonadal dysgenesis | 1 | ORPHANET |
Tgene | WT1 | C4552079 | Premature Ovarian Failure 1 | 1 | CTD_human |
Tgene | WT1 | C4704874 | Mammary Carcinoma, Human | 1 | CTD_human |