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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:CD40-LAMC3

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CD40-LAMC3
FusionPDB ID: 14501
FusionGDB2.0 ID: 14501
HgeneTgene
Gene symbol

CD40

LAMC3

Gene ID

958

10319

Gene nameCD40 moleculelaminin subunit gamma 3
SynonymsBp50|CDW40|TNFRSF5|p50OCCM
Cytomap

20q13.12

9q34.12

Type of geneprotein-codingprotein-coding
Descriptiontumor necrosis factor receptor superfamily member 5B cell surface antigen CD40B cell-associated moleculeCD40 molecule, TNF receptor superfamily member 5CD40L receptorlaminin subunit gamma-3laminin, gamma 3laminin-12 subunit gammalaminin-14 subunit gammalaminin-15 subunit gamma
Modification date2020032720200313
UniProtAcc

P25942

Main function of 5'-partner protein: FUNCTION: Receptor for TNFSF5/CD40LG (PubMed:31331973). Transduces TRAF6- and MAP3K8-mediated signals that activate ERK in macrophages and B cells, leading to induction of immunoglobulin secretion (By similarity). {ECO:0000250|UniProtKB:P27512, ECO:0000269|PubMed:31331973}.

Q9Y6N6

Main function of 5'-partner protein: FUNCTION: Binding to cells via a high affinity receptor, laminin is thought to mediate the attachment, migration and organization of cells into tissues during embryonic development by interacting with other extracellular matrix components.
Ensembl transtripts involved in fusion geneENST idsENST00000489304, ENST00000372276, 
ENST00000372285, 
ENST00000361069, 
ENST00000480883, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score2 X 2 X 2=86 X 6 X 5=180
# samples 26
** MAII scorelog2(2/8*10)=1.32192809488736log2(6/180*10)=-1.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: CD40 [Title/Abstract] AND LAMC3 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: CD40 [Title/Abstract] AND LAMC3 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CD40(44751395)-LAMC3(133901672), # samples:1
Anticipated loss of major functional domain due to fusion event.CD40-LAMC3 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.
CD40-LAMC3 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.
CD40-LAMC3 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.
CD40-LAMC3 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
HgeneCD40

GO:0023035

CD40 signaling pathway

31331973

HgeneCD40

GO:2000353

positive regulation of endothelial cell apoptotic process

12885753



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/chr20:44751395/chr9:133901672)
- 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 CD40 (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 LAMC3 (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)
ENST00000372285CD40chr2044751395+ENST00000361069LAMC3chr9133901672+61024757248291585
ENST00000372276CD40chr2044751395+ENST00000361069LAMC3chr9133901672+60584312847851585

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
ENST00000372285ENST00000361069CD40chr2044751395+LAMC3chr9133901672+0.0079962050.99200374
ENST00000372276ENST00000361069CD40chr2044751395+LAMC3chr9133901672+0.0075827980.9924172

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 CD40-LAMC3

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
CD40chr2044751395LAMC3chr9133901672431134HRSCSPGFGVKQIGKAYEITYVRLKF
CD40chr2044751395LAMC3chr9133901672475134HRSCSPGFGVKQIGKAYEITYVRLKF

