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:TNFAIP3-IL26 (FusionGDB2 ID:91965)

Fusion Gene Summary for TNFAIP3-IL26

check button Fusion gene summary
Fusion gene informationFusion gene name: TNFAIP3-IL26
Fusion gene ID: 91965
HgeneTgene
Gene symbol

TNFAIP3

IL26

Gene ID

7128

55801

Gene nameTNF alpha induced protein 3interleukin 26
SynonymsA20|AISBL|OTUD7C|TNFA1P2AK155|IL-26
Cytomap

6q23.3

12q15

Type of geneprotein-codingprotein-coding
Descriptiontumor necrosis factor alpha-induced protein 3OTU domain-containing protein 7Cputative DNA-binding protein A20tumor necrosis factor inducible protein A20tumor necrosis factor, alpha induced protein 3zinc finger protein A20interleukin-26
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000237289, ENST00000485192, 
ENST00000229134, 
Fusion gene scores* DoF score2 X 2 X 2=85 X 2 X 2=20
# samples 25
** MAII scorelog2(2/8*10)=1.32192809488736log2(5/20*10)=1.32192809488736
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: TNFAIP3 [Title/Abstract] AND IL26 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointTNFAIP3(138192659)-IL26(68595863), # samples:2
Anticipated loss of major functional domain due to fusion event.TNFAIP3-IL26 seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
TNFAIP3-IL26 seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
* 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
HgeneTNFAIP3

GO:0002237

response to molecule of bacterial origin

19912257

HgeneTNFAIP3

GO:0031397

negative regulation of protein ubiquitination

20392859

HgeneTNFAIP3

GO:0032088

negative regulation of NF-kappaB transcription factor activity

18223652

HgeneTNFAIP3

GO:0034140

negative regulation of toll-like receptor 3 signaling pathway

15474016

HgeneTNFAIP3

GO:0035871

protein K11-linked deubiquitination

23827681

HgeneTNFAIP3

GO:0043124

negative regulation of I-kappaB kinase/NF-kappaB signaling

11463333|15258597|21127049

HgeneTNFAIP3

GO:0045732

positive regulation of protein catabolic process

21127049

HgeneTNFAIP3

GO:0048662

negative regulation of smooth muscle cell proliferation

16816117

HgeneTNFAIP3

GO:0070536

protein K63-linked deubiquitination

15258597

HgeneTNFAIP3

GO:0070936

protein K48-linked ubiquitination

15258597

HgeneTNFAIP3

GO:0071108

protein K48-linked deubiquitination

23827681

HgeneTNFAIP3

GO:0071222

cellular response to lipopolysaccharide

19912257|21127049|21220427

HgeneTNFAIP3

GO:1902042

negative regulation of extrinsic apoptotic signaling pathway via death domain receptors

12167698

HgeneTNFAIP3

GO:2000352

negative regulation of endothelial cell apoptotic process

12885753

TgeneIL26

GO:0032874

positive regulation of stress-activated MAPK cascade

18483078

TgeneIL26

GO:0045944

positive regulation of transcription by RNA polymerase II

18483078

TgeneIL26

GO:0046427

positive regulation of JAK-STAT cascade

18483078

TgeneIL26

GO:0050680

negative regulation of epithelial cell proliferation

18483078

TgeneIL26

GO:0050715

positive regulation of cytokine secretion

18483078

TgeneIL26

GO:0051897

positive regulation of protein kinase B signaling

18483078

TgeneIL26

GO:0070374

positive regulation of ERK1 and ERK2 cascade

18483078


check buttonFusion gene breakpoints across TNFAIP3 (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 IL26 (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
ChimerDB4SARCTCGA-DX-A6BH-01ATNFAIP3chr6

138192659

+IL26chr12

68595863

-
ChimerDB4SARCTCGA-DX-A6BH-01ATNFAIP3chr6

138192659

-IL26chr12

68595863

-


Top

Fusion Gene ORF analysis for TNFAIP3-IL26

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
Frame-shiftENST00000237289ENST00000229134TNFAIP3chr6

138192659

+IL26chr12

68595863

-
intron-3CDSENST00000485192ENST00000229134TNFAIP3chr6

138192659

+IL26chr12

68595863

-

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 TNFAIP3-IL26


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.

Top

Fusion Protein Features for TNFAIP3-IL26


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
..
FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.

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 TNFAIP3-IL26


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 TNFAIP3-IL26


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 TNFAIP3-IL26


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 TNFAIP3-IL26


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneTNFAIP3C0024141Lupus Erythematosus, Systemic9CTD_human;ORPHANET
HgeneTNFAIP3C0003873Rheumatoid Arthritis5CTD_human
HgeneTNFAIP3C0242380Libman-Sacks Disease4CTD_human
HgeneTNFAIP3C4225218AUTOINFLAMMATORY SYNDROME, FAMILIAL, BEHCET-LIKE3CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgeneTNFAIP3C0030246Pustulosis of Palms and Soles2CTD_human
HgeneTNFAIP3C0033860Psoriasis2CTD_human
HgeneTNFAIP3C0086981Sicca Syndrome2CTD_human
HgeneTNFAIP3C1527336Sjogren's Syndrome2CTD_human
HgeneTNFAIP3C0004364Autoimmune Diseases1CTD_human
HgeneTNFAIP3C0007621Neoplastic Cell Transformation1CTD_human
HgeneTNFAIP3C0021368Inflammation1CTD_human
HgeneTNFAIP3C0024301Lymphoma, Follicular1CTD_human
HgeneTNFAIP3C0026769Multiple Sclerosis1CTD_human
HgeneTNFAIP3C0079745Lymphoma, Large-Cell, Follicular1CTD_human
HgeneTNFAIP3C0079758Lymphoma, Mixed-Cell, Follicular1CTD_human
HgeneTNFAIP3C0079765Lymphoma, Small Cleaved-Cell, Follicular1CTD_human
HgeneTNFAIP3C0079773Lymphoma, T-Cell, Cutaneous1CTD_human
HgeneTNFAIP3C0376407Granulomatous Slack Skin1CTD_human
HgeneTNFAIP3C0751324Multiple Sclerosis, Acute Fulminating1CTD_human
HgeneTNFAIP3C0751422Hereditary Autoinflammatory Diseases1CTD_human
HgeneTNFAIP3C1328840Autoimmune Lymphoproliferative Syndrome1GENOMICS_ENGLAND
HgeneTNFAIP3C1956130Lymphoma, Follicular, Grade 11CTD_human
HgeneTNFAIP3C1956131Lymphoma, Follicular, Grade 31CTD_human
HgeneTNFAIP3C1956132Lymphoma, Follicular, Grade 21CTD_human
HgeneTNFAIP3C3860213Autoinflammatory disorder1GENOMICS_ENGLAND