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Fusion Protein:ATP6V1E1-BID |
Fusion Protein Summary |
 Fusion gene summary |
| Fusion partner gene information | Fusion gene name: ATP6V1E1-BID | FusionPDB ID: 8175 | FusionGDB2.0 ID: 8175 | Hgene | Tgene | Gene symbol | ATP6V1E1 | BID | Gene ID | 529 | 637 |
| Gene name | ATPase H+ transporting V1 subunit E1 | BH3 interacting domain death agonist | |
| Synonyms | ARCL2C|ATP6E|ATP6E2|ATP6V1E|P31|Vma4 | FP497 | |
| Cytomap | 22q11.21 | 22q11.21 | |
| Type of gene | protein-coding | protein-coding | |
| Description | V-type proton ATPase subunit E 1ATPase, H+ transporting, lysosomal 31kDa, V1 subunit E1H(+)-transporting two-sector ATPase, 31kDa subunitH+-transporting ATP synthase chain E, vacuolarV-ATPase 31 kDa subunitV-ATPase subunit E 1V-ATPase, subunit Evac | BH3-interacting domain death agonistBH3 interacting domain death agonist Si6 isoformBID isoform ES(1b)BID isoform L(2)BID isoform Si6Human BID coding sequenceapoptic death agonistdesmocollin type 4p22 BID | |
| Modification date | 20200313 | 20200313 | |
| UniProtAcc | P36543 | P55957 | |
| Ensembl transtripts involved in fusion gene | ENST ids | ENST00000253413, ENST00000399796, ENST00000399798, ENST00000478963, | ENST00000399767, ENST00000399774, ENST00000473439, ENST00000342111, ENST00000399765, ENST00000551952, ENST00000317361, |
| Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0) | * DoF score | 7 X 7 X 2=98 | 8 X 6 X 7=336 |
| # samples | 7 | 9 | |
| ** MAII score | log2(7/98*10)=-0.485426827170242 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(9/336*10)=-1.90046432644909 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
| Context (manual curation of fusion genes in FusionPDB) | PubMed: ATP6V1E1 [Title/Abstract] AND BID [Title/Abstract] AND fusion [Title/Abstract] | ||
| Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0) | ATP6V1E1(18095578)-BID(18226779), # samples:1 BID(18220783)-ATP6V1E1(18096086), # samples:1 BID(18220782)-ATP6V1E1(18096086), # samples:1 | ||
| Anticipated loss of major functional domain due to fusion event. | ATP6V1E1-BID 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. ATP6V1E1-BID 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. BID-ATP6V1E1 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. BID-ATP6V1E1 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. BID-ATP6V1E1 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF. BID-ATP6V1E1 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF. BID-ATP6V1E1 seems lost the major protein functional domain in Tgene 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) |
| Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez |
| Partner | Gene | GO ID | GO term | PubMed ID |
| Tgene | BID | GO:0001836 | release of cytochrome c from mitochondria | 17052454 |
| Tgene | BID | GO:0031334 | positive regulation of protein complex assembly | 19074440|21041309 |
| Tgene | BID | GO:0090150 | establishment of protein localization to membrane | 21041309 |
| Fusion gene breakpoints across ATP6V1E1 (5'-gene) * 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 gene breakpoints across BID (3'-gene) * 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 Gene Sample Information |
| Fusion gene information from FusionGDB2.0. |
| Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0) * All genome coordinats were lifted-over on hg19. * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
| Source | Disease | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
| ChimerDB4 | LUAD | TCGA-05-4389-01A | ATP6V1E1 | chr22 | 18095578 | - | BID | chr22 | 18226779 | - |
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Fusion ORF Analysis |
| Fusion information from ORFfinder translation from full-length transcript sequence from FusionPDB. |
| 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) |
| ENST00000253413 | ATP6V1E1 | chr22 | 18095578 | - | ENST00000317361 | BID | chr22 | 18226779 | - | 2475 | 459 | 108 | 1034 | 308 |
| ENST00000399796 | ATP6V1E1 | chr22 | 18095578 | - | ENST00000317361 | BID | chr22 | 18226779 | - | 2404 | 388 | 37 | 963 | 308 |
| ENST00000399798 | ATP6V1E1 | chr22 | 18095578 | - | ENST00000317361 | BID | chr22 | 18226779 | - | 2340 | 324 | 39 | 899 | 286 |
| DeepORF 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. |
| Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
| ENST00000253413 | ENST00000317361 | ATP6V1E1 | chr22 | 18095578 | - | BID | chr22 | 18226779 | - | 0.001855796 | 0.99814427 |
| ENST00000399796 | ENST00000317361 | ATP6V1E1 | chr22 | 18095578 | - | BID | chr22 | 18226779 | - | 0.001845534 | 0.99815446 |
| ENST00000399798 | ENST00000317361 | ATP6V1E1 | chr22 | 18095578 | - | BID | chr22 | 18226779 | - | 0.001303333 | 0.99869674 |
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Fusion Amino Acid Sequences |
| For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones. |
| >FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP >8175_8175_1_ATP6V1E1-BID_ATP6V1E1_chr22_18095578_ENST00000253413_BID_chr22_18226779_ENST00000317361_length(amino acids)=308AA_BP=117 MPISLTSPFKPKLEPTVHRPSIALAMALSDADVQKQIKHMMAFIEQEANEKAEEIDAKAEEEFNIEKGRLVQTQRLKIMEYYEKKEKQIE QQKKIQMSNLMNQARLKVLRARDDLITVNNGSSLRDECITNLLVFGFLQSCSDNSFRRELDALGHELPVLAPQWEGYDELQTDGNRSSHS RLGRIEADSESQEDIIRNIARHLAQVGDSMDRSIPPGLVNGLALQLRNTSRSEEDRNRDLATALEQLLQAYPRDMEKEKTMLVLALLLAK -------------------------------------------------------------- >8175_8175_2_ATP6V1E1-BID_ATP6V1E1_chr22_18095578_ENST00000399796_BID_chr22_18226779_ENST00000317361_length(amino acids)=308AA_BP=117 MPISLTSPFKPKLEPTVHRPSIALAMALSDADVQKQIKHMMAFIEQEANEKAEEIDAKAEEEFNIEKGRLVQTQRLKIMEYYEKKEKQIE QQKKIQMSNLMNQARLKVLRARDDLITVNNGSSLRDECITNLLVFGFLQSCSDNSFRRELDALGHELPVLAPQWEGYDELQTDGNRSSHS RLGRIEADSESQEDIIRNIARHLAQVGDSMDRSIPPGLVNGLALQLRNTSRSEEDRNRDLATALEQLLQAYPRDMEKEKTMLVLALLLAK -------------------------------------------------------------- >8175_8175_3_ATP6V1E1-BID_ATP6V1E1_chr22_18095578_ENST00000399798_BID_chr22_18226779_ENST00000317361_length(amino acids)=286AA_BP=95 MPISLTSPFKPKLEPTVHRPSIALAMALSDADVQKQAEEEFNIEKGRLVQTQRLKIMEYYEKKEKQIEQQKKIQMSNLMNQARLKVLRAR DDLITVNNGSSLRDECITNLLVFGFLQSCSDNSFRRELDALGHELPVLAPQWEGYDELQTDGNRSSHSRLGRIEADSESQEDIIRNIARH LAQVGDSMDRSIPPGLVNGLALQLRNTSRSEEDRNRDLATALEQLLQAYPRDMEKEKTMLVLALLLAKKVASHTPSLLRDVFHTTVNFIN -------------------------------------------------------------- |
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Fusion Protein Functional Features |
| Four levels of functional features of fusion genes Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr22:18095578/chr22:18226779) - 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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| Main function of each fusion partner protein. (from UniProt) |
| Hgene | Tgene |
| ATP6V1E1 | BID |
| FUNCTION: Subunit of the peripheral V1 complex of vacuolar ATPase essential for assembly or catalytic function. V-ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells. | FUNCTION: The major proteolytic product p15 BID allows the release of cytochrome c (By similarity). Isoform 1, isoform 2 and isoform 4 induce ICE-like proteases and apoptosis. Isoform 3 does not induce apoptosis. Counters the protective effect of Bcl-2. {ECO:0000250|UniProtKB:P70444, ECO:0000269|PubMed:14583606}. |
| Retention 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, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at * Minus value of BPloci means that the break pointn is located before the CDS. |
| - Retained protein feature among the 13 regional features. |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
| Tgene | BID | chr22:18095578 | chr22:18226779 | ENST00000317361 | 1 | 6 | 86_100 | 50.0 | 242.0 | Motif | BH3 | |
| Tgene | BID | chr22:18095578 | chr22:18226779 | ENST00000342111 | 1 | 7 | 86_100 | 4.0 | 182.33333333333334 | Motif | BH3 | |
| Tgene | BID | chr22:18095578 | chr22:18226779 | ENST00000399765 | 0 | 4 | 86_100 | 0 | 100.0 | Motif | BH3 | |
| Tgene | BID | chr22:18095578 | chr22:18226779 | ENST00000399767 | 0 | 5 | 86_100 | 0 | 100.0 | Motif | BH3 | |
| Tgene | BID | chr22:18095578 | chr22:18226779 | ENST00000399774 | 1 | 6 | 86_100 | 4.0 | 196.0 | Motif | BH3 | |
| Tgene | BID | chr22:18095578 | chr22:18226779 | ENST00000551952 | 1 | 6 | 86_100 | 4.0 | 196.0 | Motif | BH3 |
| - Not-retained protein feature among the 13 regional features. |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
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Fusion Protein-Protein Interaction |
| Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in |
| Protein-protein interactors with each fusion partner protein in wild-type from validated records (BIOGRID-3.4.160) |
| Gene | PPI interactors |
| Protein-protein interactors based on sequence similarity (STRING) |
| Gene | STRING network |
| ATP6V1E1 | |
| BID |
| - Retained interactions in fusion protein (protein functional feature from UniProt). |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
| - Lost interactions due to fusion (protein functional feature from UniProt). |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Related Drugs to ATP6V1E1-BID |
| Drugs used for this fusion-positive patient. (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
| Hgene | Tgene | Drug | Source | PMID |
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Related Diseases to ATP6V1E1-BID |
| Diseases that have this fusion gene. (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
| Hgene | Tgene | Disease | Source | PMID |
| Diseases associated with fusion partners. (DisGeNet 4.0) |
| Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
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