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Fusion Protein:CYP2E1-AMACR |
Fusion Protein Summary |
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Fusion partner gene information | Fusion gene name: CYP2E1-AMACR | FusionPDB ID: 21055 | FusionGDB2.0 ID: 21055 | Hgene | Tgene | Gene symbol | CYP2E1 | AMACR | Gene ID | 1571 | 23600 |
Gene name | cytochrome P450 family 2 subfamily E member 1 | alpha-methylacyl-CoA racemase | |
Synonyms | CPE1|CYP2E|P450-J|P450C2E | AMACRD|CBAS4|P504S|RACE|RM | |
Cytomap | 10q26.3 | 5p13.2 | |
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 | alpha-methylacyl-CoA racemase2-methylacyl-CoA racemase | |
Modification date | 20200315 | 20200313 | |
UniProtAcc | P05181 | Q9UHK6 | |
Ensembl transtripts involved in fusion gene | ENST ids | ENST00000480558, ENST00000252945, ENST00000463117, | ENST00000335606, ENST00000382072, ENST00000382068, ENST00000382085, ENST00000426255, ENST00000441713, ENST00000502637, ENST00000512079, ENST00000514195, |
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0) | * DoF score | 8 X 5 X 3=120 | 28 X 3 X 4=336 |
# samples | 8 | 23 | |
** MAII score | log2(8/120*10)=-0.584962500721156 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(23/336*10)=-0.546827371834385 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 AMACR [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0) | CYP2E1(135342144)-AMACR(34006004), # samples:1 | ||
Anticipated loss of major functional domain due to fusion event. | CYP2E1-AMACR 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-AMACR 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-AMACR 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-AMACR 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 | 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 | AMACR | GO:0008206 | bile acid metabolic process | 10655068 |
![]() * 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 Gene Sample Information |
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![]() * 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-DD-A39W-01A | CYP2E1 | chr10 | 135342144 | + | AMACR | chr5 | 34006004 | - |
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Fusion ORF Analysis |
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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) |
ENST00000463117 | CYP2E1 | chr10 | 135342144 | + | ENST00000335606 | AMACR | chr5 | 34006004 | - | 4426 | 609 | 200 | 1510 | 436 |
ENST00000463117 | CYP2E1 | chr10 | 135342144 | + | ENST00000382072 | AMACR | chr5 | 34006004 | - | 3269 | 609 | 200 | 958 | 252 |
ENST00000252945 | CYP2E1 | chr10 | 135342144 | + | ENST00000335606 | AMACR | chr5 | 34006004 | - | 4187 | 370 | 33 | 1271 | 412 |
ENST00000252945 | CYP2E1 | chr10 | 135342144 | + | ENST00000382072 | AMACR | chr5 | 34006004 | - | 3030 | 370 | 33 | 719 | 228 |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
ENST00000463117 | ENST00000335606 | CYP2E1 | chr10 | 135342144 | + | AMACR | chr5 | 34006004 | - | 0.000288096 | 0.99971193 |
ENST00000463117 | ENST00000382072 | CYP2E1 | chr10 | 135342144 | + | AMACR | chr5 | 34006004 | - | 0.039836638 | 0.9601633 |
ENST00000252945 | ENST00000335606 | CYP2E1 | chr10 | 135342144 | + | AMACR | chr5 | 34006004 | - | 8.25E-05 | 0.9999175 |
ENST00000252945 | ENST00000382072 | CYP2E1 | chr10 | 135342144 | + | AMACR | chr5 | 34006004 | - | 0.004744016 | 0.995256 |
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Fusion Amino Acid Sequences |
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>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP >21055_21055_1_CYP2E1-AMACR_CYP2E1_chr10_135342144_ENST00000252945_AMACR_chr5_34006004_ENST00000335606_length(amino acids)=412AA_BP=112 MSALGVTVALLVWAAFLLLVSMWRQVHSSWNLPPGPFPLPIIGNLFQLELKNIPKSFTRLAQRFGPVFTLYVGSQRMVVMHGYKAVKEAL LDYKDEFSGRGDLPAFHAHRDRGVMEKLQLGPEILQRENPRLIYARLSGFGQSGSFCRLAGHDINYLALSGVLSKIGRSGENPYAPLNLL ADFAGGGLMCALGIIMALFDRTRTGKGQVIDANMVEGTAYLSSFLWKTQKLSLWEAPRGQNMLDGGAPFYTTYRTADGEFMAVGAIEPQF YELLIKGLGLKSDELPNQMSMDDWPEMKKKFADVFAEKTKAEWCQIFDGTDACVTPVLTFEEVVHHDHNKERGSFITSEEQDVSPRPAPL -------------------------------------------------------------- >21055_21055_2_CYP2E1-AMACR_CYP2E1_chr10_135342144_ENST00000252945_AMACR_chr5_34006004_ENST00000382072_length(amino acids)=228AA_BP=112 MSALGVTVALLVWAAFLLLVSMWRQVHSSWNLPPGPFPLPIIGNLFQLELKNIPKSFTRLAQRFGPVFTLYVGSQRMVVMHGYKAVKEAL LDYKDEFSGRGDLPAFHAHRDRGVMEKLQLGPEILQRENPRLIYARLSGFGQSGSFCRLAGHDINYLALSGGRNSIFKFFSVENSEIESV -------------------------------------------------------------- >21055_21055_3_CYP2E1-AMACR_CYP2E1_chr10_135342144_ENST00000463117_AMACR_chr5_34006004_ENST00000335606_length(amino acids)=436AA_BP=136 