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:UVRAG-NOM1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: UVRAG-NOM1
FusionPDB ID: 97802
FusionGDB2.0 ID: 97802
HgeneTgene
Gene symbol

UVRAG

NOM1

Gene ID

7405

64434

Gene nameUV radiation resistance associatednucleolar protein with MIF4G domain 1
SynonymsDHTX|VPS38|p63C7orf3|PPP1R113|SGD1
Cytomap

11q13.5

7q36.3

Type of geneprotein-codingprotein-coding
DescriptionUV radiation resistance-associated gene proteinbeclin 1 binding proteindisrupted in heterotaxynucleolar MIF4G domain-containing protein 1SGD1 homologprotein phosphatase 1, regulatory subunit 113
Modification date2020031320200313
UniProtAcc.

Q5C9Z4

Main function of 5'-partner protein: FUNCTION: Plays a role in targeting PPP1CA to the nucleolus. {ECO:0000269|PubMed:17965019}.
Ensembl transtripts involved in fusion geneENST idsENST00000356136, ENST00000528420, 
ENST00000531818, ENST00000532130, 
ENST00000533454, ENST00000539288, 
ENST00000525872, ENST00000538870, 
ENST00000460332, ENST00000275820, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score41 X 18 X 15=110702 X 2 X 2=8
# samples 492
** MAII scorelog2(49/11070*10)=-4.49772966266634
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/8*10)=1.32192809488736
Fusion gene context

PubMed: UVRAG [Title/Abstract] AND NOM1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: UVRAG [Title/Abstract] AND NOM1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)NOM1(156743418)-UVRAG(75776754), # samples:2
UVRAG(75728024)-NOM1(156746797), # samples:1
Anticipated loss of major functional domain due to fusion event.UVRAG-NOM1 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.
UVRAG-NOM1 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.
UVRAG-NOM1 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.
UVRAG-NOM1 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.
NOM1-UVRAG seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
NOM1-UVRAG seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
NOM1-UVRAG seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor 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
HgeneUVRAG

GO:0071900

regulation of protein serine/threonine kinase activity

22542840

HgeneUVRAG

GO:0097352

autophagosome maturation

28306502

HgeneUVRAG

GO:0097680

double-strand break repair via classical nonhomologous end joining

22542840



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/chr11:156743418/chr7:75776754)
- 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 UVRAG (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 NOM1 (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)
ENST00000356136UVRAGchr1175728024-ENST00000275820NOM1chr7156746797+641714671632937924
ENST00000528420UVRAGchr1175728024-ENST00000275820NOM1chr7156746797+61581208962678860
ENST00000533454UVRAGchr1175728024-ENST00000275820NOM1chr7156746797+58128626802332550
ENST00000531818UVRAGchr1175728024-ENST00000275820NOM1chr7156746797+599010404472510687
ENST00000532130UVRAGchr1175728024-ENST00000275820NOM1chr7156746797+5537587482057669
ENST00000539288UVRAGchr1175728024-ENST00000275820NOM1chr7156746797+56046544722124550

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
ENST00000356136ENST00000275820UVRAGchr1175728024-NOM1chr7156746797+0.0003176430.9996824
ENST00000528420ENST00000275820UVRAGchr1175728024-NOM1chr7156746797+0.000527080.9994729
ENST00000533454ENST00000275820UVRAGchr1175728024-NOM1chr7156746797+0.0011224440.9988776
ENST00000531818ENST00000275820UVRAGchr1175728024-NOM1chr7156746797+0.0014570060.998543
ENST00000532130ENST00000275820UVRAGchr1175728024-NOM1chr7156746797+0.0012356340.9987644
ENST00000539288ENST00000275820UVRAGchr1175728024-NOM1chr7156746797+0.0011639250.9988361

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 UVRAG-NOM1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
UVRAGchr1175728024NOM1chr71567467971208371DNINDKLTEKERELSEPNMASISGQL
UVRAGchr1175728024NOM1chr71567467971467435DNINDKLTEKERELSEPNMASISGQL
UVRAGchr1175728024NOM1chr7156746797587180DNINDKLTEKERELSEPNMASISGQL
UVRAGchr1175728024NOM1chr715674679765461DNINDKLTEKERELSEPNMASISGQL
UVRAGchr1175728024NOM1chr715674679786261DNINDKLTEKERELSEPNMASISGQL

