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:EIF2AK2-RMDN2

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: EIF2AK2-RMDN2
FusionPDB ID: 25664
FusionGDB2.0 ID: 25664
HgeneTgene
Gene symbol

EIF2AK2

RMDN2

Gene ID

5610

151393

Gene nameeukaryotic translation initiation factor 2 alpha kinase 2regulator of microtubule dynamics 2
SynonymsEIF2AK1|PKR|PPP1R83|PRKRBLOCK18|FAM82A|FAM82A1|PRO34163|PYST9371|RMD-2|RMD2|RMD4
Cytomap

2p22.2

2p22.2

Type of geneprotein-codingprotein-coding
Descriptioninterferon-induced, double-stranded RNA-activated protein kinaseP1/eIF-2A protein kinasedouble stranded RNA activated protein kinaseeIF-2A protein kinase 2interferon-inducible elF2alpha kinasep68 kinaseprotein kinase Rprotein kinase, interferon-indregulator of microtubule dynamics protein 2family with sequence similarity 82, member Afamily with sequence similarity 82, member A1microtubule-associated protein
Modification date2020031320200313
UniProtAcc

P19525

Main function of 5'-partner protein: FUNCTION: IFN-induced dsRNA-dependent serine/threonine-protein kinase that phosphorylates the alpha subunit of eukaryotic translation initiation factor 2 (EIF2S1/eIF-2-alpha) and plays a key role in the innate immune response to viral infection (PubMed:18835251, PubMed:19507191, PubMed:19189853, PubMed:21123651, PubMed:21072047, PubMed:22948139, PubMed:23229543, PubMed:22381929). Inhibits viral replication via the integrated stress response (ISR): EIF2S1/eIF-2-alpha phosphorylation in response to viral infection converts EIF2S1/eIF-2-alpha in a global protein synthesis inhibitor, resulting to a shutdown of cellular and viral protein synthesis, while concomitantly initiating the preferential translation of ISR-specific mRNAs, such as the transcriptional activator ATF4 (PubMed:19189853, PubMed:21123651, PubMed:22948139, PubMed:23229543). Exerts its antiviral activity on a wide range of DNA and RNA viruses including hepatitis C virus (HCV), hepatitis B virus (HBV), measles virus (MV) and herpes simplex virus 1 (HHV-1) (PubMed:11836380, PubMed:19189853, PubMed:20171114, PubMed:19840259, PubMed:21710204, PubMed:23115276, PubMed:23399035). Also involved in the regulation of signal transduction, apoptosis, cell proliferation and differentiation: phosphorylates other substrates including p53/TP53, PPP2R5A, DHX9, ILF3, IRS1 and the HHV-1 viral protein US11 (PubMed:11836380, PubMed:22214662, PubMed:19229320). In addition to serine/threonine-protein kinase activity, also has tyrosine-protein kinase activity and phosphorylates CDK1 at 'Tyr-4' upon DNA damage, facilitating its ubiquitination and proteosomal degradation (PubMed:20395957). Either as an adapter protein and/or via its kinase activity, can regulate various signaling pathways (p38 MAP kinase, NF-kappa-B and insulin signaling pathways) and transcription factors (JUN, STAT1, STAT3, IRF1, ATF3) involved in the expression of genes encoding proinflammatory cytokines and IFNs (PubMed:22948139, PubMed:23084476, PubMed:23372823). Activates the NF-kappa-B pathway via interaction with IKBKB and TRAF family of proteins and activates the p38 MAP kinase pathway via interaction with MAP2K6 (PubMed:10848580, PubMed:15121867, PubMed:15229216). Can act as both a positive and negative regulator of the insulin signaling pathway (ISP) (PubMed:20685959). Negatively regulates ISP by inducing the inhibitory phosphorylation of insulin receptor substrate 1 (IRS1) at 'Ser-312' and positively regulates ISP via phosphorylation of PPP2R5A which activates FOXO1, which in turn up-regulates the expression of insulin receptor substrate 2 (IRS2) (PubMed:20685959). Can regulate NLRP3 inflammasome assembly and the activation of NLRP3, NLRP1, AIM2 and NLRC4 inflammasomes (PubMed:22801494). Plays a role in the regulation of the cytoskeleton by binding to gelsolin (GSN), sequestering the protein in an inactive conformation away from actin (By similarity). {ECO:0000250|UniProtKB:Q03963, ECO:0000269|PubMed:10848580, ECO:0000269|PubMed:11836380, ECO:0000269|PubMed:15121867, ECO:0000269|PubMed:15229216, ECO:0000269|PubMed:18835251, ECO:0000269|PubMed:19189853, ECO:0000269|PubMed:19229320, ECO:0000269|PubMed:19507191, ECO:0000269|PubMed:19840259, ECO:0000269|PubMed:20171114, ECO:0000269|PubMed:20395957, ECO:0000269|PubMed:20685959, ECO:0000269|PubMed:21072047, ECO:0000269|PubMed:21123651, ECO:0000269|PubMed:21710204, ECO:0000269|PubMed:22214662, ECO:0000269|PubMed:22381929, ECO:0000269|PubMed:22801494, ECO:0000269|PubMed:22948139, ECO:0000269|PubMed:23084476, ECO:0000269|PubMed:23115276, ECO:0000269|PubMed:23229543, ECO:0000269|PubMed:23372823, ECO:0000269|PubMed:23399035, ECO:0000269|PubMed:32197074}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000233057, ENST00000395127, 
ENST00000405334, 
ENST00000354545, 
ENST00000402091, ENST00000406384, 
ENST00000407257, ENST00000417700, 
ENST00000469469, ENST00000234195, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score6 X 8 X 4=1928 X 7 X 2=112
# samples 99
** MAII scorelog2(9/192*10)=-1.09310940439148
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(9/112*10)=-0.315501825727929
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: EIF2AK2 [Title/Abstract] AND RMDN2 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: EIF2AK2 [Title/Abstract] AND RMDN2 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)EIF2AK2(37362627)-RMDN2(38216684), # samples:2
Anticipated loss of major functional domain due to fusion event.EIF2AK2-RMDN2 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.
EIF2AK2-RMDN2 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.
EIF2AK2-RMDN2 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.
EIF2AK2-RMDN2 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.
EIF2AK2-RMDN2 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
EIF2AK2-RMDN2 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
EIF2AK2-RMDN2 seems lost the major protein functional domain in Hgene partner, which is a kinase 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
HgeneEIF2AK2

