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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:CACNA2D3-FOXP1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CACNA2D3-FOXP1
FusionPDB ID: 12363
FusionGDB2.0 ID: 12363
HgeneTgene
Gene symbol

CACNA2D3

FOXP1

Gene ID

55799

27086

Gene namecalcium voltage-gated channel auxiliary subunit alpha2delta 3forkhead box P1
SynonymsHSA27226812CC4|HSPC215|MFH|QRF1|hFKH1B
Cytomap

3p21.1-p14.3

3p13

Type of geneprotein-codingprotein-coding
Descriptionvoltage-dependent calcium channel subunit alpha-2/delta-3calcium channel alpha2-delta3 subunitcalcium channel, voltage-dependent, alpha 2/delta 3 subunitcalcium channel, voltage-dependent, alpha 2/delta subunit 3voltage-gated calcium channel subunit aforkhead box protein P1fork head-related protein like Bglutamine-rich factor 1mac-1-regulated forkhead
Modification date2020031320200329
UniProtAcc

Q8IZS8

Main function of 5'-partner protein: FUNCTION: The alpha-2/delta subunit of voltage-dependent calcium channels regulates calcium current density and activation/inactivation kinetics of the calcium channel. Acts as a regulatory subunit for P/Q-type calcium channel (CACNA1A), N-type (CACNA1B), L-type (CACNA1C OR CACNA1D) but not T-type (CACNA1G) (By similarity). {ECO:0000250}.

Q9H334

Main function of 5'-partner protein: FUNCTION: Transcriptional repressor (PubMed:18347093, PubMed:26647308). Can act with CTBP1 to synergistically repress transcription but CTPBP1 is not essential (By similarity). Plays an important role in the specification and differentiation of lung epithelium. Acts cooperatively with FOXP4 to regulate lung secretory epithelial cell fate and regeneration by restricting the goblet cell lineage program; the function may involve regulation of AGR2. Essential transcriptional regulator of B-cell development. Involved in regulation of cardiac muscle cell proliferation. Involved in the columnar organization of spinal motor neurons. Promotes the formation of the lateral motor neuron column (LMC) and the preganglionic motor column (PGC) and is required for respective appropriate motor axon projections. The segment-appropriate generation of spinal chord motor columns requires cooperation with other Hox proteins. Can regulate PITX3 promoter activity; may promote midbrain identity in embryonic stem cell-derived dopamine neurons by regulating PITX3. Negatively regulates the differentiation of T follicular helper cells T(FH)s. Involved in maintenance of hair follicle stem cell quiescence; the function probably involves regulation of FGF18 (By similarity). Represses transcription of various pro-apoptotic genes and cooperates with NF-kappa B-signaling in promoting B-cell expansion by inhibition of caspase-dependent apoptosis (PubMed:25267198). Binds to CSF1R promoter elements and is involved in regulation of monocyte differentiation and macrophage functions; repression of CSF1R in monocytes seems to involve NCOR2 as corepressor (PubMed:15286807, PubMed:18799727, PubMed:18347093). Involved in endothelial cell proliferation, tube formation and migration indicative for a role in angiogenesis; the role in neovascularization seems to implicate suppression of SEMA5B (PubMed:24023716). Can negatively regulate androgen receptor signaling (PubMed:18640093). Acts as a transcriptional activator of the FBXL7 promoter; this activity is regulated by AURKA (PubMed:28218735). {ECO:0000250|UniProtKB:P58462, ECO:0000269|PubMed:15286807, ECO:0000269|PubMed:18640093, ECO:0000269|PubMed:18799727, ECO:0000269|PubMed:24023716, ECO:0000269|PubMed:25267198, ECO:0000269|PubMed:26647308, ECO:0000269|PubMed:28218735, ECO:0000305|PubMed:18347093, ECO:0000305|PubMed:24023716}.; FUNCTION: [Isoform 8]: Involved in transcriptional regulation in embryonic stem cells (ESCs). Stimulates expression of transcription factors that are required for pluripotency and decreases expression of differentiation-associated genes. Has distinct DNA-binding specifities as compared to the canonical form and preferentially binds DNA with the sequence 5'-CGATACAA-3' (or closely related sequences) (PubMed:21924763). Promotes ESC self-renewal and pluripotency (By similarity). {ECO:0000250|UniProtKB:P58462, ECO:0000269|PubMed:21924763}.
Ensembl transtripts involved in fusion geneENST idsENST00000288197, ENST00000415676, 
ENST00000474759, ENST00000490478, 
ENST00000478261, 
ENST00000318779, 
ENST00000468577, ENST00000472382, 
ENST00000491238, ENST00000498215, 
ENST00000318789, ENST00000475937, 
ENST00000484350, ENST00000493089, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score14 X 12 X 6=100847 X 26 X 20=24440
# samples 1552
** MAII scorelog2(15/1008*10)=-2.74846123300404
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(52/24440*10)=-5.55458885167764
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: CACNA2D3 [Title/Abstract] AND FOXP1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: CACNA2D3 [Title/Abstract] AND FOXP1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CACNA2D3(54798378)-FOXP1(71050210), # samples:3
Anticipated loss of major functional domain due to fusion event.CACNA2D3-FOXP1 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.
CACNA2D3-FOXP1 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.
CACNA2D3-FOXP1 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.
CACNA2D3-FOXP1 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.
CACNA2D3-FOXP1 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
CACNA2D3-FOXP1 seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
CACNA2D3-FOXP1 seems lost the major protein functional domain in Tgene partner, which is a CGC due to the frame-shifted ORF.
CACNA2D3-FOXP1 seems lost the major protein functional domain in Tgene partner, which is a epigenetic factor due to the frame-shifted ORF.
CACNA2D3-FOXP1 seems lost the major protein functional domain in Tgene partner, which is a transcription factor due to the frame-shifted ORF.
CACNA2D3-FOXP1 seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor due to the frame-shifted 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
TgeneFOXP1