Top

Potential FusionNeoAntigen Information of UVRAG-NOM1 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.
UVRAG-NOM1_75728024_156746797.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)
UVRAG-NOM1chr1175728024chr71567467971467HLA-B39:01ERELSEPNM0.98860.89731019
UVRAG-NOM1chr1175728024chr71567467971467HLA-B45:01RELSEPNMA0.98660.79691120
UVRAG-NOM1chr1175728024chr71567467971467HLA-B50:02RELSEPNMA0.98640.62221120
UVRAG-NOM1chr1175728024chr71567467971467HLA-B38:02ERELSEPNM0.98460.92191019
UVRAG-NOM1chr1175728024chr71567467971467HLA-A02:22KLTEKEREL0.96850.5994514
UVRAG-NOM1chr1175728024chr71567467971467HLA-A02:30KLTEKEREL0.94340.7587514
UVRAG-NOM1chr1175728024chr71567467971467HLA-A02:24KLTEKEREL0.94340.7587514
UVRAG-NOM1chr1175728024chr71567467971467HLA-A02:67KLTEKEREL0.94340.7587514
UVRAG-NOM1chr1175728024chr71567467971467HLA-A02:60KLTEKEREL0.94250.7058514
UVRAG-NOM1chr1175728024chr71567467971467HLA-A02:13KLTEKEREL0.93570.7363514
UVRAG-NOM1chr1175728024chr71567467971467HLA-A02:27KLTEKEREL0.92670.6593514
UVRAG-NOM1chr1175728024chr71567467971467HLA-A02:38KLTEKEREL0.91410.7259514
UVRAG-NOM1chr1175728024chr71567467971467HLA-A02:04KLTEKEREL0.91370.7005514
UVRAG-NOM1chr1175728024chr71567467971467HLA-A02:29KLTEKEREL0.75780.7578514
UVRAG-NOM1chr1175728024chr71567467971467HLA-A02:20KLTEKEREL0.75440.7588514
UVRAG-NOM1chr1175728024chr71567467971467HLA-B15:10ERELSEPNM0.73830.57911019
UVRAG-NOM1chr1175728024chr71567467971467HLA-B15:37ERELSEPNM0.6370.57981019
UVRAG-NOM1chr1175728024chr71567467971467HLA-B41:01RELSEPNMA0.43510.76511120
UVRAG-NOM1chr1175728024chr71567467971467HLA-B50:01RELSEPNMA0.1510.75761120
UVRAG-NOM1chr1175728024chr71567467971467HLA-B13:01KLTEKEREL0.00690.9812514
UVRAG-NOM1chr1175728024chr71567467971467HLA-B45:01TEKERELSEP0.97010.7404717
UVRAG-NOM1chr1175728024chr71567467971467HLA-B50:02TEKERELSEP0.91970.6223717
UVRAG-NOM1chr1175728024chr71567467971467HLA-B45:01ERELSEPNMA0.76030.74041020
UVRAG-NOM1chr1175728024chr71567467971467HLA-B50:01RELSEPNMAS0.61030.76461121
UVRAG-NOM1chr1175728024chr71567467971467HLA-B41:01KERELSEPNMA0.99810.6369920
UVRAG-NOM1chr1175728024chr71567467971467HLA-B50:01KERELSEPNMA0.97490.7143920
UVRAG-NOM1chr1175728024chr71567467971467HLA-B40:06RELSEPNMA0.9970.70181120
UVRAG-NOM1chr1175728024chr71567467971467HLA-B39:12ERELSEPNM0.98620.90411019
UVRAG-NOM1chr1175728024chr71567467971467HLA-A02:01KLTEKEREL0.94340.7587514
UVRAG-NOM1chr1175728024chr71567467971467HLA-B73:01ERELSEPNMA0.93850.60111020
UVRAG-NOM1chr1175728024chr71567467971467HLA-B40:06KERELSEPNMA0.99980.5311920
UVRAG-NOM1chr1175728024chr71567467971467HLA-B39:31ERELSEPNM0.98950.89671019
UVRAG-NOM1chr1175728024chr71567467971467HLA-B40:04RELSEPNMA0.96240.74561120
UVRAG-NOM1chr1175728024chr71567467971467HLA-A02:03KLTEKEREL0.93930.7434514
UVRAG-NOM1chr1175728024chr71567467971467HLA-B15:09ERELSEPNM0.74280.54251019
UVRAG-NOM1chr1175728024chr71567467971467HLA-C07:04KLTEKEREL0.63570.9478514
UVRAG-NOM1chr1175728024chr71567467971467HLA-B15:73KLTEKEREL0.42630.9294514
UVRAG-NOM1chr1175728024chr71567467971467HLA-B15:30KLTEKEREL0.35510.8246514
UVRAG-NOM1chr1175728024chr71567467971467HLA-B50:05RELSEPNMA0.1510.75761120
UVRAG-NOM1chr1175728024chr71567467971467HLA-B50:04RELSEPNMA0.1510.75761120
UVRAG-NOM1chr1175728024chr71567467971467HLA-A68:02ELSEPNMASI0.94650.67031222
UVRAG-NOM1chr1175728024chr71567467971467HLA-B50:04RELSEPNMAS0.61030.76461121
UVRAG-NOM1chr1175728024chr71567467971467HLA-B50:05RELSEPNMAS0.61030.76461121
UVRAG-NOM1chr1175728024chr71567467971467HLA-B50:05KERELSEPNMA0.97490.7143920
UVRAG-NOM1chr1175728024chr71567467971467HLA-B50:04KERELSEPNMA0.97490.7143920

Top

Potential FusionNeoAntigen Information of UVRAG-NOM1 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.
UVRAG-NOM1_75728024_156746797.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)
UVRAG-NOM1chr1175728024chr71567467971467DRB1-1103NDKLTEKERELSEPN318
UVRAG-NOM1chr1175728024chr71567467971467DRB1-1103INDKLTEKERELSEP217
UVRAG-NOM1chr1175728024chr71567467971467DRB1-1111NDKLTEKERELSEPN318
UVRAG-NOM1chr1175728024chr71567467971467DRB1-1125NDKLTEKERELSEPN318
UVRAG-NOM1chr1175728024chr71567467971467DRB1-1136NDKLTEKERELSEPN318
UVRAG-NOM1chr1175728024chr71567467971467DRB1-1141NDKLTEKERELSEPN318
UVRAG-NOM1chr1175728024chr71567467971467DRB1-1141INDKLTEKERELSEP217
UVRAG-NOM1chr1175728024chr71567467971467DRB1-1148NDKLTEKERELSEPN318
UVRAG-NOM1chr1175728024chr71567467971467DRB1-1155NDKLTEKERELSEPN318
UVRAG-NOM1chr1175728024chr71567467971467DRB1-1155INDKLTEKERELSEP217
UVRAG-NOM1chr1175728024chr71567467971467DRB1-1159NDKLTEKERELSEPN318
UVRAG-NOM1chr1175728024chr71567467971467DRB1-1159INDKLTEKERELSEP217
UVRAG-NOM1chr1175728024chr71567467971467DRB1-1163NDKLTEKERELSEPN318
UVRAG-NOM1chr1175728024chr71567467971467DRB1-1163INDKLTEKERELSEP217
UVRAG-NOM1chr1175728024chr71567467971467DRB1-1176NDKLTEKERELSEPN318
UVRAG-NOM1chr1175728024chr71567467971467DRB1-1176INDKLTEKERELSEP217
UVRAG-NOM1chr1175728024chr71567467971467DRB1-1185NDKLTEKERELSEPN318
UVRAG-NOM1chr1175728024chr71567467971467DRB1-1185INDKLTEKERELSEP217
UVRAG-NOM1chr1175728024chr71567467971467DRB1-1308NDKLTEKERELSEPN318
UVRAG-NOM1chr1175728024chr71567467971467DRB1-1318NDKLTEKERELSEPN318
UVRAG-NOM1chr1175728024chr71567467971467DRB1-1320NDKLTEKERELSEPN318
UVRAG-NOM1chr1175728024chr71567467971467DRB1-1324NDKLTEKERELSEPN318
UVRAG-NOM1chr1175728024chr71567467971467DRB1-1324INDKLTEKERELSEP217
UVRAG-NOM1chr1175728024chr71567467971467DRB1-1363NDKLTEKERELSEPN318
UVRAG-NOM1chr1175728024chr71567467971467DRB1-1370NDKLTEKERELSEPN318
UVRAG-NOM1chr1175728024chr71567467971467DRB1-1371NDKLTEKERELSEPN318
UVRAG-NOM1chr1175728024chr71567467971467DRB1-1372NDKLTEKERELSEPN318
UVRAG-NOM1chr1175728024chr71567467971467DRB1-1375NDKLTEKERELSEPN318
UVRAG-NOM1chr1175728024chr71567467971467DRB1-1375INDKLTEKERELSEP217
UVRAG-NOM1chr1175728024chr71567467971467DRB1-1376NDKLTEKERELSEPN318
UVRAG-NOM1chr1175728024chr71567467971467DRB1-1378NDKLTEKERELSEPN318
UVRAG-NOM1chr1175728024chr71567467971467DRB1-1384NDKLTEKERELSEPN318

Top

Fusion breakpoint peptide structures of UVRAG-NOM1

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
5688LTEKERELSEPNMAUVRAGNOM1chr1175728024chr71567467971467

Top

Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of UVRAG-NOM1

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-B14:023BVN5688LTEKERELSEPNMA-7.9962-8.1096
HLA-B14:023BVN5688LTEKERELSEPNMA-5.70842-6.74372
HLA-B52:013W395688LTEKERELSEPNMA-6.83737-6.95077
HLA-B52:013W395688LTEKERELSEPNMA-4.4836-5.5189
HLA-A11:014UQ25688LTEKERELSEPNMA-10.0067-10.1201
HLA-A11:014UQ25688LTEKERELSEPNMA-9.03915-10.0745
HLA-A24:025HGA5688LTEKERELSEPNMA-6.56204-6.67544
HLA-A24:025HGA5688LTEKERELSEPNMA-5.42271-6.45801
HLA-B44:053DX85688LTEKERELSEPNMA-7.85648-8.89178
HLA-B44:053DX85688LTEKERELSEPNMA-5.3978-5.5112
HLA-A02:016TDR5688LTEKERELSEPNMA-3.37154-4.40684

Top

Vaccine Design for the FusionNeoAntigens of UVRAG-NOM1

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
UVRAG-NOM1chr1175728024chr71567467971019ERELSEPNMGGAGAGAGAGTTGAGTGAACCCAACAT
UVRAG-NOM1chr1175728024chr71567467971020ERELSEPNMAGGAGAGAGAGTTGAGTGAACCCAACATGGC
UVRAG-NOM1chr1175728024chr71567467971120RELSEPNMAGAGAGAGTTGAGTGAACCCAACATGGC
UVRAG-NOM1chr1175728024chr71567467971121RELSEPNMASGAGAGAGTTGAGTGAACCCAACATGGCTTC
UVRAG-NOM1chr1175728024chr71567467971222ELSEPNMASIAGAGTTGAGTGAACCCAACATGGCTTCCAT
UVRAG-NOM1chr1175728024chr7156746797514KLTEKERELCAAACTGACGGAAAAGGAGAGAGAGTT
UVRAG-NOM1chr1175728024chr7156746797717TEKERELSEPGACGGAAAAGGAGAGAGAGTTGAGTGAACC
UVRAG-NOM1chr1175728024chr7156746797920KERELSEPNMAAAAGGAGAGAGAGTTGAGTGAACCCAACATGGC

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
UVRAG-NOM1chr1175728024chr7156746797217INDKLTEKERELSEPTATCAATGACAAACTGACGGAAAAGGAGAGAGAGTTGAGTGAACC
UVRAG-NOM1chr1175728024chr7156746797318NDKLTEKERELSEPNCAATGACAAACTGACGGAAAAGGAGAGAGAGTTGAGTGAACCCAA

Top

Information of the samples that have these potential fusion neoantigens of UVRAG-NOM1

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
SARCUVRAG-NOM1chr1175728024ENST00000356136chr7156746797ENST00000275820TCGA-JV-A75J-01A

Top

Potential target of CAR-T therapy development for UVRAG-NOM1

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 UVRAG-NOM1

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

Top

Related Diseases to UVRAG-NOM1

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