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Fusion Protein:CYP2E1-GLUL |
Fusion Protein Summary |
 Fusion gene summary |
| Fusion partner gene information | Fusion gene name: CYP2E1-GLUL | FusionPDB ID: 21058 | FusionGDB2.0 ID: 21058 | Hgene | Tgene | Gene symbol | CYP2E1 | GLUL | Gene ID | 1571 | 2752 |
| Gene name | cytochrome P450 family 2 subfamily E member 1 | glutamate-ammonia ligase | |
| Synonyms | CPE1|CYP2E|P450-J|P450C2E | GLNS|GS|PIG43|PIG59 | |
| Cytomap | 10q26.3 | 1q25.3 | |
| Type of gene | protein-coding | protein-coding | |
| Description | cytochrome P450 2E14-nitrophenol 2-hydroxylaseCYPIIE1cytochrome P450, family 2, subfamily E, polypeptide 1cytochrome P450, subfamily IIE (ethanol-inducible), polypeptide 1cytochrome P450-Jflavoprotein-linked monooxygenasemicrosomal monooxygenasexe | glutamine synthetasecell proliferation-inducing protein 59glutamate decarboxylaseglutamine synthasepalmitoyltransferase GLULproliferation-inducing protein 43 | |
| Modification date | 20200315 | 20200313 | |
| UniProtAcc | P05181 | P15104 | |
| Ensembl transtripts involved in fusion gene | ENST ids | ENST00000252945, ENST00000463117, ENST00000480558, | ENST00000339526, ENST00000491322, ENST00000311223, ENST00000331872, ENST00000417584, |
| Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0) | * DoF score | 8 X 5 X 3=120 | 18 X 16 X 6=1728 |
| # samples | 8 | 20 | |
| ** MAII score | log2(8/120*10)=-0.584962500721156 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(20/1728*10)=-3.11103131238874 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
| Context (manual curation of fusion genes in FusionPDB) | PubMed: CYP2E1 [Title/Abstract] AND GLUL [Title/Abstract] AND fusion [Title/Abstract] | ||
| Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0) | CYP2E1(135345788)-GLUL(182354691), # samples:1 | ||
| Anticipated loss of major functional domain due to fusion event. | CYP2E1-GLUL 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. CYP2E1-GLUL 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. CYP2E1-GLUL 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. CYP2E1-GLUL 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) |
| 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 |
| Hgene | CYP2E1 | GO:0002933 | lipid hydroxylation | 10553002 |
| Hgene | CYP2E1 | GO:0016098 | monoterpenoid metabolic process | 16401082 |
| Hgene | CYP2E1 | GO:0017144 | drug metabolic process | 19219744 |
| Hgene | CYP2E1 | GO:0018960 | 4-nitrophenol metabolic process | 9348445 |
| Hgene | CYP2E1 | GO:0046483 | heterocycle metabolic process | 19651758 |
| Hgene | CYP2E1 | GO:0055114 | oxidation-reduction process | 16401082|19219744 |
| Tgene | GLUL | GO:0008283 | cell proliferation | 18662667 |
| Tgene | GLUL | GO:0010594 | regulation of endothelial cell migration | 30158707 |
| Tgene | GLUL | GO:0018345 | protein palmitoylation | 30158707 |
| Tgene | GLUL | GO:1903670 | regulation of sprouting angiogenesis | 30158707 |
| Fusion gene breakpoints across CYP2E1 (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 GLUL (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 | LIHC | TCGA-UB-A7MC-01A | CYP2E1 | chr10 | 135345788 | + | GLUL | chr1 | 182354691 | - |
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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) |
| ENST00000463117 | CYP2E1 | chr10 | 135345788 | + | ENST00000331872 | GLUL | chr1 | 182354691 | - | 4140 | 920 | 200 | 1438 | 412 |
| ENST00000463117 | CYP2E1 | chr10 | 135345788 | + | ENST00000417584 | GLUL | chr1 | 182354691 | - | 4139 | 920 | 200 | 1438 | 412 |
| ENST00000463117 | CYP2E1 | chr10 | 135345788 | + | ENST00000311223 | GLUL | chr1 | 182354691 | - | 4139 | 920 | 200 | 1438 | 412 |
| ENST00000252945 | CYP2E1 | chr10 | 135345788 | + | ENST00000331872 | GLUL | chr1 | 182354691 | - | 3901 | 681 | 33 | 1199 | 388 |
| ENST00000252945 | CYP2E1 | chr10 | 135345788 | + | ENST00000417584 | GLUL | chr1 | 182354691 | - | 3900 | 681 | 33 | 1199 | 388 |
| ENST00000252945 | CYP2E1 | chr10 | 135345788 | + | ENST00000311223 | GLUL | chr1 | 182354691 | - | 3900 | 681 | 33 | 1199 | 388 |
| 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 |
| ENST00000463117 | ENST00000331872 | CYP2E1 | chr10 | 135345788 | + | GLUL | chr1 | 182354691 | - | 0.000272675 | 0.9997273 |
| ENST00000463117 | ENST00000417584 | CYP2E1 | chr10 | 135345788 | + | GLUL | chr1 | 182354691 | - | 0.000271983 | 0.999728 |
| ENST00000463117 | ENST00000311223 | CYP2E1 | chr10 | 135345788 | + | GLUL | chr1 | 182354691 | - | 0.000271983 | 0.999728 |
| ENST00000252945 | ENST00000331872 | CYP2E1 | chr10 | 135345788 | + | GLUL | chr1 | 182354691 | - | 0.000255418 | 0.9997446 |
| ENST00000252945 | ENST00000417584 | CYP2E1 | chr10 | 135345788 | + | GLUL | chr1 | 182354691 | - | 0.000255014 | 0.99974495 |
| ENST00000252945 | ENST00000311223 | CYP2E1 | chr10 | 135345788 | + | GLUL | chr1 | 182354691 | - | 0.000255014 | 0.99974495 |
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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 >21058_21058_1_CYP2E1-GLUL_CYP2E1_chr10_135345788_ENST00000252945_GLUL_chr1_182354691_ENST00000311223_length(amino acids)=388AA_BP=198 MSALGVTVALLVWAAFLLLVSMWRQVHSSWNLPPGPFPLPIIGNLFQLELKNIPKSFTRLAQRFGPVFTLYVGSQRMVVMHGYKAVKEAL LDYKDEFSGRGDLPAFHAHRDRGIIFNNGPTWKDIRRFSLTTLRNYGMGKQGNESRIQREAHFLLEALRKTQGQPFDPTFLIGCAPCNVI ADILFRKHFDYNDEKFLRLMYLFNENFHLLSTPWLQWEFQIGPCEGISMGDHLWVARFILHRVCEDFGVIATFDPKPIPGNWNGAGCHTN FSTKAMREENGLKYIEEAIEKLSKRHQYHIRAYDPKGGLDNARRLTGFHETSNINDFSAGVANRSASIRIPRTVGQEKKGYFEDRRPSAN -------------------------------------------------------------- >21058_21058_2_CYP2E1-GLUL_CYP2E1_chr10_135345788_ENST00000252945_GLUL_chr1_182354691_ENST00000331872_length(amino acids)=388AA_BP=198 MSALGVTVALLVWAAFLLLVSMWRQVHSSWNLPPGPFPLPIIGNLFQLELKNIPKSFTRLAQRFGPVFTLYVGSQRMVVMHGYKAVKEAL LDYKDEFSGRGDLPAFHAHRDRGIIFNNGPTWKDIRRFSLTTLRNYGMGKQGNESRIQREAHFLLEALRKTQGQPFDPTFLIGCAPCNVI ADILFRKHFDYNDEKFLRLMYLFNENFHLLSTPWLQWEFQIGPCEGISMGDHLWVARFILHRVCEDFGVIATFDPKPIPGNWNGAGCHTN FSTKAMREENGLKYIEEAIEKLSKRHQYHIRAYDPKGGLDNARRLTGFHETSNINDFSAGVANRSASIRIPRTVGQEKKGYFEDRRPSAN -------------------------------------------------------------- >21058_21058_3_CYP2E1-GLUL_CYP2E1_chr10_135345788_ENST00000252945_GLUL_chr1_182354691_ENST00000417584_length(amino acids)=388AA_BP=198 MSALGVTVALLVWAAFLLLVSMWRQVHSSWNLPPGPFPLPIIGNLFQLELKNIPKSFTRLAQRFGPVFTLYVGSQRMVVMHGYKAVKEAL LDYKDEFSGRGDLPAFHAHRDRGIIFNNGPTWKDIRRFSLTTLRNYGMGKQGNESRIQREAHFLLEALRKTQGQPFDPTFLIGCAPCNVI ADILFRKHFDYNDEKFLRLMYLFNENFHLLSTPWLQWEFQIGPCEGISMGDHLWVARFILHRVCEDFGVIATFDPKPIPGNWNGAGCHTN FSTKAMREENGLKYIEEAIEKLSKRHQYHIRAYDPKGGLDNARRLTGFHETSNINDFSAGVANRSASIRIPRTVGQEKKGYFEDRRPSAN -------------------------------------------------------------- >21058_21058_4_CYP2E1-GLUL_CYP2E1_chr10_135345788_ENST00000463117_GLUL_chr1_182354691_ENST00000311223_length(amino acids)=412AA_BP=222 MAPFMWQVVIQDCLPGWQQGPSGTMSALGVTVALLVWAAFLLLVSMWRQVHSSWNLPPGPFPLPIIGNLFQLELKNIPKSFTRLAQRFGP VFTLYVGSQRMVVMHGYKAVKEALLDYKDEFSGRGDLPAFHAHRDRGIIFNNGPTWKDIRRFSLTTLRNYGMGKQGNESRIQREAHFLLE ALRKTQGQPFDPTFLIGCAPCNVIADILFRKHFDYNDEKFLRLMYLFNENFHLLSTPWLQWEFQIGPCEGISMGDHLWVARFILHRVCED FGVIATFDPKPIPGNWNGAGCHTNFSTKAMREENGLKYIEEAIEKLSKRHQYHIRAYDPKGGLDNARRLTGFHETSNINDFSAGVANRSA -------------------------------------------------------------- >21058_21058_5_CYP2E1-GLUL_CYP2E1_chr10_135345788_ENST00000463117_GLUL_chr1_182354691_ENST00000331872_length(amino acids)=412AA_BP=222 MAPFMWQVVIQDCLPGWQQGPSGTMSALGVTVALLVWAAFLLLVSMWRQVHSSWNLPPGPFPLPIIGNLFQLELKNIPKSFTRLAQRFGP VFTLYVGSQRMVVMHGYKAVKEALLDYKDEFSGRGDLPAFHAHRDRGIIFNNGPTWKDIRRFSLTTLRNYGMGKQGNESRIQREAHFLLE ALRKTQGQPFDPTFLIGCAPCNVIADILFRKHFDYNDEKFLRLMYLFNENFHLLSTPWLQWEFQIGPCEGISMGDHLWVARFILHRVCED FGVIATFDPKPIPGNWNGAGCHTNFSTKAMREENGLKYIEEAIEKLSKRHQYHIRAYDPKGGLDNARRLTGFHETSNINDFSAGVANRSA -------------------------------------------------------------- >21058_21058_6_CYP2E1-GLUL_CYP2E1_chr10_135345788_ENST00000463117_GLUL_chr1_182354691_ENST00000417584_length(amino acids)=412AA_BP=222 MAPFMWQVVIQDCLPGWQQGPSGTMSALGVTVALLVWAAFLLLVSMWRQVHSSWNLPPGPFPLPIIGNLFQLELKNIPKSFTRLAQRFGP VFTLYVGSQRMVVMHGYKAVKEALLDYKDEFSGRGDLPAFHAHRDRGIIFNNGPTWKDIRRFSLTTLRNYGMGKQGNESRIQREAHFLLE ALRKTQGQPFDPTFLIGCAPCNVIADILFRKHFDYNDEKFLRLMYLFNENFHLLSTPWLQWEFQIGPCEGISMGDHLWVARFILHRVCED FGVIATFDPKPIPGNWNGAGCHTNFSTKAMREENGLKYIEEAIEKLSKRHQYHIRAYDPKGGLDNARRLTGFHETSNINDFSAGVANRSA -------------------------------------------------------------- |
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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/chr10:135345788/chr1:182354691) - 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 |
| CYP2E1 | GLUL |
| FUNCTION: A cytochrome P450 monooxygenase involved in the metabolism of fatty acids (PubMed:10553002, PubMed:18577768). Mechanistically, uses molecular oxygen inserting one oxygen atom into a substrate, and reducing the second into a water molecule, with two electrons provided by NADPH via cytochrome P450 reductase (NADPH--hemoprotein reductase) (PubMed:10553002, PubMed:18577768). Catalyzes the hydroxylation of carbon-hydrogen bonds. Hydroxylates fatty acids specifically at the omega-1 position displaying the highest catalytic activity for saturated fatty acids (PubMed:10553002, PubMed:18577768). May be involved in the oxidative metabolism of xenobiotics (Probable). {ECO:0000269|PubMed:10553002, ECO:0000269|PubMed:18577768, ECO:0000305|PubMed:9348445}. | FUNCTION: Glutamine synthetase that catalyzes the ATP-dependent conversion of glutamate and ammonia to glutamine (PubMed:30158707, PubMed:16267323). Its role depends on tissue localization: in the brain, it regulates the levels of toxic ammonia and converts neurotoxic glutamate to harmless glutamine, whereas in the liver, it is one of the enzymes responsible for the removal of ammonia (By similarity). Essential for proliferation of fetal skin fibroblasts (PubMed:18662667). Independently of its glutamine synthetase activity, required for endothelial cell migration during vascular development: acts by regulating membrane localization and activation of the GTPase RHOJ, possibly by promoting RHOJ palmitoylation (PubMed:30158707). May act as a palmitoyltransferase for RHOJ: able to autopalmitoylate and then transfer the palmitoyl group to RHOJ (PubMed:30158707). Plays a role in ribosomal 40S subunit biogenesis (PubMed:26711351). {ECO:0000250|UniProtKB:P15105, ECO:0000269|PubMed:16267323, ECO:0000269|PubMed:18662667, ECO:0000269|PubMed:26711351, ECO:0000269|PubMed:30158707}. |
