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:KAT7-NPLOC4

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: KAT7-NPLOC4
FusionPDB ID: 41251
FusionGDB2.0 ID: 41251
HgeneTgene
Gene symbol

KAT7

NPLOC4

Gene ID

11143

55666

Gene namelysine acetyltransferase 7NPL4 homolog, ubiquitin recognition factor
SynonymsHBO1|HBOA|MYST2|ZC2HC7NPL4
Cytomap

17q21.33

17q25.3

Type of geneprotein-codingprotein-coding
Descriptionhistone acetyltransferase KAT7K(lysine) acetyltransferase 7MOZ, YBF2/SAS3, SAS2 and TIP60 protein 2MYST histone acetyltransferase 2histone acetyltransferase MYST2histone acetyltransferase binding to ORC1nuclear protein localization protein 4 homologNPLOC4 ubiquitin recognition factornuclear protein localization 4 homolog
Modification date2020032720200313
UniProtAcc

O95251

Main function of 5'-partner protein: FUNCTION: Catalytic subunit of histone acetyltransferase HBO1 complexes, which specifically mediate acetylation of histone H3 at 'Lys-14' (H3K14ac), thereby regulating various processes, such as gene transcription, protein ubiquitination, immune regulation, stem cell pluripotent and self-renewal maintenance and embryonic development (PubMed:16387653, PubMed:21753189, PubMed:24065767, PubMed:26620551, PubMed:31767635, PubMed:31827282). Some complexes also catalyze acetylation of histone H4 at 'Lys-5', 'Lys-8' and 'Lys-12' (H4K5ac, H4K8ac and H4K12ac, respectively), regulating DNA replication initiation, regulating DNA replication initiation (PubMed:10438470, PubMed:19187766, PubMed:20129055, PubMed:24065767). Specificity of the HBO1 complexes is determined by the scaffold subunit: complexes containing BRPF scaffold (BRPF1, BRD1/BRPF2 or BRPF3) direct KAT7/HBO1 specificity towards H3K14ac, while complexes containing JADE (JADE1, JADE2 and JADE3) scaffold direct KAT7/HBO1 specificity towards histone H4 (PubMed:19187766, PubMed:20129055, PubMed:24065767, PubMed:26620551). H3K14ac promotes transcriptional elongation by facilitating the processivity of RNA polymerase II (PubMed:31827282). Acts as a key regulator of hematopoiesis by forming a complex with BRD1/BRPF2, directing KAT7/HBO1 specificity towards H3K14ac and promoting erythroid differentiation (PubMed:21753189). H3K14ac is also required for T-cell development (By similarity). KAT7/HBO1-mediated acetylation facilitates two consecutive steps, licensing and activation, in DNA replication initiation: H3K14ac facilitates the activation of replication origins, and histone H4 acetylation (H4K5ac, H4K8ac and H4K12ac) facilitates chromatin loading of MCM complexes, promoting DNA replication licensing (PubMed:10438470, PubMed:11278932, PubMed:18832067, PubMed:19187766, PubMed:20129055, PubMed:21856198, PubMed:24065767, PubMed:26620551). Acts as a positive regulator of centromeric CENPA assembly: recruited to centromeres and mediates histone acetylation, thereby preventing centromere inactivation mediated by SUV39H1, possibly by increasing histone turnover/exchange (PubMed:27270040). Involved in nucleotide excision repair: phosphorylation by ATR in response to ultraviolet irradiation promotes its localization to DNA damage sites, where it mediates histone acetylation to facilitate recruitment of XPC at the damaged DNA sites (PubMed:28719581). Acts as an inhibitor of NF-kappa-B independently of its histone acetyltransferase activity (PubMed:16997280). {ECO:0000250|UniProtKB:Q5SVQ0, ECO:0000269|PubMed:10438470, ECO:0000269|PubMed:11278932, ECO:0000269|PubMed:16387653, ECO:0000269|PubMed:16997280, ECO:0000269|PubMed:18832067, ECO:0000269|PubMed:19187766, ECO:0000269|PubMed:20129055, ECO:0000269|PubMed:21753189, ECO:0000269|PubMed:21856198, ECO:0000269|PubMed:24065767, ECO:0000269|PubMed:26620551, ECO:0000269|PubMed:27270040, ECO:0000269|PubMed:28719581, ECO:0000269|PubMed:31767635, ECO:0000269|PubMed:31827282}.; FUNCTION: Plays a central role in the maintenance of leukemia stem cells in acute myeloid leukemia (AML) (PubMed:31827282). Acts by mediating acetylation of histone H3 at 'Lys-14' (H3K14ac), thereby facilitating the processivity of RNA polymerase II to maintain the high expression of key genes, such as HOXA9 and HOXA10 that help to sustain the functional properties of leukemia stem cells (PubMed:31827282). {ECO:0000269|PubMed:31827282}.

