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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:RPS6KC1-LPGAT1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: RPS6KC1-LPGAT1
FusionPDB ID: 78061
FusionGDB2.0 ID: 78061
HgeneTgene
Gene symbol

RPS6KC1

LPGAT1

Gene ID

26750

9926

Gene nameribosomal protein S6 kinase C1lysophosphatidylglycerol acyltransferase 1
SynonymsRPK118|RSKL1|S6K-delta-1|S6PKh1|humS6PKh1FAM34A|FAM34A1|NET8
Cytomap

1q32.3

1q32.3

Type of geneprotein-codingprotein-coding
Descriptionribosomal protein S6 kinase delta-152 kDa ribosomal protein S6 kinaseSPHK1-binding proteinribosomal S6 kinase-like protein with two PSK domains 118 kDa proteinribosomal protein S6 kinase, 52kDa, polypeptide 1acyl-CoA:lysophosphatidylglycerol acyltransferase 1family with sequence similarity 34, member A
Modification date2020032020200313
UniProtAcc.

Q92604

Main function of 5'-partner protein: FUNCTION: Catalyzes the transfert of an acyl group from an acyl-CoA to a lysophosphatidylglycerol (LPG) leading to biosynthesis of phosphatidylglycerol, a precursor for cardiolipin synthesis (PubMed:15485873). Uses various acyl-CoAs and LPGs as substrates but demonstrates a clear preference for long chain saturated fatty acyl-CoAs and oleoyl-CoA as acyl donors (PubMed:15485873). Prefers oleoyl-LPG over palmitoyl-LPG as an acyl receptor and oleoyl-CoA over lauroyl-CoA as an acyl donor (PubMed:15485873). In vitro can also catalyzes the transfert of an acyl group from an acyl-CoA to a monoacylglycerol leading to diacylglycerol synthesis, a precursor of triacylglycerol and plays a role in hepatic triacylglycerol synthesis and secretion (By similarity). Prefers the sn-2-monoacylglycerol to rac-1-monoacylglycerol as acyl acceptor (By similarity). {ECO:0000250|UniProtKB:Q91YX5, ECO:0000269|PubMed:15485873}.
Ensembl transtripts involved in fusion geneENST idsENST00000490299, ENST00000366959, 
ENST00000366960, ENST00000543354, 
ENST00000543470, 
ENST00000366996, 
ENST00000366997, ENST00000488600, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score17 X 16 X 8=21768 X 7 X 5=280
# samples 178
** MAII scorelog2(17/2176*10)=-3.67807190511264
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/280*10)=-1.8073549220576
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: RPS6KC1 [Title/Abstract] AND LPGAT1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: RPS6KC1 [Title/Abstract] AND LPGAT1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)RPS6KC1(213251158)-LPGAT1(211966532), # samples:1
Anticipated loss of major functional domain due to fusion event.RPS6KC1-LPGAT1 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.
RPS6KC1-LPGAT1 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.
RPS6KC1-LPGAT1 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.
RPS6KC1-LPGAT1 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


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/chr1:213251158/chr1:211966532)
- 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 RPS6KC1 (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 LPGAT1 (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)
ENST00000366960RPS6KC1chr1213251158+ENST00000366997LPGAT1chr1211966532-77294121501286378
ENST00000366960RPS6KC1chr1213251158+ENST00000366996LPGAT1chr1211966532-13934121501286378
ENST00000366959RPS6KC1chr1213251158+ENST00000366997LPGAT1chr1211966532-76933761501250366
ENST00000366959RPS6KC1chr1213251158+ENST00000366996LPGAT1chr1211966532-13573761501250366

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
ENST00000366960ENST00000366997RPS6KC1chr1213251158+LPGAT1chr1211966532-0.0001604730.99983954
ENST00000366960ENST00000366996RPS6KC1chr1213251158+LPGAT1chr1211966532-0.0004117170.9995883
ENST00000366959ENST00000366997RPS6KC1chr1213251158+LPGAT1chr1211966532-0.0001801150.99981993
ENST00000366959ENST00000366996RPS6KC1chr1213251158+LPGAT1chr1211966532-0.0005344490.9994655

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 RPS6KC1-LPGAT1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
RPS6KC1chr1213251158LPGAT1chr121196653237675SELFPPFAKGIVFVMEWGEDIKAVSK
RPS6KC1chr1213251158LPGAT1chr121196653241287SELFPPFAKGIVFVMEWGEDIKAVSK

