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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:STAT1-U2SURP (FusionGDB2 ID:86629)

Fusion Gene Summary for STAT1-U2SURP

check button Fusion gene summary
Fusion gene informationFusion gene name: STAT1-U2SURP
Fusion gene ID: 86629
HgeneTgene
Gene symbol

STAT1

U2SURP

Gene ID

6772

23350

Gene namesignal transducer and activator of transcription 1U2 snRNP associated SURP domain containing
SynonymsCANDF7|IMD31A|IMD31B|IMD31C|ISGF-3|STAT91SR140|fSAPa
Cytomap

2q32.2

3q23

Type of geneprotein-codingprotein-coding
Descriptionsignal transducer and activator of transcription 1-alpha/betasignal transducer and activator of transcription 1, 91kDsignal transducer and activator of transcription 1, 91kDatranscription factor ISGF-3 components p91/p84U2 snRNP-associated SURP motif-containing protein140 kDa Ser/Arg-rich domain proteinSer/Arg-rich domain protein, 140 kDaU2-associated SR140 proteinU2-associated protein SR140functional spliceosome-associated protein a
Modification date2020032920200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000361099, ENST00000409465, 
ENST00000540176, ENST00000392322, 
ENST00000392323, 
ENST00000397933, 
ENST00000473835, ENST00000493598, 
Fusion gene scores* DoF score7 X 8 X 3=1689 X 10 X 3=270
# samples 811
** MAII scorelog2(8/168*10)=-1.0703893278914
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(11/270*10)=-1.29545588352617
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: STAT1 [Title/Abstract] AND U2SURP [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointSTAT1(191881304)-U2SURP(142772562), # 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
HgeneSTAT1

GO:0007259

JAK-STAT cascade

22002246

HgeneSTAT1

GO:0010742

macrophage derived foam cell differentiation

26504087

HgeneSTAT1

GO:0032727

positive regulation of interferon-alpha production

28753426

HgeneSTAT1

GO:0033209

tumor necrosis factor-mediated signaling pathway

10848577

HgeneSTAT1

GO:0045893

positive regulation of transcription, DNA-templated

10973496

HgeneSTAT1

GO:0051607

defense response to virus

28753426

HgeneSTAT1

GO:0060333

interferon-gamma-mediated signaling pathway

21268089

HgeneSTAT1

GO:0060337

type I interferon signaling pathway

23386060

HgeneSTAT1

GO:0071346

cellular response to interferon-gamma

23386060


check buttonFusion gene breakpoints across STAT1 (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 U2SURP (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/AAA160277STAT1chr2

191881304

+U2SURPchr3

142772562

-


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Fusion Gene ORF analysis for STAT1-U2SURP

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-3CDSENST00000361099ENST00000397933STAT1chr2

191881304

+U2SURPchr3

142772562

-
intron-3CDSENST00000361099ENST00000473835STAT1chr2

191881304

+U2SURPchr3

142772562

-
intron-3CDSENST00000361099ENST00000493598STAT1chr2

191881304

+U2SURPchr3

142772562

-
intron-3CDSENST00000409465ENST00000397933STAT1chr2

191881304

+U2SURPchr3

142772562

-
intron-3CDSENST00000409465ENST00000473835STAT1chr2

191881304

+U2SURPchr3

142772562

-
intron-3CDSENST00000409465ENST00000493598STAT1chr2

191881304

+U2SURPchr3

142772562

-
intron-3CDSENST00000540176ENST00000397933STAT1chr2

191881304

+U2SURPchr3

142772562

-
intron-3CDSENST00000540176ENST00000473835STAT1chr2

191881304

+U2SURPchr3

142772562

-
intron-3CDSENST00000540176ENST00000493598STAT1chr2

191881304

+U2SURPchr3

142772562

-
intron-3CDSENST00000392322ENST00000397933STAT1chr2

191881304

+U2SURPchr3

142772562

-
intron-3CDSENST00000392322ENST00000473835STAT1chr2

191881304

+U2SURPchr3

142772562

-
intron-3CDSENST00000392322ENST00000493598STAT1chr2

191881304

+U2SURPchr3

142772562

-
intron-3CDSENST00000392323ENST00000397933STAT1chr2

191881304

+U2SURPchr3

142772562

-
intron-3CDSENST00000392323ENST00000473835STAT1chr2

191881304

+U2SURPchr3

142772562

-
intron-3CDSENST00000392323ENST00000493598STAT1chr2

191881304

+U2SURPchr3

142772562

-

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 STAT1-U2SURP


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 STAT1-U2SURP


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


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Fusion Gene Sequence for STAT1-U2SURP


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 STAT1-U2SURP


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 STAT1-U2SURP


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 STAT1-U2SURP


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSTAT1C3151088IMMUNODEFICIENCY 31B8CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgeneSTAT1C3279990CANDIDIASIS, FAMILIAL, 78CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgeneSTAT1C4013950IMMUNODEFICIENCY 31A5CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgeneSTAT1C0003865Arthritis, Adjuvant-Induced1CTD_human
HgeneSTAT1C0003873Rheumatoid Arthritis1CTD_human
HgeneSTAT1C0006845Candidiasis, Chronic Mucocutaneous1CTD_human
HgeneSTAT1C0010823Cytomegalovirus Infections1CTD_human
HgeneSTAT1C0021400Influenza1CTD_human
HgeneSTAT1C0023890Liver Cirrhosis1CTD_human
HgeneSTAT1C0026918Mycobacterium Infections1CTD_human
HgeneSTAT1C0027627Neoplasm Metastasis1CTD_human
HgeneSTAT1C0235874Disease Exacerbation1CTD_human
HgeneSTAT1C0239946Fibrosis, Liver1CTD_human
HgeneSTAT1C0494261Combined immunodeficiency1GENOMICS_ENGLAND
HgeneSTAT1C0971858Arthritis, Collagen-Induced1CTD_human
HgeneSTAT1C0993582Arthritis, Experimental1CTD_human
HgeneSTAT1C1384666hearing impairment1CTD_human
HgeneSTAT1C1961099Precursor T-Cell Lymphoblastic Leukemia-Lymphoma1CTD_human
HgeneSTAT1C2239176Liver carcinoma1CTD_human
TgeneU2SURPC0023893Liver Cirrhosis, Experimental1CTD_human