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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:CELSR1-STK24

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CELSR1-STK24
FusionPDB ID: 15660
FusionGDB2.0 ID: 15660
HgeneTgene
Gene symbol

CELSR1

STK24

Gene ID

9620

8428

Gene namecadherin EGF LAG seven-pass G-type receptor 1serine/threonine kinase 24
SynonymsADGRC1|CDHF9|FMI2|HFMI2|ME2HEL-S-95|MST3|MST3B|STE20|STK3
Cytomap

22q13.31

13q32.2

Type of geneprotein-codingprotein-coding
Descriptioncadherin EGF LAG seven-pass G-type receptor 1adhesion G protein-coupled receptor C1cadherin family member 9cadherin, EGF LAG seven-pass G-type receptor 1 (flamingo homolog, Drosophila)flamingo homolog 2protocadherin flamingo 2serine/threonine-protein kinase 24STE20-like kinase 3STE20-like kinase MST3epididymis secretory protein Li 95mammalian STE20-like protein kinase 3serine/threonine kinase 24 (STE20 homolog, yeast)sterile 20-like kinase 3
Modification date2020032220200313
UniProtAcc

Q9NYQ6

Main function of 5'-partner protein: FUNCTION: Receptor that may have an important role in cell/cell signaling during nervous system formation.
.
Ensembl transtripts involved in fusion geneENST idsENST00000262738, ENST00000395964, 
ENST00000497509, 
ENST00000376547, 
ENST00000481288, ENST00000397517, 
ENST00000539966, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score23 X 19 X 11=480715 X 8 X 8=960
# samples 2818
** MAII scorelog2(28/4807*10)=-4.10163807119293
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(18/960*10)=-2.41503749927884
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: CELSR1 [Title/Abstract] AND STK24 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: CELSR1 [Title/Abstract] AND STK24 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CELSR1(46829289)-STK24(99127612), # samples:1
Anticipated loss of major functional domain due to fusion event.CELSR1-STK24 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.
CELSR1-STK24 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.
CELSR1-STK24 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.
CELSR1-STK24 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
TgeneSTK24

GO:0006468

protein phosphorylation

19604147

TgeneSTK24

GO:0042542

response to hydrogen peroxide

22291017

TgeneSTK24

GO:0046777

protein autophosphorylation

17046825|17657516



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/chr22:46829289/chr13:99127612)
- 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 CELSR1 (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 STK24 (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)
ENST00000262738CELSR1chr2246829289-ENST00000397517STK24chr1399127612-85494611055761858
ENST00000262738CELSR1chr2246829289-ENST00000539966STK24chr1399127612-58354611055761858

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
ENST00000262738ENST00000397517CELSR1chr2246829289-STK24chr1399127612-0.0004597380.9995403
ENST00000262738ENST00000539966CELSR1chr2246829289-STK24chr1399127612-0.0015374770.99846256

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 CELSR1-STK24

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
CELSR1chr2246829289STK24chr139912761246111537GRWHSVQVQYYNKLEPGPLDETQIAT

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Potential FusionNeoAntigen Information of CELSR1-STK24 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.
CELSR1-STK24_46829289_99127612.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)
CELSR1-STK24chr2246829289chr13991276124611HLA-B13:01VQVQYYNKL0.57250.7583514
CELSR1-STK24chr2246829289chr13991276124611HLA-B39:13VQVQYYNKL0.34310.6278514
CELSR1-STK24chr2246829289chr13991276124611HLA-B52:01VQVQYYNKL0.05350.5675514
CELSR1-STK24chr2246829289chr13991276124611HLA-B15:04VQVQYYNKL0.8030.5186514
CELSR1-STK24chr2246829289chr13991276124611HLA-B51:07VQVQYYNKL0.02420.5188514
CELSR1-STK24chr2246829289chr13991276124611HLA-B39:02VQVQYYNKL0.48080.6283514

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Potential FusionNeoAntigen Information of CELSR1-STK24 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.
CELSR1-STK24_46829289_99127612.msa