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Potential FusionNeoAntigen Information of RPS6KC1-LPGAT1 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.
RPS6KC1-LPGAT1_213251158_211966532.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)
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-B51:01FAKGIVFV0.99820.66614
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-B57:01KGIVFVMEW0.9990.9956817
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-B58:01KGIVFVMEW0.99840.9898817
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-B58:02KGIVFVMEW0.99790.9873817
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-B57:03KGIVFVMEW0.9940.9969817
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-B35:05FAKGIVFVM0.97750.7747615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-B35:03FAKGIVFVM0.96970.9589615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-B35:01FAKGIVFVM0.96940.961615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-B35:04FAKGIVFVM0.77430.9836615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-B35:02FAKGIVFVM0.77430.9836615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-B57:01FAKGIVFVMEW0.99990.9937617
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C06:03FAKGIVFV0.99980.9972614
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C12:04FAKGIVFV0.99980.9974614
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C03:08FAKGIVFVM0.99910.9098615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C03:19FAKGIVFVM0.99880.9948615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C03:07FAKGIVFVM0.9970.9943615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C15:04FAKGIVFVM0.99560.973615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C15:06FAKGIVFVM0.99480.9604615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C12:16FAKGIVFVM0.99350.9803615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-B15:21FAKGIVFVM0.99060.9747615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C12:12FAKGIVFVM0.97710.9662615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C06:03FAKGIVFVM0.97680.9971615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C12:04FAKGIVFVM0.97570.9971615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C08:13FAKGIVFVM0.94630.9784615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C08:04FAKGIVFVM0.94630.9784615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C07:05FAKGIVFVM0.9230.9685615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C03:14FAKGIVFVM0.90720.9911615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C07:27FAKGIVFVM0.8460.9704615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C08:03FAKGIVFVM0.84150.9888615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C07:95FAKGIVFVM0.83330.6658615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C02:06FAKGIVFVM0.82140.9894615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C07:19FAKGIVFVM0.81280.799615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-B35:12FAKGIVFVM0.77430.9836615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-B78:01FAKGIVFVM0.74060.7805615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C12:03FAKGIVFV0.9990.9884614
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-B51:21FAKGIVFV0.99890.6746614
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C03:03FAKGIVFVM0.99940.9947615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C03:04FAKGIVFVM0.99940.9947615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C03:02FAKGIVFVM0.99910.9886615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-B57:10KGIVFVMEW0.9990.9956817
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C03:67FAKGIVFVM0.99860.99615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C03:17FAKGIVFVM0.99750.9791615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C03:05FAKGIVFVM0.99740.9437615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C12:02FAKGIVFVM0.99560.9842615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C15:09FAKGIVFVM0.99560.973615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-B57:04KGIVFVMEW0.99550.8602817
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-B58:06KGIVFVMEW0.99410.966817
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C16:04FAKGIVFVM0.99310.9905615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-B35:11FAKGIVFVM0.99020.9718615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C12:03FAKGIVFVM0.98880.9896615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C15:02FAKGIVFVM0.98750.9417615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-B35:30FAKGIVFVM0.98050.9022615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-B35:17FAKGIVFVM0.98050.9022615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C06:17FAKGIVFVM0.97220.9967615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C06:02FAKGIVFVM0.97220.9967615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-B35:23FAKGIVFVM0.9710.9665615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-B35:77FAKGIVFVM0.96940.961615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-B35:13FAKGIVFVM0.96360.9614615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-B15:11FAKGIVFVM0.95990.9653615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-B15:08FAKGIVFVM0.95930.9593615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-B35:43FAKGIVFVM0.95280.9595615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C03:06FAKGIVFVM0.94610.9947615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C07:22FAKGIVFVM0.92840.707615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C07:17FAKGIVFVM0.90170.9813615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C16:01FAKGIVFVM0.87640.9841615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C08:01FAKGIVFVM0.84150.9888615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-B35:24FAKGIVFVM0.83470.9604615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C16:02FAKGIVFVM0.82770.9932615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-B35:09FAKGIVFVM0.77430.9836615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-B78:02FAKGIVFVM0.73420.9247615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C02:10FAKGIVFVM0.69220.9923615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C02:02FAKGIVFVM0.69220.9923615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C06:08FAKGIVFVM0.6870.9962615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-C17:01FAKGIVFVM0.2240.9588615
RPS6KC1-LPGAT1chr1213251158chr1211966532376HLA-B57:10FAKGIVFVMEW0.99990.9937617

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Potential FusionNeoAntigen Information of RPS6KC1-LPGAT1 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)

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Fusion breakpoint peptide structures of RPS6KC1-LPGAT1

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
2288FAKGIVFVMEWGEDRPS6KC1LPGAT1chr1213251158chr1211966532376

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of RPS6KC1-LPGAT1

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-B14:023BVN2288FAKGIVFVMEWGED-4.62424-5.65954
HLA-B14:023BVN2288FAKGIVFVMEWGED-4.1114-4.2248
HLA-B52:013W392288FAKGIVFVMEWGED-6.8001-6.9135
HLA-B52:013W392288FAKGIVFVMEWGED-6.46104-7.49634
HLA-A24:025HGA2288FAKGIVFVMEWGED-9.1447-9.2581
HLA-A24:025HGA2288FAKGIVFVMEWGED-6.01279-7.04809
HLA-B44:053DX82288FAKGIVFVMEWGED-5.02862-5.14202
HLA-B44:053DX82288FAKGIVFVMEWGED-4.60714-5.64244

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Vaccine Design for the FusionNeoAntigens of RPS6KC1-LPGAT1

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
RPS6KC1-LPGAT1chr1213251158chr1211966532614FAKGIVFVTTGCTAAAGGAATAGTGTTTGTGA
RPS6KC1-LPGAT1chr1213251158chr1211966532615FAKGIVFVMTTGCTAAAGGAATAGTGTTTGTGATGG
RPS6KC1-LPGAT1chr1213251158chr1211966532617FAKGIVFVMEWTTGCTAAAGGAATAGTGTTTGTGATGGAATGGG
RPS6KC1-LPGAT1chr1213251158chr1211966532817KGIVFVMEWAAGGAATAGTGTTTGTGATGGAATGGG

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

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Information of the samples that have these potential fusion neoantigens of RPS6KC1-LPGAT1

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
Non-CancerRPS6KC1-LPGAT1chr1213251158ENST00000366959chr1211966532ENST00000366996ERR315366

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Potential target of CAR-T therapy development for RPS6KC1-LPGAT1

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
TgeneLPGAT1chr1:213251158chr1:211966532ENST0000036699618342_3620371.0TransmembraneHelical
TgeneLPGAT1chr1:213251158chr1:211966532ENST0000036699718342_3620371.0TransmembraneHelical

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 RPS6KC1-LPGAT1

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 RPS6KC1-LPGAT1

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