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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:HSP90B1-ACTN4

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: HSP90B1-ACTN4
FusionPDB ID: 37815
FusionGDB2.0 ID: 37815
HgeneTgene
Gene symbol

HSP90B1

ACTN4

Gene ID

7184

81

Gene nameheat shock protein 90 beta family member 1actinin alpha 4
SynonymsECGP|GP96|GRP94|HEL-S-125m|HEL35|TRA1ACTININ-4|FSGS|FSGS1
Cytomap

12q23.3

19q13.2

Type of geneprotein-codingprotein-coding
Descriptionendoplasmin94 kDa glucose-regulated proteinendothelial cell (HBMEC) glycoproteinepididymis luminal protein 35epididymis secretory sperm binding protein Li 125mheat shock protein 90 kDa beta member 1heat shock protein 90kDa beta (Grp94), member 1heaalpha-actinin-4focal segmental glomerulosclerosis 1non-muscle alpha-actinin 4
Modification date2020032020200327
UniProtAcc

P14625

Main function of 5'-partner protein: FUNCTION: Molecular chaperone that functions in the processing and transport of secreted proteins (By similarity). When associated with CNPY3, required for proper folding of Toll-like receptors (By similarity). Functions in endoplasmic reticulum associated degradation (ERAD) (PubMed:18264092). Has ATPase activity (By similarity). May participate in the unfolding of cytosolic leaderless cargos (lacking the secretion signal sequence) such as the interleukin 1/IL-1 to facilitate their translocation into the ERGIC (endoplasmic reticulum-Golgi intermediate compartment) and secretion; the translocation process is mediated by the cargo receptor TMED10 (PubMed:32272059). {ECO:0000250|UniProtKB:P08113, ECO:0000269|PubMed:18264092, ECO:0000269|PubMed:32272059}.

O43707

Main function of 5'-partner protein: FUNCTION: F-actin cross-linking protein which is thought to anchor actin to a variety of intracellular structures. This is a bundling protein (Probable). Probably involved in vesicular trafficking via its association with the CART complex. The CART complex is necessary for efficient transferrin receptor recycling but not for EGFR degradation (PubMed:15772161). Involved in tight junction assembly in epithelial cells probably through interaction with MICALL2. Links MICALL2 to the actin cytoskeleton and recruits it to the tight junctions (By similarity). May also function as a transcriptional coactivator, stimulating transcription mediated by the nuclear hormone receptors PPARG and RARA (PubMed:22351778). {ECO:0000250|UniProtKB:P57780, ECO:0000269|PubMed:15772161, ECO:0000269|PubMed:22351778, ECO:0000305|PubMed:9508771}.
Ensembl transtripts involved in fusion geneENST idsENST00000299767, ENST00000497637, 
ENST00000252699, ENST00000390009, 
ENST00000424234, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score19 X 19 X 10=361027 X 38 X 12=12312
# samples 2548
** MAII scorelog2(25/3610*10)=-3.85199883711245
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(48/12312*10)=-4.68088692071969
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: HSP90B1 [Title/Abstract] AND ACTN4 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: HSP90B1 [Title/Abstract] AND ACTN4 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)HSP90B1(104331584)-ACTN4(39219913), # samples:1
Anticipated loss of major functional domain due to fusion event.HSP90B1-ACTN4 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.
HSP90B1-ACTN4 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.
HSP90B1-ACTN4 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.
HSP90B1-ACTN4 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
HgeneHSP90B1

GO:0001666

response to hypoxia

15620698

HgeneHSP90B1

GO:0031247

actin rod assembly

19000834

HgeneHSP90B1

GO:0043666

regulation of phosphoprotein phosphatase activity

19000834

HgeneHSP90B1

GO:0071318

cellular response to ATP

19000834

TgeneACTN4

GO:0033209

tumor necrosis factor-mediated signaling pathway

25411248

TgeneACTN4

GO:0035357

peroxisome proliferator activated receptor signaling pathway

22351778

TgeneACTN4

GO:0048384

retinoic acid receptor signaling pathway

22351778

TgeneACTN4

GO:0051272

positive regulation of cellular component movement

9508771



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/chr12:104331584/chr19:39219913)
- 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 HSP90B1 (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 ACTN4 (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)
ENST00000299767HSP90B1chr12104331584+ENST00000252699ACTN4chr1939219913+334710371821195337
ENST00000299767HSP90B1chr12104331584+ENST00000424234ACTN4chr1939219913+119610371821195338
ENST00000299767HSP90B1chr12104331584+ENST00000390009ACTN4chr1939219913+121110371821195337

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
ENST00000299767ENST00000252699HSP90B1chr12104331584+ACTN4chr1939219913+0.0006896080.9993104
ENST00000299767ENST00000424234HSP90B1chr12104331584+ACTN4chr1939219913+0.0004579010.9995421
ENST00000299767ENST00000390009HSP90B1chr12104331584+ACTN4chr1939219913+0.0005021680.9994978

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 HSP90B1-ACTN4

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
HSP90B1chr12104331584ACTN4chr19392199131037285QFINFPIYVWSSKNFITAEELRRELP

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Potential FusionNeoAntigen Information of HSP90B1-ACTN4 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.
HSP90B1-ACTN4_104331584_39219913.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)
HSP90B1-ACTN4chr12104331584chr19392199131037HLA-A02:35YVWSSKNFI0.96020.5954716
HSP90B1-ACTN4chr12104331584chr19392199131037HLA-B35:05FPIYVWSSKNF0.99860.5185415
HSP90B1-ACTN4chr12104331584chr19392199131037HLA-C07:29IYVWSSKNF0.28340.9228615
HSP90B1-ACTN4chr12104331584chr19392199131037HLA-C07:67IYVWSSKNF0.26780.9351615
HSP90B1-ACTN4chr12104331584chr19392199131037HLA-C07:80IYVWSSKNF0.26780.9351615
HSP90B1-ACTN4chr12104331584chr19392199131037HLA-C07:10IYVWSSKNF0.23230.9635615
HSP90B1-ACTN4chr12104331584chr19392199131037HLA-C07:46IYVWSSKNF0.16520.8294615
HSP90B1-ACTN4chr12104331584chr19392199131037HLA-A68:02YVWSSKNFI0.96620.5862716
HSP90B1-ACTN4chr12104331584chr19392199131037HLA-A69:01YVWSSKNFI0.95890.7532716
HSP90B1-ACTN4chr12104331584chr19392199131037HLA-C07:17IYVWSSKNF0.29290.9777615
HSP90B1-ACTN4chr12104331584chr19392199131037HLA-C07:02IYVWSSKNF0.26780.9351615
HSP90B1-ACTN4chr12104331584chr19392199131037HLA-C14:02IYVWSSKNF0.00760.9691615
HSP90B1-ACTN4chr12104331584chr19392199131037HLA-C14:03IYVWSSKNF0.00760.9691615
HSP90B1-ACTN4chr12104331584chr19392199131037HLA-B35:30FPIYVWSSKNF0.99880.7238415
HSP90B1-ACTN4chr12104331584chr19392199131037HLA-B35:17FPIYVWSSKNF0.99880.7238415

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Potential FusionNeoAntigen Information of HSP90B1-ACTN4 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.
HSP90B1-ACTN4_104331584_39219913.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)
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-0902SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-0902SSKNFITAEELRREL1025
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-0902WSSKNFITAEELRRE924
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-0908SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1114SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1120SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1179SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1182SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1302SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1323SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1334SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1339SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1341SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1373SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1374SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1386SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1386SSKNFITAEELRREL1025
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1396SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1397SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1399SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1402SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1407FPIYVWSSKNFITAE419
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1407NFPIYVWSSKNFITA318
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1407PIYVWSSKNFITAEE520
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1414FPIYVWSSKNFITAE419
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1419SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1424SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1430SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1436FPIYVWSSKNFITAE419
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1441SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1442FPIYVWSSKNFITAE419
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1444FPIYVWSSKNFITAE419
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1446SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1447SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1451SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1468FPIYVWSSKNFITAE419
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1468NFPIYVWSSKNFITA318
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1489SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1493FPIYVWSSKNFITAE419
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1494SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1498SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1510NFPIYVWSSKNFITA318
HSP90B1-ACTN4chr12104331584chr19392199131037DRB1-1510INFPIYVWSSKNFIT217
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0101SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0101SSKNFITAEELRREL1025
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0101WSSKNFITAEELRRE924
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0102SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0102SSKNFITAEELRREL1025
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0102WSSKNFITAEELRRE924
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0103SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0103SSKNFITAEELRREL1025
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0103WSSKNFITAEELRRE924
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0104SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0104SSKNFITAEELRREL1025
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0104WSSKNFITAEELRRE924
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0105SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0105SSKNFITAEELRREL1025
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0105WSSKNFITAEELRRE924
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0108NSKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0108NSSKNFITAEELRREL1025
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0108NWSSKNFITAEELRRE924
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0111SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0111SSKNFITAEELRREL1025
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0111WSSKNFITAEELRRE924
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0112SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0112SSKNFITAEELRREL1025
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0112WSSKNFITAEELRRE924
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0113SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0113SSKNFITAEELRREL1025
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0113WSSKNFITAEELRRE924
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0114SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0114SSKNFITAEELRREL1025
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0114WSSKNFITAEELRRE924
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0203SKNFITAEELRRELP1126
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0203SSKNFITAEELRREL1025
HSP90B1-ACTN4chr12104331584chr19392199131037DRB5-0203WSSKNFITAEELRRE924

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Fusion breakpoint peptide structures of HSP90B1-ACTN4

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
4089IYVWSSKNFITAEEHSP90B1ACTN4chr12104331584chr19392199131037

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of HSP90B1-ACTN4

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-B14:023BVN4089IYVWSSKNFITAEE-7.15543-7.26883
HLA-B14:023BVN4089IYVWSSKNFITAEE-4.77435-5.80965
HLA-B52:013W394089IYVWSSKNFITAEE-6.80875-6.92215
HLA-B52:013W394089IYVWSSKNFITAEE-4.20386-5.23916
HLA-A11:014UQ24089IYVWSSKNFITAEE-7.5194-8.5547
HLA-A11:014UQ24089IYVWSSKNFITAEE-6.9601-7.0735
HLA-A24:025HGA4089IYVWSSKNFITAEE-7.52403-7.63743
HLA-A24:025HGA4089IYVWSSKNFITAEE-5.82433-6.85963
HLA-B27:056PYJ4089IYVWSSKNFITAEE-3.28285-4.31815
HLA-B44:053DX84089IYVWSSKNFITAEE-5.91172-6.94702
HLA-B44:053DX84089IYVWSSKNFITAEE-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of HSP90B1-ACTN4

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
HSP90B1-ACTN4chr12104331584chr1939219913415FPIYVWSSKNFTTTCCTATTTATGTATGGAGCAGCAAGAACTTC
HSP90B1-ACTN4chr12104331584chr1939219913615IYVWSSKNFATTTATGTATGGAGCAGCAAGAACTTC
HSP90B1-ACTN4chr12104331584chr1939219913716YVWSSKNFITATGTATGGAGCAGCAAGAACTTCATC

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
HSP90B1-ACTN4chr12104331584chr19392199131025SSKNFITAEELRRELAGCAGCAAGAACTTCATCACAGCTGAGGAGCTGCGGAGAGAGCTG
HSP90B1-ACTN4chr12104331584chr19392199131126SKNFITAEELRRELPAGCAAGAACTTCATCACAGCTGAGGAGCTGCGGAGAGAGCTGCCC
HSP90B1-ACTN4chr12104331584chr1939219913217INFPIYVWSSKNFITATAAACTTTCCTATTTATGTATGGAGCAGCAAGAACTTCATCACA
HSP90B1-ACTN4chr12104331584chr1939219913318NFPIYVWSSKNFITAAACTTTCCTATTTATGTATGGAGCAGCAAGAACTTCATCACAGCT
HSP90B1-ACTN4chr12104331584chr1939219913419FPIYVWSSKNFITAETTTCCTATTTATGTATGGAGCAGCAAGAACTTCATCACAGCTGAG
HSP90B1-ACTN4chr12104331584chr1939219913520PIYVWSSKNFITAEECCTATTTATGTATGGAGCAGCAAGAACTTCATCACAGCTGAGGAG
HSP90B1-ACTN4chr12104331584chr1939219913924WSSKNFITAEELRRETGGAGCAGCAAGAACTTCATCACAGCTGAGGAGCTGCGGAGAGAG

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Information of the samples that have these potential fusion neoantigens of HSP90B1-ACTN4

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
STADHSP90B1-ACTN4chr12104331584ENST00000299767chr1939219913ENST00000252699TCGA-HU-A4H2

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Potential target of CAR-T therapy development for HSP90B1-ACTN4

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 HSP90B1-ACTN4

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 HSP90B1-ACTN4

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
TgeneACTN4C4551527Focal segmental glomerulosclerosis 19GENOMICS_ENGLAND;UNIPROT
TgeneACTN4C0007097Carcinoma1CTD_human
TgeneACTN4C0019193Hepatitis, Toxic1CTD_human
TgeneACTN4C0024667Animal Mammary Neoplasms1CTD_human
TgeneACTN4C0024668Mammary Neoplasms, Experimental1CTD_human
TgeneACTN4C0205696Anaplastic carcinoma1CTD_human
TgeneACTN4C0205697Carcinoma, Spindle-Cell1CTD_human
TgeneACTN4C0205698Undifferentiated carcinoma1CTD_human
TgeneACTN4C0205699Carcinomatosis1CTD_human
TgeneACTN4C0860207Drug-Induced Liver Disease1CTD_human
TgeneACTN4C1257925Mammary Carcinoma, Animal1CTD_human
TgeneACTN4C1262760Hepatitis, Drug-Induced1CTD_human
TgeneACTN4C1868672NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE1ORPHANET
TgeneACTN4C3658290Drug-Induced Acute Liver Injury1CTD_human
TgeneACTN4C4277682Chemical and Drug Induced Liver Injury1CTD_human
TgeneACTN4C4279912Chemically-Induced Liver Toxicity1CTD_human