Q8TAT6

Main function of 5'-partner protein: FUNCTION: The ternary complex containing UFD1, VCP and NPLOC4 binds ubiquitinated proteins and is necessary for the export of misfolded proteins from the ER to the cytoplasm, where they are degraded by the proteasome. The NPLOC4-UFD1-VCP complex regulates spindle disassembly at the end of mitosis and is necessary for the formation of a closed nuclear envelope (By similarity). Acts as a negative regulator of type I interferon production via the complex formed with VCP and UFD1, which binds to DDX58/RIG-I and recruits RNF125 to promote ubiquitination and degradation of DDX58/RIG-I (PubMed:26471729). {ECO:0000250|UniProtKB:Q9ES54, ECO:0000269|PubMed:26471729}.
Ensembl transtripts involved in fusion geneENST idsENST00000259021, ENST00000424009, 
ENST00000435742, ENST00000454930, 
ENST00000503935, ENST00000509773, 
ENST00000510819, ENST00000513980, 
ENST00000539314, ENST00000572760, 
ENST00000573876, ENST00000574344, 
ENST00000331134, ENST00000374747, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score5 X 4 X 4=8015 X 9 X 10=1350
# samples 718
** MAII scorelog2(7/80*10)=-0.192645077942396
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(18/1350*10)=-2.90689059560852
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: KAT7 [Title/Abstract] AND NPLOC4 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: KAT7 [Title/Abstract] AND NPLOC4 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)KAT7(47895373)-NPLOC4(79589304), # samples:2
Anticipated loss of major functional domain due to fusion event.KAT7-NPLOC4 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.
KAT7-NPLOC4 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.
KAT7-NPLOC4 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.
KAT7-NPLOC4 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
HgeneKAT7

GO:0006260

DNA replication

16387653

HgeneKAT7

GO:0018393

internal peptidyl-lysine acetylation

26221039

HgeneKAT7

GO:0031098

stress-activated protein kinase signaling cascade

21856198

HgeneKAT7

GO:0043966

histone H3 acetylation

16387653

HgeneKAT7

GO:0043981

histone H4-K5 acetylation

16387653

HgeneKAT7

GO:0043982

histone H4-K8 acetylation

16387653

HgeneKAT7

GO:0043983

histone H4-K12 acetylation

16387653

HgeneKAT7

GO:0043984

histone H4-K16 acetylation

16387653

HgeneKAT7

GO:1900182

positive regulation of protein localization to nucleus

24739512



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/chr17:47895373/chr17:79589304)
- 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 KAT7 (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 NPLOC4 (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)
ENST00000259021KAT7chr1747895373+ENST00000331134NPLOC4chr1779589304-553814352803165961
ENST00000259021KAT7chr1747895373+ENST00000374747NPLOC4chr1779589304-674714352803192970
ENST00000454930KAT7chr1747895373+ENST00000331134NPLOC4chr1779589304-49958921542622822
ENST00000454930KAT7chr1747895373+ENST00000374747NPLOC4chr1779589304-62048921542649831
ENST00000509773KAT7chr1747895373+ENST00000331134NPLOC4chr1779589304-50819781532708851
ENST00000509773KAT7chr1747895373+ENST00000374747NPLOC4chr1779589304-62909781532735860
ENST00000510819KAT7chr1747895373+ENST00000331134NPLOC4chr1779589304-48937901422520792
ENST00000510819KAT7chr1747895373+ENST00000374747NPLOC4chr1779589304-61027901422547801
ENST00000424009KAT7chr1747895373+ENST00000331134NPLOC4chr1779589304-529711941292924931
ENST00000424009KAT7chr1747895373+ENST00000374747NPLOC4chr1779589304-650611941292951940
ENST00000503935KAT7chr1747895373+ENST00000331134NPLOC4chr1779589304-5826172344234531003
ENST00000503935KAT7chr1747895373+ENST00000374747NPLOC4chr1779589304-7035172344234801012
ENST00000435742KAT7chr1747895373+ENST00000331134NPLOC4chr1779589304-546613631723093973
ENST00000435742KAT7chr1747895373+ENST00000374747NPLOC4chr1779589304-667513631723120982

