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:ARHGAP5-LSAMP

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ARHGAP5-LSAMP
FusionPDB ID: 6141
FusionGDB2.0 ID: 6141
HgeneTgene
Gene symbol

ARHGAP5

LSAMP

Gene ID

394

4045

Gene nameRho GTPase activating protein 5limbic system associated membrane protein
SynonymsGFI2|RhoGAP5|p190-B|p190BRhoGAPIGLON3|LAMP
Cytomap

14q12

3q13.31

Type of geneprotein-codingprotein-coding
Descriptionrho GTPase-activating protein 5growth factor independent 2p100 RasGAP-associated p105 proteinp105 RhoGAPrho-type GTPase-activating protein 5limbic system-associated membrane proteinIgLON family member 3
Modification date2020031320200313
UniProtAcc

Q13017

Main function of 5'-partner protein: FUNCTION: GTPase-activating protein for Rho family members (PubMed:8537347). {ECO:0000269|PubMed:8537347}.

Q13449

Main function of 5'-partner protein: FUNCTION: Mediates selective neuronal growth and axon targeting. Contributes to the guidance of developing axons and remodeling of mature circuits in the limbic system. Essential for normal growth of the hyppocampal mossy fiber projection (By similarity). {ECO:0000250}.
Ensembl transtripts involved in fusion geneENST idsENST00000396582, ENST00000345122, 
ENST00000432921, ENST00000433497, 
ENST00000539826, ENST00000556611, 
ENST00000498645, ENST00000490035, 
ENST00000539563, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score10 X 4 X 7=28020 X 18 X 11=3960
# samples 1234
** MAII scorelog2(12/280*10)=-1.22239242133645
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(34/3960*10)=-3.54189377882927
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: ARHGAP5 [Title/Abstract] AND LSAMP [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: ARHGAP5 [Title/Abstract] AND LSAMP [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ARHGAP5(32546641)-LSAMP(116163802), # samples:2
Anticipated loss of major functional domain due to fusion event.ARHGAP5-LSAMP 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.
ARHGAP5-LSAMP 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.
ARHGAP5-LSAMP 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.
ARHGAP5-LSAMP 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.
ARHGAP5-LSAMP seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
ARHGAP5-LSAMP seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
ARHGAP5-LSAMP 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


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/chr14:32546641/chr3:116163802)
- 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 ARHGAP5 (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 LSAMP (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)
ENST00000396582ARHGAP5chr1432546641+ENST00000539563LSAMPchr3116163802-13723622921371360

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
ENST00000396582ENST00000539563ARHGAP5chr1432546641+LSAMPchr3116163802-0.0028026830.9971973

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 ARHGAP5-LSAMP

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
ARHGAP5chr1432546641LSAMPchr311616380236223LPLRRRRRRPTLLGLPVRSVDFNRGT

Top

Potential FusionNeoAntigen Information of ARHGAP5-LSAMP 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.
ARHGAP5-LSAMP_32546641_116163802.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)
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B27:04RRPTLLGL0.99990.7448715
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B27:04RRRPTLLGL0.99960.7824615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B27:02RRRPTLLGL0.99960.5328615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B27:05RRRPTLLGL0.99950.7269615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B07:05RPTLLGLPV0.99720.5498817
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B07:02RPTLLGLPV0.99690.5533817
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-A02:13LLGLPVRSV0.98290.83121120
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-A02:11LLGLPVRSV0.97360.78591120
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-A02:27LLGLPVRSV0.97110.79441120
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-A02:04LLGLPVRSV0.95440.88071120
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-A02:19LLGLPVRSV0.94380.7741120
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B14:01RRRPTLLGL0.93580.8343615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B14:02RRRPTLLGL0.93580.8343615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-A02:38LLGLPVRSV0.89390.73981120
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-A02:35LLGLPVRSV0.89140.78751120
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B48:01RRRPTLLGL0.54580.5203615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B07:10RRRPTLLGL0.34820.7755615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B82:01RPTLLGLPV0.34620.7652817
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B81:01RPTLLGLPV0.29630.5618817
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B27:04RRRRPTLLGL0.99980.7848515
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B27:05RRRRPTLLGL0.99980.6984515
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B27:07RRRRPTLLGL0.99950.5707515
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-A02:22TLLGLPVRSV0.99470.74111020
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-A02:13TLLGLPVRSV0.99290.85331020
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-A02:27TLLGLPVRSV0.99020.79911020
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-A02:11TLLGLPVRSV0.98990.76081020
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-A02:16TLLGLPVRSV0.98930.64181020
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-A02:30TLLGLPVRSV0.98810.73451020
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-A02:24TLLGLPVRSV0.98810.73451020
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-A02:67TLLGLPVRSV0.98810.73451020
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-A02:60TLLGLPVRSV0.9880.74161020
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-A02:38TLLGLPVRSV0.97940.84541020
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-A02:04TLLGLPVRSV0.97520.83591020
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-A02:19TLLGLPVRSV0.96370.68121020
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-A02:35TLLGLPVRSV0.93120.7561020
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-A02:29TLLGLPVRSV0.86250.73211020
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-A02:20TLLGLPVRSV0.84340.74461020
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-A74:03RPTLLGLPVR0.81210.5986818
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-A74:09RPTLLGLPVR0.81210.5986818
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-A74:11RPTLLGLPVR0.81210.5986818
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B27:07RRRRRPTLLGL0.99990.6089415
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B27:05RRRRRPTLLGL0.99990.6658415
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B27:04RRRRRPTLLGL0.99990.7635415
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B27:14RRRPTLLGL0.99960.693615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-C07:05RRRPTLLGL0.99740.9302615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-C07:27RRRPTLLGL0.99690.9326615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-C07:95RRRPTLLGL0.99580.5899615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-C07:13RRRPTLLGL0.98630.9371615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-C07:29RRRPTLLGL0.98420.8744615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B27:03RRRPTLLGL0.97290.7449615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B07:12RPTLLGLPV0.95720.6402817
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B07:04RPTLLGLPV0.9020.5638817
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-C07:46RRRPTLLGL0.86190.8706615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-C07:19RRRPTLLGL0.81180.7638615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-C07:80RRRPTLLGL0.80850.949615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-C07:67RRRPTLLGL0.80850.949615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-C07:10RRRPTLLGL0.80770.9549615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B39:12RRRPTLLGL0.80060.8389615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B42:02RPTLLGLPV0.71780.7243817
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B42:01RPTLLGLPV0.68670.7179817
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B39:10RPTLLGLPV0.57750.9144817
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-C12:16RRRPTLLGL0.14080.9717615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B27:14RRRRPTLLGL0.99980.6643515
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-A02:01TLLGLPVRSV0.98810.73451020
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B27:03RRRRPTLLGL0.9880.7237515
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B27:03RRRRRPTLLGL0.99680.6995415
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B27:09RRPTLLGL0.99990.7277715
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B27:06RRPTLLGL0.99990.7147715
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B27:10RRPTLLGL0.99980.8609715
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B27:06RRRPTLLGL0.99970.7692615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B27:10RRRPTLLGL0.99960.8753615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B27:08RRRPTLLGL0.99950.6473615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B27:09RRRPTLLGL0.99910.7186615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-C07:01RRRPTLLGL0.99760.6021615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B07:22RPTLLGLPV0.99690.5533817
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B07:09RPTLLGLPV0.99680.5515817
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-A02:03LLGLPVRSV0.9960.85381120
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-C06:08RRRPTLLGL0.97620.9932615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-C07:17RRRPTLLGL0.94120.9519615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-C07:22RRRPTLLGL0.91710.7049615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B55:04RPTLLGLPV0.91660.5547817
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-C07:04RRRPTLLGL0.82240.9682615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-C07:02RRRPTLLGL0.80850.949615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B67:01RPTLLGLPV0.69990.9086817
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-C06:06RRRPTLLGL0.50570.995615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-C06:17RRRPTLLGL0.38950.9939615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-C06:02RRRPTLLGL0.38950.9939615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B82:02RPTLLGLPV0.34620.7652817
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B15:68RRRPTLLGL0.27050.6623615
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B27:10RRRRPTLLGL0.99980.8739515
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B27:08RRRRPTLLGL0.99970.611515
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B27:06RRRRPTLLGL0.99960.7818515
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B27:09RRRRPTLLGL0.99920.682515
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-A02:03TLLGLPVRSV0.9980.82781020
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-A74:01RPTLLGLPVR0.81210.5986818
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B27:06RRRRRPTLLGL0.99990.7685415
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B27:08RRRRRPTLLGL0.99990.5737415
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B27:10RRRRRPTLLGL0.99990.8601415
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B27:09RRRRRPTLLGL0.99980.6432415
ARHGAP5-LSAMPchr1432546641chr3116163802362HLA-B27:10RRPTLLGLPVR0.99970.7384718

Top

Potential FusionNeoAntigen Information of ARHGAP5-LSAMP 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.
ARHGAP5-LSAMP_32546641_116163802.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)
ARHGAP5-LSAMPchr1432546641chr3116163802362DRB1-1220RPTLLGLPVRSVDFN823
ARHGAP5-LSAMPchr1432546641chr3116163802362DRB1-1221RPTLLGLPVRSVDFN823

Top

Fusion breakpoint peptide structures of ARHGAP5-LSAMP

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
8194RRRPTLLGLPVRSVARHGAP5LSAMPchr1432546641chr3116163802362

Top

Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of ARHGAP5-LSAMP

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-B14:023BVN8194RRRPTLLGLPVRSV-7.9962-8.1096
HLA-B14:023BVN8194RRRPTLLGLPVRSV-5.70842-6.74372
HLA-B52:013W398194RRRPTLLGLPVRSV-6.83737-6.95077
HLA-B52:013W398194RRRPTLLGLPVRSV-4.4836-5.5189
HLA-A11:014UQ28194RRRPTLLGLPVRSV-10.0067-10.1201
HLA-A11:014UQ28194RRRPTLLGLPVRSV-9.03915-10.0745
HLA-A24:025HGA8194RRRPTLLGLPVRSV-6.56204-6.67544
HLA-A24:025HGA8194RRRPTLLGLPVRSV-5.42271-6.45801
HLA-B44:053DX88194RRRPTLLGLPVRSV-7.85648-8.89178
HLA-B44:053DX88194RRRPTLLGLPVRSV-5.3978-5.5112
HLA-A02:016TDR8194RRRPTLLGLPVRSV-3.37154-4.40684

Top

Vaccine Design for the FusionNeoAntigens of ARHGAP5-LSAMP

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
ARHGAP5-LSAMPchr1432546641chr31161638021020TLLGLPVRSVCGTTGTTAGGACTGCCTGTTCGCAGCGTGG
ARHGAP5-LSAMPchr1432546641chr31161638021120LLGLPVRSVTGTTAGGACTGCCTGTTCGCAGCGTGG
ARHGAP5-LSAMPchr1432546641chr3116163802415RRRRRPTLLGLGGAGACGGAGGAGACCGACGTTGTTAGGACTGC
ARHGAP5-LSAMPchr1432546641chr3116163802515RRRRPTLLGLGACGGAGGAGACCGACGTTGTTAGGACTGC
ARHGAP5-LSAMPchr1432546641chr3116163802615RRRPTLLGLGGAGGAGACCGACGTTGTTAGGACTGC
ARHGAP5-LSAMPchr1432546641chr3116163802715RRPTLLGLGGAGACCGACGTTGTTAGGACTGC
ARHGAP5-LSAMPchr1432546641chr3116163802718RRPTLLGLPVRGGAGACCGACGTTGTTAGGACTGCCTGTTCGCA
ARHGAP5-LSAMPchr1432546641chr3116163802817RPTLLGLPVGACCGACGTTGTTAGGACTGCCTGTTC
ARHGAP5-LSAMPchr1432546641chr3116163802818RPTLLGLPVRGACCGACGTTGTTAGGACTGCCTGTTCGCA

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
ARHGAP5-LSAMPchr1432546641chr3116163802823RPTLLGLPVRSVDFNGACCGACGTTGTTAGGACTGCCTGTTCGCAGCGTGGATTTTAACC

Top

Information of the samples that have these potential fusion neoantigens of ARHGAP5-LSAMP

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
SKCMARHGAP5-LSAMPchr1432546641ENST00000396582chr3116163802ENST00000539563TCGA-GF-A6C9-06A

Top

Potential target of CAR-T therapy development for ARHGAP5-LSAMP

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 ARHGAP5-LSAMP

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

Top

Related Diseases to ARHGAP5-LSAMP

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