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:SBNO2-C1D (FusionGDB2 ID:79350)

Fusion Gene Summary for SBNO2-C1D

check button Fusion gene summary
Fusion gene informationFusion gene name: SBNO2-C1D
Fusion gene ID: 79350
HgeneTgene
Gene symbol

SBNO2

C1D

Gene ID

22904

10438

Gene namestrawberry notch homolog 2C1D nuclear receptor corepressor
SynonymsKIAA0963|SNO|STNOLRP1|Rrp47|SUN-CoR|SUNCOR|hC1D
Cytomap

19p13.3

2p14

Type of geneprotein-codingprotein-coding
Descriptionprotein strawberry notch homolog 2nuclear nucleic acid-binding protein C1DC1D DNA-binding proteinC1D nuclear receptor co-repressornuclear DNA-binding proteinsmall unique nuclear receptor co-repressorsmall unique nuclear receptor corepressor
Modification date2020031320200313
UniProtAcc.

Q13901

Ensembl transtripts involved in fusion geneENST00000361757, ENST00000587024, 
ENST00000438103, 
ENST00000355848, 
ENST00000407324, ENST00000409302, 
ENST00000410067, ENST00000470189, 
Fusion gene scores* DoF score29 X 15 X 16=69606 X 4 X 7=168
# samples 3811
** MAII scorelog2(38/6960*10)=-4.19501598240514
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(11/168*10)=-0.610957709254101
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SBNO2 [Title/Abstract] AND C1D [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointSBNO2(1147308)-C1D(68274451), # samples:3
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
HgeneSBNO2

GO:0071354

cellular response to interleukin-6

25903009


check buttonFusion gene breakpoints across SBNO2 (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 C1D (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
ChimerDB4UCSTCGA-N7-A59B-01ASBNO2chr19

1147308

-C1Dchr2

68274451

-
ChimerDB4UCSTCGA-N7-A59BSBNO2chr19

1147308

-C1Dchr2

68274451

-
ChimerDB4UCSTCGA-N7-A59BSBNO2chr19

1147308

-C1Dchr2

68280269

-
ChimerDB4UCSTCGA-N8-A4POSBNO2chr19

1147308

-C1Dchr2

68274451

-
ChimerDB4UCSTCGA-N8-A4POSBNO2chr19

1147308

-C1Dchr2

68280269

-


Top

Fusion Gene ORF analysis for SBNO2-C1D

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-5UTRENST00000361757ENST00000355848SBNO2chr19

1147308

-C1Dchr2

68274451

-
5CDS-5UTRENST00000361757ENST00000407324SBNO2chr19

1147308

-C1Dchr2

68274451

-
5CDS-5UTRENST00000361757ENST00000409302SBNO2chr19

1147308

-C1Dchr2

68274451

-
5CDS-5UTRENST00000361757ENST00000409302SBNO2chr19

1147308

-C1Dchr2

68280269

-
5CDS-5UTRENST00000361757ENST00000410067SBNO2chr19

1147308

-C1Dchr2

68274451

-
5CDS-5UTRENST00000361757ENST00000470189SBNO2chr19

1147308

-C1Dchr2

68274451

-
5CDS-5UTRENST00000587024ENST00000355848SBNO2chr19

1147308

-C1Dchr2

68274451

-
5CDS-5UTRENST00000587024ENST00000407324SBNO2chr19

1147308

-C1Dchr2

68274451

-
5CDS-5UTRENST00000587024ENST00000409302SBNO2chr19

1147308

-C1Dchr2

68274451

-
5CDS-5UTRENST00000587024ENST00000409302SBNO2chr19

1147308

-C1Dchr2

68280269

-
5CDS-5UTRENST00000587024ENST00000410067SBNO2chr19

1147308

-C1Dchr2

68274451

-
5CDS-5UTRENST00000587024ENST00000470189SBNO2chr19

1147308

-C1Dchr2

68274451

-
5CDS-intronENST00000361757ENST00000355848SBNO2chr19

1147308

-C1Dchr2

68280269

-
5CDS-intronENST00000361757ENST00000407324SBNO2chr19

1147308

-C1Dchr2

68280269

-
5CDS-intronENST00000361757ENST00000410067SBNO2chr19

1147308

-C1Dchr2

68280269

-
5CDS-intronENST00000361757ENST00000470189SBNO2chr19

1147308

-C1Dchr2

68280269

-
5CDS-intronENST00000587024ENST00000355848SBNO2chr19

1147308

-C1Dchr2

68280269

-
5CDS-intronENST00000587024ENST00000407324SBNO2chr19

1147308

-C1Dchr2

68280269

-
5CDS-intronENST00000587024ENST00000410067SBNO2chr19

1147308

-C1Dchr2

68280269

-
5CDS-intronENST00000587024ENST00000470189SBNO2chr19

1147308

-C1Dchr2

68280269

-
intron-5UTRENST00000438103ENST00000355848SBNO2chr19

1147308

-C1Dchr2

68274451

-
intron-5UTRENST00000438103ENST00000407324SBNO2chr19

1147308

-C1Dchr2

68274451

-
intron-5UTRENST00000438103ENST00000409302SBNO2chr19

1147308

-C1Dchr2

68274451

-
intron-5UTRENST00000438103ENST00000409302SBNO2chr19

1147308

-C1Dchr2

68280269

-
intron-5UTRENST00000438103ENST00000410067SBNO2chr19

1147308

-C1Dchr2

68274451

-
intron-5UTRENST00000438103ENST00000470189SBNO2chr19

1147308

-C1Dchr2

68274451

-
intron-intronENST00000438103ENST00000355848SBNO2chr19

1147308

-C1Dchr2

68280269

-
intron-intronENST00000438103ENST00000407324SBNO2chr19

1147308

-C1Dchr2

68280269

-
intron-intronENST00000438103ENST00000410067SBNO2chr19

1147308

-C1Dchr2

68280269

-
intron-intronENST00000438103ENST00000470189SBNO2chr19

1147308

-C1Dchr2

68280269

-

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 SBNO2-C1D


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 SBNO2-C1D


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/:1147308/:68274451)
- 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
.C1D

Q13901

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: Plays a role in the recruitment of the RNA exosome complex to pre-rRNA to mediate the 3'-5' end processing of the 5.8S rRNA; this function may include MPHOSPH6. Can activate PRKDC not only in the presence of linear DNA but also in the presence of supercoiled DNA. Can induce apoptosis in a p53/TP53 dependent manner. May regulate the TRAX/TSN complex formation. Potentiates transcriptional repression by NR1D1 and THRB (By similarity). {ECO:0000250, ECO:0000269|PubMed:10362552, ECO:0000269|PubMed:11801738, ECO:0000269|PubMed:17412707, ECO:0000269|PubMed:9679063}.

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 SBNO2-C1D


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 SBNO2-C1D


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 SBNO2-C1D


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 SBNO2-C1D


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