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
ENST00000259021ENST00000331134KAT7chr1747895373+NPLOC4chr1779589304-0.0013651790.99863476
ENST00000259021ENST00000374747KAT7chr1747895373+NPLOC4chr1779589304-0.0007349540.999265
ENST00000454930ENST00000331134KAT7chr1747895373+NPLOC4chr1779589304-0.0041480080.995852
ENST00000454930ENST00000374747KAT7chr1747895373+NPLOC4chr1779589304-0.0019603020.99803966
ENST00000509773ENST00000331134KAT7chr1747895373+NPLOC4chr1779589304-0.002382170.9976178
ENST00000509773ENST00000374747KAT7chr1747895373+NPLOC4chr1779589304-0.0011744060.9988256
ENST00000510819ENST00000331134KAT7chr1747895373+NPLOC4chr1779589304-0.0046577380.99534225
ENST00000510819ENST00000374747KAT7chr1747895373+NPLOC4chr1779589304-0.0024371280.9975629
ENST00000424009ENST00000331134KAT7chr1747895373+NPLOC4chr1779589304-0.0017054510.99829453
ENST00000424009ENST00000374747KAT7chr1747895373+NPLOC4chr1779589304-0.0008460040.999154
ENST00000503935ENST00000331134KAT7chr1747895373+NPLOC4chr1779589304-0.0012611190.99873894
ENST00000503935ENST00000374747KAT7chr1747895373+NPLOC4chr1779589304-0.0006841360.99931586
ENST00000435742ENST00000331134KAT7chr1747895373+NPLOC4chr1779589304-0.0022355150.99776447
ENST00000435742ENST00000374747KAT7chr1747895373+NPLOC4chr1779589304-0.001245320.9987546

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 KAT7-NPLOC4

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
KAT7chr1747895373NPLOC4chr17795893041194355KYMKSQTILRRHMVAKEFGFQNNGFS
KAT7chr1747895373NPLOC4chr17795893041363397KYMKSQTILRRHMVAKEFGFQNNGFS
KAT7chr1747895373NPLOC4chr17795893041435385KYMKSQTILRRHMVAKEFGFQNNGFS
KAT7chr1747895373NPLOC4chr17795893041723427KYMKSQTILRRHMVAKEFGFQNNGFS
KAT7chr1747895373NPLOC4chr1779589304790216KYMKSQTILRRHMVAKEFGFQNNGFS
KAT7chr1747895373NPLOC4chr1779589304892246KYMKSQTILRRHMVAKEFGFQNNGFS
KAT7chr1747895373NPLOC4chr1779589304978275KYMKSQTILRRHMVAKEFGFQNNGFS

