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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:FLNA-TIMM23

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: FLNA-TIMM23
FusionPDB ID: 30650
FusionGDB2.0 ID: 30650
HgeneTgene
Gene symbol

FLNA

TIMM23

Gene ID

2316

100287932

Gene namefilamin Atranslocase of inner mitochondrial membrane 23
SynonymsABP-280|ABPX|CSBS|CVD1|FGS2|FLN|FLN-A|FLN1|FMD|MNS|NHBP|OPD|OPD1|OPD2|XLVD|XMVDTIM23
Cytomap

Xq28

10q11.22

Type of geneprotein-codingprotein-coding
Descriptionfilamin-Aactin binding protein 280alpha-filaminendothelial actin-binding proteinepididymis secretory sperm binding proteinfilamin A, alphafilamin-1non-muscle filaminmitochondrial import inner membrane translocase subunit Tim23translocase of inner mitochondrial membrane 23 homologtranslocase of the inner mitochondrial membrane
Modification date2020031320200329
UniProtAcc

P21333

Main function of 5'-partner protein: FUNCTION: Promotes orthogonal branching of actin filaments and links actin filaments to membrane glycoproteins. Anchors various transmembrane proteins to the actin cytoskeleton and serves as a scaffold for a wide range of cytoplasmic signaling proteins. Interaction with FLNB may allow neuroblast migration from the ventricular zone into the cortical plate. Tethers cell surface-localized furin, modulates its rate of internalization and directs its intracellular trafficking (By similarity). Involved in ciliogenesis. Plays a role in cell-cell contacts and adherens junctions during the development of blood vessels, heart and brain organs. Plays a role in platelets morphology through interaction with SYK that regulates ITAM- and ITAM-like-containing receptor signaling, resulting in by platelet cytoskeleton organization maintenance (By similarity). During the axon guidance process, required for growth cone collapse induced by SEMA3A-mediated stimulation of neurons (PubMed:25358863). {ECO:0000250, ECO:0000250|UniProtKB:Q8BTM8, ECO:0000269|PubMed:22121117, ECO:0000269|PubMed:25358863}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000344736, ENST00000360319, 
ENST00000369850, ENST00000369856, 
ENST00000422373, ENST00000498491, 
ENST00000374064, ENST00000374065, 
ENST00000485812, ENST00000260867, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score24 X 29 X 9=62646 X 4 X 5=120
# samples 346
** MAII scorelog2(34/6264*10)=-4.20347756115334
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/120*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: FLNA [Title/Abstract] AND TIMM23 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: FLNA [Title/Abstract] AND TIMM23 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)FLNA(153582519)-TIMM23(51612988), # samples:1
Anticipated loss of major functional domain due to fusion event.FLNA-TIMM23 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.
FLNA-TIMM23 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.
FLNA-TIMM23 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.
FLNA-TIMM23 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
HgeneFLNA

GO:0016479

negative regulation of transcription by RNA polymerase I

22307607

HgeneFLNA

GO:0030334

regulation of cell migration

16291724

HgeneFLNA

GO:0031532

actin cytoskeleton reorganization

10051605

HgeneFLNA

GO:0034394

protein localization to cell surface

18322202

HgeneFLNA

GO:0043113

receptor clustering

10692483

HgeneFLNA

GO:0043433

negative regulation of DNA-binding transcription factor activity

15684392

HgeneFLNA

GO:0044319

wound healing, spreading of cells

16291724

HgeneFLNA

GO:0045184

establishment of protein localization

18322202

HgeneFLNA

GO:0051764

actin crosslink formation

10051605

HgeneFLNA

GO:0072659

protein localization to plasma membrane

24951510

HgeneFLNA

GO:0090307

mitotic spindle assembly

18548008

HgeneFLNA

GO:1901381

positive regulation of potassium ion transmembrane transport

24951510



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:153582519/chr10:51612988)
- 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 FLNA (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 TIMM23 (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)
ENST00000360319FLNAchrX153582519-ENST00000260867TIMM23chr1051612988-63665571259411979
ENST00000422373FLNAchrX153582519-ENST00000260867TIMM23chr1051612988-6577578221361521979
ENST00000369850FLNAchrX153582519-ENST00000260867TIMM23chr1051612988-6589579420161641987
ENST00000369856FLNAchrX153582519-ENST00000260867TIMM23chr1051612988-1612817181187389
ENST00000344736FLNAchrX153582519-ENST00000260867TIMM23chr1051612988-62755480758501947

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
ENST00000360319ENST00000260867FLNAchrX153582519-TIMM23chr1051612988-0.0008073210.99919266
ENST00000422373ENST00000260867FLNAchrX153582519-TIMM23chr1051612988-0.0009517720.9990482
ENST00000369850ENST00000260867FLNAchrX153582519-TIMM23chr1051612988-0.0011925970.99880743
ENST00000369856ENST00000260867FLNAchrX153582519-TIMM23chr1051612988-0.0063907460.9936093
ENST00000344736ENST00000260867FLNAchrX153582519-TIMM23chr1051612988-0.0015883790.99841166

