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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:TRPC4AP-ADNP

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: TRPC4AP-ADNP
FusionPDB ID: 94337
FusionGDB2.0 ID: 94337
HgeneTgene
Gene symbol

TRPC4AP

ADNP

Gene ID

26133

23394

Gene nametransient receptor potential cation channel subfamily C member 4 associated proteinactivity dependent neuroprotector homeobox
SynonymsC20orf188|PPP1R158|TRRP4AP|TRUSSADNP1|HVDAS|MRD28
Cytomap

20q11.22

20q13.13

Type of geneprotein-codingprotein-coding
Descriptionshort transient receptor potential channel 4-associated proteinTNF-receptor ubiquitous scaffolding/signaling proteinTRP4-associated proteinprotein phosphatase 1, regulatory subunit 158trpc4-associated proteintumor necrosis factor receptor-associated activity-dependent neuroprotector homeobox proteinADNP homeobox 1activity-dependent neuroprotective proteinactivity-dependent neuroprotector
Modification date2020031320200322
UniProtAcc.

Q6IQ32

Main function of 5'-partner protein: FUNCTION: May be involved in transcriptional regulation.
Ensembl transtripts involved in fusion geneENST idsENST00000252015, ENST00000432634, 
ENST00000451813, ENST00000539834, 
ENST00000396029, ENST00000349014, 
ENST00000371602, ENST00000396032, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score30 X 25 X 10=750010 X 8 X 5=400
# samples 339
** MAII scorelog2(33/7500*10)=-4.50635266602479
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(9/400*10)=-2.15200309344505
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: TRPC4AP [Title/Abstract] AND ADNP [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: TRPC4AP [Title/Abstract] AND ADNP [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)TRPC4AP(33680417)-ADNP(49511049), # samples:2
Anticipated loss of major functional domain due to fusion event.TRPC4AP-ADNP 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.
TRPC4AP-ADNP 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.
TRPC4AP-ADNP 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.
TRPC4AP-ADNP 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.
TRPC4AP-ADNP seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
TRPC4AP-ADNP seems lost the major protein functional domain in Tgene partner, which is a epigenetic factor due to the frame-shifted ORF.
TRPC4AP-ADNP seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
TRPC4AP-ADNP seems lost the major protein functional domain in Tgene partner, which is a transcription factor 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
HgeneTRPC4AP

GO:0006511

ubiquitin-dependent protein catabolic process

20551172

HgeneTRPC4AP

GO:0016567

protein ubiquitination

20551172



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/chr20:33680417/chr20:49511049)
- 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 TRPC4AP (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 ADNP (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)
ENST00000451813TRPC4APchr2033680417-ENST00000396032ADNPchr2049511049-4404194533011098
ENST00000451813TRPC4APchr2033680417-ENST00000371602ADNPchr2049511049-5659194533011098
ENST00000451813TRPC4APchr2033680417-ENST00000349014ADNPchr2049511049-5659194533011098
ENST00000252015TRPC4APchr2033680417-ENST00000396032ADNPchr2049511049-44682586933651098
ENST00000252015TRPC4APchr2033680417-ENST00000371602ADNPchr2049511049-57232586933651098
ENST00000252015TRPC4APchr2033680417-ENST00000349014ADNPchr2049511049-57232586933651098
ENST00000432634TRPC4APchr2033680417-ENST00000396032ADNPchr2049511049-4404194533011098
ENST00000432634TRPC4APchr2033680417-ENST00000371602ADNPchr2049511049-5659194533011098
ENST00000432634TRPC4APchr2033680417-ENST00000349014ADNPchr2049511049-5659194533011098

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
ENST00000451813ENST00000396032TRPC4APchr2033680417-ADNPchr2049511049-0.0002932730.9997067
ENST00000451813ENST00000371602TRPC4APchr2033680417-ADNPchr2049511049-0.0002072010.9997929
ENST00000451813ENST00000349014TRPC4APchr2033680417-ADNPchr2049511049-0.0002072010.9997929
ENST00000252015ENST00000396032TRPC4APchr2033680417-ADNPchr2049511049-0.0003238440.9996762
ENST00000252015ENST00000371602TRPC4APchr2033680417-ADNPchr2049511049-0.0002286590.9997713
ENST00000252015ENST00000349014TRPC4APchr2033680417-ADNPchr2049511049-0.0002286590.9997713
ENST00000432634ENST00000396032TRPC4APchr2033680417-ADNPchr2049511049-0.0002932730.9997067
ENST00000432634ENST00000371602TRPC4APchr2033680417-ADNPchr2049511049-0.0002072010.9997929
ENST00000432634ENST00000349014TRPC4APchr2033680417-ADNPchr2049511049-0.0002072010.9997929

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 TRPC4AP-ADNP

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
TRPC4APchr2033680417ADNPchr204951104919463GQLTGRGLVRAVQDYRTKPFCCSACP
TRPC4APchr2033680417ADNPchr204951104925863GQLTGRGLVRAVQDYRTKPFCCSACP

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Potential FusionNeoAntigen Information of TRPC4AP-ADNP 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.
TRPC4AP-ADNP_33680417_49511049.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)
TRPC4AP-ADNPchr2033680417chr2049511049258HLA-B15:01GLVRAVQDY0.99190.8131615
TRPC4AP-ADNPchr2033680417chr2049511049258HLA-A30:08RAVQDYRTK0.95910.6055918
TRPC4AP-ADNPchr2033680417chr2049511049258HLA-B15:25GLVRAVQDY0.9270.8695615
TRPC4AP-ADNPchr2033680417chr2049511049258HLA-B15:03VQDYRTKPF0.80310.69671120
TRPC4AP-ADNPchr2033680417chr2049511049258HLA-C08:15VQDYRTKPF0.99620.96781120
TRPC4AP-ADNPchr2033680417chr2049511049258HLA-B15:07GLVRAVQDY0.94130.6655615
TRPC4AP-ADNPchr2033680417chr2049511049258HLA-B15:05GLVRAVQDY0.49550.8514615
TRPC4AP-ADNPchr2033680417chr2049511049258HLA-C08:02VQDYRTKPF0.99620.96781120
TRPC4AP-ADNPchr2033680417chr2049511049258HLA-B15:27GLVRAVQDY0.9920.8658615
TRPC4AP-ADNPchr2033680417chr2049511049258HLA-B15:125GLVRAVQDY0.99190.8131615
TRPC4AP-ADNPchr2033680417chr2049511049258HLA-B15:34GLVRAVQDY0.99190.8131615
TRPC4AP-ADNPchr2033680417chr2049511049258HLA-B15:50GLVRAVQDY0.99190.807615
TRPC4AP-ADNPchr2033680417chr2049511049258HLA-B15:33GLVRAVQDY0.99190.8131615
TRPC4AP-ADNPchr2033680417chr2049511049258HLA-B15:135GLVRAVQDY0.99160.8478615
TRPC4AP-ADNPchr2033680417chr2049511049258HLA-B15:35GLVRAVQDY0.970.8621615
TRPC4AP-ADNPchr2033680417chr2049511049258HLA-A30:01RAVQDYRTK0.95930.7488918
TRPC4AP-ADNPchr2033680417chr2049511049258HLA-B15:39GLVRAVQDY0.93330.7627615
TRPC4AP-ADNPchr2033680417chr2049511049258HLA-B15:53VQDYRTKPF0.80950.83321120
TRPC4AP-ADNPchr2033680417chr2049511049258HLA-B15:54VQDYRTKPF0.75940.79491120
TRPC4AP-ADNPchr2033680417chr2049511049258HLA-B48:02VQDYRTKPF0.63030.89131120
TRPC4AP-ADNPchr2033680417chr2049511049258HLA-B15:20GLVRAVQDY0.49830.9085615

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Potential FusionNeoAntigen Information of TRPC4AP-ADNP in HLA II

check button Multiple sequence alignments of the potential FusionNeoAntigens per fusion breakpoints. If the MSA is empty, then it means that there were predicted fusion neoantigens in this fusion breakpoint, but those predicted fusion neoantigens were not across the breakpoint, which is not fusion-specific.

check button Potential FusionNeoAntigen Information
* We used NetMHCIIpan v4.1 (%rank<0.5).
Fusion geneHchrHbpTgeneTchrTbpHLA IIFusionNeoAntigen peptideNeoantigen start (at BP 13)Neoantigen end (at BP 13)

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Fusion breakpoint peptide structures of TRPC4AP-ADNP

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
2971GLVRAVQDYRTKPFTRPC4APADNPchr2033680417chr2049511049258

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of TRPC4AP-ADNP

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-B14:023BVN2971GLVRAVQDYRTKPF-7.15543-7.26883
HLA-B14:023BVN2971GLVRAVQDYRTKPF-4.77435-5.80965
HLA-B52:013W392971GLVRAVQDYRTKPF-6.80875-6.92215
HLA-B52:013W392971GLVRAVQDYRTKPF-4.20386-5.23916
HLA-A11:014UQ22971GLVRAVQDYRTKPF-7.5194-8.5547
HLA-A11:014UQ22971GLVRAVQDYRTKPF-6.9601-7.0735
HLA-A24:025HGA2971GLVRAVQDYRTKPF-7.52403-7.63743
HLA-A24:025HGA2971GLVRAVQDYRTKPF-5.82433-6.85963
HLA-B27:056PYJ2971GLVRAVQDYRTKPF-3.28285-4.31815
HLA-B44:053DX82971GLVRAVQDYRTKPF-5.91172-6.94702
HLA-B44:053DX82971GLVRAVQDYRTKPF-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of TRPC4AP-ADNP

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
TRPC4AP-ADNPchr2033680417chr20495110491120VQDYRTKPFGTGCAGGACTATCGGACAAAACCTTTC
TRPC4AP-ADNPchr2033680417chr2049511049615GLVRAVQDYGGCCTGGTCCGGGCGGTGCAGGACTAT
TRPC4AP-ADNPchr2033680417chr2049511049918RAVQDYRTKCGGGCGGTGCAGGACTATCGGACAAAA

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

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Information of the samples that have these potential fusion neoantigens of TRPC4AP-ADNP

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
LUADTRPC4AP-ADNPchr2033680417ENST00000252015chr2049511049ENST00000349014TCGA-91-6831-01A

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Potential target of CAR-T therapy development for TRPC4AP-ADNP

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 TRPC4AP-ADNP

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 TRPC4AP-ADNP

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