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Fusion Protein:IFT81-INSR |
Fusion Gene and Fusion Protein Summary |
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Fusion partner gene information | Fusion gene name: IFT81-INSR | FusionPDB ID: 38451 | FusionGDB2.0 ID: 38451 | Hgene | Tgene | Gene symbol | IFT81 | INSR | Gene ID | 28981 | 3643 |
Gene name | intraflagellar transport 81 | insulin receptor | |
Synonyms | CDV-1|CDV-1R|CDV1|CDV1R|DV1|SRTD19 | CD220|HHF5 | |
Cytomap | 12q24.11 | 19p13.2 | |
Type of gene | protein-coding | protein-coding | |
Description | intraflagellar transport protein 81 homologcarnitine deficiency-associated gene expressed in ventricle 1carnitine deficiency-associated protein expressed in ventricle 1 | insulin receptorIR | |
Modification date | 20200313 | 20200313 | |
UniProtAcc | Q8WYA0 Main function of 5'-partner protein: FUNCTION: Component of the intraflagellar transport (IFT) complex B: together with IFT74, forms a tubulin-binding module that specifically mediates transport of tubulin within the cilium. Binds tubulin via its CH (calponin-homology)-like region (PubMed:23990561). Required for ciliogenesis (PubMed:27666822, PubMed:23990561). Required for proper regulation of SHH signaling (PubMed:27666822). {ECO:0000269|PubMed:23990561, ECO:0000269|PubMed:27666822}. | P06213 Main function of 5'-partner protein: FUNCTION: Receptor tyrosine kinase which mediates the pleiotropic actions of insulin. Binding of insulin leads to phosphorylation of several intracellular substrates, including, insulin receptor substrates (IRS1, 2, 3, 4), SHC, GAB1, CBL and other signaling intermediates. Each of these phosphorylated proteins serve as docking proteins for other signaling proteins that contain Src-homology-2 domains (SH2 domain) that specifically recognize different phosphotyrosine residues, including the p85 regulatory subunit of PI3K and SHP2. Phosphorylation of IRSs proteins lead to the activation of two main signaling pathways: the PI3K-AKT/PKB pathway, which is responsible for most of the metabolic actions of insulin, and the Ras-MAPK pathway, which regulates expression of some genes and cooperates with the PI3K pathway to control cell growth and differentiation. Binding of the SH2 domains of PI3K to phosphotyrosines on IRS1 leads to the activation of PI3K and the generation of phosphatidylinositol-(3, 4, 5)-triphosphate (PIP3), a lipid second messenger, which activates several PIP3-dependent serine/threonine kinases, such as PDPK1 and subsequently AKT/PKB. The net effect of this pathway is to produce a translocation of the glucose transporter SLC2A4/GLUT4 from cytoplasmic vesicles to the cell membrane to facilitate glucose transport. Moreover, upon insulin stimulation, activated AKT/PKB is responsible for: anti-apoptotic effect of insulin by inducing phosphorylation of BAD; regulates the expression of gluconeogenic and lipogenic enzymes by controlling the activity of the winged helix or forkhead (FOX) class of transcription factors. Another pathway regulated by PI3K-AKT/PKB activation is mTORC1 signaling pathway which regulates cell growth and metabolism and integrates signals from insulin. AKT mediates insulin-stimulated protein synthesis by phosphorylating TSC2 thereby activating mTORC1 pathway. The Ras/RAF/MAP2K/MAPK pathway is mainly involved in mediating cell growth, survival and cellular differentiation of insulin. Phosphorylated IRS1 recruits GRB2/SOS complex, which triggers the activation of the Ras/RAF/MAP2K/MAPK pathway. In addition to binding insulin, the insulin receptor can bind insulin-like growth factors (IGFI and IGFII). Isoform Short has a higher affinity for IGFII binding. When present in a hybrid receptor with IGF1R, binds IGF1. PubMed:12138094 shows that hybrid receptors composed of IGF1R and INSR isoform Long are activated with a high affinity by IGF1, with low affinity by IGF2 and not significantly activated by insulin, and that hybrid receptors composed of IGF1R and INSR isoform Short are activated by IGF1, IGF2 and insulin. In contrast, PubMed:16831875 shows that hybrid receptors composed of IGF1R and INSR isoform Long and hybrid receptors composed of IGF1R and INSR isoform Short have similar binding characteristics, both bind IGF1 and have a low affinity for insulin. In adipocytes, inhibits lipolysis (By similarity). {ECO:0000250|UniProtKB:P15208, ECO:0000269|PubMed:12138094, ECO:0000269|PubMed:16314505, ECO:0000269|PubMed:16831875, ECO:0000269|PubMed:8257688, ECO:0000269|PubMed:8276809, ECO:0000269|PubMed:8452530, ECO:0000269|PubMed:9428692}. | |
Ensembl transtripts involved in fusion gene | ENST ids | ENST00000549009, ENST00000242591, ENST00000361948, ENST00000552912, | ENST00000302850, ENST00000341500, |
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0) | * DoF score | 6 X 6 X 5=180 | 20 X 13 X 8=2080 |
# samples | 6 | 20 | |
** MAII score | log2(6/180*10)=-1.58496250072116 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(20/2080*10)=-3.37851162325373 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Fusion gene context | PubMed: IFT81 [Title/Abstract] AND INSR [Title/Abstract] AND fusion [Title/Abstract] | ||
Fusion neoantigen context | PubMed: IFT81 [Title/Abstract] AND INSR [Title/Abstract] AND neoantigen [Title/Abstract] | ||
Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0) | IFT81(110574665)-INSR(7184648), # samples:2 | ||
Anticipated loss of major functional domain due to fusion event. | IFT81-INSR 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. IFT81-INSR 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. IFT81-INSR 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. IFT81-INSR 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 |
Tgene | INSR | GO:0001934 | positive regulation of protein phosphorylation | 7556070 |
Tgene | INSR | GO:0002092 | positive regulation of receptor internalization | 25401701 |
Tgene | INSR | GO:0007186 | G protein-coupled receptor signaling pathway | 9092559 |
Tgene | INSR | GO:0008284 | positive regulation of cell proliferation | 17925406 |
Tgene | INSR | GO:0008286 | insulin receptor signaling pathway | 6849137|8440175|20455999 |
Tgene | INSR | GO:0018108 | peptidyl-tyrosine phosphorylation | 8496180 |
Tgene | INSR | GO:0032148 | activation of protein kinase B activity | 7556070 |
Tgene | INSR | GO:0032869 | cellular response to insulin stimulus | 8440175 |
Tgene | INSR | GO:0043410 | positive regulation of MAPK cascade | 20455999 |
Tgene | INSR | GO:0045725 | positive regulation of glycogen biosynthetic process | 17925406 |
Tgene | INSR | GO:0046326 | positive regulation of glucose import | 3518947 |
Tgene | INSR | GO:0046777 | protein autophosphorylation | 6849137|8496180 |
Tgene | INSR | GO:0060267 | positive regulation of respiratory burst | 9092559 |
![]() Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr12:110574665/chr19:7184648) - 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) |
ENST00000552912 | IFT81 | chr12 | 110574665 | + | ENST00000341500 | INSR | chr19 | 7184648 | - | 9173 | 911 | 130 | 4371 | 1413 |
ENST00000552912 | IFT81 | chr12 | 110574665 | + | ENST00000302850 | INSR | chr19 | 7184648 | - | 4837 | 911 | 130 | 4407 | 1425 |
ENST00000242591 | IFT81 | chr12 | 110574665 | + | ENST00000341500 | INSR | chr19 | 7184648 | - | 9549 | 1287 | 506 | 4747 | 1413 |
ENST00000242591 | IFT81 | chr12 | 110574665 | + | ENST00000302850 | INSR | chr19 | 7184648 | - | 5213 | 1287 | 506 | 4783 | 1425 |
ENST00000361948 | IFT81 | chr12 | 110574665 | + | ENST00000341500 | INSR | chr19 | 7184648 | - | 9591 | 1329 | 548 | 4789 | 1413 |
ENST00000361948 | IFT81 | chr12 | 110574665 | + | ENST00000302850 | INSR | chr19 | 7184648 | - | 5255 | 1329 | 548 | 4825 | 1425 |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
ENST00000552912 | ENST00000341500 | IFT81 | chr12 | 110574665 | + | INSR | chr19 | 7184648 | - | 0.00018766 | 0.9998123 |
ENST00000552912 | ENST00000302850 | IFT81 | chr12 | 110574665 | + | INSR | chr19 | 7184648 | - | 0.001494486 | 0.9985056 |
ENST00000242591 | ENST00000341500 | IFT81 | chr12 | 110574665 | + | INSR | chr19 | 7184648 | - | 0.000275455 | 0.99972457 |
ENST00000242591 | ENST00000302850 | IFT81 | chr12 | 110574665 | + | INSR | chr19 | 7184648 | - | 0.001947399 | 0.9980526 |
ENST00000361948 | ENST00000341500 | IFT81 | chr12 | 110574665 | + | INSR | chr19 | 7184648 | - | 0.000296929 | 0.999703 |
ENST00000361948 | ENST00000302850 | IFT81 | chr12 | 110574665 | + | INSR | chr19 | 7184648 | - | 0.002113861 | 0.9978861 |
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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 IFT81-INSR |