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 FLNA-TIMM23

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
FLNAchrX153582519TIMM23chr105161298854801823LHEMDIRYDNMHIPGAAFGAMNGLRL
FLNAchrX153582519TIMM23chr105161298855711855LHEMDIRYDNMHIPGAAFGAMNGLRL
FLNAchrX153582519TIMM23chr105161298857821855LHEMDIRYDNMHIPGAAFGAMNGLRL
FLNAchrX153582519TIMM23chr105161298857941863LHEMDIRYDNMHIPGAAFGAMNGLRL
FLNAchrX153582519TIMM23chr1051612988817265LHEMDIRYDNMHIPGAAFGAMNGLRL

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Potential FusionNeoAntigen Information of FLNA-TIMM23 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.
FLNA-TIMM23_153582519_51612988.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)
FLNA-TIMM23chrX153582519chr10516129885480HLA-B39:24MHIPGAAF0.99940.50651018
FLNA-TIMM23chrX153582519chr10516129885480HLA-B39:01MHIPGAAF0.99880.94461018
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:10MHIPGAAF0.99840.53531018
FLNA-TIMM23chrX153582519chr10516129885480HLA-B38:02MHIPGAAF0.99790.97011018
FLNA-TIMM23chrX153582519chr10516129885480HLA-B38:01MHIPGAAF0.99750.96611018
FLNA-TIMM23chrX153582519chr10516129885480HLA-B14:01MHIPGAAF0.9940.91461018
FLNA-TIMM23chrX153582519chr10516129885480HLA-B14:02MHIPGAAF0.9940.91461018
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:18MHIPGAAF0.98760.75541018
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:37MHIPGAAF0.98220.56891018
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:01NMHIPGAAF0.99840.899918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:02NMHIPGAAF0.98650.9361918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:25NMHIPGAAF0.98240.9178918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B35:01IPGAAFGAM0.97520.93471221
FLNA-TIMM23chrX153582519chr10516129885480HLA-B35:03IPGAAFGAM0.95390.93561221
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:03NMHIPGAAF0.91420.746918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B35:05IPGAAFGAM0.90720.68841221
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:18NMHIPGAAF0.84420.6975918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B35:02IPGAAFGAM0.74780.97411221
FLNA-TIMM23chrX153582519chr10516129885480HLA-B35:04IPGAAFGAM0.74780.97411221
FLNA-TIMM23chrX153582519chr10516129885480HLA-B39:06MHIPGAAFGA0.99860.98041020
FLNA-TIMM23chrX153582519chr10516129885480HLA-B39:01MHIPGAAFGAM0.99980.98251021
FLNA-TIMM23chrX153582519chr10516129885480HLA-B39:24MHIPGAAFGAM0.99980.82251021
FLNA-TIMM23chrX153582519chr10516129885480HLA-B38:01MHIPGAAFGAM0.99920.9931021
FLNA-TIMM23chrX153582519chr10516129885480HLA-B38:02MHIPGAAFGAM0.99920.9931021
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:10MHIPGAAFGAM0.99890.73131021
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:18MHIPGAAFGAM0.99770.83821021
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:37MHIPGAAFGAM0.9870.74811021
FLNA-TIMM23chrX153582519chr10516129885480HLA-B39:09MHIPGAAF0.9990.80121018
FLNA-TIMM23chrX153582519chr10516129885480HLA-B39:12MHIPGAAF0.99840.9491018
FLNA-TIMM23chrX153582519chr10516129885480HLA-B39:05MHIPGAAF0.99710.92991018
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:21MHIPGAAF0.95850.94631018
FLNA-TIMM23chrX153582519chr10516129885480HLA-B14:03MHIPGAAF0.88450.92311018
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:07NMHIPGAAF0.99760.6768918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:21NMHIPGAAF0.98430.9168918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:04NMHIPGAAF0.98090.8789918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:31NMHIPGAAF0.94160.8965918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:05NMHIPGAAF0.89640.8871918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B35:12IPGAAFGAM0.74780.97411221
FLNA-TIMM23chrX153582519chr10516129885480HLA-B39:10IPGAAFGAM0.5260.98131221
FLNA-TIMM23chrX153582519chr10516129885480HLA-B42:02IPGAAFGAM0.43260.87551221
FLNA-TIMM23chrX153582519chr10516129885480HLA-B42:01IPGAAFGAM0.39280.86771221
FLNA-TIMM23chrX153582519chr10516129885480HLA-B39:09MHIPGAAFGAM0.99980.95151021
FLNA-TIMM23chrX153582519chr10516129885480HLA-B73:01IRYDNMHIPGA0.99960.6588516
FLNA-TIMM23chrX153582519chr10516129885480HLA-B39:05MHIPGAAFGAM0.99920.97921021
FLNA-TIMM23chrX153582519chr10516129885480HLA-B39:31MHIPGAAF0.99850.94421018
FLNA-TIMM23chrX153582519chr10516129885480HLA-B38:05MHIPGAAF0.99750.96611018
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:09MHIPGAAF0.99350.67421018
FLNA-TIMM23chrX153582519chr10516129885480HLA-B39:11MHIPGAAF0.94320.92021018
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:11NMHIPGAAF0.99850.8387918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:33NMHIPGAAF0.99840.899918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:125NMHIPGAAF0.99840.899918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:34NMHIPGAAF0.99840.899918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:08NMHIPGAAF0.99840.8623918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:27NMHIPGAAF0.99840.8941918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:135NMHIPGAAF0.99830.8777918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B35:43NMHIPGAAF0.9980.8635918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:24NMHIPGAAF0.99720.8197918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:35NMHIPGAAF0.99710.8699918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:50NMHIPGAAF0.99670.9462918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:53NMHIPGAAF0.99640.8772918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:54NMHIPGAAF0.99380.847918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B35:11NMHIPGAAF0.98610.915918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:39NMHIPGAAF0.98140.8362918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:12NMHIPGAAF0.98120.8482918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:68NMHIPGAAF0.98080.5811918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B35:77IPGAAFGAM0.97520.93471221
FLNA-TIMM23chrX153582519chr10516129885480HLA-B35:23IPGAAFGAM0.9740.92761221
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:13NMHIPGAAF0.95330.6361918
FLNA-TIMM23chrX153582519chr10516129885480HLA-C03:02NMHIPGAAF0.95240.9652918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B35:20NMHIPGAAF0.92780.9374918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B35:17IPGAAFGAM0.90930.82551221
FLNA-TIMM23chrX153582519chr10516129885480HLA-B35:30IPGAAFGAM0.90930.82551221
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:20NMHIPGAAF0.9030.9255918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:73NMHIPGAAF0.89950.689918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B35:11IPGAAFGAM0.89280.91761221
FLNA-TIMM23chrX153582519chr10516129885480HLA-B35:28NMHIPGAAF0.88150.9263918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:30NMHIPGAAF0.82170.8675918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B35:09IPGAAFGAM0.74780.97411221
FLNA-TIMM23chrX153582519chr10516129885480HLA-B48:02NMHIPGAAF0.66280.9143918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B56:05IPGAAFGAM0.59570.52251221
FLNA-TIMM23chrX153582519chr10516129885480HLA-B67:01IPGAAFGAM0.59080.97241221
FLNA-TIMM23chrX153582519chr10516129885480HLA-B18:04NMHIPGAAF0.46420.9298918
FLNA-TIMM23chrX153582519chr10516129885480HLA-B35:43IPGAAFGAM0.04370.88591221
FLNA-TIMM23chrX153582519chr10516129885480HLA-B39:31MHIPGAAFGAM0.99980.98241021
FLNA-TIMM23chrX153582519chr10516129885480HLA-B38:05MHIPGAAFGAM0.99920.9931021
FLNA-TIMM23chrX153582519chr10516129885480HLA-B15:09MHIPGAAFGAM0.99640.85671021
FLNA-TIMM23chrX153582519chr10516129885480HLA-B39:11MHIPGAAFGAM0.96620.95651021

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Potential FusionNeoAntigen Information of FLNA-TIMM23 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 FLNA-TIMM23

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
8347RYDNMHIPGAAFGAFLNATIMM23chrX153582519chr10516129885480

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of FLNA-TIMM23

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

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Vaccine Design for the FusionNeoAntigens of FLNA-TIMM23

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
FLNA-TIMM23chrX153582519chr10516129881018MHIPGAAFACATCCCAGGGGCTGCGTTTGGTG
FLNA-TIMM23chrX153582519chr10516129881020MHIPGAAFGAACATCCCAGGGGCTGCGTTTGGTGCAATGA
FLNA-TIMM23chrX153582519chr10516129881021MHIPGAAFGAMACATCCCAGGGGCTGCGTTTGGTGCAATGAATG
FLNA-TIMM23chrX153582519chr10516129881221IPGAAFGAMCAGGGGCTGCGTTTGGTGCAATGAATG
FLNA-TIMM23chrX153582519chr1051612988516IRYDNMHIPGAGCTATGACAACATGCACATCCCAGGGGCTGCGT
FLNA-TIMM23chrX153582519chr1051612988918NMHIPGAAFTGCACATCCCAGGGGCTGCGTTTGGTG

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 FLNA-TIMM23

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
STADFLNA-TIMM23chrX153582519ENST00000344736chr1051612988ENST00000260867TCGA-BR-8365-01A

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Potential target of CAR-T therapy development for FLNA-TIMM23

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
TgeneTIMM23chrX:153582519chr10:51612988ENST0000026086727125_1450210.0TransmembraneHelical
TgeneTIMM23chrX:153582519chr10:51612988ENST0000026086727181_1970210.0TransmembraneHelical

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 FLNA-TIMM23

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 FLNA-TIMM23

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