GO:0002903

negative regulation of B cell apoptotic process

25267198

TgeneFOXP1

GO:0010629

negative regulation of gene expression

30111844

TgeneFOXP1

GO:0030316

osteoclast differentiation

18799727

TgeneFOXP1

GO:0032496

response to lipopolysaccharide

18799727

TgeneFOXP1

GO:0032680

regulation of tumor necrosis factor production

18799727

TgeneFOXP1

GO:0035926

chemokine (C-C motif) ligand 2 secretion

18799727

TgeneFOXP1

GO:0036035

osteoclast development

18799727

TgeneFOXP1

GO:0042116

macrophage activation

18799727

TgeneFOXP1

GO:0042117

monocyte activation

18799727

TgeneFOXP1

GO:0045655

regulation of monocyte differentiation

15286807

TgeneFOXP1

GO:0045892

negative regulation of transcription, DNA-templated

20950788

TgeneFOXP1

GO:0050706

regulation of interleukin-1 beta secretion

18799727

TgeneFOXP1

GO:0050727

regulation of inflammatory response

18799727

TgeneFOXP1

GO:0060766

negative regulation of androgen receptor signaling pathway

18640093

TgeneFOXP1

GO:1900424

regulation of defense response to bacterium

18799727

TgeneFOXP1

GO:1901256

regulation of macrophage colony-stimulating factor production

18799727

TgeneFOXP1

GO:2001182

regulation of interleukin-12 secretion

18799727



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/chr3:54798378/chr3:71050210)
- 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 CACNA2D3 (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 FOXP1 (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)
ENST00000415676CACNA2D3chr354798378+ENST00000318789FOXP1chr371037228-702414981182469783
ENST00000415676CACNA2D3chr354798378+ENST00000475937FOXP1chr371037228-497214981182469783
ENST00000415676CACNA2D3chr354798378+ENST00000493089FOXP1chr371037228-251014981182466782
ENST00000415676CACNA2D3chr354798378+ENST00000484350FOXP1chr371037228-250614981182469783
ENST00000288197CACNA2D3chr354798378+ENST00000318789FOXP1chr371037228-69541428482399783
ENST00000288197CACNA2D3chr354798378+ENST00000475937FOXP1chr371037228-49021428482399783
ENST00000288197CACNA2D3chr354798378+ENST00000493089FOXP1chr371037228-24401428482396782
ENST00000288197CACNA2D3chr354798378+ENST00000484350FOXP1chr371037228-24361428482399783
ENST00000474759CACNA2D3chr354798378+ENST00000318789FOXP1chr371037228-69541428482399783
ENST00000474759CACNA2D3chr354798378+ENST00000475937FOXP1chr371037228-49021428482399783
ENST00000474759CACNA2D3chr354798378+ENST00000493089FOXP1chr371037228-24401428482396782
ENST00000474759CACNA2D3chr354798378+ENST00000484350FOXP1chr371037228-24361428482399783
ENST00000490478CACNA2D3chr354798378+ENST00000318789FOXP1chr371037228-683613101252281718
ENST00000490478CACNA2D3chr354798378+ENST00000475937FOXP1chr371037228-478413101252281718
ENST00000490478CACNA2D3chr354798378+ENST00000493089FOXP1chr371037228-232213101252278717
ENST00000490478CACNA2D3chr354798378+ENST00000484350FOXP1chr371037228-231813101252281718

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
ENST00000415676ENST00000318789CACNA2D3chr354798378+FOXP1chr371037228-0.0003960020.99960405
ENST00000415676ENST00000475937CACNA2D3chr354798378+FOXP1chr371037228-0.0007763680.9992236
ENST00000415676ENST00000493089CACNA2D3chr354798378+FOXP1chr371037228-0.0040628830.9959371
ENST00000415676ENST00000484350CACNA2D3chr354798378+FOXP1chr371037228-0.0045035020.9954965
ENST00000288197ENST00000318789CACNA2D3chr354798378+FOXP1chr371037228-0.0003993740.9996006
ENST00000288197ENST00000475937CACNA2D3chr354798378+FOXP1chr371037228-0.0007414870.99925846
ENST00000288197ENST00000493089CACNA2D3chr354798378+FOXP1chr371037228-0.0034999890.9965
ENST00000288197ENST00000484350CACNA2D3chr354798378+FOXP1chr371037228-0.0038522460.99614775
ENST00000474759ENST00000318789CACNA2D3chr354798378+FOXP1chr371037228-0.0003993740.9996006
ENST00000474759ENST00000475937CACNA2D3chr354798378+FOXP1chr371037228-0.0007414870.99925846
ENST00000474759ENST00000493089CACNA2D3chr354798378+FOXP1chr371037228-0.0034999890.9965
ENST00000474759ENST00000484350CACNA2D3chr354798378+FOXP1chr371037228-0.0038522460.99614775
ENST00000490478ENST00000318789CACNA2D3chr354798378+FOXP1chr371037228-0.0005806950.99941933
ENST00000490478ENST00000475937CACNA2D3chr354798378+FOXP1chr371037228-0.0010402520.9989598
ENST00000490478ENST00000493089CACNA2D3chr354798378+FOXP1chr371037228-0.0038290810.99617094
ENST00000490478ENST00000484350CACNA2D3chr354798378+FOXP1chr371037228-0.0038943880.9961056

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 CACNA2D3-FOXP1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
CACNA2D3chr354798378FOXP1chr3710372281310395HDVVWTEAYIDSTLAKDKERLQAMMT
CACNA2D3chr354798378FOXP1chr3710372281428460HDVVWTEAYIDSTLAKDKERLQAMMT
CACNA2D3chr354798378FOXP1chr3710372281498460HDVVWTEAYIDSTLAKDKERLQAMMT

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Potential FusionNeoAntigen Information of CACNA2D3-FOXP1 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.
CACNA2D3-FOXP1_54798378_71037228.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)
CACNA2D3-FOXP1chr354798378chr3710372281428HLA-B47:01TEAYIDSTL0.88030.5308514
CACNA2D3-FOXP1chr354798378chr3710372281428HLA-A02:22TLAKDKERL0.86770.64031221
CACNA2D3-FOXP1chr354798378chr3710372281428HLA-B18:01TEAYIDSTL0.72940.919514
CACNA2D3-FOXP1chr354798378chr3710372281428HLA-B39:13TEAYIDSTL0.51450.8675514
CACNA2D3-FOXP1chr354798378chr3710372281428HLA-B41:01TEAYIDSTL0.4340.827514
CACNA2D3-FOXP1chr354798378chr3710372281428HLA-B38:02TEAYIDSTL0.41470.9237514
CACNA2D3-FOXP1chr354798378chr3710372281428HLA-B45:01TEAYIDSTLA0.97360.7356515
CACNA2D3-FOXP1chr354798378chr3710372281428HLA-B50:01TEAYIDSTLA0.75430.7027515
CACNA2D3-FOXP1chr354798378chr3710372281428HLA-B39:08TEAYIDSTL0.66450.7521514
CACNA2D3-FOXP1chr354798378chr3710372281428HLA-B39:05TEAYIDSTL0.41950.8791514
CACNA2D3-FOXP1chr354798378chr3710372281428HLA-B40:04TEAYIDSTL0.99790.6973514
CACNA2D3-FOXP1chr354798378chr3710372281428HLA-A30:01AYIDSTLAK0.82760.8008716
CACNA2D3-FOXP1chr354798378chr3710372281428HLA-B18:04TEAYIDSTL0.80960.9332514
CACNA2D3-FOXP1chr354798378chr3710372281428HLA-B18:07TEAYIDSTL0.77420.8537514
CACNA2D3-FOXP1chr354798378chr3710372281428HLA-B18:05TEAYIDSTL0.72940.919514
CACNA2D3-FOXP1chr354798378chr3710372281428HLA-B18:08TEAYIDSTL0.6960.8816514
CACNA2D3-FOXP1chr354798378chr3710372281428HLA-B18:06TEAYIDSTL0.6870.9287514
CACNA2D3-FOXP1chr354798378chr3710372281428HLA-B39:11TEAYIDSTL0.67190.7804514
CACNA2D3-FOXP1chr354798378chr3710372281428HLA-B18:11TEAYIDSTL0.66620.8803514
CACNA2D3-FOXP1chr354798378chr3710372281428HLA-B18:03TEAYIDSTL0.59150.9119514
CACNA2D3-FOXP1chr354798378chr3710372281428HLA-B39:31TEAYIDSTL0.49350.8879514
CACNA2D3-FOXP1chr354798378chr3710372281428HLA-B39:02TEAYIDSTL0.48020.8749514
CACNA2D3-FOXP1chr354798378chr3710372281428HLA-B50:05TEAYIDSTLA0.75430.7027515
CACNA2D3-FOXP1chr354798378chr3710372281428HLA-B50:04TEAYIDSTLA0.75430.7027515

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Potential FusionNeoAntigen Information of CACNA2D3-FOXP1 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.
CACNA2D3-FOXP1_54798378_71037228.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)
CACNA2D3-FOXP1chr354798378chr3710372281428DRB1-0903TEAYIDSTLAKDKER520
CACNA2D3-FOXP1chr354798378chr3710372281428DRB1-0908TEAYIDSTLAKDKER520
CACNA2D3-FOXP1chr354798378chr3710372281428DRB1-0908WTEAYIDSTLAKDKE419

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Fusion breakpoint peptide structures of CACNA2D3-FOXP1

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
1558EAYIDSTLAKDKERCACNA2D3FOXP1chr354798378chr3710372281428

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of CACNA2D3-FOXP1

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-B14:023BVN1558EAYIDSTLAKDKER-7.9962-8.1096
HLA-B14:023BVN1558EAYIDSTLAKDKER-5.70842-6.74372
HLA-B52:013W391558EAYIDSTLAKDKER-6.83737-6.95077
HLA-B52:013W391558EAYIDSTLAKDKER-4.4836-5.5189
HLA-A11:014UQ21558EAYIDSTLAKDKER-10.0067-10.1201
HLA-A11:014UQ21558EAYIDSTLAKDKER-9.03915-10.0745
HLA-A24:025HGA1558EAYIDSTLAKDKER-6.56204-6.67544
HLA-A24:025HGA1558EAYIDSTLAKDKER-5.42271-6.45801
HLA-B44:053DX81558EAYIDSTLAKDKER-7.85648-8.89178
HLA-B44:053DX81558EAYIDSTLAKDKER-5.3978-5.5112
HLA-A02:016TDR1558EAYIDSTLAKDKER-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of CACNA2D3-FOXP1

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
CACNA2D3-FOXP1chr354798378chr3710372281221TLAKDKERLACTCTTGCAAAAGACAAAGAACGCCTG
CACNA2D3-FOXP1chr354798378chr371037228514TEAYIDSTLACCGAAGCTTACATTGACAGCACTCTT
CACNA2D3-FOXP1chr354798378chr371037228515TEAYIDSTLAACCGAAGCTTACATTGACAGCACTCTTGCA
CACNA2D3-FOXP1chr354798378chr371037228716AYIDSTLAKGCTTACATTGACAGCACTCTTGCAAAA

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
CACNA2D3-FOXP1chr354798378chr371037228419WTEAYIDSTLAKDKETGGACCGAAGCTTACATTGACAGCACTCTTGCAAAAGACAAAGAA
CACNA2D3-FOXP1chr354798378chr371037228520TEAYIDSTLAKDKERACCGAAGCTTACATTGACAGCACTCTTGCAAAAGACAAAGAACGC

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Information of the samples that have these potential fusion neoantigens of CACNA2D3-FOXP1

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
BRCACACNA2D3-FOXP1chr354798378ENST00000288197chr371037228ENST00000318789TCGA-A2-A0CX-01A

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Potential target of CAR-T therapy development for CACNA2D3-FOXP1

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 CACNA2D3-FOXP1

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 CACNA2D3-FOXP1

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