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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:MTF2-GPSM2 (FusionGDB2 ID:55647)

Fusion Gene Summary for MTF2-GPSM2

check button Fusion gene summary
Fusion gene informationFusion gene name: MTF2-GPSM2
Fusion gene ID: 55647
HgeneTgene
Gene symbol

MTF2

GPSM2

Gene ID

22823

29899

Gene namemetal response element binding transcription factor 2G protein signaling modulator 2
SynonymsM96|PCL2|TDRD19A|dJ976O13.2CMCS|DFNB82|LGN|PINS
Cytomap

1p22.1

1p13.3

Type of geneprotein-codingprotein-coding
Descriptionmetal-response element-binding transcription factor 2hPCl2metal regulatory transcription factor 2metal-response element DNA-binding protein M96polycomb-like 2polycomb-like protein 2putative DNA binding proteintudor domain containing 19AG-protein-signaling modulator 2G-protein signalling modulator 2 (AGS3-like, C. elegans)mosaic protein LGN
Modification date2020031320200313
UniProtAcc

Q9Y483

P81274

Ensembl transtripts involved in fusion geneENST00000471953, ENST00000370298, 
ENST00000370303, ENST00000540243, 
ENST00000545708, 
ENST00000264126, 
ENST00000406462, 
Fusion gene scores* DoF score11 X 4 X 6=2643 X 4 X 2=24
# samples 133
** MAII scorelog2(13/264*10)=-1.02202630633
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
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: MTF2 [Title/Abstract] AND GPSM2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointMTF2(93545088)-GPSM2(109427897), # samples:3
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 MTF2 (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 GPSM2 (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
ChimerDB4BRCATCGA-A8-A08I-01AMTF2chr1

93545088

+GPSM2chr1

109417955

+
ChimerDB4BRCATCGA-A8-A08I-01AMTF2chr1

93545088

-GPSM2chr1

109427897

+
ChimerDB4BRCATCGA-A8-A08I-01AMTF2chr1

93545088

+GPSM2chr1

109427897

+


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Fusion Gene ORF analysis for MTF2-GPSM2

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
3UTR-5UTRENST00000471953ENST00000264126MTF2chr1

93545088

+GPSM2chr1

109427897

+
3UTR-5UTRENST00000471953ENST00000406462MTF2chr1

93545088

+GPSM2chr1

109427897

+
3UTR-intronENST00000471953ENST00000264126MTF2chr1

93545088

+GPSM2chr1

109417955

+
3UTR-intronENST00000471953ENST00000406462MTF2chr1

93545088

+GPSM2chr1

109417955

+
5CDS-5UTRENST00000370298ENST00000264126MTF2chr1

93545088

+GPSM2chr1

109427897

+
5CDS-5UTRENST00000370298ENST00000406462MTF2chr1

93545088

+GPSM2chr1

109427897

+
5CDS-5UTRENST00000370303ENST00000264126MTF2chr1

93545088

+GPSM2chr1

109427897

+
5CDS-5UTRENST00000370303ENST00000406462MTF2chr1

93545088

+GPSM2chr1

109427897

+
5CDS-intronENST00000370298ENST00000264126MTF2chr1

93545088

+GPSM2chr1

109417955

+
5CDS-intronENST00000370298ENST00000406462MTF2chr1

93545088

+GPSM2chr1

109417955

+
5CDS-intronENST00000370303ENST00000264126MTF2chr1

93545088

+GPSM2chr1

109417955

+
5CDS-intronENST00000370303ENST00000406462MTF2chr1

93545088

+GPSM2chr1

109417955

+
5UTR-5UTRENST00000540243ENST00000264126MTF2chr1

93545088

+GPSM2chr1

109427897

+
5UTR-5UTRENST00000540243ENST00000406462MTF2chr1

93545088

+GPSM2chr1

109427897

+
5UTR-5UTRENST00000545708ENST00000264126MTF2chr1

93545088

+GPSM2chr1

109427897

+
5UTR-5UTRENST00000545708ENST00000406462MTF2chr1

93545088

+GPSM2chr1

109427897

+
5UTR-intronENST00000540243ENST00000264126MTF2chr1

93545088

+GPSM2chr1

109417955

+
5UTR-intronENST00000540243ENST00000406462MTF2chr1

93545088

+GPSM2chr1

109417955

+
5UTR-intronENST00000545708ENST00000264126MTF2chr1

93545088

+GPSM2chr1

109417955

+
5UTR-intronENST00000545708ENST00000406462MTF2chr1

93545088

+GPSM2chr1

109417955

+

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 MTF2-GPSM2


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.
genomic feature of top 1%

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Fusion Protein Features for MTF2-GPSM2


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/:93545088/:109427897)
- 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
MTF2

Q9Y483

GPSM2

P81274

FUNCTION: Polycomb group (PcG) protein that specifically binds histone H3 trimethylated at 'Lys-36' (H3K36me3) and recruits the PRC2 complex, thus enhancing PRC2 H3K27me3 methylation activity (PubMed:23142980, PubMed:23228662, PubMed:31959557). Regulates the transcriptional networks during embryonic stem cell self-renewal and differentiation (By similarity). Promotes recruitment of the PRC2 complex to the inactive X chromosome in differentiating XX ES cells and PRC2 recruitment to target genes in undifferentiated ES cells (By similarity). Required to repress Hox genes by enhancing H3K27me3 methylation of the PRC2 complex (By similarity). In some conditions may act as an inhibitor of PRC2 activity: able to activate the CDKN2A gene and promote cellular senescence by suppressing the catalytic activity of the PRC2 complex locally (By similarity). Binds to the metal-regulating-element (MRE) of MT1A gene promoter (By similarity). {ECO:0000250|UniProtKB:Q02395, ECO:0000269|PubMed:23142980, ECO:0000269|PubMed:23228662, ECO:0000269|PubMed:31959557}.FUNCTION: Plays an important role in mitotic spindle pole organization via its interaction with NUMA1 (PubMed:11781568, PubMed:15632202, PubMed:21816348). Required for cortical dynein-dynactin complex recruitment during metaphase (PubMed:22327364). Plays a role in metaphase spindle orientation (PubMed:22327364). Plays also an important role in asymmetric cell divisions (PubMed:21816348). Has guanine nucleotide dissociation inhibitor (GDI) activity towards G(i) alpha proteins, such as GNAI1 and GNAI3, and thereby regulates their activity (By similarity). {ECO:0000250|UniProtKB:Q8VDU0, ECO:0000269|PubMed:11781568, ECO:0000269|PubMed:15632202, ECO:0000269|PubMed:21816348, ECO:0000269|PubMed:22327364}.

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 MTF2-GPSM2


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 MTF2-GPSM2


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 MTF2-GPSM2


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 MTF2-GPSM2


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