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Potential FusionNeoAntigen Information of CD40-LAMC3 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.
CD40-LAMC3_44751395_133901672.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)
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:03VKQIGKAY0.96330.5844917
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:01GVKQIGKAY0.99860.7207817
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:25GVKQIGKAY0.9870.7719817
CD40-LAMC3chr2044751395chr9133901672431HLA-B13:02KQIGKAYEI0.97450.56181019
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:02GVKQIGKAY0.96960.8059817
CD40-LAMC3chr2044751395chr9133901672431HLA-A32:13KQIGKAYEI0.96310.84481019
CD40-LAMC3chr2044751395chr9133901672431HLA-B13:01KQIGKAYEI0.90590.86451019
CD40-LAMC3chr2044751395chr9133901672431HLA-B47:01KQIGKAYEI0.85760.5341019
CD40-LAMC3chr2044751395chr9133901672431HLA-B38:01KQIGKAYEI0.68570.82271019
CD40-LAMC3chr2044751395chr9133901672431HLA-B38:02KQIGKAYEI0.66330.80241019
CD40-LAMC3chr2044751395chr9133901672431HLA-B39:13KQIGKAYEI0.66030.7431019
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:03GVKQIGKAY0.570.5614817
CD40-LAMC3chr2044751395chr9133901672431HLA-B52:01KQIGKAYEI0.11870.83731019
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:01FGVKQIGKAY0.99660.7069717
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:02FGVKQIGKAY0.98420.7826717
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:01KQIGKAYEITY10.73991021
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:25KQIGKAYEITY0.99840.77781021
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:03KQIGKAYEITY0.96890.55511021
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:07GVKQIGKAY0.99540.5013817
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:21GVKQIGKAY0.97170.7324817
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:04KQIGKAYEI0.95550.82631019
CD40-LAMC3chr2044751395chr9133901672431HLA-C02:06KQIGKAYEI0.87720.93731019
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:04GVKQIGKAY0.81180.7819817
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:05GVKQIGKAY0.76550.6542817
CD40-LAMC3chr2044751395chr9133901672431HLA-B39:08KQIGKAYEI0.72620.7721019
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:31GVKQIGKAY0.64580.6808817
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:04KQIGKAYEITY0.99940.76561021
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:07GFGVKQIGKAY0.99650.6782617
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:05KQIGKAYEITY0.99190.77121021
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:125GVKQIGKAY0.99860.7207817
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:33GVKQIGKAY0.99860.7207817
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:34GVKQIGKAY0.99860.7207817
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:27GVKQIGKAY0.99850.7638817
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:135GVKQIGKAY0.99830.7512817
CD40-LAMC3chr2044751395chr9133901672431HLA-B27:06KQIGKAYEI0.99760.62261019
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:50GVKQIGKAY0.99640.6808817
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:11GVKQIGKAY0.99640.6624817
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:08GVKQIGKAY0.99610.6587817
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:24KQIGKAYEI0.99580.84471019
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:35GVKQIGKAY0.99530.7594817
CD40-LAMC3chr2044751395chr9133901672431HLA-A32:01KQIGKAYEI0.9950.82581019
CD40-LAMC3chr2044751395chr9133901672431HLA-B35:43GVKQIGKAY0.99430.6565817
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:24GVKQIGKAY0.9930.784817
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:39GVKQIGKAY0.98660.6492817
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:73KQIGKAYEI0.98550.85891019
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:35IGKAYEITY0.98470.70721221
CD40-LAMC3chr2044751395chr9133901672431HLA-C06:08KQIGKAYEI0.97980.98441019
CD40-LAMC3chr2044751395chr9133901672431HLA-C06:06KQIGKAYEI0.97870.97791019
CD40-LAMC3chr2044751395chr9133901672431HLA-C06:02KQIGKAYEI0.97150.98471019
CD40-LAMC3chr2044751395chr9133901672431HLA-C06:17KQIGKAYEI0.97150.98471019
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:30KQIGKAYEI0.96010.81831019
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:53GVKQIGKAY0.960.6857817
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:12GVKQIGKAY0.95310.7422817
CD40-LAMC3chr2044751395chr9133901672431HLA-C07:04KQIGKAYEI0.92250.91531019
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:20GVKQIGKAY0.79130.7714817
CD40-LAMC3chr2044751395chr9133901672431HLA-B39:02KQIGKAYEI0.78530.7381019
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:54GVKQIGKAY0.75770.6306817
CD40-LAMC3chr2044751395chr9133901672431HLA-B38:05KQIGKAYEI0.68570.82271019
CD40-LAMC3chr2044751395chr9133901672431HLA-B35:28GVKQIGKAY0.68190.7826817
CD40-LAMC3chr2044751395chr9133901672431HLA-C12:02GVKQIGKAY0.45690.9079817
CD40-LAMC3chr2044751395chr9133901672431HLA-C02:10GVKQIGKAY0.07930.9618817
CD40-LAMC3chr2044751395chr9133901672431HLA-C02:02GVKQIGKAY0.07930.9618817
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:125FGVKQIGKAY0.99660.7069717
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:27FGVKQIGKAY0.99660.7402717
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:33FGVKQIGKAY0.99660.7069717
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:34FGVKQIGKAY0.99660.7069717
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:135FGVKQIGKAY0.9960.7601717
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:50FGVKQIGKAY0.99510.7349717
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:11FGVKQIGKAY0.9950.6538717
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:08FGVKQIGKAY0.99480.6556717
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:35FGVKQIGKAY0.99310.7358717
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:12FGVKQIGKAY0.97330.7884717
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:34KQIGKAYEITY10.73991021
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:27KQIGKAYEITY10.77381021
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:135KQIGKAYEITY10.76221021
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:24KQIGKAYEITY10.79291021
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:50KQIGKAYEITY10.73381021
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:125KQIGKAYEITY10.73991021
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:33KQIGKAYEITY10.73991021
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:12KQIGKAYEITY0.99990.64981021
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:53KQIGKAYEITY0.99960.7011021
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:54KQIGKAYEITY0.99950.65121021
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:35KQIGKAYEITY0.99940.75481021
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:39KQIGKAYEITY0.99850.64921021
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:35GFGVKQIGKAY0.99540.8725617
CD40-LAMC3chr2044751395chr9133901672431HLA-B15:20KQIGKAYEITY0.99250.8451021
CD40-LAMC3chr2044751395chr9133901672431HLA-B35:28KQIGKAYEITY0.98920.8581021
CD40-LAMC3chr2044751395chr9133901672431HLA-A32:01KQIGKAYEITY0.97650.79951021
CD40-LAMC3chr2044751395chr9133901672431HLA-B48:02KQIGKAYEITY0.93170.8281021

