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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:DNA2-POMT1 (FusionGDB2 ID:23296)

Fusion Gene Summary for DNA2-POMT1

check button Fusion gene summary
Fusion gene informationFusion gene name: DNA2-POMT1
Fusion gene ID: 23296
HgeneTgene
Gene symbol

DNA2

POMT1

Gene ID

1763

10585

Gene nameDNA replication helicase/nuclease 2protein O-mannosyltransferase 1
SynonymsDNA2L|hDNA2LGMD2K|LGMDR11|MDDGA1|MDDGB1|MDDGC1|RT
Cytomap

10q21.3

9q34.13

Type of geneprotein-codingprotein-coding
DescriptionDNA replication ATP-dependent helicase/nuclease DNA2DNA replication ATP-dependent helicase-like homologDNA replication helicase 2 homologDNA2 DNA replication helicase 2-likeDNA2-like helicaseprotein O-mannosyl-transferase 1dolichyl-phosphate-mannose--protein mannosyltransferase 1testis tissue sperm-binding protein Li 57ptruncated O-mannosyl-transferase 1 variant SV3DEL
Modification date2020032220200328
UniProtAcc

P51530

.
Ensembl transtripts involved in fusion geneENST00000358410, ENST00000399179, 
ENST00000399180, 
ENST00000341012, 
ENST00000372228, ENST00000402686, 
ENST00000404875, ENST00000423007, 
ENST00000354713, ENST00000419118, 
ENST00000485278, ENST00000541219, 
Fusion gene scores* DoF score4 X 4 X 2=323 X 4 X 2=24
# samples 43
** MAII scorelog2(4/32*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(3/24*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: DNA2 [Title/Abstract] AND POMT1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointDNA2(70176996)-POMT1(134399186), # samples:1
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
HgeneDNA2

GO:0000729

DNA double-strand break processing

21325134

HgeneDNA2

GO:0006264

mitochondrial DNA replication

18995831|19487465

HgeneDNA2

GO:0006284

base-excision repair

18995831

HgeneDNA2

GO:0033567

DNA replication, Okazaki fragment processing

22570407

HgeneDNA2

GO:0043137

DNA replication, removal of RNA primer

18995831

HgeneDNA2

GO:0043504

mitochondrial DNA repair

19487465

HgeneDNA2

GO:0045740

positive regulation of DNA replication

18995831


check buttonFusion gene breakpoints across DNA2 (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 POMT1 (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
ChiTaRS5.0N/ACB049905DNA2chr10

70176996

-POMT1chr9

134399186

-


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Fusion Gene ORF analysis for DNA2-POMT1

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
intron-3UTRENST00000358410ENST00000341012DNA2chr10

70176996

-POMT1chr9

134399186

-
intron-3UTRENST00000358410ENST00000372228DNA2chr10

70176996

-POMT1chr9

134399186

-
intron-3UTRENST00000358410ENST00000402686DNA2chr10

70176996

-POMT1chr9

134399186

-
intron-3UTRENST00000358410ENST00000404875DNA2chr10

70176996

-POMT1chr9

134399186

-
intron-3UTRENST00000358410ENST00000423007DNA2chr10

70176996

-POMT1chr9

134399186

-
intron-3UTRENST00000399179ENST00000341012DNA2chr10

70176996

-POMT1chr9

134399186

-
intron-3UTRENST00000399179ENST00000372228DNA2chr10

70176996

-POMT1chr9

134399186

-
intron-3UTRENST00000399179ENST00000402686DNA2chr10

70176996

-POMT1chr9

134399186

-
intron-3UTRENST00000399179ENST00000404875DNA2chr10

70176996

-POMT1chr9

134399186

-
intron-3UTRENST00000399179ENST00000423007DNA2chr10

70176996

-POMT1chr9

134399186

-
intron-3UTRENST00000399180ENST00000341012DNA2chr10

70176996

-POMT1chr9

134399186

-
intron-3UTRENST00000399180ENST00000372228DNA2chr10

70176996

-POMT1chr9

134399186

-
intron-3UTRENST00000399180ENST00000402686DNA2chr10

70176996

-POMT1chr9

134399186

-
intron-3UTRENST00000399180ENST00000404875DNA2chr10

70176996

-POMT1chr9

134399186

-
intron-3UTRENST00000399180ENST00000423007DNA2chr10

70176996

-POMT1chr9

134399186

-
intron-intronENST00000358410ENST00000354713DNA2chr10

70176996

-POMT1chr9

134399186

-
intron-intronENST00000358410ENST00000419118DNA2chr10

70176996

-POMT1chr9

134399186

-
intron-intronENST00000358410ENST00000485278DNA2chr10

70176996

-POMT1chr9

134399186

-
intron-intronENST00000358410ENST00000541219DNA2chr10

70176996

-POMT1chr9

134399186

-
intron-intronENST00000399179ENST00000354713DNA2chr10

70176996

-POMT1chr9

134399186

-
intron-intronENST00000399179ENST00000419118DNA2chr10

70176996

-POMT1chr9

134399186

-
intron-intronENST00000399179ENST00000485278DNA2chr10

70176996

-POMT1chr9

134399186

-
intron-intronENST00000399179ENST00000541219DNA2chr10

70176996

-POMT1chr9

134399186

-
intron-intronENST00000399180ENST00000354713DNA2chr10

70176996

-POMT1chr9

134399186

-
intron-intronENST00000399180ENST00000419118DNA2chr10

70176996

-POMT1chr9

134399186

-
intron-intronENST00000399180ENST00000485278DNA2chr10

70176996

-POMT1chr9

134399186

-
intron-intronENST00000399180ENST00000541219DNA2chr10

70176996

-POMT1chr9

134399186

-

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 DNA2-POMT1


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 DNA2-POMT1


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/:70176996/:134399186)
- 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
DNA2

P51530

.
FUNCTION: Key enzyme involved in DNA replication and DNA repair in nucleus and mitochondrion. Involved in Okazaki fragments processing by cleaving long flaps that escape FEN1: flaps that are longer than 27 nucleotides are coated by replication protein A complex (RPA), leading to recruit DNA2 which cleaves the flap until it is too short to bind RPA and becomes a substrate for FEN1. Also involved in 5'-end resection of DNA during double-strand break (DSB) repair: recruited by BLM and mediates the cleavage of 5'-ssDNA, while the 3'-ssDNA cleavage is prevented by the presence of RPA. Also involved in DNA replication checkpoint independently of Okazaki fragments processing. Possesses different enzymatic activities, such as single-stranded DNA (ssDNA)-dependent ATPase, 5'-3' helicase and endonuclease activities. While the ATPase and endonuclease activities are well-defined and play a key role in Okazaki fragments processing and DSB repair, the 5'-3' DNA helicase activity is subject to debate. According to various reports, the helicase activity is weak and its function remains largely unclear. Helicase activity may promote the motion of DNA2 on the flap, helping the nuclease function. {ECO:0000269|PubMed:16595799, ECO:0000269|PubMed:16595800, ECO:0000269|PubMed:18995831, ECO:0000269|PubMed:19487465, ECO:0000269|PubMed:21325134, ECO:0000269|PubMed:21572043, ECO:0000269|PubMed:22570407, ECO:0000269|PubMed:22570476}.FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}.

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 DNA2-POMT1


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 DNA2-POMT1


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 DNA2-POMT1


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 DNA2-POMT1


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