check button Potential FusionNeoAntigen Information
* We used NetMHCIIpan v4.1 (%rank<0.5).
Fusion geneHchrHbpTgeneTchrTbpHLA IIFusionNeoAntigen peptideNeoantigen start (at BP 13)Neoantigen end (at BP 13)
CELSR1-STK24chr2246829289chr13991276124611DRB1-0101VQYYNKLEPGPLDET722
CELSR1-STK24chr2246829289chr13991276124611DRB1-0101QVQYYNKLEPGPLDE621
CELSR1-STK24chr2246829289chr13991276124611DRB1-0105VQYYNKLEPGPLDET722
CELSR1-STK24chr2246829289chr13991276124611DRB1-0105QVQYYNKLEPGPLDE621
CELSR1-STK24chr2246829289chr13991276124611DRB1-0107VQYYNKLEPGPLDET722
CELSR1-STK24chr2246829289chr13991276124611DRB1-0107QVQYYNKLEPGPLDE621
CELSR1-STK24chr2246829289chr13991276124611DRB1-0109VQYYNKLEPGPLDET722
CELSR1-STK24chr2246829289chr13991276124611DRB1-0111VQYYNKLEPGPLDET722
CELSR1-STK24chr2246829289chr13991276124611DRB1-0111QVQYYNKLEPGPLDE621
CELSR1-STK24chr2246829289chr13991276124611DRB1-0115VQYYNKLEPGPLDET722
CELSR1-STK24chr2246829289chr13991276124611DRB1-0117VQYYNKLEPGPLDET722
CELSR1-STK24chr2246829289chr13991276124611DRB1-0117QVQYYNKLEPGPLDE621
CELSR1-STK24chr2246829289chr13991276124611DRB1-0119VQYYNKLEPGPLDET722
CELSR1-STK24chr2246829289chr13991276124611DRB1-0119QVQYYNKLEPGPLDE621
CELSR1-STK24chr2246829289chr13991276124611DRB1-0121VQYYNKLEPGPLDET722
CELSR1-STK24chr2246829289chr13991276124611DRB1-0125VQYYNKLEPGPLDET722
CELSR1-STK24chr2246829289chr13991276124611DRB1-0125QVQYYNKLEPGPLDE621
CELSR1-STK24chr2246829289chr13991276124611DRB1-0127VQYYNKLEPGPLDET722
CELSR1-STK24chr2246829289chr13991276124611DRB1-0127QVQYYNKLEPGPLDE621
CELSR1-STK24chr2246829289chr13991276124611DRB1-0129VQYYNKLEPGPLDET722
CELSR1-STK24chr2246829289chr13991276124611DRB1-0131VQYYNKLEPGPLDET722
CELSR1-STK24chr2246829289chr13991276124611DRB1-0131QVQYYNKLEPGPLDE621
CELSR1-STK24chr2246829289chr13991276124611DRB1-1216VQYYNKLEPGPLDET722
CELSR1-STK24chr2246829289chr13991276124611DRB1-1216QVQYYNKLEPGPLDE621

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Fusion breakpoint peptide structures of CELSR1-STK24

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
7633QVQYYNKLEPGPLDCELSR1STK24chr2246829289chr13991276124611

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of CELSR1-STK24

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-B14:023BVN7633QVQYYNKLEPGPLD-6.66017-6.77357
HLA-B14:023BVN7633QVQYYNKLEPGPLD-3.48242-4.51772
HLA-B27:093CZF7633QVQYYNKLEPGPLD10000.110000
HLA-B52:013W397633QVQYYNKLEPGPLD-5.06127-5.17467
HLA-B52:013W397633QVQYYNKLEPGPLD-4.23673-5.27203
HLA-B18:014JQV7633QVQYYNKLEPGPLD-3.70535-3.81875
HLA-A11:014UQ27633QVQYYNKLEPGPLD-8.9083-9.0217
HLA-A11:014UQ27633QVQYYNKLEPGPLD-5.86986-6.90516
HLA-A24:025HGA7633QVQYYNKLEPGPLD-6.45287-6.56627
HLA-A24:025HGA7633QVQYYNKLEPGPLD-6.01305-7.04835
HLA-B27:056PYJ7633QVQYYNKLEPGPLD-4.82238-5.85768
HLA-B27:056PYJ7633QVQYYNKLEPGPLD-4.78695-4.90035
HLA-B27:036PZ57633QVQYYNKLEPGPLD-5.33736-5.45076
HLA-B27:036PZ57633QVQYYNKLEPGPLD-2.16924-3.20454
HLA-B44:053DX87633QVQYYNKLEPGPLD-5.3498-5.4632
HLA-B44:053DX87633QVQYYNKLEPGPLD-3.28888-4.32418
HLA-A02:016TDR7633QVQYYNKLEPGPLD-2.20851-3.24381

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Vaccine Design for the FusionNeoAntigens of CELSR1-STK24

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
CELSR1-STK24chr2246829289chr1399127612514VQVQYYNKLGTGCAGGTGCAGTACTACAACAAGTTA

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
CELSR1-STK24chr2246829289chr1399127612621QVQYYNKLEPGPLDECAGGTGCAGTACTACAACAAGTTAGAACCTGGCCCATTAGATGAA
CELSR1-STK24chr2246829289chr1399127612722VQYYNKLEPGPLDETGTGCAGTACTACAACAAGTTAGAACCTGGCCCATTAGATGAAACC

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Information of the samples that have these potential fusion neoantigens of CELSR1-STK24

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
OVCELSR1-STK24chr2246829289ENST00000262738chr1399127612ENST00000397517TCGA-23-1029

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Potential target of CAR-T therapy development for CELSR1-STK24

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
CELSR1chr2246829289ENST00000262738STK24chr1399127612ENST00000397517

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Related Drugs to CELSR1-STK24

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 CELSR1-STK24

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