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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:INTS7-SDCCAG8 (FusionGDB2 ID:39982)

Fusion Gene Summary for INTS7-SDCCAG8

check button Fusion gene summary
Fusion gene informationFusion gene name: INTS7-SDCCAG8
Fusion gene ID: 39982
HgeneTgene
Gene symbol

INTS7

SDCCAG8

Gene ID

25896

10806

Gene nameintegrator complex subunit 7SHH signaling and ciliogenesis regulator SDCCAG8
SynonymsC1orf73|INT7BBS16|CCCAP|CCCAP SLSN7|HSPC085|NPHP10|NY-CO-8|SLSN7|hCCCAP
Cytomap

1q32.3

1q43-q44

Type of geneprotein-codingprotein-coding
Descriptionintegrator complex subunit 7serologically defined colon cancer antigen 8Bardet-Biedl syndrome 16antigen NY-CO-8centrosomal colon cancer autoantigen proteinnephrocystin 10
Modification date2020031320200313
UniProtAcc

Q9NVH2

.
Ensembl transtripts involved in fusion geneENST00000366992, ENST00000366993, 
ENST00000366994, ENST00000440600, 
ENST00000469606, 
ENST00000343783, 
ENST00000391846, ENST00000496361, 
ENST00000355875, ENST00000366541, 
Fusion gene scores* DoF score3 X 2 X 3=1822 X 19 X 10=4180
# samples 326
** MAII scorelog2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(26/4180*10)=-4.00691941393979
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: INTS7 [Title/Abstract] AND SDCCAG8 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointINTS7(212208686)-SDCCAG8(243433407), # samples:1
Anticipated loss of major functional domain due to fusion event.INTS7-SDCCAG8 seems lost the major protein functional domain in Hgene partner, which is a essential gene 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
HgeneINTS7

GO:0016180

snRNA processing

16239144

HgeneINTS7

GO:0071479

cellular response to ionizing radiation

21659603


check buttonFusion gene breakpoints across INTS7 (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 SDCCAG8 (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
ChimerDB4STADTCGA-CD-A48C-01AINTS7chr1

212208686

-SDCCAG8chr1

243433407

+


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Fusion Gene ORF analysis for INTS7-SDCCAG8

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-intronENST00000366992ENST00000343783INTS7chr1

212208686

-SDCCAG8chr1

243433407

+
5CDS-intronENST00000366992ENST00000391846INTS7chr1

212208686

-SDCCAG8chr1

243433407

+
5CDS-intronENST00000366992ENST00000496361INTS7chr1

212208686

-SDCCAG8chr1

243433407

+
5CDS-intronENST00000366993ENST00000343783INTS7chr1

212208686

-SDCCAG8chr1

243433407

+
5CDS-intronENST00000366993ENST00000391846INTS7chr1

212208686

-SDCCAG8chr1

243433407

+
5CDS-intronENST00000366993ENST00000496361INTS7chr1

212208686

-SDCCAG8chr1

243433407

+
5CDS-intronENST00000366994ENST00000343783INTS7chr1

212208686

-SDCCAG8chr1

243433407

+
5CDS-intronENST00000366994ENST00000391846INTS7chr1

212208686

-SDCCAG8chr1

243433407

+
5CDS-intronENST00000366994ENST00000496361INTS7chr1

212208686

-SDCCAG8chr1

243433407

+
5CDS-intronENST00000440600ENST00000343783INTS7chr1

212208686

-SDCCAG8chr1

243433407

+
5CDS-intronENST00000440600ENST00000391846INTS7chr1

212208686

-SDCCAG8chr1

243433407

+
5CDS-intronENST00000440600ENST00000496361INTS7chr1

212208686

-SDCCAG8chr1

243433407

+
5UTR-3CDSENST00000469606ENST00000355875INTS7chr1

212208686

-SDCCAG8chr1

243433407

+
5UTR-3CDSENST00000469606ENST00000366541INTS7chr1

212208686

-SDCCAG8chr1

243433407

+
5UTR-intronENST00000469606ENST00000343783INTS7chr1

212208686

-SDCCAG8chr1

243433407

+
5UTR-intronENST00000469606ENST00000391846INTS7chr1

212208686

-SDCCAG8chr1

243433407

+
5UTR-intronENST00000469606ENST00000496361INTS7chr1

212208686

-SDCCAG8chr1

243433407

+
Frame-shiftENST00000366992ENST00000355875INTS7chr1

212208686

-SDCCAG8chr1

243433407

+
Frame-shiftENST00000366992ENST00000366541INTS7chr1

212208686

-SDCCAG8chr1

243433407

+
Frame-shiftENST00000366993ENST00000355875INTS7chr1

212208686

-SDCCAG8chr1

243433407

+
Frame-shiftENST00000366993ENST00000366541INTS7chr1

212208686

-SDCCAG8chr1

243433407

+
Frame-shiftENST00000366994ENST00000355875INTS7chr1

212208686

-SDCCAG8chr1

243433407

+
Frame-shiftENST00000366994ENST00000366541INTS7chr1

212208686

-SDCCAG8chr1

243433407

+
Frame-shiftENST00000440600ENST00000355875INTS7chr1

212208686

-SDCCAG8chr1

243433407

+
Frame-shiftENST00000440600ENST00000366541INTS7chr1

212208686

-SDCCAG8chr1

243433407

+

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 INTS7-SDCCAG8


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)
INTS7chr1212208685-SDCCAG8chr1243433406+0.0572772620.94272274
INTS7chr1212208685-SDCCAG8chr1243433406+0.0572772620.94272274

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.
genomic feature of top 1%

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Fusion Protein Features for INTS7-SDCCAG8


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/:212208686/:243433407)
- 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
INTS7

Q9NVH2

.
FUNCTION: Component of the Integrator (INT) complex, a complex involved in the small nuclear RNAs (snRNA) U1 and U2 transcription and in their 3'-box-dependent processing. The Integrator complex is associated with the C-terminal domain (CTD) of RNA polymerase II largest subunit (POLR2A) and is recruited to the U1 and U2 snRNAs genes (Probable). Plays a role in DNA damage response (DDR) signaling during the S phase (PubMed:21659603). May be not involved in the recruitment of cytoplasmic dynein to the nuclear envelope by different components of the INT complex (PubMed:23904267). {ECO:0000269|PubMed:21659603, ECO:0000269|PubMed:23904267, ECO:0000305|PubMed:16239144}.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


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Fusion Gene Sequence for INTS7-SDCCAG8


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 INTS7-SDCCAG8


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 INTS7-SDCCAG8


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 INTS7-SDCCAG8


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