UTHEALTH HOME    ABOUT SBMI    A-Z    WEBMAIL    INSIDE THE UNIVERSITY
FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Terms of Use

Center for Computational Systems Medicine level1
leaf

Fusion Gene Summary

leaf

Fusion Gene Sample Information

leaf

Fusion ORF Analysis

leaf

Fusion Amino Acid Sequences

leaf

Fusion Protein Functional Features

leaf

Fusion Protein-Protein Interaction

leaf

Related drugs with this fusion protein

leaf

Related disease with this fusion protein

Fusion Protein:CYP2E1-AMACR

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CYP2E1-AMACR
FusionPDB ID: 21055
FusionGDB2.0 ID: 21055
HgeneTgene
Gene symbol

CYP2E1

AMACR

Gene ID

1571

23600

Gene namecytochrome P450 family 2 subfamily E member 1alpha-methylacyl-CoA racemase
SynonymsCPE1|CYP2E|P450-J|P450C2EAMACRD|CBAS4|P504S|RACE|RM
Cytomap

10q26.3

5p13.2

Type of geneprotein-codingprotein-coding
Descriptioncytochrome P450 2E14-nitrophenol 2-hydroxylaseCYPIIE1cytochrome P450, family 2, subfamily E, polypeptide 1cytochrome P450, subfamily IIE (ethanol-inducible), polypeptide 1cytochrome P450-Jflavoprotein-linked monooxygenasemicrosomal monooxygenasexealpha-methylacyl-CoA racemase2-methylacyl-CoA racemase
Modification date2020031520200313
UniProtAcc

P05181

Q9UHK6

Ensembl transtripts involved in fusion geneENST idsENST00000480558, 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 score8 X 5 X 3=12028 X 3 X 4=336
# samples 823
** MAII scorelog2(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)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
HgeneCYP2E1

GO:0002933

lipid hydroxylation

10553002

HgeneCYP2E1

GO:0016098

monoterpenoid metabolic process

16401082

HgeneCYP2E1

GO:0017144

drug metabolic process

19219744

HgeneCYP2E1

GO:0018960

4-nitrophenol metabolic process

9348445

HgeneCYP2E1

GO:0046483

heterocycle metabolic process

19651758

HgeneCYP2E1

GO:0055114

oxidation-reduction process

16401082|19219744

TgeneAMACR

GO:0008206

bile acid metabolic process

10655068


check buttonFusion 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.
all structure

check buttonFusion gene breakpoints across AMACR (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


Top

Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
check button 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4LIHCTCGA-DD-A39W-01ACYP2E1chr10

135342144

+AMACRchr5

34006004

-


Top

Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000463117CYP2E1chr10135342144+ENST00000335606AMACRchr534006004-44266092001510436
ENST00000463117CYP2E1chr10135342144+ENST00000382072AMACRchr534006004-3269609200958252
ENST00000252945CYP2E1chr10135342144+ENST00000335606AMACRchr534006004-4187370331271412
ENST00000252945CYP2E1chr10135342144+ENST00000382072AMACRchr534006004-303037033719228

check buttonDeepORF 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.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score
ENST00000463117ENST00000335606CYP2E1chr10135342144+AMACRchr534006004-0.0002880960.99971193
ENST00000463117ENST00000382072CYP2E1chr10135342144+AMACRchr534006004-0.0398366380.9601633
ENST00000252945ENST00000335606CYP2E1chr10135342144+AMACRchr534006004-8.25E-050.9999175
ENST00000252945ENST00000382072CYP2E1chr10135342144+AMACRchr534006004-0.0047440160.995256

Top

Fusion Amino Acid Sequences


check button 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

>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

--------------------------------------------------------------

Top

Fusion Protein Functional Features


check button Four levels of functional features of fusion genes
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.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
CYP2E1

P05181

AMACR

Q9UHK6

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}.

check buttonRetention 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

download page

* Minus value of BPloci means that the break pointn is located before the CDS.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgeneAMACRchr10:135342144chr5:34006004ENST0000033560605380_38282.33333333333333383.0MotifMicrobody targeting signal
TgeneAMACRchr10:135342144chr5:34006004ENST0000038207204380_38282.33333333333333199.0MotifMicrobody targeting signal
TgeneAMACRchr10:135342144chr5:34006004ENST0000038208506380_38282.33333333333333395.0MotifMicrobody targeting signal
TgeneAMACRchr10:135342144chr5:34006004ENST0000044171304380_38282.33333333333333230.0MotifMicrobody targeting signal
TgeneAMACRchr10:135342144chr5:34006004ENST0000033560605121_12682.33333333333333383.0RegionSubstrate binding
TgeneAMACRchr10:135342144chr5:34006004ENST0000038207204121_12682.33333333333333199.0RegionSubstrate binding
TgeneAMACRchr10:135342144chr5:34006004ENST0000038208506121_12682.33333333333333395.0RegionSubstrate binding
TgeneAMACRchr10:135342144chr5:34006004ENST0000044171304121_12682.33333333333333230.0RegionSubstrate binding

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneCYP2E1chr10:135342144chr5:34006004ENST00000252945+29298_303112.33333333333333494.0RegionSubstrate binding
HgeneCYP2E1chr10:135342144chr5:34006004ENST00000463117+411298_303112.33333333333333494.0RegionSubstrate binding
TgeneAMACRchr10:135342144chr5:34006004ENST000003356060555_5882.33333333333333383.0RegionSubstrate binding
TgeneAMACRchr10:135342144chr5:34006004ENST000003820720455_5882.33333333333333199.0RegionSubstrate binding
TgeneAMACRchr10:135342144chr5:34006004ENST000003820850655_5882.33333333333333395.0RegionSubstrate binding
TgeneAMACRchr10:135342144chr5:34006004ENST000004417130455_5882.33333333333333230.0RegionSubstrate binding


Top

Fusion Protein-Protein Interaction


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page.


check button Protein-protein interactors with each fusion partner protein in wild-type from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
CYP2E1
AMACR


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


Top

Related Drugs to CYP2E1-AMACR


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

Top

Related Diseases to CYP2E1-AMACR


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource