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:SLC1A5-STAT6 (FusionGDB2 ID:82410)

Fusion Gene Summary for SLC1A5-STAT6

check button Fusion gene summary
Fusion gene informationFusion gene name: SLC1A5-STAT6
Fusion gene ID: 82410
HgeneTgene
Gene symbol

SLC1A5

STAT6

Gene ID

6510

6778

Gene namesolute carrier family 1 member 5signal transducer and activator of transcription 6
SynonymsAAAT|ASCT2|ATBO|M7V1|M7VS1|R16|RDRCD12S1644|IL-4-STAT|STAT6B|STAT6C
Cytomap

19q13.32

12q13.3

Type of geneprotein-codingprotein-coding
Descriptionneutral amino acid transporter B(0)ATB(0)RD114 virus receptorRD114/simian type D retrovirus receptorbaboon M7 virus receptorneutral amino acid transporter Bsodium-dependent neutral amino acid transporter type 2solute carrier family 1 (neutral aminosignal transducer and activator of transcription 6STAT, interleukin4-inducedsignal transducer and activator of transcription 6, interleukin-4 inducedtranscription factor IL-4 STAT
Modification date2020031520200329
UniProtAcc.

P42226

Ensembl transtripts involved in fusion geneENST00000434726, ENST00000542575, 
ENST00000594991, ENST00000412532, 
ENST00000300134, ENST00000454075, 
ENST00000537215, ENST00000538913, 
ENST00000543873, ENST00000556155, 
Fusion gene scores* DoF score9 X 8 X 3=21642 X 21 X 17=14994
# samples 1046
** MAII scorelog2(10/216*10)=-1.11103131238874
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(46/14994*10)=-5.02660763586348
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SLC1A5 [Title/Abstract] AND STAT6 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointSLC1A5(47278142)-STAT6(57496773), # 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
HgeneSLC1A5

GO:0006868

glutamine transport

29872227

HgeneSLC1A5

GO:0070207

protein homotrimerization

29872227

TgeneSTAT6

GO:0045944

positive regulation of transcription by RNA polymerase II

8810328


check buttonFusion gene breakpoints across SLC1A5 (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 STAT6 (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
ChimerDB4PRADTCGA-CH-5743-01ASLC1A5chr19

47278142

-STAT6chr12

57496773

-


Top

Fusion Gene ORF analysis for SLC1A5-STAT6

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-intronENST00000434726ENST00000300134SLC1A5chr19

47278142

-STAT6chr12

57496773

-
5CDS-intronENST00000434726ENST00000454075SLC1A5chr19

47278142

-STAT6chr12

57496773

-
5CDS-intronENST00000434726ENST00000537215SLC1A5chr19

47278142

-STAT6chr12

57496773

-
5CDS-intronENST00000434726ENST00000538913SLC1A5chr19

47278142

-STAT6chr12

57496773

-
5CDS-intronENST00000434726ENST00000543873SLC1A5chr19

47278142

-STAT6chr12

57496773

-
5CDS-intronENST00000434726ENST00000556155SLC1A5chr19

47278142

-STAT6chr12

57496773

-
5CDS-intronENST00000542575ENST00000300134SLC1A5chr19

47278142

-STAT6chr12

57496773

-
5CDS-intronENST00000542575ENST00000454075SLC1A5chr19

47278142

-STAT6chr12

57496773

-
5CDS-intronENST00000542575ENST00000537215SLC1A5chr19

47278142

-STAT6chr12

57496773

-
5CDS-intronENST00000542575ENST00000538913SLC1A5chr19

47278142

-STAT6chr12

57496773

-
5CDS-intronENST00000542575ENST00000543873SLC1A5chr19

47278142

-STAT6chr12

57496773

-
5CDS-intronENST00000542575ENST00000556155SLC1A5chr19

47278142

-STAT6chr12

57496773

-
5CDS-intronENST00000594991ENST00000300134SLC1A5chr19

47278142

-STAT6chr12

57496773

-
5CDS-intronENST00000594991ENST00000454075SLC1A5chr19

47278142

-STAT6chr12

57496773

-
5CDS-intronENST00000594991ENST00000537215SLC1A5chr19

47278142

-STAT6chr12

57496773

-
5CDS-intronENST00000594991ENST00000538913SLC1A5chr19

47278142

-STAT6chr12

57496773

-
5CDS-intronENST00000594991ENST00000543873SLC1A5chr19

47278142

-STAT6chr12

57496773

-
5CDS-intronENST00000594991ENST00000556155SLC1A5chr19

47278142

-STAT6chr12

57496773

-
intron-intronENST00000412532ENST00000300134SLC1A5chr19

47278142

-STAT6chr12

57496773

-
intron-intronENST00000412532ENST00000454075SLC1A5chr19

47278142

-STAT6chr12

57496773

-
intron-intronENST00000412532ENST00000537215SLC1A5chr19

47278142

-STAT6chr12

57496773

-
intron-intronENST00000412532ENST00000538913SLC1A5chr19

47278142

-STAT6chr12

57496773

-
intron-intronENST00000412532ENST00000543873SLC1A5chr19

47278142

-STAT6chr12

57496773

-
intron-intronENST00000412532ENST00000556155SLC1A5chr19

47278142

-STAT6chr12

57496773

-

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 SLC1A5-STAT6


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 SLC1A5-STAT6


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/:47278142/:57496773)
- 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
.STAT6

P42226

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: Carries out a dual function: signal transduction and activation of transcription. Involved in IL4/interleukin-4- and IL3/interleukin-3-mediated signaling. {ECO:0000269|PubMed:17210636}.

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 SLC1A5-STAT6


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 SLC1A5-STAT6


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 SLC1A5-STAT6


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 SLC1A5-STAT6


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource