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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:REPS2-GLRA2

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: REPS2-GLRA2
FusionPDB ID: 73476
FusionGDB2.0 ID: 73476
HgeneTgene
Gene symbol

REPS2

GLRA2

Gene ID

9185

2742

Gene nameRALBP1 associated Eps domain containing 2glycine receptor alpha 2
SynonymsPOB1GLR
Cytomap

Xp22.2

Xp22.2

Type of geneprotein-codingprotein-coding
DescriptionralBP1-associated Eps domain-containing protein 2RALBP1-interacting protein 2partner of Ral-binding protein 1partner of RalBP1glycine receptor subunit alpha-2glycine receptor alpha 2 subunitglycine receptor, alpha-2 polypeptide
Modification date2020031320200313
UniProtAcc.

P23416

Main function of 5'-partner protein: FUNCTION: Glycine receptors are ligand-gated chloride channels. Channel opening is triggered by extracellular glycine (PubMed:2155780, PubMed:15302677, PubMed:16144831, PubMed:23895467, PubMed:25445488). Channel opening is also triggered by taurine and beta-alanine (PubMed:15302677). Plays a role in the down-regulation of neuronal excitability. Contributes to the generation of inhibitory postsynaptic currents (PubMed:25445488). Plays a role in cellular responses to ethanol (PubMed:23895467). {ECO:0000269|PubMed:15302677, ECO:0000269|PubMed:16144831, ECO:0000269|PubMed:2155780, ECO:0000269|PubMed:23895467, ECO:0000269|PubMed:25445488}.
Ensembl transtripts involved in fusion geneENST idsENST00000469714, ENST00000303843, 
ENST00000357277, ENST00000380064, 
ENST00000218075, ENST00000355020, 
ENST00000443437, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score13 X 9 X 10=11702 X 2 X 2=8
# samples 192
** MAII scorelog2(19/1170*10)=-2.62243720613982
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/8*10)=1.32192809488736
Fusion gene context

PubMed: REPS2 [Title/Abstract] AND GLRA2 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: REPS2 [Title/Abstract] AND GLRA2 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)REPS2(17121902)-GLRA2(14708832), # samples:3
Anticipated loss of major functional domain due to fusion event.REPS2-GLRA2 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.
REPS2-GLRA2 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.
REPS2-GLRA2 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.
REPS2-GLRA2 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
TgeneGLRA2

GO:0007218

neuropeptide signaling pathway

2155780

TgeneGLRA2

GO:0034220

ion transmembrane transport

2155780

TgeneGLRA2

GO:0071230

cellular response to amino acid stimulus

2155780

TgeneGLRA2

GO:0071294

cellular response to zinc ion

23895467

TgeneGLRA2

GO:0071361

cellular response to ethanol

23895467

TgeneGLRA2

GO:1902476

chloride transmembrane transport

23895467



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:17121902/chrX:14708832)
- 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 REPS2 (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 GLRA2 (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)
ENST00000357277REPS2chrX17121902+ENST00000443437GLRA2chrX14708832+350217491712177668
ENST00000357277REPS2chrX17121902+ENST00000218075GLRA2chrX14708832+350517491712177668
ENST00000357277REPS2chrX17121902+ENST00000355020GLRA2chrX14708832+226317491712177668
ENST00000303843REPS2chrX17121902+ENST00000443437GLRA2chrX14708832+3328157502003667
ENST00000303843REPS2chrX17121902+ENST00000218075GLRA2chrX14708832+3331157502003667
ENST00000303843REPS2chrX17121902+ENST00000355020GLRA2chrX14708832+2089157502003667
ENST00000380064REPS2chrX17121902+ENST00000443437GLRA2chrX14708832+29301177671605512
ENST00000380064REPS2chrX17121902+ENST00000218075GLRA2chrX14708832+29331177671605512
ENST00000380064REPS2chrX17121902+ENST00000355020GLRA2chrX14708832+16911177671605512

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
ENST00000357277ENST00000443437REPS2chrX17121902+GLRA2chrX14708832+0.0004096090.99959046
ENST00000357277ENST00000218075REPS2chrX17121902+GLRA2chrX14708832+0.0004108760.99958915
ENST00000357277ENST00000355020REPS2chrX17121902+GLRA2chrX14708832+0.0044683740.99553156
ENST00000303843ENST00000443437REPS2chrX17121902+GLRA2chrX14708832+0.0002887940.9997112
ENST00000303843ENST00000218075REPS2chrX17121902+GLRA2chrX14708832+0.0002911140.99970883
ENST00000303843ENST00000355020REPS2chrX17121902+GLRA2chrX14708832+0.0033770460.9966229
ENST00000380064ENST00000443437REPS2chrX17121902+GLRA2chrX14708832+0.0004018250.9995982
ENST00000380064ENST00000218075REPS2chrX17121902+GLRA2chrX14708832+0.0004043330.9995957
ENST00000380064ENST00000355020REPS2chrX17121902+GLRA2chrX14708832+0.0034022120.9965978

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 REPS2-GLRA2

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
REPS2chrX17121902GLRA2chrX147088321177368LPPPPALPPRPCPSQVSYVKAIDIWM
REPS2chrX17121902GLRA2chrX147088321575523LPPPPALPPRPCPSQVSYVKAIDIWM
REPS2chrX17121902GLRA2chrX147088321749524LPPPPALPPRPCPSQVSYVKAIDIWM

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Potential FusionNeoAntigen Information of REPS2-GLRA2 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.
REPS2-GLRA2_17121902_14708832.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)
REPS2-GLRA2chrX17121902chrX147088321575HLA-B35:01RPCPSQVSY0.98060.7996918
REPS2-GLRA2chrX17121902chrX147088321575HLA-B15:02RPCPSQVSY0.95190.8796918
REPS2-GLRA2chrX17121902chrX147088321575HLA-B35:08RPCPSQVSY0.94820.7187918
REPS2-GLRA2chrX17121902chrX147088321575HLA-B35:05RPCPSQVSY0.85580.5229918
REPS2-GLRA2chrX17121902chrX147088321575HLA-B15:18RPCPSQVSY0.58940.6163918
REPS2-GLRA2chrX17121902chrX147088321575HLA-B55:01LPPRPCPSQV0.82160.5171616
REPS2-GLRA2chrX17121902chrX147088321575HLA-B07:05ALPPRPCPSQV0.86150.5081516
REPS2-GLRA2chrX17121902chrX147088321575HLA-B07:02ALPPRPCPSQV0.85920.5647516
REPS2-GLRA2chrX17121902chrX147088321575HLA-B15:31RPCPSQVSY0.97610.8228918
REPS2-GLRA2chrX17121902chrX147088321575HLA-B15:21RPCPSQVSY0.95030.8484918
REPS2-GLRA2chrX17121902chrX147088321575HLA-B07:04ALPPRPCPSQV0.91470.5653516
REPS2-GLRA2chrX17121902chrX147088321575HLA-B35:77RPCPSQVSY0.98060.7996918
REPS2-GLRA2chrX17121902chrX147088321575HLA-B35:23RPCPSQVSY0.97890.7113918
REPS2-GLRA2chrX17121902chrX147088321575HLA-B35:20RPCPSQVSY0.9780.8486918
REPS2-GLRA2chrX17121902chrX147088321575HLA-B35:11RPCPSQVSY0.9570.8254918
REPS2-GLRA2chrX17121902chrX147088321575HLA-B15:20RPCPSQVSY0.94840.8462918
REPS2-GLRA2chrX17121902chrX147088321575HLA-B35:28RPCPSQVSY0.93210.846918
REPS2-GLRA2chrX17121902chrX147088321575HLA-B35:30RPCPSQVSY0.92790.67918
REPS2-GLRA2chrX17121902chrX147088321575HLA-B35:17RPCPSQVSY0.92790.67918
REPS2-GLRA2chrX17121902chrX147088321575HLA-B35:24RPCPSQVSY0.90430.808918
REPS2-GLRA2chrX17121902chrX147088321575HLA-B15:13RPCPSQVSY0.72770.5869918
REPS2-GLRA2chrX17121902chrX147088321575HLA-B15:11RPCPSQVSY0.41320.8178918
REPS2-GLRA2chrX17121902chrX147088321575HLA-B15:08RPCPSQVSY0.41220.7946918
REPS2-GLRA2chrX17121902chrX147088321575HLA-B35:43RPCPSQVSY0.37470.8015918
REPS2-GLRA2chrX17121902chrX147088321575HLA-B18:04RPCPSQVSY0.2830.8567918
REPS2-GLRA2chrX17121902chrX147088321575HLA-B18:07RPCPSQVSY0.07660.8015918
REPS2-GLRA2chrX17121902chrX147088321575HLA-B18:08RPCPSQVSY0.05010.7768918
REPS2-GLRA2chrX17121902chrX147088321575HLA-B67:01RPCPSQVSY0.0420.6592918
REPS2-GLRA2chrX17121902chrX147088321575HLA-B51:13LPPRPCPSQV0.92020.5603616
REPS2-GLRA2chrX17121902chrX147088321575HLA-B51:21LPPRPCPSQV0.79370.5119616
REPS2-GLRA2chrX17121902chrX147088321575HLA-B59:01LPPRPCPSQV0.76920.753616
REPS2-GLRA2chrX17121902chrX147088321575HLA-A02:03ALPPRPCPSQV0.9790.6042516
REPS2-GLRA2chrX17121902chrX147088321575HLA-B07:26ALPPRPCPSQV0.93580.5354516
REPS2-GLRA2chrX17121902chrX147088321575HLA-B07:22ALPPRPCPSQV0.85920.5647516

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Potential FusionNeoAntigen Information of REPS2-GLRA2 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.
REPS2-GLRA2_17121902_14708832.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)
REPS2-GLRA2chrX17121902chrX147088321575DRB1-0701CPSQVSYVKAIDIWM1126
REPS2-GLRA2chrX17121902chrX147088321575DRB1-0701PCPSQVSYVKAIDIW1025
REPS2-GLRA2chrX17121902chrX147088321575DRB1-0703CPSQVSYVKAIDIWM1126
REPS2-GLRA2chrX17121902chrX147088321575DRB1-0703PCPSQVSYVKAIDIW1025
REPS2-GLRA2chrX17121902chrX147088321575DRB1-0705CPSQVSYVKAIDIWM1126
REPS2-GLRA2chrX17121902chrX147088321575DRB1-0705PCPSQVSYVKAIDIW1025
REPS2-GLRA2chrX17121902chrX147088321575DRB1-0707CPSQVSYVKAIDIWM1126
REPS2-GLRA2chrX17121902chrX147088321575DRB1-0707PCPSQVSYVKAIDIW1025
REPS2-GLRA2chrX17121902chrX147088321575DRB1-0708CPSQVSYVKAIDIWM1126
REPS2-GLRA2chrX17121902chrX147088321575DRB1-0708PCPSQVSYVKAIDIW1025
REPS2-GLRA2chrX17121902chrX147088321575DRB1-0709CPSQVSYVKAIDIWM1126
REPS2-GLRA2chrX17121902chrX147088321575DRB1-0709PCPSQVSYVKAIDIW1025
REPS2-GLRA2chrX17121902chrX147088321575DRB1-0711CPSQVSYVKAIDIWM1126
REPS2-GLRA2chrX17121902chrX147088321575DRB1-0712CPSQVSYVKAIDIWM1126
REPS2-GLRA2chrX17121902chrX147088321575DRB1-0712PCPSQVSYVKAIDIW1025
REPS2-GLRA2chrX17121902chrX147088321575DRB1-0713CPSQVSYVKAIDIWM1126
REPS2-GLRA2chrX17121902chrX147088321575DRB1-0713PCPSQVSYVKAIDIW1025
REPS2-GLRA2chrX17121902chrX147088321575DRB1-0714CPSQVSYVKAIDIWM1126
REPS2-GLRA2chrX17121902chrX147088321575DRB1-0714PCPSQVSYVKAIDIW1025
REPS2-GLRA2chrX17121902chrX147088321575DRB1-0715CPSQVSYVKAIDIWM1126
REPS2-GLRA2chrX17121902chrX147088321575DRB1-0715PCPSQVSYVKAIDIW1025
REPS2-GLRA2chrX17121902chrX147088321575DRB1-0716CPSQVSYVKAIDIWM1126
REPS2-GLRA2chrX17121902chrX147088321575DRB1-0716PCPSQVSYVKAIDIW1025
REPS2-GLRA2chrX17121902chrX147088321575DRB1-0717CPSQVSYVKAIDIWM1126
REPS2-GLRA2chrX17121902chrX147088321575DRB1-0717PCPSQVSYVKAIDIW1025
REPS2-GLRA2chrX17121902chrX147088321575DRB1-0719CPSQVSYVKAIDIWM1126
REPS2-GLRA2chrX17121902chrX147088321575DRB1-0719PCPSQVSYVKAIDIW1025

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Fusion breakpoint peptide structures of REPS2-GLRA2

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
5406LPPRPCPSQVSYVKREPS2GLRA2chrX17121902chrX147088321575

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of REPS2-GLRA2

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-B14:023BVN5406LPPRPCPSQVSYVK-7.15543-7.26883
HLA-B14:023BVN5406LPPRPCPSQVSYVK-4.77435-5.80965
HLA-B52:013W395406LPPRPCPSQVSYVK-6.80875-6.92215
HLA-B52:013W395406LPPRPCPSQVSYVK-4.20386-5.23916
HLA-A11:014UQ25406LPPRPCPSQVSYVK-7.5194-8.5547
HLA-A11:014UQ25406LPPRPCPSQVSYVK-6.9601-7.0735
HLA-A24:025HGA5406LPPRPCPSQVSYVK-7.52403-7.63743
HLA-A24:025HGA5406LPPRPCPSQVSYVK-5.82433-6.85963
HLA-B27:056PYJ5406LPPRPCPSQVSYVK-3.28285-4.31815
HLA-B44:053DX85406LPPRPCPSQVSYVK-5.91172-6.94702
HLA-B44:053DX85406LPPRPCPSQVSYVK-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of REPS2-GLRA2

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
REPS2-GLRA2chrX17121902chrX14708832516ALPPRPCPSQVCCTCCAAGACCTTGTCCATCACAGGTCTCCTAT
REPS2-GLRA2chrX17121902chrX14708832616LPPRPCPSQVCCAAGACCTTGTCCATCACAGGTCTCCTAT
REPS2-GLRA2chrX17121902chrX14708832918RPCPSQVSYTGTCCATCACAGGTCTCCTATGTAAAA

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
REPS2-GLRA2chrX17121902chrX147088321025PCPSQVSYVKAIDIWCCATCACAGGTCTCCTATGTAAAAGCGATTGACATCTGGATGGCG
REPS2-GLRA2chrX17121902chrX147088321126CPSQVSYVKAIDIWMTCACAGGTCTCCTATGTAAAAGCGATTGACATCTGGATGGCGGTG

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Information of the samples that have these potential fusion neoantigens of REPS2-GLRA2

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
SARCREPS2-GLRA2chrX17121902ENST00000303843chrX14708832ENST00000218075TCGA-X6-A8C6-01A

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Potential target of CAR-T therapy development for REPS2-GLRA2

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
TgeneGLRA2chrX:17121902chrX:14708832ENST0000021807569316_3360453.0TransmembraneHelical%3B Name%3D3
TgeneGLRA2chrX:17121902chrX:14708832ENST0000021807569421_4410453.0TransmembraneHelical%3B Name%3D4
TgeneGLRA2chrX:17121902chrX:14708832ENST0000035502069316_3360453.0TransmembraneHelical%3B Name%3D3
TgeneGLRA2chrX:17121902chrX:14708832ENST0000035502069421_4410453.0TransmembraneHelical%3B Name%3D4
TgeneGLRA2chrX:17121902chrX:14708832ENST00000443437811257_2780364.0TransmembraneHelical%3B Name%3D1
TgeneGLRA2chrX:17121902chrX:14708832ENST00000443437811284_3040364.0TransmembraneHelical%3B Name%3D2
TgeneGLRA2chrX:17121902chrX:14708832ENST00000443437811316_3360364.0TransmembraneHelical%3B Name%3D3
TgeneGLRA2chrX:17121902chrX:14708832ENST00000443437811421_4410364.0TransmembraneHelical%3B Name%3D4

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 REPS2-GLRA2

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 REPS2-GLRA2

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