GO:0006468

protein phosphorylation

19189853

HgeneEIF2AK2

GO:0017148

negative regulation of translation

12882984

HgeneEIF2AK2

GO:0035455

response to interferon-alpha

19840259

HgeneEIF2AK2

GO:0046777

protein autophosphorylation

22801494

HgeneEIF2AK2

GO:0051092

positive regulation of NF-kappaB transcription factor activity

15121867



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/chr2:37362627/chr2:38216684)
- 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 EIF2AK2 (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 RMDN2 (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)
ENST00000405334EIF2AK2chr237362627-ENST00000234195RMDN2chr238216684+132978501181393

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
ENST00000405334ENST00000234195EIF2AK2chr237362627-RMDN2chr238216684+0.00048780.9995122

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 EIF2AK2-RMDN2

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
EIF2AK2chr237362627RMDN2chr238216684785261LPDMKETKYTVDKRYAVLCGYVSEFE

Top

Potential FusionNeoAntigen Information of EIF2AK2-RMDN2 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.
EIF2AK2-RMDN2_37362627_38216684.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)
EIF2AK2-RMDN2chr237362627chr238216684785HLA-B27:02KRYAVLCGY0.99950.78341221
EIF2AK2-RMDN2chr237362627chr238216684785HLA-B27:05KRYAVLCGY0.99940.84981221
EIF2AK2-RMDN2chr237362627chr238216684785HLA-B27:04KRYAVLCGY0.99940.93961221
EIF2AK2-RMDN2chr237362627chr238216684785HLA-B27:07KRYAVLCGY0.95180.60591221
EIF2AK2-RMDN2chr237362627chr238216684785HLA-B15:03TKYTVDKRY0.12280.5166615
EIF2AK2-RMDN2chr237362627chr238216684785HLA-B44:03KETKYTVDKRY0.99890.8826415
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C04:07TVDKRYAVL0.99980.8703918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C05:09TVDKRYAVL0.99980.9372918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C04:10TVDKRYAVL0.99980.8558918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C01:17TVDKRYAVL0.99970.9352918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C08:15TVDKRYAVL0.99970.9632918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C15:06YTVDKRYAV0.99930.7635817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C15:04YTVDKRYAV0.99920.8119817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C03:07YTVDKRYAV0.99880.9373817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C04:06YTVDKRYAV0.99860.737817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-B27:14KRYAVLCGY0.99810.82481221
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C03:19TVDKRYAVL0.99780.9755918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C01:30TVDKRYAVL0.99720.9371918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C03:08TVDKRYAVL0.99720.8456918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C03:07TVDKRYAVL0.99690.9603918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-B27:03KRYAVLCGY0.99640.85291221
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C15:06TVDKRYAVL0.99620.8528918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C03:19YTVDKRYAV0.99460.9699817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C07:95KRYAVLCGY0.9910.78941221
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C06:03YTVDKRYAV0.990.9767817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C12:04YTVDKRYAV0.98970.9776817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C04:06TVDKRYAVL0.98750.8697918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C03:08YTVDKRYAV0.98560.7762817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C08:13YTVDKRYAV0.9780.9427817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C08:04YTVDKRYAV0.9780.9427817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C08:13TVDKRYAVL0.97350.9586918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C08:04TVDKRYAVL0.97350.9586918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-B14:03TVDKRYAVL0.96570.6789918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C04:14TVDKRYAVL0.95530.9039918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C07:13TVDKRYAVL0.95420.8898918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C02:06YTVDKRYAV0.9510.9537817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C12:12YTVDKRYAV0.94380.8572817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C08:03YTVDKRYAV0.93770.9403817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C07:27KRYAVLCGY0.93450.96911221
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C07:05KRYAVLCGY0.88410.97341221
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C07:29TVDKRYAVL0.8710.8612918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C08:03TVDKRYAVL0.85280.967918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C07:19KRYAVLCGY0.81260.87991221
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C07:67KRYAVLCGY0.74830.96671221
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C07:80KRYAVLCGY0.74830.96671221
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C07:10KRYAVLCGY0.73190.98391221
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C07:46KRYAVLCGY0.67370.93941221
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C03:14YTVDKRYAV0.57030.946817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C12:16KRYAVLCGY0.01510.98151221
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C04:03TVDKRYAVL0.99980.9012918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C01:03TVDKRYAVL0.99980.9393918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C04:01TVDKRYAVL0.99980.8703918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C05:01TVDKRYAVL0.99980.9372918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C18:01TVDKRYAVL0.99980.8935918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C01:02TVDKRYAVL0.99970.9369918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C08:02TVDKRYAVL0.99970.9632918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C15:02YTVDKRYAV0.99960.7349817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-B27:08KRYAVLCGY0.99940.83031221
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C15:05YTVDKRYAV0.99940.7506817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-B27:10KRYAVLCGY0.99930.96831221
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C15:09YTVDKRYAV0.99920.8119817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C03:03TVDKRYAVL0.99820.9782918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C03:04TVDKRYAVL0.99820.9782918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C03:67TVDKRYAVL0.99560.967918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C03:05TVDKRYAVL0.99540.8932918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C16:02YTVDKRYAV0.9950.9651817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C15:05TVDKRYAVL0.99490.8813918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C07:01KRYAVLCGY0.99450.81791221
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C03:06YTVDKRYAV0.99410.9713817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C03:17YTVDKRYAV0.99380.9239817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C03:05YTVDKRYAV0.9920.8763817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C04:04TVDKRYAVL0.9840.8628918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C16:04YTVDKRYAV0.98190.9078817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-B27:09KRYAVLCGY0.98130.83081221
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C06:02YTVDKRYAV0.97830.9755817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C06:17YTVDKRYAV0.97830.9755817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C06:06YTVDKRYAV0.97620.9607817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C07:04TVDKRYAVL0.97370.9058918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C03:03YTVDKRYAV0.95770.9715817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C03:04YTVDKRYAV0.95770.9715817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C12:03YTVDKRYAV0.95410.95817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C08:01YTVDKRYAV0.93770.9403817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C03:06TVDKRYAVL0.93030.9826918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C16:01YTVDKRYAV0.91270.9375817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C03:67YTVDKRYAV0.89190.9565817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C07:04YTVDKRYAV0.87580.695817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-B07:13TVDKRYAVL0.8590.7544918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C08:01TVDKRYAVL0.85280.967918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C02:02YTVDKRYAV0.84750.9514817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C02:10YTVDKRYAV0.84750.9514817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C06:08YTVDKRYAV0.84370.977817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C17:01YTVDKRYAV0.77180.8728817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C07:02KRYAVLCGY0.74830.96671221
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C07:22KRYAVLCGY0.74720.8381221
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C12:02YTVDKRYAV0.70310.9139817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-B07:13YTVDKRYAV0.5730.5517817
EIF2AK2-RMDN2chr237362627chr238216684785HLA-C17:01TVDKRYAVL0.52620.9057918
EIF2AK2-RMDN2chr237362627chr238216684785HLA-B48:02TKYTVDKRY0.20990.7589615
EIF2AK2-RMDN2chr237362627chr238216684785HLA-B15:53TKYTVDKRY0.02030.7395615
EIF2AK2-RMDN2chr237362627chr238216684785HLA-B15:54TKYTVDKRY0.01360.7214615
EIF2AK2-RMDN2chr237362627chr238216684785HLA-B15:68KRYAVLCGY0.00390.85811221
EIF2AK2-RMDN2chr237362627chr238216684785HLA-A25:01ETKYTVDKRY0.92870.6064515
EIF2AK2-RMDN2chr237362627chr238216684785HLA-B44:13KETKYTVDKRY0.99890.8826415
EIF2AK2-RMDN2chr237362627chr238216684785HLA-B44:26KETKYTVDKRY0.99890.8826415
EIF2AK2-RMDN2chr237362627chr238216684785HLA-B44:07KETKYTVDKRY0.99890.8826415

Top

Potential FusionNeoAntigen Information of EIF2AK2-RMDN2 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.
EIF2AK2-RMDN2_37362627_38216684.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)
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-0305MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-0305ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-0305KETKYTVDKRYAVLC419
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-0305DMKETKYTVDKRYAV217
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-0305TKYTVDKRYAVLCGY621
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-0338MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-0338ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-0338KETKYTVDKRYAVLC419
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-0338DMKETKYTVDKRYAV217
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-0340MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-0340ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-0340KETKYTVDKRYAVLC419
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-0340DMKETKYTVDKRYAV217
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-0340TKYTVDKRYAVLCGY621
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-0466ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-0466MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-0840MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1114ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1120ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1153MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1153ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1153KETKYTVDKRYAVLC419
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1168ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1173ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1173MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1173KETKYTVDKRYAVLC419
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1179ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1179MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1179KETKYTVDKRYAVLC419
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1179DMKETKYTVDKRYAV217
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1182ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1182MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1182KETKYTVDKRYAVLC419
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1302ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1303MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1303ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-13100MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-13101MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-13101ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-13101KETKYTVDKRYAVLC419
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-13101DMKETKYTVDKRYAV217
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1310MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1310ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1310KETKYTVDKRYAVLC419
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1310DMKETKYTVDKRYAV217
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1323ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1329ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1331MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1331ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1331KETKYTVDKRYAVLC419
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1333MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1333ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1333KETKYTVDKRYAVLC419
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1333DMKETKYTVDKRYAV217
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1334ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1336ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1336MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1337ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1337MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1337KETKYTVDKRYAVLC419
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1338MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1338ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1338KETKYTVDKRYAVLC419
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1339ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1341ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1341MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1341KETKYTVDKRYAVLC419
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1346MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1365MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1365ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1365KETKYTVDKRYAVLC419
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1366MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1366ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1366KETKYTVDKRYAVLC419
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1373ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1374ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1385ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1385MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1385KETKYTVDKRYAVLC419
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1386ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1386MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1388MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1388ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1390MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1390ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1395MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1395ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1396ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1396MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1396KETKYTVDKRYAVLC419
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1397ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1399ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1402ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1402MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1407MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1407ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1407KETKYTVDKRYAVLC419
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1407DMKETKYTVDKRYAV217
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1409MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1409ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1409KETKYTVDKRYAVLC419
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1413MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1413ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1414MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1414ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1414KETKYTVDKRYAVLC419
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1419ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1419MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1419KETKYTVDKRYAVLC419
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1424ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1424MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1430ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1430MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1430KETKYTVDKRYAVLC419
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1436MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1436ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1436KETKYTVDKRYAVLC419
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1441ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1441MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1442MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1442ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1442KETKYTVDKRYAVLC419
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1444MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1444ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1444KETKYTVDKRYAVLC419
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1447ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1447MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1447KETKYTVDKRYAVLC419
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1448MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1448ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1449MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1449ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1449KETKYTVDKRYAVLC419
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1451MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1451ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1451KETKYTVDKRYAVLC419
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1468MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1468ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1468KETKYTVDKRYAVLC419
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1469MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1469ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1493MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1493ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1493KETKYTVDKRYAVLC419
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1493DMKETKYTVDKRYAV217
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1494ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB1-1494MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB3-0114MKETKYTVDKRYAVL318
EIF2AK2-RMDN2chr237362627chr238216684785DRB3-0114ETKYTVDKRYAVLCG520
EIF2AK2-RMDN2chr237362627chr238216684785DRB3-0114KETKYTVDKRYAVLC419
EIF2AK2-RMDN2chr237362627chr238216684785DRB3-0114DMKETKYTVDKRYAV217