| 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 | GLUL | chr10:135345788 | chr1:182354691 | ENST00000311223 | 5 | 8 | 203_208 | 201.0 | 374.0 | Nucleotide binding | ATP | |
| Tgene | GLUL | chr10:135345788 | chr1:182354691 | ENST00000311223 | 5 | 8 | 255_257 | 201.0 | 374.0 | Nucleotide binding | ATP | |
| Tgene | GLUL | chr10:135345788 | chr1:182354691 | ENST00000311223 | 5 | 8 | 336_338 | 201.0 | 374.0 | Nucleotide binding | ADP | |
| Tgene | GLUL | chr10:135345788 | chr1:182354691 | ENST00000331872 | 4 | 7 | 203_208 | 201.0 | 374.0 | Nucleotide binding | ATP | |
| Tgene | GLUL | chr10:135345788 | chr1:182354691 | ENST00000331872 | 4 | 7 | 255_257 | 201.0 | 374.0 | Nucleotide binding | ATP | |
| Tgene | GLUL | chr10:135345788 | chr1:182354691 | ENST00000331872 | 4 | 7 | 336_338 | 201.0 | 374.0 | Nucleotide binding | ADP | |
| Tgene | GLUL | chr10:135345788 | chr1:182354691 | ENST00000339526 | 4 | 7 | 203_208 | 201.0 | 374.0 | Nucleotide binding | ATP | |
| Tgene | GLUL | chr10:135345788 | chr1:182354691 | ENST00000339526 | 4 | 7 | 255_257 | 201.0 | 374.0 | Nucleotide binding | ATP | |
| Tgene | GLUL | chr10:135345788 | chr1:182354691 | ENST00000339526 | 4 | 7 | 336_338 | 201.0 | 374.0 | Nucleotide binding | ADP | |
| Tgene | GLUL | chr10:135345788 | chr1:182354691 | ENST00000417584 | 4 | 7 | 203_208 | 201.0 | 374.0 | Nucleotide binding | ATP | |
| Tgene | GLUL | chr10:135345788 | chr1:182354691 | ENST00000417584 | 4 | 7 | 255_257 | 201.0 | 374.0 | Nucleotide binding | ATP | |
| Tgene | GLUL | chr10:135345788 | chr1:182354691 | ENST00000417584 | 4 | 7 | 336_338 | 201.0 | 374.0 | Nucleotide binding | ADP | |
| Tgene | GLUL | chr10:135345788 | chr1:182354691 | ENST00000311223 | 5 | 8 | 246_247 | 201.0 | 374.0 | Region | L-glutamate binding | |
| Tgene | GLUL | chr10:135345788 | chr1:182354691 | ENST00000331872 | 4 | 7 | 246_247 | 201.0 | 374.0 | Region | L-glutamate binding | |
| Tgene | GLUL | chr10:135345788 | chr1:182354691 | ENST00000339526 | 4 | 7 | 246_247 | 201.0 | 374.0 | Region | L-glutamate binding | |
| Tgene | GLUL | chr10:135345788 | chr1:182354691 | ENST00000417584 | 4 | 7 | 246_247 | 201.0 | 374.0 | Region | L-glutamate binding |
| - 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 |
| Hgene | CYP2E1 | chr10:135345788 | chr1:182354691 | ENST00000252945 | + | 4 | 9 | 298_303 | 216.0 | 494.0 | Region | Substrate binding |
| Hgene | CYP2E1 | chr10:135345788 | chr1:182354691 | ENST00000463117 | + | 6 | 11 | 298_303 | 216.0 | 494.0 | Region | Substrate binding |
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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 |
| CYP2E1 | |
| GLUL |
| - 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 CYP2E1-GLUL |
| 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 CYP2E1-GLUL |
| 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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