FusionNeoAntigen Logo

Home

Download

Statistics

Examples

Help

Contact

Terms of Use

Center for Computational Systems Medicine
leaf

Fusion Gene and Fusion Protein Summary

leaf

Fusion Amino Acid Sequences (multiple BPs and multiple gene isoforms)

leaf

Fusion Protein Breakpoint Sequences - (for the Screening of the FusionNeoAntigens)

leaf

Potential FusionNeoAntigens in HLA I - (netMHCpan v4.1 + deepHLApan v1.1)

leaf

Potential FusionNeoAntigens in HLA II - (netMHCIIpan v4.1)

leaf

Fusion Breakpoint 14 AA Peptide Structure - (RoseTTAFold)

leaf

Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D - (Glide)

leaf

Vaccine Design for the FusionNeoAntigens (RNA/protein sequences)

leaf

Potential target of CAR-T therapy development

leaf

Information on the samples that have these potential fusion neoantigens

leaf

Fusion Protein Targeting Drugs - (Manual Curation)

leaf

Fusion Protein Related diseases - (Manual Curation)

Fusion Protein:SH3KBP1-ZNF92

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: SH3KBP1-ZNF92
FusionPDB ID: 81504
FusionGDB2.0 ID: 81504
HgeneTgene
Gene symbol

SH3KBP1

ZNF92

Gene ID

30011

168374

Gene nameSH3 domain containing kinase binding protein 1zinc finger protein 92
SynonymsAGMX2|CD2BP3|CIN85|GIG10|HSB-1|HSB1|IMD61|MIG18HEL-203|HPF12|HTF12|TF12
Cytomap

Xp22.12

7q11.21

Type of geneprotein-codingprotein-coding
DescriptionSH3 domain-containing kinase-binding protein 1CD2-binding protein 3SH3-domain kinase binding protein 1Src family kinase-binding protein 1c-Cbl-interacting proteincbl-interacting protein of 85 kDahuman Src family kinase-binding protein 1migration-inzinc finger protein 92epididymis luminal protein 203zinc finger protein HTF12
Modification date2020032720200313
UniProtAcc

SHKBP1

Main function of 5'-partner protein: 707
.
Ensembl transtripts involved in fusion geneENST idsENST00000379697, ENST00000379698, 
ENST00000397821, ENST00000379716, 
ENST00000477102, ENST00000541422, 
ENST00000357512, ENST00000431504, 
ENST00000450302, ENST00000328747, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score14 X 14 X 5=9803 X 4 X 3=36
# samples 153
** MAII scorelog2(15/980*10)=-2.70781924850669
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/36*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: SH3KBP1 [Title/Abstract] AND ZNF92 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: SH3KBP1 [Title/Abstract] AND ZNF92 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)SH3KBP1(19701941)-ZNF92(64852815), # samples:2
Anticipated loss of major functional domain due to fusion event.SH3KBP1-ZNF92 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.
SH3KBP1-ZNF92 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.
SH3KBP1-ZNF92 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.
SH3KBP1-ZNF92 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.
SH3KBP1-ZNF92 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
SH3KBP1-ZNF92 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


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/chrX:19701941/chr7:64852815)
- 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 SH3KBP1 (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 ZNF92 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


Top

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)
ENST00000397821SH3KBP1chrX19701941-ENST00000328747ZNF92chr764852815+402510172912774827
ENST00000379698SH3KBP1chrX19701941-ENST00000328747ZNF92chr764852815+3690682672439790
ENST00000379697SH3KBP1chrX19701941-ENST00000328747ZNF92chr764852815+401510071492764871

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
ENST00000397821ENST00000328747SH3KBP1chrX19701941-ZNF92chr764852815+0.0001398610.99986017
ENST00000379698ENST00000328747SH3KBP1chrX19701941-ZNF92chr764852815+0.0005240770.9994759
ENST00000379697ENST00000328747SH3KBP1chrX19701941-ZNF92chr764852815+8.97E-050.99991024

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

Top

Fusion Protein Breakpoint Sequences for SH3KBP1-ZNF92

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
SH3KBP1chrX19701941ZNF92chr7648528151007286SIEVENDFLPVEKGPLTFRDVKIEFS
SH3KBP1chrX19701941ZNF92chr7648528151007448VKVFHKFPNVNRNKIRHTGKKPFKCK
SH3KBP1chrX19701941ZNF92chr7648528151007451FHKFPNVNRNKIRHTGKKPFKCKNRG
SH3KBP1chrX19701941ZNF92chr7648528151017242SIEVENDFLPVEKGPLTFRDVKIEFS
SH3KBP1chrX19701941ZNF92chr7648528151017404VKVFHKFPNVNRNKIRHTGKKPFKCK
SH3KBP1chrX19701941ZNF92chr7648528151017407FHKFPNVNRNKIRHTGKKPFKCKNRG
SH3KBP1chrX19701941ZNF92chr764852815682205SIEVENDFLPVEKGPLTFRDVKIEFS
SH3KBP1chrX19701941ZNF92chr764852815682367VKVFHKFPNVNRNKIRHTGKKPFKCK
SH3KBP1chrX19701941ZNF92chr764852815682370FHKFPNVNRNKIRHTGKKPFKCKNRG

Top

Potential FusionNeoAntigen Information of SH3KBP1-ZNF92 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.
SH3KBP1-ZNF92_19701941_64852815.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)
SH3KBP1-ZNF92chrX19701941chr7648528151007HLA-B35:03FPNVNRNKI0.94890.8726615
SH3KBP1-ZNF92chrX19701941chr7648528151007HLA-B35:02FPNVNRNKI0.90350.7984615
SH3KBP1-ZNF92chrX19701941chr7648528151007HLA-B35:04FPNVNRNKI0.90350.7984615
SH3KBP1-ZNF92chrX19701941chr7648528151007HLA-B08:01FPNVNRNKI0.8890.5854615
SH3KBP1-ZNF92chrX19701941chr7648528151007HLA-B08:09FPNVNRNKI0.84460.619615
SH3KBP1-ZNF92chrX19701941chr7648528151007HLA-B51:07FPNVNRNKI0.96470.5109615
SH3KBP1-ZNF92chrX19701941chr7648528151007HLA-B42:02FPNVNRNKI0.9570.5786615
SH3KBP1-ZNF92chrX19701941chr7648528151007HLA-B42:01FPNVNRNKI0.91260.5774615
SH3KBP1-ZNF92chrX19701941chr7648528151007HLA-B35:12FPNVNRNKI0.90350.7984615
SH3KBP1-ZNF92chrX19701941chr7648528151007HLA-B73:01NRNKIRHTG0.8340.7461019
SH3KBP1-ZNF92chrX19701941chr7648528151007HLA-B39:10FPNVNRNKI0.34490.8249615
SH3KBP1-ZNF92chrX19701941chr7648528151007HLA-A30:01RNKIRHTGK0.97670.80111120
SH3KBP1-ZNF92chrX19701941chr7648528151007HLA-A30:01KFPNVNRNK0.94770.7693514
SH3KBP1-ZNF92chrX19701941chr7648528151007HLA-B35:09FPNVNRNKI0.90350.7984615
SH3KBP1-ZNF92chrX19701941chr7648528151007HLA-B08:18FPNVNRNKI0.8890.5854615
SH3KBP1-ZNF92chrX19701941chr7648528151007HLA-B08:12FPNVNRNKI0.58670.7375615
SH3KBP1-ZNF92chrX19701941chr7648528151007HLA-B67:01FPNVNRNKI0.55720.5578615

Top

Potential FusionNeoAntigen Information of SH3KBP1-ZNF92 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.
SH3KBP1-ZNF92_19701941_64852815.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)
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1114VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1120VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1168VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1182VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1186VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1302VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1316VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1323VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1329VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1331RNKIRHTGKKPFKCK1126
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1331VNRNKIRHTGKKPFK924
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1331NRNKIRHTGKKPFKC1025
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1334VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1339VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1341VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1343RNKIRHTGKKPFKCK1126
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1343VNRNKIRHTGKKPFK924
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1343NRNKIRHTGKKPFKC1025
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1354RNKIRHTGKKPFKCK1126
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1354VNRNKIRHTGKKPFK924
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1354NRNKIRHTGKKPFKC1025
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1367VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1373VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1374VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1376RNKIRHTGKKPFKCK1126
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1377VNRNKIRHTGKKPFK924
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1377RNKIRHTGKKPFKCK1126
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1386VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1396VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1397VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1399VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1416RNKIRHTGKKPFKCK1126
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1416VNRNKIRHTGKKPFK924
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1424VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1424KVFHKFPNVNRNKIR116
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1446VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1502VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1508VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1511VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1514VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1515VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1519VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1526VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1530VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1531VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1538VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1539VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1544VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1547VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB1-1610VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB5-0101VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB5-0102VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB5-0102KVFHKFPNVNRNKIR116
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB5-0103VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB5-0103KVFHKFPNVNRNKIR116
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB5-0104VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB5-0105VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB5-0106VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB5-0108NVKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB5-0108NKVFHKFPNVNRNKIR116
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB5-0111VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB5-0111KVFHKFPNVNRNKIR116
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB5-0113VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB5-0114VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB5-0202VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB5-0203VKVFHKFPNVNRNKI015
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB5-0203KVFHKFPNVNRNKIR116
SH3KBP1-ZNF92chrX19701941chr7648528151007DRB5-0204VKVFHKFPNVNRNKI015