MAPFMWQVVIQDCLPGWQQGPSGTMSALGVTVALLVWAAFLLLVSMWRQVHSSWNLPPGPFPLPIIGNLFQLELKNIPKSFTRLAQRFGP VFTLYVGSQRMVVMHGYKAVKEALLDYKDEFSGRGDLPAFHAHRDRGVMEKLQLGPEILQRENPRLIYARLSGFGQSGSFCRLAGHDINY LALSGVLSKIGRSGENPYAPLNLLADFAGGGLMCALGIIMALFDRTRTGKGQVIDANMVEGTAYLSSFLWKTQKLSLWEAPRGQNMLDGG APFYTTYRTADGEFMAVGAIEPQFYELLIKGLGLKSDELPNQMSMDDWPEMKKKFADVFAEKTKAEWCQIFDGTDACVTPVLTFEEVVHH -------------------------------------------------------------- >21055_21055_4_CYP2E1-AMACR_CYP2E1_chr10_135342144_ENST00000463117_AMACR_chr5_34006004_ENST00000382072_length(amino acids)=252AA_BP=136 MAPFMWQVVIQDCLPGWQQGPSGTMSALGVTVALLVWAAFLLLVSMWRQVHSSWNLPPGPFPLPIIGNLFQLELKNIPKSFTRLAQRFGP VFTLYVGSQRMVVMHGYKAVKEALLDYKDEFSGRGDLPAFHAHRDRGVMEKLQLGPEILQRENPRLIYARLSGFGQSGSFCRLAGHDINY -------------------------------------------------------------- |
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Fusion Protein Functional Features |
![]() Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr10:135342144/chr5:34006004) - 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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Hgene | Tgene |
CYP2E1 | AMACR |
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: Catalyzes the interconversion of (R)- and (S)-stereoisomers of alpha-methyl-branched-chain fatty acyl-CoA esters (PubMed:7649182, PubMed:10655068, PubMed:11060359). Acts only on coenzyme A thioesters, not on free fatty acids, and accepts as substrates a wide range of alpha-methylacyl-CoAs, including pristanoyl-CoA, trihydroxycoprostanoyl-CoA (an intermediate in bile acid synthesis), and arylpropionic acids like the anti-inflammatory drug ibuprofen (2-(4-isobutylphenyl)propionic acid) but neither 3-methyl-branched nor linear-chain acyl-CoAs (PubMed:7649182, PubMed:10655068, PubMed:11060359). {ECO:0000269|PubMed:10655068, ECO:0000269|PubMed:11060359, ECO:0000269|PubMed:7649182}. |
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- 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 | AMACR | chr10:135342144 | chr5:34006004 | ENST00000335606 | 0 | 5 | 380_382 | 82.33333333333333 | 383.0 | Motif | Microbody targeting signal | |
Tgene | AMACR | chr10:135342144 | chr5:34006004 | ENST00000382072 | 0 | 4 | 380_382 | 82.33333333333333 | 199.0 | Motif | Microbody targeting signal | |
Tgene | AMACR | chr10:135342144 | chr5:34006004 | ENST00000382085 | 0 | 6 | 380_382 | 82.33333333333333 | 395.0 | Motif | Microbody targeting signal | |
Tgene | AMACR | chr10:135342144 | chr5:34006004 | ENST00000441713 | 0 | 4 | 380_382 | 82.33333333333333 | 230.0 | Motif | Microbody targeting signal | |
Tgene | AMACR | chr10:135342144 | chr5:34006004 | ENST00000335606 | 0 | 5 | 121_126 | 82.33333333333333 | 383.0 | Region | Substrate binding | |
Tgene | AMACR | chr10:135342144 | chr5:34006004 | ENST00000382072 | 0 | 4 | 121_126 | 82.33333333333333 | 199.0 | Region | Substrate binding | |
Tgene | AMACR | chr10:135342144 | chr5:34006004 | ENST00000382085 | 0 | 6 | 121_126 | 82.33333333333333 | 395.0 | Region | Substrate binding | |
Tgene | AMACR | chr10:135342144 | chr5:34006004 | ENST00000441713 | 0 | 4 | 121_126 | 82.33333333333333 | 230.0 | Region | Substrate 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 | chr10:135342144 | chr5:34006004 | ENST00000252945 | + | 2 | 9 | 298_303 | 112.33333333333333 | 494.0 | Region | Substrate binding |
Hgene | CYP2E1 | chr10:135342144 | chr5:34006004 | ENST00000463117 | + | 4 | 11 | 298_303 | 112.33333333333333 | 494.0 | Region | Substrate binding |
Tgene | AMACR | chr10:135342144 | chr5:34006004 | ENST00000335606 | 0 | 5 | 55_58 | 82.33333333333333 | 383.0 | Region | Substrate binding | |
Tgene | AMACR | chr10:135342144 | chr5:34006004 | ENST00000382072 | 0 | 4 | 55_58 | 82.33333333333333 | 199.0 | Region | Substrate binding | |
Tgene | AMACR | chr10:135342144 | chr5:34006004 | ENST00000382085 | 0 | 6 | 55_58 | 82.33333333333333 | 395.0 | Region | Substrate binding | |
Tgene | AMACR | chr10:135342144 | chr5:34006004 | ENST00000441713 | 0 | 4 | 55_58 | 82.33333333333333 | 230.0 | Region | Substrate binding |
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Fusion Protein-Protein Interaction |
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Gene | PPI interactors |
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Gene | STRING network |
CYP2E1 | |
AMACR |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Related Drugs to CYP2E1-AMACR |
![]() (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Drug | Source | PMID |
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Related Diseases to CYP2E1-AMACR |
![]() (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Disease | Source | PMID |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |