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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:IL7-GSS (FusionGDB2 ID:39427)

Fusion Gene Summary for IL7-GSS

check button Fusion gene summary
Fusion gene informationFusion gene name: IL7-GSS
Fusion gene ID: 39427
HgeneTgene
Gene symbol

IL7

GSS

Gene ID

3574

5621

Gene nameinterleukin 7prion protein
SynonymsIL-7ASCR|AltPrP|CD230|CJD|GSS|KURU|PRIP|PrP|PrP27-30|PrP33-35C|PrPc|p27-30
Cytomap

8q21.13

20p13

Type of geneprotein-codingprotein-coding
Descriptioninterleukin-7major prion proteinalternative prion proteinCD230 antigenprion-related protein
Modification date2020031320200315
UniProtAcc.

P48637

Ensembl transtripts involved in fusion geneENST00000263851, ENST00000520269, 
ENST00000379113, ENST00000519833, 
ENST00000541183, 
ENST00000216951, 
ENST00000541098, ENST00000451957, 
Fusion gene scores* DoF score1 X 1 X 1=19 X 8 X 3=216
# samples 19
** MAII scorelog2(1/1*10)=3.32192809488736log2(9/216*10)=-1.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: IL7 [Title/Abstract] AND GSS [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointIL7(79627472)-GSS(33530340), # 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
HgeneIL7

GO:0001961

positive regulation of cytokine-mediated signaling pathway

11418668

HgeneIL7

GO:0019221

cytokine-mediated signaling pathway

11418668

HgeneIL7

GO:0032722

positive regulation of chemokine production

11418668

TgeneGSS

GO:0050731

positive regulation of peptidyl-tyrosine phosphorylation

22820466

TgeneGSS

GO:0071280

cellular response to copper ion

16254249


check buttonFusion gene breakpoints across IL7 (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 GSS (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
ChiTaRS5.0N/AAI802443IL7chr8

79627472

-GSSchr20

33530340

+


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Fusion Gene ORF analysis for IL7-GSS

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
intron-3CDSENST00000263851ENST00000216951IL7chr8

79627472

-GSSchr20

33530340

+
intron-3CDSENST00000263851ENST00000541098IL7chr8

79627472

-GSSchr20

33530340

+
intron-intronENST00000263851ENST00000451957IL7chr8

79627472

-GSSchr20

33530340

+
intron-3CDSENST00000520269ENST00000216951IL7chr8

79627472

-GSSchr20

33530340

+
intron-3CDSENST00000520269ENST00000541098IL7chr8

79627472

-GSSchr20

33530340

+
intron-intronENST00000520269ENST00000451957IL7chr8

79627472

-GSSchr20

33530340

+
intron-3CDSENST00000379113ENST00000216951IL7chr8

79627472

-GSSchr20

33530340

+
intron-3CDSENST00000379113ENST00000541098IL7chr8

79627472

-GSSchr20

33530340

+
intron-intronENST00000379113ENST00000451957IL7chr8

79627472

-GSSchr20

33530340

+
intron-3CDSENST00000519833ENST00000216951IL7chr8

79627472

-GSSchr20

33530340

+
intron-3CDSENST00000519833ENST00000541098IL7chr8

79627472

-GSSchr20

33530340

+
intron-intronENST00000519833ENST00000451957IL7chr8

79627472

-GSSchr20

33530340

+
intron-3CDSENST00000541183ENST00000216951IL7chr8

79627472

-GSSchr20

33530340

+
intron-3CDSENST00000541183ENST00000541098IL7chr8

79627472

-GSSchr20

33530340

+
intron-intronENST00000541183ENST00000451957IL7chr8

79627472

-GSSchr20

33530340

+

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 IL7-GSS


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.

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Fusion Protein Features for IL7-GSS


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
.GSS

P48637

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


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Fusion Gene Sequence for IL7-GSS


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 IL7-GSS


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 IL7-GSS


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneGSSP48637DB06151AcetylcysteineStimulatorSmall moleculeApproved|Investigational
TgeneGSSP48637DB09130CopperSmall moleculeApproved|Investigational
TgeneGSSP48637DB00143GlutathioneSmall moleculeApproved|Investigational|Nutraceutical
TgeneGSSP48637DB00151CysteineSmall moleculeApproved|Nutraceutical
TgeneGSSP48637DB00145GlycineSubstrateSmall moleculeApproved|Nutraceutical|Vet_approved

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Related Diseases for IL7-GSS


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneIL7C0014522Epidermodysplasia Verruciformis1ORPHANET
HgeneIL7C0024312Lymphopenia1CTD_human
HgeneIL7C0026769Multiple Sclerosis1CTD_human
HgeneIL7C0751324Multiple Sclerosis, Acute Fulminating1CTD_human
TgeneGSSC0398746Gluthathione synthetase deficiency15CLINGEN;CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
TgeneGSSC1856399Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to5CTD_human;GENOMICS_ENGLAND;ORPHANET
TgeneGSSC0520572Enzymopathy2GENOMICS_ENGLAND
TgeneGSSC0007097Carcinoma1CTD_human
TgeneGSSC0011616Contact Dermatitis1CTD_human
TgeneGSSC0024667Animal Mammary Neoplasms1CTD_human
TgeneGSSC0024668Mammary Neoplasms, Experimental1CTD_human
TgeneGSSC0026636Mouth Diseases1CTD_human
TgeneGSSC0162351Contact hypersensitivity1CTD_human
TgeneGSSC0205696Anaplastic carcinoma1CTD_human
TgeneGSSC0205697Carcinoma, Spindle-Cell1CTD_human
TgeneGSSC0205698Undifferentiated carcinoma1CTD_human
TgeneGSSC0205699Carcinomatosis1CTD_human
TgeneGSSC1257925Mammary Carcinoma, Animal1CTD_human