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Potential FusionNeoAntigen Information of CD40-LAMC3 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.
CD40-LAMC3_44751395_133901672.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)
CD40-LAMC3chr2044751395chr9133901672431DRB1-0802SPGFGVKQIGKAYEI419
CD40-LAMC3chr2044751395chr9133901672431DRB1-0802CSPGFGVKQIGKAYE318
CD40-LAMC3chr2044751395chr9133901672431DRB1-0806GFGVKQIGKAYEITY621
CD40-LAMC3chr2044751395chr9133901672431DRB1-0806PGFGVKQIGKAYEIT520
CD40-LAMC3chr2044751395chr9133901672431DRB1-0809SPGFGVKQIGKAYEI419
CD40-LAMC3chr2044751395chr9133901672431DRB1-0809CSPGFGVKQIGKAYE318
CD40-LAMC3chr2044751395chr9133901672431DRB1-0810GFGVKQIGKAYEITY621
CD40-LAMC3chr2044751395chr9133901672431DRB1-0810PGFGVKQIGKAYEIT520
CD40-LAMC3chr2044751395chr9133901672431DRB1-0812GFGVKQIGKAYEITY621
CD40-LAMC3chr2044751395chr9133901672431DRB1-0812PGFGVKQIGKAYEIT520
CD40-LAMC3chr2044751395chr9133901672431DRB1-0821SPGFGVKQIGKAYEI419
CD40-LAMC3chr2044751395chr9133901672431DRB1-0821CSPGFGVKQIGKAYE318
CD40-LAMC3chr2044751395chr9133901672431DRB1-0822GFGVKQIGKAYEITY621
CD40-LAMC3chr2044751395chr9133901672431DRB1-0822PGFGVKQIGKAYEIT520
CD40-LAMC3chr2044751395chr9133901672431DRB1-0822SPGFGVKQIGKAYEI419
CD40-LAMC3chr2044751395chr9133901672431DRB1-1358GFGVKQIGKAYEITY621
CD40-LAMC3chr2044751395chr9133901672431DRB1-1358PGFGVKQIGKAYEIT520
CD40-LAMC3chr2044751395chr9133901672431DRB1-1381GFGVKQIGKAYEITY621
CD40-LAMC3chr2044751395chr9133901672431DRB1-1381PGFGVKQIGKAYEIT520
CD40-LAMC3chr2044751395chr9133901672431DRB1-1389PGFGVKQIGKAYEIT520
CD40-LAMC3chr2044751395chr9133901672431DRB1-1389GFGVKQIGKAYEITY621
CD40-LAMC3chr2044751395chr9133901672431DRB1-1427SPGFGVKQIGKAYEI419

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Fusion breakpoint peptide structures of CD40-LAMC3

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
2773GFGVKQIGKAYEITCD40LAMC3chr2044751395chr9133901672431

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of CD40-LAMC3

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-B14:023BVN2773GFGVKQIGKAYEIT-7.9962-8.1096
HLA-B14:023BVN2773GFGVKQIGKAYEIT-5.70842-6.74372
HLA-B52:013W392773GFGVKQIGKAYEIT-6.83737-6.95077
HLA-B52:013W392773GFGVKQIGKAYEIT-4.4836-5.5189
HLA-A11:014UQ22773GFGVKQIGKAYEIT-10.0067-10.1201
HLA-A11:014UQ22773GFGVKQIGKAYEIT-9.03915-10.0745
HLA-A24:025HGA2773GFGVKQIGKAYEIT-6.56204-6.67544
HLA-A24:025HGA2773GFGVKQIGKAYEIT-5.42271-6.45801
HLA-B44:053DX82773GFGVKQIGKAYEIT-7.85648-8.89178
HLA-B44:053DX82773GFGVKQIGKAYEIT-5.3978-5.5112
HLA-A02:016TDR2773GFGVKQIGKAYEIT-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of CD40-LAMC3

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
CD40-LAMC3chr2044751395chr91339016721019KQIGKAYEIAGCAGATTGGGAAGGCTTATGAGATCA
CD40-LAMC3chr2044751395chr91339016721021KQIGKAYEITYAGCAGATTGGGAAGGCTTATGAGATCACGTATG
CD40-LAMC3chr2044751395chr91339016721221IGKAYEITYTTGGGAAGGCTTATGAGATCACGTATG
CD40-LAMC3chr2044751395chr9133901672617GFGVKQIGKAYGCTTTGGGGTCAAGCAGATTGGGAAGGCTTATG
CD40-LAMC3chr2044751395chr9133901672717FGVKQIGKAYTTGGGGTCAAGCAGATTGGGAAGGCTTATG
CD40-LAMC3chr2044751395chr9133901672817GVKQIGKAYGGGTCAAGCAGATTGGGAAGGCTTATG
CD40-LAMC3chr2044751395chr9133901672917VKQIGKAYTCAAGCAGATTGGGAAGGCTTATG

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
CD40-LAMC3chr2044751395chr9133901672318CSPGFGVKQIGKAYEGCTCGCCCGGCTTTGGGGTCAAGCAGATTGGGAAGGCTTATGAGA
CD40-LAMC3chr2044751395chr9133901672419SPGFGVKQIGKAYEICGCCCGGCTTTGGGGTCAAGCAGATTGGGAAGGCTTATGAGATCA
CD40-LAMC3chr2044751395chr9133901672520PGFGVKQIGKAYEITCCGGCTTTGGGGTCAAGCAGATTGGGAAGGCTTATGAGATCACGT
CD40-LAMC3chr2044751395chr9133901672621GFGVKQIGKAYEITYGCTTTGGGGTCAAGCAGATTGGGAAGGCTTATGAGATCACGTATG

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Information of the samples that have these potential fusion neoantigens of CD40-LAMC3

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
GBMCD40-LAMC3chr2044751395ENST00000372276chr9133901672ENST00000361069TCGA-28-5215-01A

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Potential target of CAR-T therapy development for CD40-LAMC3

check button Predicted 3D structure. We used RoseTTAFold.
89_CD40-LAMC3_t000_.e2e.pdb


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
CD40chr2044751395ENST00000372276LAMC3chr9133901672ENST00000361069

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Related Drugs to CD40-LAMC3

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 CD40-LAMC3

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