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Fusion Protein:ERN1-EIF3C |
Fusion Gene and Fusion Protein Summary |
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Fusion partner gene information | Fusion gene name: ERN1-EIF3C | FusionPDB ID: 27441 | FusionGDB2.0 ID: 27441 | Hgene | Tgene | Gene symbol | ERN1 | EIF3C | Gene ID | 2081 | 8663 |
Gene name | endoplasmic reticulum to nucleus signaling 1 | eukaryotic translation initiation factor 3 subunit C | |
Synonyms | IRE1|IRE1P|IRE1a|hIRE1p | EIF3CL|EIF3S8|eIF3-p110 | |
Cytomap | 17q23.3 | 16p11.2 | |
Type of gene | protein-coding | protein-coding | |
Description | serine/threonine-protein kinase/endoribonuclease IRE1ER to nucleus signalling 1inositol-requiring 1inositol-requiring enzyme 1inositol-requiring protein 1ire1-alphaprotein kinase/endoribonuclease | eukaryotic translation initiation factor 3 subunit Ccell migration-inducing protein 17eIF3 p110eukaryotic translation initiation factor 3 subunit 8eukaryotic translation initiation factor 3, subunit 8 (110kD)eukaryotic translation initiation factor 3 | |
Modification date | 20200329 | 20200322 | |
UniProtAcc | O75460 Main function of 5'-partner protein: FUNCTION: Serine/threonine-protein kinase and endoribonuclease that acts as a key sensor for the endoplasmic reticulum unfolded protein response (UPR) (PubMed:11779464, PubMed:11175748, PubMed:12637535, PubMed:9637683, PubMed:21317875, PubMed:28128204). In unstressed cells, the endoplasmic reticulum luminal domain is maintained in its inactive monomeric state by binding to the endoplasmic reticulum chaperone HSPA5/BiP (PubMed:21317875). Accumulation of misfolded proteins in the endoplasmic reticulum causes release of HSPA5/BiP, allowing the luminal domain to homodimerize, promoting autophosphorylation of the kinase domain and subsequent activation of the endoribonuclease activity (PubMed:21317875). The endoribonuclease activity is specific for XBP1 mRNA and excises 26 nucleotides from XBP1 mRNA (PubMed:11779464, PubMed:24508390, PubMed:21317875). The resulting spliced transcript of XBP1 encodes a transcriptional activator protein that up-regulates expression of UPR target genes (PubMed:11779464, PubMed:24508390, PubMed:21317875). Acts as an upstream signal for ER stress-induced GORASP2-mediated unconventional (ER/Golgi-independent) trafficking of CFTR to cell membrane by modulating the expression and localization of SEC16A (PubMed:21884936, PubMed:28067262). {ECO:0000269|PubMed:11175748, ECO:0000269|PubMed:11779464, ECO:0000269|PubMed:12637535, ECO:0000269|PubMed:21317875, ECO:0000269|PubMed:21884936, ECO:0000269|PubMed:28067262, ECO:0000269|PubMed:28128204, ECO:0000269|PubMed:9637683, ECO:0000305|PubMed:24508390}. | B5ME19 Main function of 5'-partner protein: FUNCTION: Component of the eukaryotic translation initiation factor 3 (eIF-3) complex, which is required for several steps in the initiation of protein synthesis. The eIF-3 complex associates with the 40S ribosome and facilitates the recruitment of eIF-1, eIF-1A, eIF-2:GTP:methionyl-tRNAi and eIF-5 to form the 43S pre-initiation complex (43S PIC). The eIF-3 complex stimulates mRNA recruitment to the 43S PIC and scanning of the mRNA for AUG recognition. The eIF-3 complex is also required for disassembly and recycling of post-termination ribosomal complexes and subsequently prevents premature joining of the 40S and 60S ribosomal subunits prior to initiation. The eIF-3 complex specifically targets and initiates translation of a subset of mRNAs involved in cell proliferation, including cell cycling, differentiation and apoptosis, and uses different modes of RNA stem-loop binding to exert either translational activation or repression. {ECO:0000250|UniProtKB:Q99613}. | |
Ensembl transtripts involved in fusion gene | ENST ids | ENST00000433197, ENST00000577567, ENST00000606895, | ENST00000565099, ENST00000331666, ENST00000395587, ENST00000564243, ENST00000566501, ENST00000566866, |
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0) | * DoF score | 7 X 9 X 7=441 | 8 X 8 X 3=192 |
# samples | 10 | 8 | |
** MAII score | log2(10/441*10)=-2.1407786557828 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(8/192*10)=-1.26303440583379 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Fusion gene context | PubMed: ERN1 [Title/Abstract] AND EIF3C [Title/Abstract] AND fusion [Title/Abstract] | ||
Fusion neoantigen context | PubMed: ERN1 [Title/Abstract] AND EIF3C [Title/Abstract] AND neoantigen [Title/Abstract] | ||
Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0) | ERN1(62144031)-EIF3C(28734485), # samples:1 | ||
Anticipated loss of major functional domain due to fusion event. | ERN1-EIF3C 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. ERN1-EIF3C 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. ERN1-EIF3C 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. ERN1-EIF3C 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) |
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Partner | Gene | GO ID | GO term | PubMed ID |
Hgene | ERN1 | GO:0001935 | endothelial cell proliferation | 23529610 |
Hgene | ERN1 | GO:0006468 | protein phosphorylation | 9637683 |
Hgene | ERN1 | GO:0007257 | activation of JUN kinase activity | 10650002 |
Hgene | ERN1 | GO:0033120 | positive regulation of RNA splicing | 11779464|19622636 |
Hgene | ERN1 | GO:0034620 | cellular response to unfolded protein | 19328063 |
Hgene | ERN1 | GO:0034976 | response to endoplasmic reticulum stress | 10650002 |
Hgene | ERN1 | GO:0035924 | cellular response to vascular endothelial growth factor stimulus | 23529610 |
Hgene | ERN1 | GO:0036289 | peptidyl-serine autophosphorylation | 20103773 |
Hgene | ERN1 | GO:0036498 | IRE1-mediated unfolded protein response | 9637683|11779465|19328063|29198525 |
Hgene | ERN1 | GO:0046777 | protein autophosphorylation | 9637683|19328063 |
Hgene | ERN1 | GO:0070054 | mRNA splicing, via endonucleolytic cleavage and ligation | 11779464|19328063|19622636|21317875 |
Hgene | ERN1 | GO:0071333 | cellular response to glucose stimulus | 20103773 |
Hgene | ERN1 | GO:0098787 | mRNA cleavage involved in mRNA processing | 21317875 |
Hgene | ERN1 | GO:1901142 | insulin metabolic process | 20103773 |
Tgene | EIF3C | GO:0006413 | translational initiation | 17581632 |
![]() Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr17:62144031/chr16:28734485) - 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. |
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![]() * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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![]() * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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Fusion Amino Acid Sequences |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | Seq length (transcript) | BP loci (transcript) | Predicted start (transcript) | Predicted stop (transcript) | Seq length (amino acids) |
ENST00000433197 | ERN1 | chr17 | 62144031 | - | ENST00000566501 | EIF3C | chr16 | 28734485 | + | 2989 | 938 | 27 | 2903 | 958 |
ENST00000433197 | ERN1 | chr17 | 62144031 | - | ENST00000331666 | EIF3C | chr16 | 28734485 | + | 3121 | 938 | 27 | 2903 | 958 |
ENST00000433197 | ERN1 | chr17 | 62144031 | - | ENST00000395587 | EIF3C | chr16 | 28734485 | + | 3118 | 938 | 27 | 2903 | 958 |
ENST00000433197 | ERN1 | chr17 | 62144031 | - | ENST00000564243 | EIF3C | chr16 | 28734485 | + | 2987 | 938 | 27 | 2903 | 958 |
ENST00000433197 | ERN1 | chr17 | 62144031 | - | ENST00000566866 | EIF3C | chr16 | 28734485 | + | 2988 | 938 | 27 | 2903 | 958 |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
ENST00000433197 | ENST00000566501 | ERN1 | chr17 | 62144031 | - | EIF3C | chr16 | 28734485 | + | 0.001573235 | 0.9984268 |
ENST00000433197 | ENST00000331666 | ERN1 | chr17 | 62144031 | - | EIF3C | chr16 | 28734485 | + | 0.00154331 | 0.9984567 |
ENST00000433197 | ENST00000395587 | ERN1 | chr17 | 62144031 | - | EIF3C | chr16 | 28734485 | + | 0.001554107 | 0.9984459 |
ENST00000433197 | ENST00000564243 | ERN1 | chr17 | 62144031 | - | EIF3C | chr16 | 28734485 | + | 0.001586165 | 0.9984138 |
ENST00000433197 | ENST00000566866 | ERN1 | chr17 | 62144031 | - | EIF3C | chr16 | 28734485 | + | 0.001590474 | 0.99840957 |
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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 ERN1-EIF3C |
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Hgene | Hchr | Hbp | Tgene | Tchr | Tbp | Length(fusion protein) | BP in fusion protein | Peptide |
ERN1 | chr17 | 62144031 | EIF3C | chr16 | 28734485 | 938 | 304 | PFPKETEAKSKLTAPTTDEDKKAAEK |
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Potential FusionNeoAntigen Information of ERN1-EIF3C in HLA I |
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ERN1-EIF3C_62144031_28734485.msa |
![]() * We used NetMHCpan v4.1 (%rank<0.5) and deepHLApan v1.1 (immunogenic score>0.5) |
Fusion gene | Hchr | Hbp | Tgene | Tchr | Tbp | HLA I | FusionNeoAntigen peptide | Binding score | Immunogenic score | Neoantigen start (at BP 13) | Neoantigen end (at BP 13) |
ERN1-EIF3C | chr17 | 62144031 | chr16 | 28734485 | 938 | HLA-B45:01 | TEAKSKLTA | 0.9971 | 0.8273 | 5 | 14 |
ERN1-EIF3C | chr17 | 62144031 | chr16 | 28734485 | 938 | HLA-B50:02 | TEAKSKLTA | 0.9937 | 0.7187 | 5 | 14 |
ERN1-EIF3C | chr17 | 62144031 | chr16 | 28734485 | 938 | HLA-A30:08 | KSKLTAPTT | 0.9792 | 0.8643 | 8 | 17 |
ERN1-EIF3C | chr17 | 62144031 | chr16 | 28734485 | 938 | HLA-B08:09 | EAKSKLTAP | 0.969 | 0.501 | 6 | 15 |
ERN1-EIF3C | chr17 | 62144031 | chr16 | 28734485 | 938 | HLA-B41:01 | TEAKSKLTA | 0.6667 | 0.7162 | 5 | 14 |
ERN1-EIF3C | chr17 | 62144031 | chr16 | 28734485 | 938 | HLA-B50:01 | TEAKSKLTA | 0.2448 | 0.7303 | 5 | 14 |
ERN1-EIF3C | chr17 | 62144031 | chr16 | 28734485 | 938 | HLA-B45:01 | TEAKSKLTAP | 0.9734 | 0.8796 | 5 | 15 |
ERN1-EIF3C | chr17 | 62144031 | chr16 | 28734485 | 938 | HLA-B41:01 | TEAKSKLTAP | 0.9182 | 0.7385 | 5 | 15 |
ERN1-EIF3C | chr17 | 62144031 | chr16 | 28734485 | 938 | HLA-B50:02 | TEAKSKLTAP | 0.8931 | 0.7254 | 5 | 15 |
ERN1-EIF3C | chr17 | 62144031 | chr16 | 28734485 | 938 | HLA-B41:01 | ETEAKSKLTA | 0.7805 | 0.7989 | 4 | 14 |
ERN1-EIF3C | chr17 | 62144031 | chr16 | 28734485 | 938 | HLA-B45:01 | ETEAKSKLTA | 0.7448 | 0.896 | 4 | 14 |
ERN1-EIF3C | chr17 | 62144031 | chr16 | 28734485 | 938 | HLA-B50:02 | ETEAKSKLTA | 0.7298 | 0.6721 | 4 | 14 |
ERN1-EIF3C | chr17 | 62144031 | chr16 | 28734485 | 938 | HLA-B45:01 | KETEAKSKLTA | 0.9996 | 0.8721 | 3 | 14 |
ERN1-EIF3C | chr17 | 62144031 | chr16 | 28734485 | 938 | HLA-B50:02 | KETEAKSKLTA | 0.9987 | 0.7195 | 3 | 14 |
ERN1-EIF3C | chr17 | 62144031 | chr16 | 28734485 | 938 | HLA-B41:01 | KETEAKSKLTA | 0.9986 | 0.8663 | 3 | 14 |
ERN1-EIF3C | chr17 | 62144031 | chr16 | 28734485 | 938 | HLA-B50:01 | KETEAKSKLTA | 0.9939 | 0.7585 | 3 | 14 |
ERN1-EIF3C | chr17 | 62144031 | chr16 | 28734485 | 938 | HLA-B40:06 | TEAKSKLTA | 0.9972 | 0.5071 | 5 | 14 |
ERN1-EIF3C | chr17 | 62144031 | chr16 | 28734485 | 938 | HLA-A30:01 | KSKLTAPTT | 0.9803 | 0.9304 | 8 | 17 |
ERN1-EIF3C | chr17 | 62144031 | chr16 | 28734485 | 938 | HLA-B40:04 | TEAKSKLTA | 0.9497 | 0.675 | 5 | 14 |
ERN1-EIF3C | chr17 | 62144031 | chr16 | 28734485 | 938 | HLA-B50:05 | TEAKSKLTA | 0.2448 | 0.7303 | 5 | 14 |
ERN1-EIF3C | chr17 | 62144031 | chr16 | 28734485 | 938 | HLA-B50:04 | TEAKSKLTA | 0.2448 | 0.7303 | 5 | 14 |
ERN1-EIF3C | chr17 | 62144031 | chr16 | 28734485 | 938 | HLA-B50:05 | KETEAKSKLTA | 0.9939 | 0.7585 | 3 | 14 |
ERN1-EIF3C | chr17 | 62144031 | chr16 | 28734485 | 938 | HLA-B50:04 | KETEAKSKLTA | 0.9939 | 0.7585 | 3 | 14 |
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Potential FusionNeoAntigen Information of ERN1-EIF3C in HLA II |
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![]() * We used NetMHCIIpan v4.1 (%rank<0.5). |
Fusion gene | Hchr | Hbp | Tgene | Tchr | Tbp | HLA II | FusionNeoAntigen peptide | Neoantigen start (at BP 13) | Neoantigen end (at BP 13) |
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Fusion breakpoint peptide structures of ERN1-EIF3C |
![]() * 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 name | BPseq | Hgene | Tgene | Hchr | Hbp | Tchr | Tbp | AAlen |
1529 | EAKSKLTAPTTDED | ERN1 | EIF3C | chr17 | 62144031 | chr16 | 28734485 | 938 |
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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of ERN1-EIF3C |
![]() * We used Glide to predict the interaction between HLAs and neoantigens. |
HLA allele | PDB ID | File name | BPseq | Docking score | Glide score |
HLA-B14:02 | 3BVN | 1529 | EAKSKLTAPTTDED | -4.49634 | -4.50354 |
HLA-B52:01 | 3W39 | 1529 | EAKSKLTAPTTDED | -4.85976 | -4.86696 |
HLA-A11:01 | 4UQ2 | 1529 | EAKSKLTAPTTDED | -6.83409 | -6.84129 |
HLA-A24:02 | 5HGA | 1529 | EAKSKLTAPTTDED | -7.42139 | -7.42859 |
HLA-B27:05 | 6PYJ | 1529 | EAKSKLTAPTTDED | -5.73102 | -5.73822 |
HLA-B44:05 | 3DX8 | 1529 | EAKSKLTAPTTDED | -5.02455 | -5.03175 |
HLA-A02:01 | 6TDR | 1529 | EAKSKLTAPTTDED | -6.90764 | -6.91484 |
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Vaccine Design for the FusionNeoAntigens of ERN1-EIF3C |
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Fusion gene | Hchr | Hbp | Tchr | Tbp | Start in +/-13AA | End in +/-13AA | FusionNeoAntigen peptide sequence | FusionNeoAntigen RNA sequence |
ERN1-EIF3C | chr17 | 62144031 | chr16 | 28734485 | 3 | 14 | KETEAKSKLTA | CAAGGAGACAGAGGCCAAGAGCAAGCTGACGGC |
ERN1-EIF3C | chr17 | 62144031 | chr16 | 28734485 | 4 | 14 | ETEAKSKLTA | GGAGACAGAGGCCAAGAGCAAGCTGACGGC |
ERN1-EIF3C | chr17 | 62144031 | chr16 | 28734485 | 5 | 14 | TEAKSKLTA | GACAGAGGCCAAGAGCAAGCTGACGGC |
ERN1-EIF3C | chr17 | 62144031 | chr16 | 28734485 | 5 | 15 | TEAKSKLTAP | GACAGAGGCCAAGAGCAAGCTGACGGCACC |
ERN1-EIF3C | chr17 | 62144031 | chr16 | 28734485 | 6 | 15 | EAKSKLTAP | AGAGGCCAAGAGCAAGCTGACGGCACC |
ERN1-EIF3C | chr17 | 62144031 | chr16 | 28734485 | 8 | 17 | KSKLTAPTT | CAAGAGCAAGCTGACGGCACCCACCAC |
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Fusion gene | Hchr | Hbp | Tchr | Tbp | Start in +/-13AA | End in +/-13AA | FusionNeoAntigen peptide | FusionNEoAntigen RNA sequence |
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Information of the samples that have these potential fusion neoantigens of ERN1-EIF3C |
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Cancer type | Fusion gene | Hchr | Hbp | Henst | Tchr | Tbp | Tenst | Sample |
BRCA | ERN1-EIF3C | chr17 | 62144031 | ENST00000433197 | chr16 | 28734485 | ENST00000331666 | TCGA-AO-A0J7-01A |
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Potential target of CAR-T therapy development for ERN1-EIF3C |
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![]() * Minus value of BPloci means that the break point is located before the CDS. |
- In-frame and retained 'Transmembrane'. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
![]() * 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. |
Hgene | Hchr | Hbp | Henst | Tgene | Tchr | Tbp | Tenst | DeepLoc result |
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Related Drugs to ERN1-EIF3C |
![]() (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Drug | Source | PMID |
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Related Diseases to ERN1-EIF3C |
![]() (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Disease | Source | PMID |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |