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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:HDAC4-SATB2

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: HDAC4-SATB2
FusionPDB ID: 35838
FusionGDB2.0 ID: 35838
HgeneTgene
Gene symbol

HDAC4

SATB2

Gene ID

9759

23314

Gene namehistone deacetylase 4SATB homeobox 2
SynonymsAHO3|BDMR|HA6116|HD4|HDAC-4|HDAC-A|HDACAGLSS
Cytomap

2q37.3

2q33.1

Type of geneprotein-codingprotein-coding
Descriptionhistone deacetylase 4histone deacetylase ADNA-binding protein SATB2SATB family member 2special AT-rich sequence-binding protein 2
Modification date2020032920200313
UniProtAcc

P56524

Main function of 5'-partner protein: FUNCTION: Responsible for the deacetylation of lysine residues on the N-terminal part of the core histones (H2A, H2B, H3 and H4). Histone deacetylation gives a tag for epigenetic repression and plays an important role in transcriptional regulation, cell cycle progression and developmental events. Histone deacetylases act via the formation of large multiprotein complexes. Involved in muscle maturation via its interaction with the myocyte enhancer factors such as MEF2A, MEF2C and MEF2D. Involved in the MTA1-mediated epigenetic regulation of ESR1 expression in breast cancer. Deacetylates HSPA1A and HSPA1B at 'Lys-77' leading to their preferential binding to co-chaperone STUB1 (PubMed:27708256). {ECO:0000269|PubMed:10523670, ECO:0000269|PubMed:24413532, ECO:0000269|PubMed:27708256}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000345617, ENST00000541256, 
ENST00000543185, ENST00000553145, 
ENST00000260926, ENST00000457245, 
ENST00000417098, ENST00000428695, 
ENST00000443023, ENST00000484124, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score13 X 10 X 9=11704 X 6 X 3=72
# samples 157
** MAII scorelog2(15/1170*10)=-2.96347412397489
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/72*10)=-0.0406419844973459
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: HDAC4 [Title/Abstract] AND SATB2 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: HDAC4 [Title/Abstract] AND SATB2 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)HDAC4(240158289)-SATB2(200325255), # samples:1
HDAC4(240158289)-SATB2(200298237), # samples:1
Anticipated loss of major functional domain due to fusion event.HDAC4-SATB2 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.
HDAC4-SATB2 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.
HDAC4-SATB2 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.
HDAC4-SATB2 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
HgeneHDAC4

GO:0000122

negative regulation of transcription by RNA polymerase II

10869435|16236793

HgeneHDAC4

GO:0006338

chromatin remodeling

18850004

HgeneHDAC4

GO:0006476

protein deacetylation

27708256

HgeneHDAC4

GO:0016575

histone deacetylation

10869435

HgeneHDAC4

GO:0033235

positive regulation of protein sumoylation

17696781

HgeneHDAC4

GO:0034983

peptidyl-lysine deacetylation

18614528

HgeneHDAC4

GO:0045892

negative regulation of transcription, DNA-templated

10869435

HgeneHDAC4

GO:0070932

histone H3 deacetylation

12590135

HgeneHDAC4

GO:0070933

histone H4 deacetylation

12590135



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/chr2:240158289/chr2:200325255)
- 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 HDAC4 (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 SATB2 (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)
ENST00000345617HDAC4chr2240158289-ENST00000417098SATB2chr2200298237-56308867832918711

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
ENST00000345617ENST00000417098HDAC4chr2240158289-SATB2chr2200298237-0.0007291110.99927086

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 HDAC4-SATB2

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
HDAC4chr2240158289SATB2chr220029823788634LLNPARVNHMPSTGLMIPVFCVVEQL

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Potential FusionNeoAntigen Information of HDAC4-SATB2 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.
HDAC4-SATB2_240158289_200298237.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)
HDAC4-SATB2chr2240158289chr2200298237886HLA-B39:01NHMPSTGL0.99980.9619715
HDAC4-SATB2chr2240158289chr2200298237886HLA-B39:24NHMPSTGL0.99980.6186715
HDAC4-SATB2chr2240158289chr2200298237886HLA-B38:01NHMPSTGL0.99960.9748715
HDAC4-SATB2chr2240158289chr2200298237886HLA-B38:02NHMPSTGL0.99960.9798715
HDAC4-SATB2chr2240158289chr2200298237886HLA-B15:10NHMPSTGL0.99950.5786715
HDAC4-SATB2chr2240158289chr2200298237886HLA-B39:06NHMPSTGL0.99930.8915715
HDAC4-SATB2chr2240158289chr2200298237886HLA-B15:37NHMPSTGL0.9940.6344715
HDAC4-SATB2chr2240158289chr2200298237886HLA-B51:01MPSTGLMI0.990.5193917
HDAC4-SATB2chr2240158289chr2200298237886HLA-B14:02NHMPSTGL0.97060.9521715
HDAC4-SATB2chr2240158289chr2200298237886HLA-B14:01NHMPSTGL0.97060.9521715
HDAC4-SATB2chr2240158289chr2200298237886HLA-B15:18NHMPSTGL0.9230.649715
HDAC4-SATB2chr2240158289chr2200298237886HLA-B39:01NHMPSTGLM0.99850.9647716
HDAC4-SATB2chr2240158289chr2200298237886HLA-B39:24NHMPSTGLM0.99720.6091716
HDAC4-SATB2chr2240158289chr2200298237886HLA-B15:10NHMPSTGLM0.99580.5472716
HDAC4-SATB2chr2240158289chr2200298237886HLA-B38:02NHMPSTGLM0.99540.9815716
HDAC4-SATB2chr2240158289chr2200298237886HLA-B38:01NHMPSTGLM0.99490.9771716
HDAC4-SATB2chr2240158289chr2200298237886HLA-B39:06NHMPSTGLM0.98890.9022716
HDAC4-SATB2chr2240158289chr2200298237886HLA-B15:37NHMPSTGLM0.97740.6155716
HDAC4-SATB2chr2240158289chr2200298237886HLA-B15:17STGLMIPVF0.96740.86671120
HDAC4-SATB2chr2240158289chr2200298237886HLA-B14:02NHMPSTGLM0.92320.9611716
HDAC4-SATB2chr2240158289chr2200298237886HLA-B14:01NHMPSTGLM0.92320.9611716
HDAC4-SATB2chr2240158289chr2200298237886HLA-B57:03STGLMIPVF0.88290.96681120
HDAC4-SATB2chr2240158289chr2200298237886HLA-B15:18NHMPSTGLM0.78580.6316716
HDAC4-SATB2chr2240158289chr2200298237886HLA-B39:01NHMPSTGLMI0.99790.9685717
HDAC4-SATB2chr2240158289chr2200298237886HLA-B39:24NHMPSTGLMI0.99760.6202717
HDAC4-SATB2chr2240158289chr2200298237886HLA-B39:06NHMPSTGLMI0.99730.9051717
HDAC4-SATB2chr2240158289chr2200298237886HLA-B38:02NHMPSTGLMI0.99710.9809717
HDAC4-SATB2chr2240158289chr2200298237886HLA-B38:01NHMPSTGLMI0.9970.9738717
HDAC4-SATB2chr2240158289chr2200298237886HLA-B15:37NHMPSTGLMI0.94510.5593717
HDAC4-SATB2chr2240158289chr2200298237886HLA-B15:10VNHMPSTGLM0.87490.5545616
HDAC4-SATB2chr2240158289chr2200298237886HLA-B38:01VNHMPSTGLM0.5730.991616
HDAC4-SATB2chr2240158289chr2200298237886HLA-B27:05ARVNHMPSTGL10.5688415
HDAC4-SATB2chr2240158289chr2200298237886HLA-B27:04ARVNHMPSTGL10.8403415
HDAC4-SATB2chr2240158289chr2200298237886HLA-B27:07ARVNHMPSTGL0.99980.7121415
HDAC4-SATB2chr2240158289chr2200298237886HLA-B35:01MPSTGLMIPVF0.99950.9198920
HDAC4-SATB2chr2240158289chr2200298237886HLA-B35:08MPSTGLMIPVF0.99930.8845920
HDAC4-SATB2chr2240158289chr2200298237886HLA-B35:05MPSTGLMIPVF0.99880.7041920
HDAC4-SATB2chr2240158289chr2200298237886HLA-B35:03MPSTGLMIPVF0.99790.9066920
HDAC4-SATB2chr2240158289chr2200298237886HLA-B35:04MPSTGLMIPVF0.98950.9647920
HDAC4-SATB2chr2240158289chr2200298237886HLA-B35:02MPSTGLMIPVF0.98950.9647920
HDAC4-SATB2chr2240158289chr2200298237886HLA-B39:09NHMPSTGL0.99980.8865715
HDAC4-SATB2chr2240158289chr2200298237886HLA-B39:12NHMPSTGL0.99970.9616715
HDAC4-SATB2chr2240158289chr2200298237886HLA-B39:05NHMPSTGL0.99960.9512715
HDAC4-SATB2chr2240158289chr2200298237886HLA-C01:30HMPSTGLM0.77250.9787816
HDAC4-SATB2chr2240158289chr2200298237886HLA-B14:03NHMPSTGL0.60040.9456715
HDAC4-SATB2chr2240158289chr2200298237886HLA-B39:09NHMPSTGLM0.99860.8846716
HDAC4-SATB2chr2240158289chr2200298237886HLA-B39:12NHMPSTGLM0.99830.9655716
HDAC4-SATB2chr2240158289chr2200298237886HLA-B54:01MPSTGLMIP0.99570.5472918
HDAC4-SATB2chr2240158289chr2200298237886HLA-B39:05NHMPSTGLM0.99550.957716
HDAC4-SATB2chr2240158289chr2200298237886HLA-C01:17HMPSTGLMI0.28210.9767817
HDAC4-SATB2chr2240158289chr2200298237886HLA-B14:03NHMPSTGLM0.22690.9442716
HDAC4-SATB2chr2240158289chr2200298237886HLA-B15:21NHMPSTGLM0.18820.8551716
HDAC4-SATB2chr2240158289chr2200298237886HLA-C01:30HMPSTGLMI0.1470.9798817
HDAC4-SATB2chr2240158289chr2200298237886HLA-B54:01MPSTGLMIPV0.99870.5996919
HDAC4-SATB2chr2240158289chr2200298237886HLA-B39:05NHMPSTGLMI0.99620.9621717
HDAC4-SATB2chr2240158289chr2200298237886HLA-B27:03ARVNHMPSTGL0.99870.6214415
HDAC4-SATB2chr2240158289chr2200298237886HLA-B35:12MPSTGLMIPVF0.98950.9647920
HDAC4-SATB2chr2240158289chr2200298237886HLA-B39:31NHMPSTGL0.99980.9619715
HDAC4-SATB2chr2240158289chr2200298237886HLA-B38:05NHMPSTGL0.99960.9748715
HDAC4-SATB2chr2240158289chr2200298237886HLA-B15:09NHMPSTGL0.99920.6786715
HDAC4-SATB2chr2240158289chr2200298237886HLA-B39:11NHMPSTGL0.99120.8924715
HDAC4-SATB2chr2240158289chr2200298237886HLA-B78:02MPSTGLMI0.98970.9177917
HDAC4-SATB2chr2240158289chr2200298237886HLA-B51:21MPSTGLMI0.98430.5491917
HDAC4-SATB2chr2240158289chr2200298237886HLA-C01:02HMPSTGLM0.98290.9753816
HDAC4-SATB2chr2240158289chr2200298237886HLA-B51:09MPSTGLMI0.97940.5233917
HDAC4-SATB2chr2240158289chr2200298237886HLA-B59:01MPSTGLMI0.94870.5004917
HDAC4-SATB2chr2240158289chr2200298237886HLA-B39:31NHMPSTGLM0.99810.9647716
HDAC4-SATB2chr2240158289chr2200298237886HLA-B38:05NHMPSTGLM0.99490.9771716
HDAC4-SATB2chr2240158289chr2200298237886HLA-B15:09NHMPSTGLM0.98440.6556716
HDAC4-SATB2chr2240158289chr2200298237886HLA-B57:02STGLMIPVF0.89920.92151120
HDAC4-SATB2chr2240158289chr2200298237886HLA-B39:11NHMPSTGLM0.8930.8574716
HDAC4-SATB2chr2240158289chr2200298237886HLA-C01:02HMPSTGLMI0.17640.9763817
HDAC4-SATB2chr2240158289chr2200298237886HLA-C01:03HMPSTGLMI0.08860.9102817
HDAC4-SATB2chr2240158289chr2200298237886HLA-B38:05NHMPSTGLMI0.9970.9738717
HDAC4-SATB2chr2240158289chr2200298237886HLA-B15:09NHMPSTGLMI0.99250.63717
HDAC4-SATB2chr2240158289chr2200298237886HLA-B38:05VNHMPSTGLM0.5730.991616
HDAC4-SATB2chr2240158289chr2200298237886HLA-B15:09VNHMPSTGLM0.5450.7207616
HDAC4-SATB2chr2240158289chr2200298237886HLA-B27:08ARVNHMPSTGL10.547415
HDAC4-SATB2chr2240158289chr2200298237886HLA-B27:10ARVNHMPSTGL10.8673415
HDAC4-SATB2chr2240158289chr2200298237886HLA-B27:09ARVNHMPSTGL0.99990.5546415
HDAC4-SATB2chr2240158289chr2200298237886HLA-B27:06ARVNHMPSTGL0.99990.8512415
HDAC4-SATB2chr2240158289chr2200298237886HLA-B35:77MPSTGLMIPVF0.99950.9198920
HDAC4-SATB2chr2240158289chr2200298237886HLA-B35:23MPSTGLMIPVF0.99950.934920
HDAC4-SATB2chr2240158289chr2200298237886HLA-B35:17MPSTGLMIPVF0.99880.8517920
HDAC4-SATB2chr2240158289chr2200298237886HLA-B35:30MPSTGLMIPVF0.99880.8517920
HDAC4-SATB2chr2240158289chr2200298237886HLA-B35:11MPSTGLMIPVF0.99790.9455920
HDAC4-SATB2chr2240158289chr2200298237886HLA-B55:04MPSTGLMIPVF0.99680.5115920
HDAC4-SATB2chr2240158289chr2200298237886HLA-B35:09MPSTGLMIPVF0.98950.9647920
HDAC4-SATB2chr2240158289chr2200298237886HLA-B35:24MPSTGLMIPVF0.98830.8942920
HDAC4-SATB2chr2240158289chr2200298237886HLA-B15:08MPSTGLMIPVF0.9610.918920
HDAC4-SATB2chr2240158289chr2200298237886HLA-B35:43MPSTGLMIPVF0.96060.9193920
HDAC4-SATB2chr2240158289chr2200298237886HLA-B15:11MPSTGLMIPVF0.95710.9064920

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Potential FusionNeoAntigen Information of HDAC4-SATB2 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 HDAC4-SATB2

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
10138VNHMPSTGLMIPVFHDAC4SATB2chr2240158289chr2200298237886

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of HDAC4-SATB2

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-B14:023BVN10138VNHMPSTGLMIPVF-7.9962-8.1096
HLA-B14:023BVN10138VNHMPSTGLMIPVF-5.70842-6.74372
HLA-B52:013W3910138VNHMPSTGLMIPVF-6.83737-6.95077
HLA-B52:013W3910138VNHMPSTGLMIPVF-4.4836-5.5189
HLA-A11:014UQ210138VNHMPSTGLMIPVF-10.0067-10.1201
HLA-A11:014UQ210138VNHMPSTGLMIPVF-9.03915-10.0745
HLA-A24:025HGA10138VNHMPSTGLMIPVF-6.56204-6.67544
HLA-A24:025HGA10138VNHMPSTGLMIPVF-5.42271-6.45801
HLA-B44:053DX810138VNHMPSTGLMIPVF-7.85648-8.89178
HLA-B44:053DX810138VNHMPSTGLMIPVF-5.3978-5.5112
HLA-B35:011A1N10138VNHMPSTGLMIPVF-6.27422-6.38762
HLA-B35:011A1N10138VNHMPSTGLMIPVF-5.27424-6.30954
HLA-A02:016TDR10138VNHMPSTGLMIPVF-3.37154-4.40684

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Vaccine Design for the FusionNeoAntigens of HDAC4-SATB2

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
HDAC4-SATB2chr2240158289chr22002982371120STGLMIPVFGCACGGGTTTGATGATTCCTGTCTTTT
HDAC4-SATB2chr2240158289chr2200298237415ARVNHMPSTGLCCCGCGTGAACCACATGCCCAGCACGGGTTTGA
HDAC4-SATB2chr2240158289chr2200298237616VNHMPSTGLMTGAACCACATGCCCAGCACGGGTTTGATGA
HDAC4-SATB2chr2240158289chr2200298237715NHMPSTGLACCACATGCCCAGCACGGGTTTGA
HDAC4-SATB2chr2240158289chr2200298237716NHMPSTGLMACCACATGCCCAGCACGGGTTTGATGA
HDAC4-SATB2chr2240158289chr2200298237717NHMPSTGLMIACCACATGCCCAGCACGGGTTTGATGATTC
HDAC4-SATB2chr2240158289chr2200298237816HMPSTGLMACATGCCCAGCACGGGTTTGATGA
HDAC4-SATB2chr2240158289chr2200298237817HMPSTGLMIACATGCCCAGCACGGGTTTGATGATTC
HDAC4-SATB2chr2240158289chr2200298237917MPSTGLMITGCCCAGCACGGGTTTGATGATTC
HDAC4-SATB2chr2240158289chr2200298237918MPSTGLMIPTGCCCAGCACGGGTTTGATGATTCCTG
HDAC4-SATB2chr2240158289chr2200298237919MPSTGLMIPVTGCCCAGCACGGGTTTGATGATTCCTGTCT
HDAC4-SATB2chr2240158289chr2200298237920MPSTGLMIPVFTGCCCAGCACGGGTTTGATGATTCCTGTCTTTT

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 HDAC4-SATB2

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
BLCAHDAC4-SATB2chr2240158289ENST00000345617chr2200298237ENST00000417098TCGA-BL-A13J-01A

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Potential target of CAR-T therapy development for HDAC4-SATB2

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 HDAC4-SATB2

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 HDAC4-SATB2

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