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Hgene | Hchr | Hbp | Tgene | Tchr | Tbp | Length(fusion protein) | BP in fusion protein | Peptide |
IFT81 | chr12 | 110574665 | INSR | chr19 | 7184648 | 1287 | 261 | SMRQAAADAKPEICPTICKSHGCTAE |
IFT81 | chr12 | 110574665 | INSR | chr19 | 7184648 | 1329 | 261 | SMRQAAADAKPEICPTICKSHGCTAE |
IFT81 | chr12 | 110574665 | INSR | chr19 | 7184648 | 911 | 261 | SMRQAAADAKPEICPTICKSHGCTAE |
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Potential FusionNeoAntigen Information of IFT81-INSR in HLA I |
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IFT81-INSR_110574665_7184648.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) |
IFT81-INSR | chr12 | 110574665 | chr19 | 7184648 | 1287 | HLA-B52:01 | AKPEICPTI | 0.0822 | 0.8637 | 8 | 17 |
IFT81-INSR | chr12 | 110574665 | chr19 | 7184648 | 1287 | HLA-C08:15 | AADAKPEIC | 0.998 | 0.9436 | 5 | 14 |
IFT81-INSR | chr12 | 110574665 | chr19 | 7184648 | 1287 | HLA-B51:07 | DAKPEICPTI | 0.9862 | 0.7639 | 7 | 17 |
IFT81-INSR | chr12 | 110574665 | chr19 | 7184648 | 1287 | HLA-C08:02 | AADAKPEIC | 0.998 | 0.9436 | 5 | 14 |
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Potential FusionNeoAntigen Information of IFT81-INSR 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 IFT81-INSR |
![]() * 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 |
96 | ADAKPEICPTICKS | IFT81 | INSR | chr12 | 110574665 | chr19 | 7184648 | 1287 |
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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of IFT81-INSR |
![]() * 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 | 96 | ADAKPEICPTICKS | -7.23149 | -7.46669 |
HLA-B14:02 | 3BVN | 96 | ADAKPEICPTICKS | -5.32844 | -5.99034 |
HLA-B52:01 | 3W39 | 96 | ADAKPEICPTICKS | -6.06486 | -6.30006 |
HLA-B52:01 | 3W39 | 96 | ADAKPEICPTICKS | -3.50061 | -4.16251 |
HLA-A11:01 | 4UQ2 | 96 | ADAKPEICPTICKS | -7.21586 | -7.87776 |
HLA-A24:02 | 5HGA | 96 | ADAKPEICPTICKS | -7.89571 | -8.13091 |
HLA-A24:02 | 5HGA | 96 | ADAKPEICPTICKS | -4.02532 | -4.68722 |
HLA-B27:05 | 6PYJ | 96 | ADAKPEICPTICKS | -6.15548 | -6.81738 |
HLA-B27:05 | 6PYJ | 96 | ADAKPEICPTICKS | -0.382212 | -0.617412 |
HLA-B44:05 | 3DX8 | 96 | ADAKPEICPTICKS | -5.889 | -6.1242 |
HLA-B44:05 | 3DX8 | 96 | ADAKPEICPTICKS | -4.51633 | -5.17823 |
HLA-A02:01 | 6TDR | 96 | ADAKPEICPTICKS | -3.58478 | -4.24668 |
HLA-A02:01 | 6TDR | 96 | ADAKPEICPTICKS | -2.484 | -2.7192 |
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Vaccine Design for the FusionNeoAntigens of IFT81-INSR |
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Fusion gene | Hchr | Hbp | Tchr | Tbp | Start in +/-13AA | End in +/-13AA | FusionNeoAntigen peptide sequence | FusionNeoAntigen RNA sequence |
IFT81-INSR | chr12 | 110574665 | chr19 | 7184648 | 5 | 14 | AADAKPEIC | CTGCAGCAGATGCAAAGCCTGAAATTT |
IFT81-INSR | chr12 | 110574665 | chr19 | 7184648 | 7 | 17 | DAKPEICPTI | CAGATGCAAAGCCTGAAATTTGCCCGACCA |
IFT81-INSR | chr12 | 110574665 | chr19 | 7184648 | 8 | 17 | AKPEICPTI | ATGCAAAGCCTGAAATTTGCCCGACCA |
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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 IFT81-INSR |
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Cancer type | Fusion gene | Hchr | Hbp | Henst | Tchr | Tbp | Tenst | Sample |
SARC | IFT81-INSR | chr12 | 110574665 | ENST00000242591 | chr19 | 7184648 | ENST00000302850 | TCGA-3B-A9HS-01A |
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Potential target of CAR-T therapy development for IFT81-INSR |
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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 |
Tgene | INSR | chr12:110574665 | chr19:7184648 | ENST00000302850 | 1 | 22 | 957_979 | 0 | 1383.0 | Transmembrane | Helical | |
Tgene | INSR | chr12:110574665 | chr19:7184648 | ENST00000341500 | 1 | 21 | 957_979 | 0 | 1371.0 | Transmembrane | Helical |
![]() * 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 IFT81-INSR |
![]() (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Drug | Source | PMID |
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Related Diseases to IFT81-INSR |
![]() (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Disease | Source | PMID |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |