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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:CYP4F3-PTMS

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CYP4F3-PTMS
FusionPDB ID: 21097
FusionGDB2.0 ID: 21097
HgeneTgene
Gene symbol

CYP4F3

PTMS

Gene ID

4051

5763

Gene namecytochrome P450 family 4 subfamily F member 3parathymosin
SynonymsCPF3|CYP4F|CYPIVF3|LTB4HParaT
Cytomap

19p13.12

12p13.31

Type of geneprotein-codingprotein-coding
Descriptioncytochrome P450 4F320-HETE synthase20-hydroxyeicosatetraenoic acid synthasecytochrome P-450cytochrome P450, family 4, subfamily F, polypeptide 3cytochrome P450, subfamily IVF, polypeptide 3 (leukotriene B4 omega hydroxylase)cytochrome P450-LTB-omegaparathymosin
Modification date2020031320200313
UniProtAcc

Q08477

.
Ensembl transtripts involved in fusion geneENST idsENST00000221307, ENST00000585846, 
ENST00000586182, ENST00000591058, 
ENST00000588886, 
ENST00000538057, 
ENST00000309083, ENST00000389462, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score1 X 1 X 1=116 X 10 X 10=1600
# samples 116
** MAII scorelog2(1/1*10)=3.32192809488736log2(16/1600*10)=-3.32192809488736
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: CYP4F3 [Title/Abstract] AND PTMS [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CYP4F3(15752423)-PTMS(6878769), # samples:1
Anticipated loss of major functional domain due to fusion event.CYP4F3-PTMS 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.
CYP4F3-PTMS 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

check buttonFusion gene breakpoints across CYP4F3 (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 PTMS (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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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-EP-A2KB-01ACYP4F3chr19

15752423

+PTMSchr12

6878769

+


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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)
ENST00000586182CYP4F3chr1915752423+ENST00000389462PTMSchr126878769+6292325641188
ENST00000586182CYP4F3chr1915752423+ENST00000309083PTMSchr126878769+9972325671189
ENST00000591058CYP4F3chr1915752423+ENST00000389462PTMSchr126878769+6422455772192
ENST00000591058CYP4F3chr1915752423+ENST00000309083PTMSchr126878769+10102455802193
ENST00000221307CYP4F3chr1915752423+ENST00000389462PTMSchr126878769+6422455772192
ENST00000221307CYP4F3chr1915752423+ENST00000309083PTMSchr126878769+10102455802193
ENST00000585846CYP4F3chr1915752423+ENST00000389462PTMSchr126878769+70230563783184
ENST00000585846CYP4F3chr1915752423+ENST00000309083PTMSchr126878769+1070305858292188

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
ENST00000586182ENST00000389462CYP4F3chr1915752423+PTMSchr126878769+0.0251407230.97485936
ENST00000586182ENST00000309083CYP4F3chr1915752423+PTMSchr126878769+0.0037243870.99627566
ENST00000591058ENST00000389462CYP4F3chr1915752423+PTMSchr126878769+0.0269859020.9730142
ENST00000591058ENST00000309083CYP4F3chr1915752423+PTMSchr126878769+0.0030552190.9969447
ENST00000221307ENST00000389462CYP4F3chr1915752423+PTMSchr126878769+0.0269859020.9730142
ENST00000221307ENST00000309083CYP4F3chr1915752423+PTMSchr126878769+0.0030552190.9969447
ENST00000585846ENST00000389462CYP4F3chr1915752423+PTMSchr126878769+0.034681680.96531826
ENST00000585846ENST00000309083CYP4F3chr1915752423+PTMSchr126878769+0.0035662060.99643373

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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

>21097_21097_1_CYP4F3-PTMS_CYP4F3_chr19_15752423_ENST00000221307_PTMS_chr12_6878769_ENST00000309083_length(amino acids)=193AA_BP=1
MDLAAPTPTSRPREASQPQPVGRGSRRCPIFCLLPFGIRFILLFGSSLQRGPFIILFFFFLIFFFPFIFLLSILGSFFFFLLSPVLLLLH
HFFLSLFPACLLLHLLLLLLQVQAQVTQEPIPFRGLRETPEAAAVVIEGIGPGQDAGQEPGGPNQQQEQPRGCCHWPKAQRGQAQLWHPS

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

>21097_21097_2_CYP4F3-PTMS_CYP4F3_chr19_15752423_ENST00000221307_PTMS_chr12_6878769_ENST00000389462_length(amino acids)=192AA_BP=0
MPHFLSSAVWDPLHPPLRQLSSARALHHPLLLLPHLLLPLHLPPLHPRQFLLLPPQPRSPPPVGTRRGSSLRLAACLAHHHHQWDWSLHH
FFLSLFPACLLLHLLLLLLQVQAQVTQEPIPFRGLRETPEAAAVVIEGIGPGQDAGQEPGGPNQQQEQPRGCCHWPKAQRGQAQLWHPSV

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

>21097_21097_3_CYP4F3-PTMS_CYP4F3_chr19_15752423_ENST00000585846_PTMS_chr12_6878769_ENST00000309083_length(amino acids)=188AA_BP=0
MRLVGEGEREQRERGAIGGQLESSDGAGQEVEQWQSEGGGRSVWRGGNEKAGEKEEGGSSGAGPRAGSQVKSGWTWLPPPPPPGPERPPN
PSLLAGAHADAPFSVFCRLGSASSSSSAALFSAGPSSSSSSSSSSSSSPSSSSSPSSAVSSSSSSAPFSSSSTTSFFRSFRLAFSSTFSF

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

>21097_21097_4_CYP4F3-PTMS_CYP4F3_chr19_15752423_ENST00000585846_PTMS_chr12_6878769_ENST00000389462_length(amino acids)=184AA_BP=0
MPHFLSSAVWDPLHPPLRQLSSARALHHPLLLLPHLLLPLHLPPLHPRQFLLLPPQPRSPPPVGTRRGSSLRLAACLAHHHHQWDWSLHH
FFLSLFPACLLLHLLLLLLQVQAQVTQEPIPFRGLRETPEAAAVVIEGIGPGQDAGQEPGGPNQQQEQPRGCCHWPKAQRGQAQLWHPAG

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

>21097_21097_5_CYP4F3-PTMS_CYP4F3_chr19_15752423_ENST00000586182_PTMS_chr12_6878769_ENST00000309083_length(amino acids)=189AA_BP=1
MDLAAPTPTSRPREASQPQPVGRGSRRCPIFCLLPFGIRFILLFGSSLQRGPFIILFFFFLIFFFPFIFLLSILGSFFFFLLSPVLLLLH
HFFLSLFPACLLLHLLLLLLQVQAQVTQEPIPFRGLRETPEAAAVVIEGIGPGQDAGQEPGGPNQQQEQPRGCCHWPKAQRGQAQLWHPC

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

>21097_21097_6_CYP4F3-PTMS_CYP4F3_chr19_15752423_ENST00000586182_PTMS_chr12_6878769_ENST00000389462_length(amino acids)=188AA_BP=0
MPHFLSSAVWDPLHPPLRQLSSARALHHPLLLLPHLLLPLHLPPLHPRQFLLLPPQPRSPPPVGTRRGSSLRLAACLAHHHHQWDWSLHH
FFLSLFPACLLLHLLLLLLQVQAQVTQEPIPFRGLRETPEAAAVVIEGIGPGQDAGQEPGGPNQQQEQPRGCCHWPKAQRGQAQLWHPCP

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

>21097_21097_7_CYP4F3-PTMS_CYP4F3_chr19_15752423_ENST00000591058_PTMS_chr12_6878769_ENST00000309083_length(amino acids)=193AA_BP=1
MDLAAPTPTSRPREASQPQPVGRGSRRCPIFCLLPFGIRFILLFGSSLQRGPFIILFFFFLIFFFPFIFLLSILGSFFFFLLSPVLLLLH
HFFLSLFPACLLLHLLLLLLQVQAQVTQEPIPFRGLRETPEAAAVVIEGIGPGQDAGQEPGGPNQQQEQPRGCCHWPKAQRGQAQLWHPS

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

>21097_21097_8_CYP4F3-PTMS_CYP4F3_chr19_15752423_ENST00000591058_PTMS_chr12_6878769_ENST00000389462_length(amino acids)=192AA_BP=0
MPHFLSSAVWDPLHPPLRQLSSARALHHPLLLLPHLLLPLHLPPLHPRQFLLLPPQPRSPPPVGTRRGSSLRLAACLAHHHHQWDWSLHH
FFLSLFPACLLLHLLLLLLQVQAQVTQEPIPFRGLRETPEAAAVVIEGIGPGQDAGQEPGGPNQQQEQPRGCCHWPKAQRGQAQLWHPSV

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

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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/chr19:15752423/chr12:6878769)
- 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
CYP4F3

