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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:CD9-CD9 (FusionGDB2 ID:HG928TG928)

Fusion Gene Summary for CD9-CD9

check button Fusion gene summary
Fusion gene informationFusion gene name: CD9-CD9
Fusion gene ID: hg928tg928
HgeneTgene
Gene symbol

CD9

CD9

Gene ID

928

928

Gene nameCD9 moleculeCD9 molecule
SynonymsBTCC-1|DRAP-27|MIC3|MRP-1|TSPAN-29|TSPAN29BTCC-1|DRAP-27|MIC3|MRP-1|TSPAN-29|TSPAN29
Cytomap('CD9')('CD9')

12p13.31

12p13.31

Type of geneprotein-codingprotein-coding
DescriptionCD9 antigen5H9 antigenBA-2/p24 antigenCD9 antigen (p24)antigen CD9cell growth-inhibiting gene 2 proteinleukocyte antigen MIC3motility related protein-1tetraspanin-29CD9 antigen5H9 antigenBA-2/p24 antigenCD9 antigen (p24)antigen CD9cell growth-inhibiting gene 2 proteinleukocyte antigen MIC3motility related protein-1tetraspanin-29
Modification date2020032720200327
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000009180, ENST00000382518, 
ENST00000382515, ENST00000481267, 
ENST00000481267, ENST00000009180, 
ENST00000382515, ENST00000382518, 
Fusion gene scores* DoF score13 X 11 X 7=10018 X 7 X 6=336
# samples 148
** MAII scorelog2(14/1001*10)=-2.83794324189103
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/336*10)=-2.0703893278914
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CD9 [Title/Abstract] AND CD9 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCD9(6309683)-CD9(6342592), # 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
HgeneCD9

GO:0007155

cell adhesion

7511626

HgeneCD9

GO:0007342

fusion of sperm to egg plasma membrane involved in single fertilization

14575715

HgeneCD9

GO:0051271

negative regulation of cellular component movement

8478605

HgeneCD9

GO:0090331

negative regulation of platelet aggregation

18541721

TgeneCD9

GO:0007155

cell adhesion

7511626

TgeneCD9

GO:0007342

fusion of sperm to egg plasma membrane involved in single fertilization

14575715

TgeneCD9

GO:0051271

negative regulation of cellular component movement

8478605

TgeneCD9

GO:0090331

negative regulation of platelet aggregation

18541721


check buttonFusion gene breakpoints across CD9 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure
check buttonFusion gene breakpoints across CD9 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

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


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Fusion Gene ORF analysis for CD9-CD9

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

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 CD9-CD9


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.
genomic feature

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Fusion Protein Features for CD9-CD9


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/chr12:6309683/chr12:6342592)
- 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
TgeneCD9chr12:6309683chr12:6342592ENST0000000918008112_1950229.0Topological domainExtracellular
TgeneCD9chr12:6309683chr12:6342592ENST0000000918008222_2280229.0Topological domainCytoplasmic
TgeneCD9chr12:6309683chr12:6342592ENST00000009180082_120229.0Topological domainCytoplasmic
TgeneCD9chr12:6309683chr12:6342592ENST000000091800834_550229.0Topological domainExtracellular
TgeneCD9chr12:6309683chr12:6342592ENST000000091800877_870229.0Topological domainCytoplasmic
TgeneCD9chr12:6309683chr12:6342592ENST0000038251809112_1950229.0Topological domainExtracellular
TgeneCD9chr12:6309683chr12:6342592ENST0000038251809222_2280229.0Topological domainCytoplasmic
TgeneCD9chr12:6309683chr12:6342592ENST00000382518092_120229.0Topological domainCytoplasmic
TgeneCD9chr12:6309683chr12:6342592ENST000003825180934_550229.0Topological domainExtracellular
TgeneCD9chr12:6309683chr12:6342592ENST000003825180977_870229.0Topological domainCytoplasmic
TgeneCD9chr12:6309683chr12:6342592ENST000000091800813_330229.0TransmembraneHelical
TgeneCD9chr12:6309683chr12:6342592ENST0000000918008196_2210229.0TransmembraneHelical
TgeneCD9chr12:6309683chr12:6342592ENST000000091800856_760229.0TransmembraneHelical
TgeneCD9chr12:6309683chr12:6342592ENST000000091800888_1110229.0TransmembraneHelical
TgeneCD9chr12:6309683chr12:6342592ENST000003825180913_330229.0TransmembraneHelical
TgeneCD9chr12:6309683chr12:6342592ENST0000038251809196_2210229.0TransmembraneHelical
TgeneCD9chr12:6309683chr12:6342592ENST000003825180956_760229.0TransmembraneHelical
TgeneCD9chr12:6309683chr12:6342592ENST000003825180988_1110229.0TransmembraneHelical

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneCD9chr12:6309683chr12:6342592ENST00000009180-18112_1950229.0Topological domainExtracellular
HgeneCD9chr12:6309683chr12:6342592ENST00000009180-18222_2280229.0Topological domainCytoplasmic
HgeneCD9chr12:6309683chr12:6342592ENST00000009180-182_120229.0Topological domainCytoplasmic
HgeneCD9chr12:6309683chr12:6342592ENST00000009180-1834_550229.0Topological domainExtracellular
HgeneCD9chr12:6309683chr12:6342592ENST00000009180-1877_870229.0Topological domainCytoplasmic
HgeneCD9chr12:6309683chr12:6342592ENST00000382518-19112_1950229.0Topological domainExtracellular
HgeneCD9chr12:6309683chr12:6342592ENST00000382518-19222_2280229.0Topological domainCytoplasmic
HgeneCD9chr12:6309683chr12:6342592ENST00000382518-192_120229.0Topological domainCytoplasmic
HgeneCD9chr12:6309683chr12:6342592ENST00000382518-1934_550229.0Topological domainExtracellular
HgeneCD9chr12:6309683chr12:6342592ENST00000382518-1977_870229.0Topological domainCytoplasmic
HgeneCD9chr12:6309683chr12:6342592ENST00000009180-1813_330229.0TransmembraneHelical
HgeneCD9chr12:6309683chr12:6342592ENST00000009180-18196_2210229.0TransmembraneHelical
HgeneCD9chr12:6309683chr12:6342592ENST00000009180-1856_760229.0TransmembraneHelical
HgeneCD9chr12:6309683chr12:6342592ENST00000009180-1888_1110229.0TransmembraneHelical
HgeneCD9chr12:6309683chr12:6342592ENST00000382518-1913_330229.0TransmembraneHelical
HgeneCD9chr12:6309683chr12:6342592ENST00000382518-19196_2210229.0TransmembraneHelical
HgeneCD9chr12:6309683chr12:6342592ENST00000382518-1956_760229.0TransmembraneHelical
HgeneCD9chr12:6309683chr12:6342592ENST00000382518-1988_1110229.0TransmembraneHelical


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Fusion Gene Sequence for CD9-CD9


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 CD9-CD9


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 CD9-CD9


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 CD9-CD9


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCD9C0007131Non-Small Cell Lung Carcinoma1CTD_human
HgeneCD9C0009402Colorectal Carcinoma1CTD_human
HgeneCD9C0009404Colorectal Neoplasms1CTD_human
HgeneCD9C0017636Glioblastoma1CTD_human
HgeneCD9C0023467Leukemia, Myelocytic, Acute1CTD_human
HgeneCD9C0023890Liver Cirrhosis1CTD_human
HgeneCD9C0026998Acute Myeloid Leukemia, M11CTD_human
HgeneCD9C0027654Embryonal Neoplasm1CTD_human
HgeneCD9C0027658Neoplasms, Germ Cell and Embryonal1CTD_human
HgeneCD9C0027746Nerve Degeneration1CTD_human
HgeneCD9C0033578Prostatic Neoplasms1CTD_human
HgeneCD9C0205851Germ cell tumor1CTD_human
HgeneCD9C0205852Neoplasms, Embryonal and Mixed1CTD_human
HgeneCD9C0239946Fibrosis, Liver1CTD_human
HgeneCD9C0334588Giant Cell Glioblastoma1CTD_human
HgeneCD9C0376358Malignant neoplasm of prostate1CTD_human
HgeneCD9C0740345Germ Cell Cancer1CTD_human
HgeneCD9C0751364Cancer, Embryonal1CTD_human
HgeneCD9C0751365Cancer, Embryonal and Mixed1CTD_human
HgeneCD9C1621958Glioblastoma Multiforme1CTD_human
HgeneCD9C1879321Acute Myeloid Leukemia (AML-M2)1CTD_human
TgeneC0007131Non-Small Cell Lung Carcinoma1CTD_human
TgeneC0009402Colorectal Carcinoma1CTD_human
TgeneC0009404Colorectal Neoplasms1CTD_human
TgeneC0017636Glioblastoma1CTD_human
TgeneC0023467Leukemia, Myelocytic, Acute1CTD_human
TgeneC0023890Liver Cirrhosis1CTD_human
TgeneC0026998Acute Myeloid Leukemia, M11CTD_human
TgeneC0027654Embryonal Neoplasm1CTD_human
TgeneC0027658Neoplasms, Germ Cell and Embryonal1CTD_human
TgeneC0027746Nerve Degeneration1CTD_human
TgeneC0033578Prostatic Neoplasms1CTD_human
TgeneC0205851Germ cell tumor1CTD_human
TgeneC0205852Neoplasms, Embryonal and Mixed1CTD_human
TgeneC0239946Fibrosis, Liver1CTD_human
TgeneC0334588Giant Cell Glioblastoma1CTD_human
TgeneC0376358Malignant neoplasm of prostate1CTD_human
TgeneC0740345Germ Cell Cancer1CTD_human
TgeneC0751364Cancer, Embryonal1CTD_human
TgeneC0751365Cancer, Embryonal and Mixed1CTD_human
TgeneC1621958Glioblastoma Multiforme1CTD_human
TgeneC1879321Acute Myeloid Leukemia (AML-M2)1CTD_human