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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:NOTCH2-PSMA5

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: NOTCH2-PSMA5
FusionPDB ID: 59767
FusionGDB2.0 ID: 59767
HgeneTgene
Gene symbol

NOTCH2

PSMA5

Gene ID

4853

5686

Gene namenotch receptor 2proteasome 20S subunit alpha 5
SynonymsAGS2|HJCYS|hN2PSC5|ZETA
Cytomap

1p12

1p13.3

Type of geneprotein-codingprotein-coding
Descriptionneurogenic locus notch homolog protein 2Notch homolog 2notch 2proteasome subunit alpha type-5epididymis tissue sperm binding protein Li 11nmacropain subunit zetamacropain zeta chainmulticatalytic endopeptidase complex zeta chainproteasome (prosome, macropain) subunit, alpha type, 5proteasome alpha 5 subunitpr
Modification date2020032920200327
UniProtAcc

P0DPK3

Main function of 5'-partner protein: FUNCTION: Human-specific protein that promotes neural progenitor proliferation and evolutionary expansion of the brain neocortex by regulating the Notch signaling pathway (PubMed:29856954, PubMed:29856955, PubMed:29561261). Able to promote neural progenitor self-renewal, possibly by down-regulating neuronal differentiation genes, thereby delaying the differentiation of neuronal progenitors and leading to an overall final increase in neuronal production (PubMed:29856954, PubMed:29856955). Acts by enhancing the Notch signaling pathway via two different mechanisms that probably work in parallel to reach the same effect (PubMed:29856954, PubMed:29856955). Enhances Notch signaling pathway in a non-cell-autonomous manner via direct interaction with NOTCH2 (PubMed:29856954). Also promotes Notch signaling pathway in a cell-autonomous manner through inhibition of cis DLL1-NOTCH2 interactions, which promotes neuronal differentiation (PubMed:29856955). {ECO:0000269|PubMed:29561261, ECO:0000269|PubMed:29856954, ECO:0000269|PubMed:29856955}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000256646, ENST00000493703, 
ENST00000602566, 
ENST00000490870, 
ENST00000538610, ENST00000271308, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score26 X 22 X 14=80087 X 6 X 4=168
# samples 358
** MAII scorelog2(35/8008*10)=-4.51601514700366
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/168*10)=-1.0703893278914
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: NOTCH2 [Title/Abstract] AND PSMA5 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: NOTCH2 [Title/Abstract] AND PSMA5 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)NOTCH2(120611948)-PSMA5(109964548), # samples:3
Anticipated loss of major functional domain due to fusion event.NOTCH2-PSMA5 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.
NOTCH2-PSMA5 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.
NOTCH2-PSMA5 seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
NOTCH2-PSMA5 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
NOTCH2-PSMA5 seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
NOTCH2-PSMA5 seems lost the major protein functional domain in Tgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
NOTCH2-PSMA5 seems lost the major protein functional domain in Tgene partner, which is a essential gene 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
HgeneNOTCH2

GO:0007050

cell cycle arrest

11306509

HgeneNOTCH2

GO:0007219

Notch signaling pathway

11306509|25985737

HgeneNOTCH2

GO:0010629

negative regulation of gene expression

11306509

HgeneNOTCH2

GO:0010838

positive regulation of keratinocyte proliferation

18469519

HgeneNOTCH2

GO:0045967

negative regulation of growth rate

11306509

HgeneNOTCH2

GO:0046579

positive regulation of Ras protein signal transduction

11306509

HgeneNOTCH2

GO:0070374

positive regulation of ERK1 and ERK2 cascade

11306509

HgeneNOTCH2

GO:2000249

regulation of actin cytoskeleton reorganization

18469519



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/chr1:120611948/chr1:109964548)
- 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 NOTCH2 (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 PSMA5 (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)
ENST00000256646NOTCH2chr1120611947-ENST00000271308PSMA5chr1109957985-3905293173922249
ENST00000256646NOTCH2chr1120611948-ENST00000271308PSMA5chr1109957985-3905293173922249

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
ENST00000256646ENST00000271308NOTCH2chr1120611947-PSMA5chr1109957985-0.001253920.99874604
ENST00000256646ENST00000271308NOTCH2chr1120611948-PSMA5chr1109957985-0.001253920.99874604

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 NOTCH2-PSMA5

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
NOTCH2chr1120611947PSMA5chr110995798529340CWRSGCAARPPRMLGSTAIGIQTSEG
NOTCH2chr1120611948PSMA5chr110995798529340CWRSGCAARPPRMLGSTAIGIQTSEG