Top

Fusion breakpoint peptide structures of EIF2AK2-RMDN2

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
9450TKYTVDKRYAVLCGEIF2AK2RMDN2chr237362627chr238216684785

Top

Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of EIF2AK2-RMDN2

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-B14:023BVN9450TKYTVDKRYAVLCG-6.11479-7.15009
HLA-B14:023BVN9450TKYTVDKRYAVLCG-4.76706-4.88046
HLA-B52:013W399450TKYTVDKRYAVLCG-6.87405-6.98745
HLA-B52:013W399450TKYTVDKRYAVLCG-5.3619-6.3972
HLA-A11:014UQ29450TKYTVDKRYAVLCG-9.79836-9.91176
HLA-A24:025HGA9450TKYTVDKRYAVLCG-8.83847-8.95187
HLA-A24:025HGA9450TKYTVDKRYAVLCG-8.05027-9.08557
HLA-B44:053DX89450TKYTVDKRYAVLCG-7.51915-7.63255
HLA-B44:053DX89450TKYTVDKRYAVLCG-4.45384-5.48914
HLA-A02:016TDR9450TKYTVDKRYAVLCG-2.8902-3.9255

Top

Vaccine Design for the FusionNeoAntigens of EIF2AK2-RMDN2

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
EIF2AK2-RMDN2chr237362627chr2382166841221KRYAVLCGYGAGGTATGCAGTTTTGTGTGGCTATGT
EIF2AK2-RMDN2chr237362627chr238216684415KETKYTVDKRYAGAAACAAAGTATACTGTGGACAAGAGGTATGC
EIF2AK2-RMDN2chr237362627chr238216684515ETKYTVDKRYAACAAAGTATACTGTGGACAAGAGGTATGC
EIF2AK2-RMDN2chr237362627chr238216684615TKYTVDKRYAAAGTATACTGTGGACAAGAGGTATGC
EIF2AK2-RMDN2chr237362627chr238216684817YTVDKRYAVTACTGTGGACAAGAGGTATGCAGTTTT
EIF2AK2-RMDN2chr237362627chr238216684918TVDKRYAVLTGTGGACAAGAGGTATGCAGTTTTGTG

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
EIF2AK2-RMDN2chr237362627chr238216684217DMKETKYTVDKRYAVCATGAAAGAAACAAAGTATACTGTGGACAAGAGGTATGCAGTTTT
EIF2AK2-RMDN2chr237362627chr238216684318MKETKYTVDKRYAVLGAAAGAAACAAAGTATACTGTGGACAAGAGGTATGCAGTTTTGTG
EIF2AK2-RMDN2chr237362627chr238216684419KETKYTVDKRYAVLCAGAAACAAAGTATACTGTGGACAAGAGGTATGCAGTTTTGTGTGG
EIF2AK2-RMDN2chr237362627chr238216684520ETKYTVDKRYAVLCGAACAAAGTATACTGTGGACAAGAGGTATGCAGTTTTGTGTGGCTA
EIF2AK2-RMDN2chr237362627chr238216684621TKYTVDKRYAVLCGYAAAGTATACTGTGGACAAGAGGTATGCAGTTTTGTGTGGCTATGT

Top

Information of the samples that have these potential fusion neoantigens of EIF2AK2-RMDN2

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
BRCAEIF2AK2-RMDN2chr237362627ENST00000405334chr238216684ENST00000234195TCGA-D8-A142-01A

Top

Potential target of CAR-T therapy development for EIF2AK2-RMDN2

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 EIF2AK2-RMDN2

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

Top

Related Diseases to EIF2AK2-RMDN2

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