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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:KRAS-IFLTD1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: KRAS-IFLTD1
FusionPDB ID: 43431
FusionGDB2.0 ID: 43433
HgeneTgene
Gene symbol

KRAS

IFLTD1

Gene ID

3845

160492

Gene nameKRAS proto-oncogene, GTPaselamin tail domain containing 1
Synonyms'C-K-RAS|C-K-RAS|CFC2|K-RAS2A|K-RAS2B|K-RAS4A|K-RAS4B|K-Ras|K-Ras 2|KI-RAS|KRAS1|KRAS2|NS|NS3|OES|RALD|RASK2|c-Ki-ras|c-Ki-ras2IFLTD1|LMNARS1|PAS1C1
Cytomap

12p12.1

12p12.1

Type of geneprotein-codingprotein-coding
DescriptionGTPase KRasK-ras p21 proteinKirsten rat sarcoma viral oncogene homologKirsten rat sarcoma viral proto-oncogenePR310 c-K-ras oncogenec-Kirsten-ras proteincellular c-Ki-ras2 proto-oncogenecellular transforming proto-oncogeneoncogene KRAS2transformilamin tail domain-containing protein 1intermediate filament tail domain containing 1intermediate filament tail domain-containing protein 1
Modification date2020032920200313
UniProtAcc

P01116

Main function of 5'-partner protein: FUNCTION: Ras proteins bind GDP/GTP and possess intrinsic GTPase activity (PubMed:20949621). Plays an important role in the regulation of cell proliferation (PubMed:23698361, PubMed:22711838). Plays a role in promoting oncogenic events by inducing transcriptional silencing of tumor suppressor genes (TSGs) in colorectal cancer (CRC) cells in a ZNF304-dependent manner (PubMed:24623306). {ECO:0000269|PubMed:20949621, ECO:0000269|PubMed:22711838, ECO:0000269|PubMed:23698361, ECO:0000269|PubMed:24623306, ECO:0000305}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000256078, ENST00000311936, 
ENST00000556131, ENST00000557334, 
ENST00000282881, ENST00000539744, 
ENST00000413632, ENST00000445693, 
ENST00000458174, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score6 X 2 X 5=608 X 5 X 5=200
# samples 68
** MAII scorelog2(6/60*10)=0log2(8/200*10)=-1.32192809488736
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: KRAS [Title/Abstract] AND IFLTD1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: KRAS [Title/Abstract] AND IFLTD1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)KRAS(25398208)-IFLTD1(25656734), # samples:2
Anticipated loss of major functional domain due to fusion event.KRAS-IFLTD1 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.
KRAS-IFLTD1 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.
KRAS-IFLTD1 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.
KRAS-IFLTD1 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.
KRAS-IFLTD1 seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
KRAS-IFLTD1 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target 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/chr12:25398208/chr12:25656734)
- 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 KRAS (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 IFLTD1 (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)
ENST00000311936KRASchr1225398208-ENST00000458174IFLTD1chr1225656734-546303257086
ENST00000311936KRASchr1225398208-ENST00000445693IFLTD1chr1225656734-64830337964589
ENST00000311936KRASchr1225398208-ENST00000413632IFLTD1chr1225656734-511303257086
ENST00000557334KRASchr1225398208-ENST00000458174IFLTD1chr1225656734-551308262287
ENST00000557334KRASchr1225398208-ENST00000445693IFLTD1chr1225656734-65330838465089
ENST00000557334KRASchr1225398208-ENST00000413632IFLTD1chr1225656734-516308262287
ENST00000256078KRASchr1225398208-ENST00000458174IFLTD1chr1225656734-4181755524061
ENST00000256078KRASchr1225398208-ENST00000445693IFLTD1chr1225656734-52017525151789
ENST00000256078KRASchr1225398208-ENST00000413632IFLTD1chr1225656734-3831755529780
ENST00000556131KRASchr1225398208-ENST00000282881IFLTD1chr1225656734-7302883361112
ENST00000556131KRASchr1225398208-ENST00000539744IFLTD1chr1225656734-70228810235383