Q08477

.
FUNCTION: A cytochrome P450 monooxygenase involved in the metabolism of various endogenous substrates, including fatty acids and their oxygenated derivatives (oxylipins) (PubMed:8486631, PubMed:9675028, PubMed:11461919, PubMed:15145985, PubMed:16547005, PubMed:16820285, PubMed:18182499, PubMed:18065749, 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 (CPR; NADPH-ferrihemoprotein reductase) (PubMed:9675028). May play a role in inactivation of proinflammatory and anti-inflammatory oxylipins during the resolution of inflammation (PubMed:8486631, PubMed:9675028, PubMed:11461919, PubMed:15145985, PubMed:15364545, PubMed:16547005, PubMed:16820285, PubMed:18182499, PubMed:18065749, PubMed:18577768). {ECO:0000269|PubMed:11461919, ECO:0000269|PubMed:15145985, ECO:0000269|PubMed:15364545, ECO:0000269|PubMed:16547005, ECO:0000269|PubMed:16820285, ECO:0000269|PubMed:18065749, ECO:0000269|PubMed:18182499, ECO:0000269|PubMed:18577768, ECO:0000269|PubMed:8486631, ECO:0000269|PubMed:9675028}.; FUNCTION: [Isoform CYP4F3A]: Catalyzes predominantly the oxidation of the terminal carbon (omega-oxidation) of oxylipins in myeloid cells, displaying higher affinity for arachidonate metabolite leukotriene B4 (LTB4) (PubMed:8486631, PubMed:9675028, PubMed:11461919, PubMed:15364545). Inactivates LTB4 via three successive oxidative transformations to 20-hydroxy-LTB4, then to 20-oxo-LTB4 and to 20-carboxy-LTB4 (PubMed:9675028). Has omega-hydroxylase activity toward long-chain fatty acid epoxides with preference for 8,9-epoxy-(5Z,11Z,14Z)-eicosatrienoate (EET) and 9,10-epoxyoctadecanoate (PubMed:15145985). Omega-hydroxylates monohydroxy polyunsaturated fatty acids (PUFAs), including hydroxyeicosatetraenoates (HETEs) and hydroxyeicosapentaenoates (HEPEs), to dihydroxy compounds (PubMed:15364545, PubMed:9675028). Contributes to the degradation of saturated very long-chain fatty acids (VLCFAs) such as docosanoic acid, by catalyzing successive omega-oxidations to the corresponding dicarboxylic acid, thereby initiating chain shortening (PubMed:18182499). Has low hydroxylase activity toward PUFAs (PubMed:18577768, PubMed:11461919). {ECO:0000269|PubMed:11461919, ECO:0000269|PubMed:15145985, ECO:0000269|PubMed:15364545, ECO:0000269|PubMed:18182499, ECO:0000269|PubMed:18577768, ECO:0000269|PubMed:8486631, ECO:0000269|PubMed:9675028}.; FUNCTION: [Isoform CYP4F3B]: Catalyzes predominantly the oxidation of the terminal carbon (omega-oxidation) of polyunsaturated fatty acids (PUFAs) (PubMed:11461919, PubMed:16820285, PubMed:18577768). Participates in the conversion of arachidonic acid to 20-hydroxyeicosatetraenoic acid (20-HETE), a signaling molecule acting both as vasoconstrictive and natriuretic with overall effect on arterial blood pressure (PubMed:11461919, PubMed:16820285, PubMed:18577768). Has high omega-hydroxylase activity toward other PUFAs, including eicosatrienoic acid (ETA), eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) (PubMed:16820285, PubMed:18577768). Can also catalyze the oxidation of the penultimate carbon (omega-1 oxidation) of PUFAs with lower efficiency (PubMed:18577768). Contributes to the degradation of saturated very long-chain fatty acids (VLCFAs) such as docosanoic acid and hexacosanoic acid, by catalyzing successive omega-oxidations to the corresponding dicarboxylic acids, thereby initiating chain shortening (PubMed:16547005, PubMed:18182499). Omega-hydroxylates long-chain 3-hydroxy fatty acids, likely initiating the oxidative conversion to the corresponding 3-hydroxydicarboxylic fatty acids (PubMed:18065749). Has omega-hydroxylase activity toward long-chain fatty acid epoxides with preference for 8,9-epoxy-(5Z,11Z,14Z)-eicosatrienoate (EET) and 9,10-epoxyoctadecanoate (PubMed:15145985). {ECO:0000269|PubMed:11461919, ECO:0000269|PubMed:15145985, ECO:0000269|PubMed:16547005, ECO:0000269|PubMed:16820285, ECO:0000269|PubMed:18065749, ECO:0000269|PubMed:18182499, ECO:0000269|PubMed:18577768}.FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.

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
HgeneCYP4F3chr19:15752423chr12:6878769ENST00000221307+21311_3166.0521.0TransmembraneHelical
HgeneCYP4F3chr19:15752423chr12:6878769ENST00000585846+11211_3166.0521.0TransmembraneHelical
HgeneCYP4F3chr19:15752423chr12:6878769ENST00000586182+21311_3166.0521.0TransmembraneHelical
HgeneCYP4F3chr19:15752423chr12:6878769ENST00000591058+21311_3166.0521.0TransmembraneHelical
TgenePTMSchr19:15752423chr12:6878769ENST000003090830536_9015.0103.0Compositional biasNote=Asp/Glu-rich (acidic)

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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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
CYP4F3
PTMS


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


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Related Drugs to CYP4F3-PTMS


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

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Related Diseases to CYP4F3-PTMS


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