Fusion Gene Studies
in Kim Lab

FusionBase FusionGDB FusionGDB2 FusionPDB FusionNeoAntigen FusionAI FusionNW FGviewer Publication Contact
FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

Fusion Gene Summary

leaf

Fusion Gene ORF analysis

leaf

Fusion Genomic Features

leaf

Fusion Protein Features

leaf

Fusion Gene Sequence

leaf

Fusion Gene PPI analysis

leaf

Related Drugs

leaf

Related Diseases

Fusion gene:TNFAIP6-TNFAIP6 (FusionGDB2 ID:HG7130TG7130)

Fusion Gene Summary for TNFAIP6-TNFAIP6

check button Fusion gene summary
Fusion gene informationFusion gene name: TNFAIP6-TNFAIP6
Fusion gene ID: hg7130tg7130
HgeneTgene
Gene symbol

TNFAIP6

TNFAIP6

Gene ID

7130

7130

Gene nameTNF alpha induced protein 6TNF alpha induced protein 6
SynonymsTSG-6|TSG6TSG-6|TSG6
Cytomap('TNFAIP6')('TNFAIP6')

2q23.3

2q23.3

Type of geneprotein-codingprotein-coding
Descriptiontumor necrosis factor-inducible gene 6 proteinTNF-stimulated gene 6 proteinhyaluronate-binding proteintumor necrosis factor alpha-inducible protein 6tumor necrosis factor, alpha induced protein 6tumor necrosis factor-stimulated gene-6 proteintumor necrosis factor-inducible gene 6 proteinTNF-stimulated gene 6 proteinhyaluronate-binding proteintumor necrosis factor alpha-inducible protein 6tumor necrosis factor, alpha induced protein 6tumor necrosis factor-stimulated gene-6 protein
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000243347, ENST00000243347, 
Fusion gene scores* DoF score2 X 2 X 2=82 X 2 X 2=8
# samples 22
** MAII scorelog2(2/8*10)=1.32192809488736log2(2/8*10)=1.32192809488736
Context

PubMed: TNFAIP6 [Title/Abstract] AND TNFAIP6 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointTNFAIP6(152236317)-TNFAIP6(152236312), # 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
HgeneTNFAIP6

GO:0050728

negative regulation of inflammatory response

21569482

TgeneTNFAIP6

GO:0050728

negative regulation of inflammatory response

21569482



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/AAA484887TNFAIP6chr2

152236317

+TNFAIP6chr2

152236312

-


Top

Fusion Gene ORF analysis for TNFAIP6-TNFAIP6

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-3UTRENST00000243347ENST00000243347TNFAIP6chr2

152236317

+TNFAIP6chr2

152236312

-

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

Top

Fusion Genomic Features for TNFAIP6-TNFAIP6


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)


Top

Fusion Protein Features for TNFAIP6-TNFAIP6


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/:152236317/:152236312)
- 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


Top

Fusion Gene Sequence for TNFAIP6-TNFAIP6


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.

Top

Fusion Gene PPI Analysis for TNFAIP6-TNFAIP6


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


Top

Related Drugs for TNFAIP6-TNFAIP6


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

Top

Related Diseases for TNFAIP6-TNFAIP6


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneTNFAIP6C0162820Dermatitis, Allergic Contact2CTD_human
HgeneTNFAIP6C0021400Influenza1CTD_human
HgeneTNFAIP6C0037274Dermatologic disorders1CTD_human
HgeneTNFAIP6C0087031Juvenile-Onset Still Disease1CTD_human
HgeneTNFAIP6C0238281Middle Cerebral Artery Syndrome1CTD_human
HgeneTNFAIP6C0242488Acute Lung Injury1CTD_human
HgeneTNFAIP6C0274861Arsenic Poisoning, Inorganic1CTD_human
HgeneTNFAIP6C0274862Nervous System, Organic Arsenic Poisoning1CTD_human
HgeneTNFAIP6C0311375Arsenic Poisoning1CTD_human
HgeneTNFAIP6C0740376Middle Cerebral Artery Thrombosis1CTD_human
HgeneTNFAIP6C0740391Middle Cerebral Artery Occlusion1CTD_human
HgeneTNFAIP6C0740392Infarction, Middle Cerebral Artery1CTD_human
HgeneTNFAIP6C0751845Middle Cerebral Artery Embolus1CTD_human
HgeneTNFAIP6C0751846Left Middle Cerebral Artery Infarction1CTD_human
HgeneTNFAIP6C0751847Embolic Infarction, Middle Cerebral Artery1CTD_human
HgeneTNFAIP6C0751848Thrombotic Infarction, Middle Cerebral Artery1CTD_human
HgeneTNFAIP6C0751849Right Middle Cerebral Artery Infarction1CTD_human
HgeneTNFAIP6C0751851Arsenic Encephalopathy1CTD_human
HgeneTNFAIP6C0751852Arsenic Induced Polyneuropathy1CTD_human
HgeneTNFAIP6C3495559Juvenile arthritis1CTD_human
HgeneTNFAIP6C3714758Juvenile psoriatic arthritis1CTD_human
HgeneTNFAIP6C4552091Polyarthritis, Juvenile, Rheumatoid Factor Negative1CTD_human
HgeneTNFAIP6C4704862Polyarthritis, Juvenile, Rheumatoid Factor Positive1CTD_human
TgeneC0162820Dermatitis, Allergic Contact2CTD_human
TgeneC0021400Influenza1CTD_human
TgeneC0037274Dermatologic disorders1CTD_human
TgeneC0087031Juvenile-Onset Still Disease1CTD_human
TgeneC0238281Middle Cerebral Artery Syndrome1CTD_human
TgeneC0242488Acute Lung Injury1CTD_human
TgeneC0274861Arsenic Poisoning, Inorganic1CTD_human
TgeneC0274862Nervous System, Organic Arsenic Poisoning1CTD_human
TgeneC0311375Arsenic Poisoning1CTD_human
TgeneC0740376Middle Cerebral Artery Thrombosis1CTD_human
TgeneC0740391Middle Cerebral Artery Occlusion1CTD_human
TgeneC0740392Infarction, Middle Cerebral Artery1CTD_human
TgeneC0751845Middle Cerebral Artery Embolus1CTD_human
TgeneC0751846Left Middle Cerebral Artery Infarction1CTD_human
TgeneC0751847Embolic Infarction, Middle Cerebral Artery1CTD_human
TgeneC0751848Thrombotic Infarction, Middle Cerebral Artery1CTD_human
TgeneC0751849Right Middle Cerebral Artery Infarction1CTD_human
TgeneC0751851Arsenic Encephalopathy1CTD_human
TgeneC0751852Arsenic Induced Polyneuropathy1CTD_human
TgeneC3495559Juvenile arthritis1CTD_human
TgeneC3714758Juvenile psoriatic arthritis1CTD_human
TgeneC4552091Polyarthritis, Juvenile, Rheumatoid Factor Negative1CTD_human
TgeneC4704862Polyarthritis, Juvenile, Rheumatoid Factor Positive1CTD_human