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
ENST00000311936ENST00000458174KRASchr1225398208-IFLTD1chr1225656734-0.0506708550.9493291
ENST00000311936ENST00000445693KRASchr1225398208-IFLTD1chr1225656734-0.083120760.91687924
ENST00000311936ENST00000413632KRASchr1225398208-IFLTD1chr1225656734-0.065153880.9348461
ENST00000557334ENST00000458174KRASchr1225398208-IFLTD1chr1225656734-0.0493001340.9506999
ENST00000557334ENST00000445693KRASchr1225398208-IFLTD1chr1225656734-0.063237860.9367622
ENST00000557334ENST00000413632KRASchr1225398208-IFLTD1chr1225656734-0.054552920.9454471
ENST00000256078ENST00000458174KRASchr1225398208-IFLTD1chr1225656734-0.165731340.8342686
ENST00000256078ENST00000445693KRASchr1225398208-IFLTD1chr1225656734-0.132999180.86700076
ENST00000256078ENST00000413632KRASchr1225398208-IFLTD1chr1225656734-0.092967010.90703297
ENST00000556131ENST00000282881KRASchr1225398208-IFLTD1chr1225656734-0.095145880.9048542
ENST00000556131ENST00000539744KRASchr1225398208-IFLTD1chr1225656734-0.093312950.9066871

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 KRAS-IFLTD1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
KRASchr1225398208IFLTD1chr122565673417540QNHFVDEYDPTIEGLRKRRHLSHKSN
KRASchr1225398208IFLTD1chr122565673428862QNHFVDEYDPTIEGLRKRRHLSHKSN

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Potential FusionNeoAntigen Information of KRAS-IFLTD1 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.
KRAS-IFLTD1_25398208_25656734.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)
KRAS-IFLTD1chr1225398208chr1225656734175HLA-B45:01DEYDPTIEG0.92560.7824514
KRAS-IFLTD1chr1225398208chr1225656734175HLA-B18:01DEYDPTIEG0.89690.9394514
KRAS-IFLTD1chr1225398208chr1225656734175HLA-B50:02DEYDPTIEG0.71770.5466514
KRAS-IFLTD1chr1225398208chr1225656734175HLA-B39:01EYDPTIEGL0.60940.7132615
KRAS-IFLTD1chr1225398208chr1225656734175HLA-B38:01EYDPTIEGL0.51320.7386615
KRAS-IFLTD1chr1225398208chr1225656734175HLA-B38:02EYDPTIEGL0.5110.7522615
KRAS-IFLTD1chr1225398208chr1225656734175HLA-B15:37EYDPTIEGL0.38230.5487615
KRAS-IFLTD1chr1225398208chr1225656734175HLA-B44:03DEYDPTIEGL0.95450.9241515
KRAS-IFLTD1chr1225398208chr1225656734175HLA-B18:01DEYDPTIEGL0.94230.9028515
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C04:07YDPTIEGL0.99980.6021715
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C04:10YDPTIEGL0.99970.5939715
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C08:15YDPTIEGL0.99960.8656715
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C04:14YDPTIEGL0.9880.5831715
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C04:10EYDPTIEGL0.99890.5748615
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C04:07EYDPTIEGL0.99870.5681615
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C07:29EYDPTIEGL0.92830.8781615
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C07:13EYDPTIEGL0.91470.8965615
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C07:10EYDPTIEGL0.88640.9504615
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C07:27EYDPTIEGL0.88310.9292615
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C07:80EYDPTIEGL0.8570.9278615
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C07:67EYDPTIEGL0.8570.9278615
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C07:19EYDPTIEGL0.82710.5052615
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C07:46EYDPTIEGL0.80270.8046615
KRAS-IFLTD1chr1225398208chr1225656734175HLA-B39:12EYDPTIEGL0.66190.7263615
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C04:14EYDPTIEGL0.55510.5864615
KRAS-IFLTD1chr1225398208chr1225656734175HLA-B39:05EYDPTIEGL0.46390.6634615
KRAS-IFLTD1chr1225398208chr1225656734175HLA-B14:03EYDPTIEGL0.45180.5613615
KRAS-IFLTD1chr1225398208chr1225656734175HLA-B51:07DEYDPTIEGL0.83820.5966515
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C04:07VDEYDPTIEGL10.5726415
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C04:10VDEYDPTIEGL10.5754415
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C04:14VDEYDPTIEGL0.99950.582415
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C04:03YDPTIEGL0.99980.6516715
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C04:01YDPTIEGL0.99980.6021715
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C18:01YDPTIEGL0.99970.6198715
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C08:02YDPTIEGL0.99960.8656715
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C04:03EYDPTIEGL0.99910.6057615
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C04:01EYDPTIEGL0.99870.5681615
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C18:01EYDPTIEGL0.99830.5809615
KRAS-IFLTD1chr1225398208chr1225656734175HLA-B18:05DEYDPTIEG0.89690.9394514
KRAS-IFLTD1chr1225398208chr1225656734175HLA-B18:06DEYDPTIEG0.87990.9431514
KRAS-IFLTD1chr1225398208chr1225656734175HLA-B18:03DEYDPTIEG0.86470.9339514
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C07:02EYDPTIEGL0.8570.9278615
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C07:17EYDPTIEGL0.85540.9531615
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C14:02EYDPTIEGL0.82450.9051615
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C14:03EYDPTIEGL0.82450.9051615
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C03:67EYDPTIEGL0.7970.9663615
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C06:06EYDPTIEGL0.78040.9711615
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C04:04EYDPTIEGL0.70520.6986615
KRAS-IFLTD1chr1225398208chr1225656734175HLA-B39:31EYDPTIEGL0.65950.7115615
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C07:04EYDPTIEGL0.52230.7599615
KRAS-IFLTD1chr1225398208chr1225656734175HLA-B38:05EYDPTIEGL0.51320.7386615
KRAS-IFLTD1chr1225398208chr1225656734175HLA-B40:04DEYDPTIEGL0.97360.5218515
KRAS-IFLTD1chr1225398208chr1225656734175HLA-B18:04DEYDPTIEGL0.96850.9144515
KRAS-IFLTD1chr1225398208chr1225656734175HLA-B18:07DEYDPTIEGL0.96150.874515
KRAS-IFLTD1chr1225398208chr1225656734175HLA-B44:13DEYDPTIEGL0.95450.9241515
KRAS-IFLTD1chr1225398208chr1225656734175HLA-B44:07DEYDPTIEGL0.95450.9241515
KRAS-IFLTD1chr1225398208chr1225656734175HLA-B44:26DEYDPTIEGL0.95450.9241515
KRAS-IFLTD1chr1225398208chr1225656734175HLA-B18:08DEYDPTIEGL0.94930.8123515
KRAS-IFLTD1chr1225398208chr1225656734175HLA-B18:05DEYDPTIEGL0.94230.9028515
KRAS-IFLTD1chr1225398208chr1225656734175HLA-B18:06DEYDPTIEGL0.93750.905515
KRAS-IFLTD1chr1225398208chr1225656734175HLA-B18:03DEYDPTIEGL0.9270.894515
KRAS-IFLTD1chr1225398208chr1225656734175HLA-B39:31DEYDPTIEGL0.88810.8632515
KRAS-IFLTD1chr1225398208chr1225656734175HLA-B18:11DEYDPTIEGL0.84360.8683515
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C18:01VDEYDPTIEGL10.6086415
KRAS-IFLTD1chr1225398208chr1225656734175HLA-C04:01VDEYDPTIEGL10.5726415

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Potential FusionNeoAntigen Information of KRAS-IFLTD1 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.
KRAS-IFLTD1_25398208_25656734.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)
KRAS-IFLTD1chr1225398208chr1225656734175DRB1-0828DPTIEGLRKRRHLSH823
KRAS-IFLTD1chr1225398208chr1225656734175DRB1-1103DPTIEGLRKRRHLSH823
KRAS-IFLTD1chr1225398208chr1225656734175DRB1-1103YDPTIEGLRKRRHLS722
KRAS-IFLTD1chr1225398208chr1225656734175DRB1-1106DPTIEGLRKRRHLSH823
KRAS-IFLTD1chr1225398208chr1225656734175DRB1-1106YDPTIEGLRKRRHLS722
KRAS-IFLTD1chr1225398208chr1225656734175DRB1-1121DPTIEGLRKRRHLSH823
KRAS-IFLTD1chr1225398208chr1225656734175DRB1-1125DPTIEGLRKRRHLSH823
KRAS-IFLTD1chr1225398208chr1225656734175DRB1-1141DPTIEGLRKRRHLSH823
KRAS-IFLTD1chr1225398208chr1225656734175DRB1-1147DPTIEGLRKRRHLSH823
KRAS-IFLTD1chr1225398208chr1225656734175DRB1-1147YDPTIEGLRKRRHLS722
KRAS-IFLTD1chr1225398208chr1225656734175DRB1-1155DPTIEGLRKRRHLSH823
KRAS-IFLTD1chr1225398208chr1225656734175DRB1-1157DPTIEGLRKRRHLSH823
KRAS-IFLTD1chr1225398208chr1225656734175DRB1-1159DPTIEGLRKRRHLSH823
KRAS-IFLTD1chr1225398208chr1225656734175DRB1-1159YDPTIEGLRKRRHLS722
KRAS-IFLTD1chr1225398208chr1225656734175DRB1-1163DPTIEGLRKRRHLSH823
KRAS-IFLTD1chr1225398208chr1225656734175DRB1-1163YDPTIEGLRKRRHLS722
KRAS-IFLTD1chr1225398208chr1225656734175DRB1-1167DPTIEGLRKRRHLSH823
KRAS-IFLTD1chr1225398208chr1225656734175DRB1-1176DPTIEGLRKRRHLSH823
KRAS-IFLTD1chr1225398208chr1225656734175DRB1-1176YDPTIEGLRKRRHLS722
KRAS-IFLTD1chr1225398208chr1225656734175DRB1-1184DPTIEGLRKRRHLSH823
KRAS-IFLTD1chr1225398208chr1225656734175DRB1-1185DPTIEGLRKRRHLSH823
KRAS-IFLTD1chr1225398208chr1225656734175DRB1-1185YDPTIEGLRKRRHLS722
KRAS-IFLTD1chr1225398208chr1225656734175DRB1-1192DPTIEGLRKRRHLSH823
KRAS-IFLTD1chr1225398208chr1225656734175DRB1-1192YDPTIEGLRKRRHLS722
KRAS-IFLTD1chr1225398208chr1225656734175DRB1-1204DPTIEGLRKRRHLSH823
KRAS-IFLTD1chr1225398208chr1225656734175DRB1-1204YDPTIEGLRKRRHLS722
KRAS-IFLTD1chr1225398208chr1225656734175DRB1-1209DPTIEGLRKRRHLSH823
KRAS-IFLTD1chr1225398208chr1225656734175DRB1-1209YDPTIEGLRKRRHLS722
KRAS-IFLTD1chr1225398208chr1225656734175DRB1-1318DPTIEGLRKRRHLSH823
KRAS-IFLTD1chr1225398208chr1225656734175DRB1-1324DPTIEGLRKRRHLSH823
KRAS-IFLTD1chr1225398208chr1225656734175DRB1-1324YDPTIEGLRKRRHLS722

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Fusion breakpoint peptide structures of KRAS-IFLTD1

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
2255EYDPTIEGLRKRRHKRASIFLTD1chr1225398208chr1225656734175

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of KRAS-IFLTD1

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-B14:023BVN2255EYDPTIEGLRKRRH-5.49577-5.60917
HLA-B14:023BVN2255EYDPTIEGLRKRRH-4.37152-5.40682
HLA-B52:013W392255EYDPTIEGLRKRRH-6.90336-7.01676
HLA-B52:013W392255EYDPTIEGLRKRRH-4.80833-5.84363
HLA-A11:014UQ22255EYDPTIEGLRKRRH-9.82261-9.93601
HLA-A24:025HGA2255EYDPTIEGLRKRRH-9.78612-9.89952
HLA-A24:025HGA2255EYDPTIEGLRKRRH-4.98992-6.02522
HLA-B27:056PYJ2255EYDPTIEGLRKRRH-5.31553-6.35083
HLA-B44:053DX82255EYDPTIEGLRKRRH-5.70582-5.81922
HLA-B44:053DX82255EYDPTIEGLRKRRH-4.32241-5.35771

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Vaccine Design for the FusionNeoAntigens of KRAS-IFLTD1

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
KRAS-IFLTD1chr1225398208chr1225656734415VDEYDPTIEGLGTGGACGAATATGATCCAACAATAGAGGGTCTA
KRAS-IFLTD1chr1225398208chr1225656734514DEYDPTIEGGACGAATATGATCCAACAATAGAGGGT
KRAS-IFLTD1chr1225398208chr1225656734515DEYDPTIEGLGACGAATATGATCCAACAATAGAGGGTCTA
KRAS-IFLTD1chr1225398208chr1225656734615EYDPTIEGLGAATATGATCCAACAATAGAGGGTCTA
KRAS-IFLTD1chr1225398208chr1225656734715YDPTIEGLTATGATCCAACAATAGAGGGTCTA

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
KRAS-IFLTD1chr1225398208chr1225656734722YDPTIEGLRKRRHLSTATGATCCAACAATAGAGGGTCTAAGAAAAAGAAGACATCTGAGT
KRAS-IFLTD1chr1225398208chr1225656734823DPTIEGLRKRRHLSHGATCCAACAATAGAGGGTCTAAGAAAAAGAAGACATCTGAGTCAC

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Information of the samples that have these potential fusion neoantigens of KRAS-IFLTD1

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
OVKRAS-IFLTD1chr1225398208ENST00000256078chr1225656734ENST00000413632TCGA-13-1511-01A

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Potential target of CAR-T therapy development for KRAS-IFLTD1

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

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Related Drugs to KRAS-IFLTD1

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 KRAS-IFLTD1

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