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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:FBLN7-ALOXE3 (FusionGDB2 ID:29468)

Fusion Gene Summary for FBLN7-ALOXE3

check button Fusion gene summary
Fusion gene informationFusion gene name: FBLN7-ALOXE3
Fusion gene ID: 29468
HgeneTgene
Gene symbol

FBLN7

ALOXE3

Gene ID

129804

59344

Gene namefibulin 7arachidonate lipoxygenase 3
SynonymsTM14ARCI3|E-LOX|eLOX-3|eLOX3
Cytomap

2q13-q14.1

17p13.1

Type of geneprotein-codingprotein-coding
Descriptionfibulin-7FIBL-7hydroperoxide isomerase ALOXE3Epidermal lipoxygenase-3e-LOX-3epidermal LOX-3epidermal lipoxygenaseepidermis-type lipoxygenase 3hydroperoxy icosatetraenoate dehydratase
Modification date2020031320200313
UniProtAcc

Q53RD9

.
Ensembl transtripts involved in fusion geneENST00000331203, ENST00000409903, 
ENST00000409667, ENST00000409450, 
ENST00000472377, 
ENST00000380149, 
ENST00000448843, ENST00000318227, 
Fusion gene scores* DoF score3 X 3 X 2=181 X 1 X 1=1
# samples 31
** MAII scorelog2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(1/1*10)=3.32192809488736
Context

PubMed: FBLN7 [Title/Abstract] AND ALOXE3 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointFBLN7(112942916)-ALOXE3(8012572), # samples:1
Anticipated loss of major functional domain due to fusion event.FBLN7-ALOXE3 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
FBLN7-ALOXE3 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)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
TgeneALOXE3

GO:0006665

sphingolipid metabolic process

21558561

TgeneALOXE3

GO:0019369

arachidonic acid metabolic process

12881489|17045234

TgeneALOXE3

GO:0019372

lipoxygenase pathway

20921226

TgeneALOXE3

GO:0043651

linoleic acid metabolic process

12881489|17045234

TgeneALOXE3

GO:0051122

hepoxilin biosynthetic process

12881489|17045234


check buttonFusion gene breakpoints across FBLN7 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across ALOXE3 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

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
ChimerDB4SARCTCGA-DX-A6YQ-01AFBLN7chr2

112942916

+ALOXE3chr17

8012572

-


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Fusion Gene ORF analysis for FBLN7-ALOXE3

check button Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
Frame-shiftENST00000331203ENST00000380149FBLN7chr2

112942916

+ALOXE3chr17

8012572

-
Frame-shiftENST00000331203ENST00000448843FBLN7chr2

112942916

+ALOXE3chr17

8012572

-
Frame-shiftENST00000331203ENST00000318227FBLN7chr2

112942916

+ALOXE3chr17

8012572

-
Frame-shiftENST00000409903ENST00000380149FBLN7chr2

112942916

+ALOXE3chr17

8012572

-
Frame-shiftENST00000409903ENST00000448843FBLN7chr2

112942916

+ALOXE3chr17

8012572

-
Frame-shiftENST00000409903ENST00000318227FBLN7chr2

112942916

+ALOXE3chr17

8012572

-
Frame-shiftENST00000409667ENST00000380149FBLN7chr2

112942916

+ALOXE3chr17

8012572

-
Frame-shiftENST00000409667ENST00000448843FBLN7chr2

112942916

+ALOXE3chr17

8012572

-
Frame-shiftENST00000409667ENST00000318227FBLN7chr2

112942916

+ALOXE3chr17

8012572

-
Frame-shiftENST00000409450ENST00000380149FBLN7chr2

112942916

+ALOXE3chr17

8012572

-
Frame-shiftENST00000409450ENST00000448843FBLN7chr2

112942916

+ALOXE3chr17

8012572

-
Frame-shiftENST00000409450ENST00000318227FBLN7chr2

112942916

+ALOXE3chr17

8012572

-
intron-3CDSENST00000472377ENST00000380149FBLN7chr2

112942916

+ALOXE3chr17

8012572

-
intron-3CDSENST00000472377ENST00000448843FBLN7chr2

112942916

+ALOXE3chr17

8012572

-
intron-3CDSENST00000472377ENST00000318227FBLN7chr2

112942916

+ALOXE3chr17

8012572

-

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

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

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Fusion Genomic Features for FBLN7-ALOXE3


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.

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Fusion Protein Features for FBLN7-ALOXE3


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
FBLN7

Q53RD9

.
FUNCTION: An adhesion molecule that interacts with extracellular matrix molecules in developing teeth and may play important roles in differentiation and maintenance of odontoblasts as well as in dentin formation. {ECO:0000250}.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.
- In-frame and retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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Fusion Gene Sequence for FBLN7-ALOXE3


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for FBLN7-ALOXE3


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 (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs for FBLN7-ALOXE3


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for FBLN7-ALOXE3


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneALOXE3C0079154Congenital Nonbullous Ichthyosiform Erythroderma5CTD_human;ORPHANET
TgeneALOXE3C3539888ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 35GENOMICS_ENGLAND;UNIPROT
TgeneALOXE3C0020758Congenital ichthyosis1CTD_human
TgeneALOXE3C0033578Prostatic Neoplasms1CTD_human
TgeneALOXE3C0239849Harlequin Fetus1CTD_human
TgeneALOXE3C0376358Malignant neoplasm of prostate1CTD_human
TgeneALOXE3C1855789Self-Healing Collodion Baby1ORPHANET
TgeneALOXE3C3536797Ichthyosis Congenita II1CTD_human
TgeneALOXE3C3543867Collodion Fetus1CTD_human
TgeneALOXE3C4551630Ichthyosis Congenita I1CTD_human