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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:ZBTB4-ACADVL (FusionGDB2 ID:99741)

Fusion Gene Summary for ZBTB4-ACADVL

check button Fusion gene summary
Fusion gene informationFusion gene name: ZBTB4-ACADVL
Fusion gene ID: 99741
HgeneTgene
Gene symbol

ZBTB4

ACADVL

Gene ID

57659

37

Gene namezinc finger and BTB domain containing 4acyl-CoA dehydrogenase very long chain
SynonymsKAISO-L1|ZNF903ACAD6|LCACD|VLCAD
Cytomap

17p13.1

17p13.1

Type of geneprotein-codingprotein-coding
Descriptionzinc finger and BTB domain-containing protein 4KAISO-like zinc finger protein 1very long-chain specific acyl-CoA dehydrogenase, mitochondrialacyl-Coenzyme A dehydrogenase, very long chain
Modification date2020031320200313
UniProtAcc.

P49748

Ensembl transtripts involved in fusion geneENST00000380599, ENST00000311403, 
ENST00000543245, ENST00000356839, 
ENST00000350303, ENST00000581562, 
Fusion gene scores* DoF score8 X 7 X 4=22411 X 12 X 7=924
# samples 812
** MAII scorelog2(8/224*10)=-1.48542682717024
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(12/924*10)=-2.94485844580754
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ZBTB4 [Title/Abstract] AND ACADVL [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointZBTB4(7382775)-ACADVL(7123923), # samples:2
Anticipated loss of major functional domain due to fusion event.
* 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
HgeneZBTB4

GO:0000122

negative regulation of transcription by RNA polymerase II

16354688

HgeneZBTB4

GO:0006974

cellular response to DNA damage stimulus

19448668

HgeneZBTB4

GO:0045892

negative regulation of transcription, DNA-templated

16354688

TgeneACADVL

GO:0033539

fatty acid beta-oxidation using acyl-CoA dehydrogenase

7668252


check buttonFusion gene breakpoints across ZBTB4 (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 ACADVL (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
ChimerDB4GBMTCGA-06-2558-01AZBTB4chr17

7382775

-ACADVLchr17

7123923

+
ChimerDB4GBMTCGA-06-2558-01AZBTB4chr17

7382775

-ACADVLchr17

7123923

+


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Fusion Gene ORF analysis for ZBTB4-ACADVL

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
5UTR-3CDSENST00000380599ENST00000543245ZBTB4chr17

7382775

-ACADVLchr17

7123923

+
5UTR-3CDSENST00000380599ENST00000356839ZBTB4chr17

7382775

-ACADVLchr17

7123923

+
5UTR-3CDSENST00000380599ENST00000350303ZBTB4chr17

7382775

-ACADVLchr17

7123923

+
5UTR-3UTRENST00000380599ENST00000581562ZBTB4chr17

7382775

-ACADVLchr17

7123923

+
intron-3CDSENST00000311403ENST00000543245ZBTB4chr17

7382775

-ACADVLchr17

7123923

+
intron-3CDSENST00000311403ENST00000356839ZBTB4chr17

7382775

-ACADVLchr17

7123923

+
intron-3CDSENST00000311403ENST00000350303ZBTB4chr17

7382775

-ACADVLchr17

7123923

+
intron-3UTRENST00000311403ENST00000581562ZBTB4chr17

7382775

-ACADVLchr17

7123923

+

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 ZBTB4-ACADVL


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)
ZBTB4chr177382774-ACADVLchr177123922+2.98E-050.9999702
ZBTB4chr177382774-ACADVLchr177123922+2.98E-050.9999702

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 ZBTB4-ACADVL


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
.ACADVL

P49748

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.FUNCTION: Very long-chain specific acyl-CoA dehydrogenase is one of the acyl-CoA dehydrogenases that catalyze the first step of mitochondrial fatty acid beta-oxidation, an aerobic process breaking down fatty acids into acetyl-CoA and allowing the production of energy from fats (PubMed:7668252, PubMed:9461620, PubMed:18227065, PubMed:9839948, PubMed:9599005). The first step of fatty acid beta-oxidation consists in the removal of one hydrogen from C-2 and C-3 of the straight-chain fatty acyl-CoA thioester, resulting in the formation of trans-2-enoyl-CoA (PubMed:7668252, PubMed:9461620, PubMed:18227065, PubMed:9839948). Among the different mitochondrial acyl-CoA dehydrogenases, very long-chain specific acyl-CoA dehydrogenase acts specifically on acyl-CoAs with saturated 12 to 24 carbons long primary chains (PubMed:21237683, PubMed:9839948). {ECO:0000269|PubMed:18227065, ECO:0000269|PubMed:21237683, ECO:0000269|PubMed:7668252, ECO:0000269|PubMed:9461620, ECO:0000269|PubMed:9599005, ECO:0000269|PubMed:9839948}.

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 ZBTB4-ACADVL


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 ZBTB4-ACADVL


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 ZBTB4-ACADVL


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 ZBTB4-ACADVL


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneZBTB4C0023893Liver Cirrhosis, Experimental1CTD_human
TgeneACADVLC3887523Very long chain acyl-CoA dehydrogenase deficiency15CLINGEN;CTD_human;GENOMICS_ENGLAND;UNIPROT
TgeneACADVLC0003129Anoxemia1CTD_human
TgeneACADVLC0003130Anoxia1CTD_human
TgeneACADVLC0242184Hypoxia1CTD_human
TgeneACADVLC0270984Metabolic myopathy1GENOMICS_ENGLAND
TgeneACADVLC0369183Erythrocyte Mean Corpuscular Hemoglobin Test1GENOMICS_ENGLAND
TgeneACADVLC0700292Hypoxemia1CTD_human
TgeneACADVLC1261502Finding of Mean Corpuscular Hemoglobin1GENOMICS_ENGLAND