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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:DLGAP1-METTL4 (FusionGDB2 ID:23133)

Fusion Gene Summary for DLGAP1-METTL4

check button Fusion gene summary
Fusion gene informationFusion gene name: DLGAP1-METTL4
Fusion gene ID: 23133
HgeneTgene
Gene symbol

DLGAP1

METTL4

Gene ID

9229

64863

Gene nameDLG associated protein 1methyltransferase like 4
SynonymsDAP-1|DAP-1-ALPHA|DAP-1-BETA|DAP1|DLGAP1A|DLGAP1B|GKAP|SAPAP1HsT661
Cytomap

18p11.31

18p11.32

Type of geneprotein-codingprotein-coding
Descriptiondisks large-associated protein 1PSD-95/SAP90 binding protein 1SAP90/PSD-95-associated protein 1discs large homolog associated protein 1guanylate kinase-associated proteinN(6)-adenine-specific DNA methyltransferase METTL4methyltransferase-like protein 4
Modification date2020031320200313
UniProtAcc

O14490

Q8N3J2

Ensembl transtripts involved in fusion geneENST00000315677, ENST00000400145, 
ENST00000400147, ENST00000400149, 
ENST00000400150, ENST00000400155, 
ENST00000515196, ENST00000534970, 
ENST00000539435, ENST00000581527, 
ENST00000581699, ENST00000584874, 
ENST00000478161, 
ENST00000319888, 
ENST00000574538, 
Fusion gene scores* DoF score37 X 27 X 8=79927 X 3 X 4=84
# samples 377
** MAII scorelog2(37/7992*10)=-4.43295940727611
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/84*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: DLGAP1 [Title/Abstract] AND METTL4 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointDLGAP1(3814059)-METTL4(2567653), # 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

check buttonFusion gene breakpoints across DLGAP1 (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 METTL4 (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-A1KU-01ADLGAP1chr18

3814059

-METTL4chr18

2567653

-


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Fusion Gene ORF analysis for DLGAP1-METTL4

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
5CDS-5UTRENST00000315677ENST00000319888DLGAP1chr18

3814059

-METTL4chr18

2567653

-
5CDS-5UTRENST00000315677ENST00000574538DLGAP1chr18

3814059

-METTL4chr18

2567653

-
5CDS-5UTRENST00000400145ENST00000319888DLGAP1chr18

3814059

-METTL4chr18

2567653

-
5CDS-5UTRENST00000400145ENST00000574538DLGAP1chr18

3814059

-METTL4chr18

2567653

-
5CDS-5UTRENST00000400147ENST00000319888DLGAP1chr18

3814059

-METTL4chr18

2567653

-
5CDS-5UTRENST00000400147ENST00000574538DLGAP1chr18

3814059

-METTL4chr18

2567653

-
5CDS-5UTRENST00000400149ENST00000319888DLGAP1chr18

3814059

-METTL4chr18

2567653

-
5CDS-5UTRENST00000400149ENST00000574538DLGAP1chr18

3814059

-METTL4chr18

2567653

-
5CDS-5UTRENST00000400150ENST00000319888DLGAP1chr18

3814059

-METTL4chr18

2567653

-
5CDS-5UTRENST00000400150ENST00000574538DLGAP1chr18

3814059

-METTL4chr18

2567653

-
5CDS-5UTRENST00000400155ENST00000319888DLGAP1chr18

3814059

-METTL4chr18

2567653

-
5CDS-5UTRENST00000400155ENST00000574538DLGAP1chr18

3814059

-METTL4chr18

2567653

-
5CDS-5UTRENST00000515196ENST00000319888DLGAP1chr18

3814059

-METTL4chr18

2567653

-
5CDS-5UTRENST00000515196ENST00000574538DLGAP1chr18

3814059

-METTL4chr18

2567653

-
5CDS-5UTRENST00000534970ENST00000319888DLGAP1chr18

3814059

-METTL4chr18

2567653

-
5CDS-5UTRENST00000534970ENST00000574538DLGAP1chr18

3814059

-METTL4chr18

2567653

-
5CDS-5UTRENST00000539435ENST00000319888DLGAP1chr18

3814059

-METTL4chr18

2567653

-
5CDS-5UTRENST00000539435ENST00000574538DLGAP1chr18

3814059

-METTL4chr18

2567653

-
5CDS-5UTRENST00000581527ENST00000319888DLGAP1chr18

3814059

-METTL4chr18

2567653

-
5CDS-5UTRENST00000581527ENST00000574538DLGAP1chr18

3814059

-METTL4chr18

2567653

-
5CDS-5UTRENST00000581699ENST00000319888DLGAP1chr18

3814059

-METTL4chr18

2567653

-
5CDS-5UTRENST00000581699ENST00000574538DLGAP1chr18

3814059

-METTL4chr18

2567653

-
5CDS-5UTRENST00000584874ENST00000319888DLGAP1chr18

3814059

-METTL4chr18

2567653

-
5CDS-5UTRENST00000584874ENST00000574538DLGAP1chr18

3814059

-METTL4chr18

2567653

-
5UTR-5UTRENST00000478161ENST00000319888DLGAP1chr18

3814059

-METTL4chr18

2567653

-
5UTR-5UTRENST00000478161ENST00000574538DLGAP1chr18

3814059

-METTL4chr18

2567653

-

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 DLGAP1-METTL4


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 DLGAP1-METTL4


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/:3814059/:2567653)
- 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
DLGAP1

O14490

METTL4

Q8N3J2

FUNCTION: Part of the postsynaptic scaffold in neuronal cells.FUNCTION: N(6)-adenine-specific methyltransferase that can methylate both RNAs and DNA (PubMed:31913360, PubMed:32183942). Acts as a N(6)-adenine-specific RNA methyltransferase by catalyzing formation of N6,2'-O-dimethyladenosine (m6A(m)) on internal positions of U2 small nuclear RNA (snRNA): methylates the 6th position of adenine residues with a pre-deposited 2'-O-methylation (PubMed:31913360). Internal m6A(m) methylation of snRNAs regulates RNA splicing (PubMed:31913360). Also able to act as a N(6)-adenine-specific DNA methyltransferase by mediating methylation of DNA on the 6th position of adenine (N(6)-methyladenosine) (PubMed:32183942). The existence of N(6)-methyladenosine (m6A) on DNA is however unclear in mammals, and additional evidences are required to confirm the role of the N(6)-adenine-specific DNA methyltransferase activity of METTL4 in vivo (PubMed:32203414). Acts as a regulator of mitochondrial transcript levels and mitochondrial DNA (mtDNA) copy number by mediating mtDNA N(6)-methylation: m6A on mtDNA reduces transcription by repressing TFAM DNA-binding and bending (PubMed:32183942). N(6)-methyladenosine deposition by METTL4 regulates Polycomb silencing by triggering ubiquitination and degradation of sensor proteins ASXL1 and MPND, leading to inactivation of the PR-DUB complex and subsequent preservation of Polycomb silencing (By similarity). {ECO:0000250|UniProtKB:Q3U034, ECO:0000269|PubMed:31913360, ECO:0000269|PubMed:32183942, ECO:0000269|PubMed:32203414}.

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 DLGAP1-METTL4


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 DLGAP1-METTL4


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 DLGAP1-METTL4


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 DLGAP1-METTL4


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