Top

Fusion breakpoint peptide structures of SH3KBP1-ZNF92

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
2504FPNVNRNKIRHTGKSH3KBP1ZNF92chrX19701941chr7648528151007

Top

Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of SH3KBP1-ZNF92

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-B14:023BVN2504FPNVNRNKIRHTGK-7.9962-8.1096
HLA-B14:023BVN2504FPNVNRNKIRHTGK-5.70842-6.74372
HLA-B52:013W392504FPNVNRNKIRHTGK-6.83737-6.95077
HLA-B52:013W392504FPNVNRNKIRHTGK-4.4836-5.5189
HLA-A11:014UQ22504FPNVNRNKIRHTGK-10.0067-10.1201
HLA-A11:014UQ22504FPNVNRNKIRHTGK-9.03915-10.0745
HLA-A24:025HGA2504FPNVNRNKIRHTGK-6.56204-6.67544
HLA-A24:025HGA2504FPNVNRNKIRHTGK-5.42271-6.45801
HLA-B44:053DX82504FPNVNRNKIRHTGK-7.85648-8.89178
HLA-B44:053DX82504FPNVNRNKIRHTGK-5.3978-5.5112
HLA-A02:016TDR2504FPNVNRNKIRHTGK-3.37154-4.40684

Top

Vaccine Design for the FusionNeoAntigens of SH3KBP1-ZNF92

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
SH3KBP1-ZNF92chrX19701941chr7648528151019NRNKIRHTGGTAGAAAAGGGACCACTGACATTTAGG
SH3KBP1-ZNF92chrX19701941chr7648528151120RNKIRHTGKGAAAAGGGACCACTGACATTTAGGGAT
SH3KBP1-ZNF92chrX19701941chr764852815514KFPNVNRNKAATGACTTTCTGCCGGTAGAAAAGGGA
SH3KBP1-ZNF92chrX19701941chr764852815615FPNVNRNKIGACTTTCTGCCGGTAGAAAAGGGACCA

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
SH3KBP1-ZNF92chrX19701941chr764852815015VKVFHKFPNVNRNKITCAATTGAAGTAGAAAATGACTTTCTGCCGGTAGAAAAGGGACCA
SH3KBP1-ZNF92chrX19701941chr764852815116KVFHKFPNVNRNKIRATTGAAGTAGAAAATGACTTTCTGCCGGTAGAAAAGGGACCACTG
SH3KBP1-ZNF92chrX19701941chr7648528151025NRNKIRHTGKKPFKCGTAGAAAAGGGACCACTGACATTTAGGGATGTGAAAATAGAATTC
SH3KBP1-ZNF92chrX19701941chr7648528151126RNKIRHTGKKPFKCKGAAAAGGGACCACTGACATTTAGGGATGTGAAAATAGAATTCTCT
SH3KBP1-ZNF92chrX19701941chr764852815924VNRNKIRHTGKKPFKCCGGTAGAAAAGGGACCACTGACATTTAGGGATGTGAAAATAGAA

Top

Information of the samples that have these potential fusion neoantigens of SH3KBP1-ZNF92

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
SARCSH3KBP1-ZNF92chrX19701941ENST00000379697chr764852815ENST00000328747TCGA-IE-A4EJ-01A

Top

Potential target of CAR-T therapy development for SH3KBP1-ZNF92

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

Top

Related Drugs to SH3KBP1-ZNF92

check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

Top

Related Diseases to SH3KBP1-ZNF92

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