Top

Potential FusionNeoAntigen Information of KAT7-NPLOC4 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.
KAT7-NPLOC4_47895373_79589304.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)
KAT7-NPLOC4chr1747895373chr17795893041435HLA-B08:09ILRRHMVA0.99870.8005715
KAT7-NPLOC4chr1747895373chr17795893041435HLA-B38:01RHMVAKEF0.9740.89551018
KAT7-NPLOC4chr1747895373chr17795893041435HLA-B15:18RHMVAKEF0.9620.60541018
KAT7-NPLOC4chr1747895373chr17795893041435HLA-B27:04RRHMVAKEF0.99980.644918
KAT7-NPLOC4chr1747895373chr17795893041435HLA-B27:05RRHMVAKEF0.99980.6722918
KAT7-NPLOC4chr1747895373chr17795893041435HLA-B27:07RRHMVAKEF0.99840.5329918
KAT7-NPLOC4chr1747895373chr17795893041435HLA-B08:01TILRRHMVA0.9950.7309615
KAT7-NPLOC4chr1747895373chr17795893041435HLA-B08:09TILRRHMVA0.99360.7963615
KAT7-NPLOC4chr1747895373chr17795893041435HLA-A30:08ILRRHMVAK0.98710.6956716
KAT7-NPLOC4chr1747895373chr17795893041435HLA-A74:03ILRRHMVAK0.7810.5516716
KAT7-NPLOC4chr1747895373chr17795893041435HLA-A74:09ILRRHMVAK0.7810.5516716
KAT7-NPLOC4chr1747895373chr17795893041435HLA-A74:11ILRRHMVAK0.7810.5516716
KAT7-NPLOC4chr1747895373chr17795893041435HLA-B15:03RRHMVAKEF0.30480.692918
KAT7-NPLOC4chr1747895373chr17795893041435HLA-B15:18RRHMVAKEF0.2680.6345918
KAT7-NPLOC4chr1747895373chr17795893041435HLA-B27:05RRHMVAKEFGF10.5463920
KAT7-NPLOC4chr1747895373chr17795893041435HLA-B27:04RRHMVAKEFGF10.6986920
KAT7-NPLOC4chr1747895373chr17795893041435HLA-B27:14RRHMVAKEF0.99980.6368918
KAT7-NPLOC4chr1747895373chr17795893041435HLA-C07:95RRHMVAKEF0.99740.6292918
KAT7-NPLOC4chr1747895373chr17795893041435HLA-B27:03RRHMVAKEF0.99720.7094918
KAT7-NPLOC4chr1747895373chr17795893041435HLA-C07:05RRHMVAKEF0.99650.9472918
KAT7-NPLOC4chr1747895373chr17795893041435HLA-C07:27RRHMVAKEF0.99120.938918
KAT7-NPLOC4chr1747895373chr17795893041435HLA-C07:80RRHMVAKEF0.81340.9229918
KAT7-NPLOC4chr1747895373chr17795893041435HLA-C07:67RRHMVAKEF0.81340.9229918
KAT7-NPLOC4chr1747895373chr17795893041435HLA-C07:19RRHMVAKEF0.81030.6981918
KAT7-NPLOC4chr1747895373chr17795893041435HLA-C07:46RRHMVAKEF0.81030.8217918
KAT7-NPLOC4chr1747895373chr17795893041435HLA-C07:10RRHMVAKEF0.80070.9523918
KAT7-NPLOC4chr1747895373chr17795893041435HLA-C12:16RRHMVAKEF0.08020.9698918
KAT7-NPLOC4chr1747895373chr17795893041435HLA-B27:03RRHMVAKEFGF0.99960.5903920
KAT7-NPLOC4chr1747895373chr17795893041435HLA-B38:05RHMVAKEF0.9740.89551018
KAT7-NPLOC4chr1747895373chr17795893041435HLA-B27:10RRHMVAKEF0.99980.8092918
KAT7-NPLOC4chr1747895373chr17795893041435HLA-B27:08RRHMVAKEF0.99980.5347918
KAT7-NPLOC4chr1747895373chr17795893041435HLA-B27:06RRHMVAKEF0.99960.6545918
KAT7-NPLOC4chr1747895373chr17795893041435HLA-C07:01RRHMVAKEF0.99830.6194918
KAT7-NPLOC4chr1747895373chr17795893041435HLA-B27:09RRHMVAKEF0.99780.6093918
KAT7-NPLOC4chr1747895373chr17795893041435HLA-B08:18TILRRHMVA0.9950.7309615
KAT7-NPLOC4chr1747895373chr17795893041435HLA-A30:01ILRRHMVAK0.98780.8247716
KAT7-NPLOC4chr1747895373chr17795893041435HLA-C07:17RRHMVAKEF0.97250.9499918
KAT7-NPLOC4chr1747895373chr17795893041435HLA-A68:02QTILRRHMV0.94740.7867514
KAT7-NPLOC4chr1747895373chr17795893041435HLA-C06:08RRHMVAKEF0.91690.9856918
KAT7-NPLOC4chr1747895373chr17795893041435HLA-C07:02RRHMVAKEF0.81340.9229918
KAT7-NPLOC4chr1747895373chr17795893041435HLA-C07:22RRHMVAKEF0.80720.7098918
KAT7-NPLOC4chr1747895373chr17795893041435HLA-A74:01ILRRHMVAK0.7810.5516716
KAT7-NPLOC4chr1747895373chr17795893041435HLA-C06:06RRHMVAKEF0.17110.992918
KAT7-NPLOC4chr1747895373chr17795893041435HLA-B15:68RRHMVAKEF0.08090.5881918
KAT7-NPLOC4chr1747895373chr17795893041435HLA-B15:54RRHMVAKEF0.06720.7549918
KAT7-NPLOC4chr1747895373chr17795893041435HLA-C06:17RRHMVAKEF0.06510.9892918
KAT7-NPLOC4chr1747895373chr17795893041435HLA-C06:02RRHMVAKEF0.06510.9892918
KAT7-NPLOC4chr1747895373chr17795893041435HLA-B27:10RRHMVAKEFGF10.8264920
KAT7-NPLOC4chr1747895373chr17795893041435HLA-B27:06RRHMVAKEFGF10.6935920

