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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:GPSM1-TMC6 (FusionGDB2 ID:HG26086TG11322)

Fusion Gene Summary for GPSM1-TMC6

check button Fusion gene summary
Fusion gene informationFusion gene name: GPSM1-TMC6
Fusion gene ID: hg26086tg11322
HgeneTgene
Gene symbol

GPSM1

TMC6

Gene ID

26086

11322

Gene nameG protein signaling modulator 1transmembrane channel like 6
SynonymsAGS3EV1|EVER1|EVIN1|LAK-4P
Cytomap('GPSM1')('TMC6')

9q34.3

17q25.3

Type of geneprotein-codingprotein-coding
DescriptionG-protein-signaling modulator 1G-protein signalling modulator 1 (AGS3-like, C. elegans)activator of G-protein signaling 3transmembrane channel-like protein 6epidermodysplasia verruciformis 1epidermodysplasia verruciformis protein 1expressed in activated T/LAK lymphocytesprotein LAK-4
Modification date2020031320200320
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000392945, ENST00000440944, 
ENST00000392944, ENST00000429455, 
Fusion gene scores* DoF score2 X 3 X 2=123 X 3 X 3=27
# samples 33
** MAII scorelog2(3/12*10)=1.32192809488736
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: GPSM1 [Title/Abstract] AND TMC6 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointGPSM1(139234272)-TMC6(76122987), # 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
HgeneGPSM1

GO:0016239

positive regulation of macroautophagy

12642577

HgeneGPSM1

GO:0034260

negative regulation of GTPase activity

11024022

HgeneGPSM1

GO:1905098

negative regulation of guanyl-nucleotide exchange factor activity

11024022



check button Fusion gene information
* 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
ChimerDB4Non-CancerERR315486GPSM1chr9

139234272

+TMC6chr17

76122987

-


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Fusion Gene ORF analysis for GPSM1-TMC6

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-5UTRENST00000392945ENST00000306591GPSM1chr9

139234272

+TMC6chr17

76122987

-
5CDS-5UTRENST00000392945ENST00000322914GPSM1chr9

139234272

+TMC6chr17

76122987

-
5CDS-5UTRENST00000392945ENST00000322933GPSM1chr9

139234272

+TMC6chr17

76122987

-
5CDS-5UTRENST00000392945ENST00000392467GPSM1chr9

139234272

+TMC6chr17

76122987

-
5CDS-5UTRENST00000392945ENST00000590602GPSM1chr9

139234272

+TMC6chr17

76122987

-
5CDS-5UTRENST00000440944ENST00000306591GPSM1chr9

139234272

+TMC6chr17

76122987

-
5CDS-5UTRENST00000440944ENST00000322914GPSM1chr9

139234272

+TMC6chr17

76122987

-
5CDS-5UTRENST00000440944ENST00000322933GPSM1chr9

139234272

+TMC6chr17

76122987

-
5CDS-5UTRENST00000440944ENST00000392467GPSM1chr9

139234272

+TMC6chr17

76122987

-
5CDS-5UTRENST00000440944ENST00000590602GPSM1chr9

139234272

+TMC6chr17

76122987

-
5CDS-intronENST00000392945ENST00000589553GPSM1chr9

139234272

+TMC6chr17

76122987

-
5CDS-intronENST00000392945ENST00000591436GPSM1chr9

139234272

+TMC6chr17

76122987

-
5CDS-intronENST00000392945ENST00000592076GPSM1chr9

139234272

+TMC6chr17

76122987

-
5CDS-intronENST00000440944ENST00000589553GPSM1chr9

139234272

+TMC6chr17

76122987

-
5CDS-intronENST00000440944ENST00000591436GPSM1chr9

139234272

+TMC6chr17

76122987

-
5CDS-intronENST00000440944ENST00000592076GPSM1chr9

139234272

+TMC6chr17

76122987

-
intron-5UTRENST00000392944ENST00000306591GPSM1chr9

139234272

+TMC6chr17

76122987

-
intron-5UTRENST00000392944ENST00000322914GPSM1chr9

139234272

+TMC6chr17

76122987

-
intron-5UTRENST00000392944ENST00000322933GPSM1chr9

139234272

+TMC6chr17

76122987

-
intron-5UTRENST00000392944ENST00000392467GPSM1chr9

139234272

+TMC6chr17

76122987

-
intron-5UTRENST00000392944ENST00000590602GPSM1chr9

139234272

+TMC6chr17

76122987

-
intron-5UTRENST00000429455ENST00000306591GPSM1chr9

139234272

+TMC6chr17

76122987

-
intron-5UTRENST00000429455ENST00000322914GPSM1chr9

139234272

+TMC6chr17

76122987

-
intron-5UTRENST00000429455ENST00000322933GPSM1chr9

139234272

+TMC6chr17

76122987

-
intron-5UTRENST00000429455ENST00000392467GPSM1chr9

139234272

+TMC6chr17

76122987

-
intron-5UTRENST00000429455ENST00000590602GPSM1chr9

139234272

+TMC6chr17

76122987

-
intron-intronENST00000392944ENST00000589553GPSM1chr9

139234272

+TMC6chr17

76122987

-
intron-intronENST00000392944ENST00000591436GPSM1chr9

139234272

+TMC6chr17

76122987

-
intron-intronENST00000392944ENST00000592076GPSM1chr9

139234272

+TMC6chr17

76122987

-
intron-intronENST00000429455ENST00000589553GPSM1chr9

139234272

+TMC6chr17

76122987

-
intron-intronENST00000429455ENST00000591436GPSM1chr9

139234272

+TMC6chr17

76122987

-
intron-intronENST00000429455ENST00000592076GPSM1chr9

139234272

+TMC6chr17

76122987

-

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 GPSM1-TMC6


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)


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Fusion Protein Features for GPSM1-TMC6


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/:139234272/:76122987)
- 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
..
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}.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 GPSM1-TMC6


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 GPSM1-TMC6


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 GPSM1-TMC6


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 GPSM1-TMC6


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneGPSM1C0009171Cocaine Abuse1CTD_human
HgeneGPSM1C0236736Cocaine-Related Disorders1CTD_human
HgeneGPSM1C0600427Cocaine Dependence1CTD_human
TgeneC4722564EPIDERMODYSPLASIA VERRUCIFORMIS, SUSCEPTIBILITY TO, 13GENOMICS_ENGLAND
TgeneC0014522Epidermodysplasia Verruciformis1CTD_human;GENOMICS_ENGLAND;ORPHANET