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Potential FusionNeoAntigen Information of NOTCH2-PSMA5 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.
NOTCH2-PSMA5_120611947_109957985.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)
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-A30:08AARPPRMLG0.90820.8282615
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-B07:05RPPRMLGSTA0.99760.5855818
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-B07:02RPPRMLGSTA0.99740.5982818
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-B07:02RPPRMLGSTAI0.99980.5179819
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-B07:02ARPPRMLGSTA0.9940.6648718
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-C12:12AARPPRML0.99540.9573614
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-C06:03AARPPRML0.99070.9945614
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-C03:08CAARPPRML0.99710.7625514
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-C03:07CAARPPRML0.99540.929514
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-C03:19CAARPPRML0.99160.9634514
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-C15:06CAARPPRML0.98250.904514
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-C02:06CAARPPRML0.82250.9354514
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-C12:12CAARPPRML0.79470.9242514
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-C06:03CAARPPRML0.69380.9923514
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-C12:04CAARPPRML0.69020.9935514
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-B07:12RPPRMLGSTA0.98040.7233818
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-B07:04RPPRMLGSTA0.94580.6253818
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-B07:12RPPRMLGSTAI0.99670.6864819
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-B07:04RPPRMLGSTAI0.99510.5504819
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-B07:04ARPPRMLGSTA0.9920.6964718
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-B42:01RPPRMLGSTAI0.8730.7436819
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-C03:05AARPPRML0.99840.8826614
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-C03:17AARPPRML0.99790.9679614
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-B07:13AARPPRML0.9970.8835614
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-C12:03AARPPRML0.98040.9879614
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-C16:01AARPPRML0.95230.9862614
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-C03:05CAARPPRML0.99550.8223514
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-C03:03CAARPPRML0.99520.9641514
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-C03:04CAARPPRML0.99520.9641514
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-C03:17CAARPPRML0.99480.9571514
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-C15:05CAARPPRML0.96370.8688514
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-C15:02CAARPPRML0.96130.8077514
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-B07:13CAARPPRML0.95680.8588514
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-C16:04CAARPPRML0.93690.9828514
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-A30:01AARPPRMLG0.92610.9095615
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-C03:06CAARPPRML0.80330.9702514
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-C16:01CAARPPRML0.75060.9812514
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-C12:03CAARPPRML0.74390.9803514
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-C16:02CAARPPRML0.71640.9925514
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-B07:22RPPRMLGSTA0.99740.5982818
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-B07:09RPPRMLGSTA0.99530.6068818
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-B07:22RPPRMLGSTAI0.99980.5179819
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-B07:09RPPRMLGSTAI0.99970.5273819
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-B07:22ARPPRMLGSTA0.9940.6648718
NOTCH2-PSMA5chr1120611947chr1109957985293HLA-B67:01RPPRMLGSTAI0.57060.6625819

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Potential FusionNeoAntigen Information of NOTCH2-PSMA5 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.
NOTCH2-PSMA5_120611947_109957985.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)
NOTCH2-PSMA5chr1120611947chr1109957985293DRB1-0701PPRMLGSTAIGIQTS924
NOTCH2-PSMA5chr1120611947chr1109957985293DRB1-0701RPPRMLGSTAIGIQT823
NOTCH2-PSMA5chr1120611947chr1109957985293DRB1-0703PPRMLGSTAIGIQTS924
NOTCH2-PSMA5chr1120611947chr1109957985293DRB1-0703RPPRMLGSTAIGIQT823
NOTCH2-PSMA5chr1120611947chr1109957985293DRB1-0704PPRMLGSTAIGIQTS924
NOTCH2-PSMA5chr1120611947chr1109957985293DRB1-0705PPRMLGSTAIGIQTS924
NOTCH2-PSMA5chr1120611947chr1109957985293DRB1-0705RPPRMLGSTAIGIQT823
NOTCH2-PSMA5chr1120611947chr1109957985293DRB1-0707PPRMLGSTAIGIQTS924
NOTCH2-PSMA5chr1120611947chr1109957985293DRB1-0707RPPRMLGSTAIGIQT823
NOTCH2-PSMA5chr1120611947chr1109957985293DRB1-0708PPRMLGSTAIGIQTS924
NOTCH2-PSMA5chr1120611947chr1109957985293DRB1-0708RPPRMLGSTAIGIQT823
NOTCH2-PSMA5chr1120611947chr1109957985293DRB1-0709PPRMLGSTAIGIQTS924
NOTCH2-PSMA5chr1120611947chr1109957985293DRB1-0709RPPRMLGSTAIGIQT823
NOTCH2-PSMA5chr1120611947chr1109957985293DRB1-0711PPRMLGSTAIGIQTS924
NOTCH2-PSMA5chr1120611947chr1109957985293DRB1-0712PPRMLGSTAIGIQTS924
NOTCH2-PSMA5chr1120611947chr1109957985293DRB1-0712RPPRMLGSTAIGIQT823
NOTCH2-PSMA5chr1120611947chr1109957985293DRB1-0713PPRMLGSTAIGIQTS924
NOTCH2-PSMA5chr1120611947chr1109957985293DRB1-0713RPPRMLGSTAIGIQT823
NOTCH2-PSMA5chr1120611947chr1109957985293DRB1-0714PPRMLGSTAIGIQTS924
NOTCH2-PSMA5chr1120611947chr1109957985293DRB1-0714RPPRMLGSTAIGIQT823
NOTCH2-PSMA5chr1120611947chr1109957985293DRB1-0715PPRMLGSTAIGIQTS924
NOTCH2-PSMA5chr1120611947chr1109957985293DRB1-0715RPPRMLGSTAIGIQT823
NOTCH2-PSMA5chr1120611947chr1109957985293DRB1-0716PPRMLGSTAIGIQTS924
NOTCH2-PSMA5chr1120611947chr1109957985293DRB1-0716RPPRMLGSTAIGIQT823
NOTCH2-PSMA5chr1120611947chr1109957985293DRB1-0717PPRMLGSTAIGIQTS924
NOTCH2-PSMA5chr1120611947chr1109957985293DRB1-0717RPPRMLGSTAIGIQT823
NOTCH2-PSMA5chr1120611947chr1109957985293DRB1-0719PPRMLGSTAIGIQTS924
NOTCH2-PSMA5chr1120611947chr1109957985293DRB1-0719RPPRMLGSTAIGIQT823
NOTCH2-PSMA5chr1120611947chr1109957985293DRB1-0904PPRMLGSTAIGIQTS924
NOTCH2-PSMA5chr1120611947chr1109957985293DRB1-0906PPRMLGSTAIGIQTS924

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Fusion breakpoint peptide structures of NOTCH2-PSMA5

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
68AARPPRMLGSTAIGNOTCH2PSMA5chr1120611947chr1109957985293

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of NOTCH2-PSMA5

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-B14:023BVN68AARPPRMLGSTAIG-7.15543-7.26883
HLA-B14:023BVN68AARPPRMLGSTAIG-4.77435-5.80965
HLA-B52:013W3968AARPPRMLGSTAIG-6.80875-6.92215
HLA-B52:013W3968AARPPRMLGSTAIG-4.20386-5.23916
HLA-A11:014UQ268AARPPRMLGSTAIG-7.5194-8.5547
HLA-A11:014UQ268AARPPRMLGSTAIG-6.9601-7.0735
HLA-A24:025HGA68AARPPRMLGSTAIG-7.52403-7.63743
HLA-A24:025HGA68AARPPRMLGSTAIG-5.82433-6.85963
HLA-B27:056PYJ68AARPPRMLGSTAIG-3.28285-4.31815
HLA-B44:053DX868AARPPRMLGSTAIG-5.91172-6.94702
HLA-B44:053DX868AARPPRMLGSTAIG-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of NOTCH2-PSMA5

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
NOTCH2-PSMA5chr1120611947chr1109957985514CAARPPRMLTGTGCTGCGCGGCCCCCGCGCATGCTT
NOTCH2-PSMA5chr1120611947chr1109957985614AARPPRMLGCTGCGCGGCCCCCGCGCATGCTT
NOTCH2-PSMA5chr1120611947chr1109957985615AARPPRMLGGCTGCGCGGCCCCCGCGCATGCTTGGT
NOTCH2-PSMA5chr1120611947chr1109957985718ARPPRMLGSTAGCGCGGCCCCCGCGCATGCTTGGTTCTACAGCC
NOTCH2-PSMA5chr1120611947chr1109957985818RPPRMLGSTACGGCCCCCGCGCATGCTTGGTTCTACAGCC
NOTCH2-PSMA5chr1120611947chr1109957985819RPPRMLGSTAICGGCCCCCGCGCATGCTTGGTTCTACAGCCATT

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
NOTCH2-PSMA5chr1120611947chr1109957985823RPPRMLGSTAIGIQTCGGCCCCCGCGCATGCTTGGTTCTACAGCCATTGGGATCCAGACA
NOTCH2-PSMA5chr1120611947chr1109957985924PPRMLGSTAIGIQTSCCCCCGCGCATGCTTGGTTCTACAGCCATTGGGATCCAGACATCA

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Information of the samples that have these potential fusion neoantigens of NOTCH2-PSMA5

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
OVNOTCH2-PSMA5chr1120611947ENST00000256646chr1109957985ENST00000271308TCGA-36-1574

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Potential target of CAR-T therapy development for NOTCH2-PSMA5

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 NOTCH2-PSMA5

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 NOTCH2-PSMA5

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