Top

Potential FusionNeoAntigen Information of KAT7-NPLOC4 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)

Top

Fusion breakpoint peptide structures of KAT7-NPLOC4

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
9407TILRRHMVAKEFGFKAT7NPLOC4chr1747895373chr17795893041435

Top

Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of KAT7-NPLOC4

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-B14:023BVN9407TILRRHMVAKEFGF-7.9962-8.1096
HLA-B14:023BVN9407TILRRHMVAKEFGF-5.70842-6.74372
HLA-B52:013W399407TILRRHMVAKEFGF-6.83737-6.95077
HLA-B52:013W399407TILRRHMVAKEFGF-4.4836-5.5189
HLA-A11:014UQ29407TILRRHMVAKEFGF-10.0067-10.1201
HLA-A11:014UQ29407TILRRHMVAKEFGF-9.03915-10.0745
HLA-A24:025HGA9407TILRRHMVAKEFGF-6.56204-6.67544
HLA-A24:025HGA9407TILRRHMVAKEFGF-5.42271-6.45801
HLA-B44:053DX89407TILRRHMVAKEFGF-7.85648-8.89178
HLA-B44:053DX89407TILRRHMVAKEFGF-5.3978-5.5112
HLA-A02:016TDR9407TILRRHMVAKEFGF-3.37154-4.40684

Top

Vaccine Design for the FusionNeoAntigens of KAT7-NPLOC4

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
KAT7-NPLOC4chr1747895373chr17795893041018RHMVAKEFCGGCACATGGTTGCAAAGGAGTTT
KAT7-NPLOC4chr1747895373chr1779589304514QTILRRHMVCAAACGATACTCCGCCGGCACATGGTT
KAT7-NPLOC4chr1747895373chr1779589304615TILRRHMVAACGATACTCCGCCGGCACATGGTTGCA
KAT7-NPLOC4chr1747895373chr1779589304715ILRRHMVAATACTCCGCCGGCACATGGTTGCA
KAT7-NPLOC4chr1747895373chr1779589304716ILRRHMVAKATACTCCGCCGGCACATGGTTGCAAAG
KAT7-NPLOC4chr1747895373chr1779589304918RRHMVAKEFCGCCGGCACATGGTTGCAAAGGAGTTT
KAT7-NPLOC4chr1747895373chr1779589304920RRHMVAKEFGFCGCCGGCACATGGTTGCAAAGGAGTTTGGCTTC

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

Top

Information of the samples that have these potential fusion neoantigens of KAT7-NPLOC4

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
KIRCKAT7-NPLOC4chr1747895373ENST00000259021chr1779589304ENST00000331134TCGA-BP-4983-01A

Top

Potential target of CAR-T therapy development for KAT7-NPLOC4

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 KAT7-NPLOC4

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

Top

Related Diseases to KAT7-NPLOC4

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