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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:SDCBP-ANKRD31 (FusionGDB2 ID:79832)

Fusion Gene Summary for SDCBP-ANKRD31

check button Fusion gene summary
Fusion gene informationFusion gene name: SDCBP-ANKRD31
Fusion gene ID: 79832
HgeneTgene
Gene symbol

SDCBP

ANKRD31

Gene ID

6386

256006

Gene namesyndecan binding proteinankyrin repeat domain 31
SynonymsMDA-9|MDA9|ST1|SYCL|TACIP18-
Cytomap

8q12.1

5q13.3

Type of geneprotein-codingprotein-coding
Descriptionsyntenin-1melanoma differentiation associated protein-9pro-TGF-alpha cytoplasmic domain-interacting protein 18scaffold protein Pbp1syndecan binding protein (syntenin)syndecan-binding protein 1ankyrin repeat domain-containing protein 31putative ankyrin repeat domain-containing protein 31
Modification date2020032720200313
UniProtAcc.

Q8N7Z5

Ensembl transtripts involved in fusion geneENST00000260130, ENST00000413219, 
ENST00000422546, ENST00000447182, 
ENST00000523483, ENST00000424270, 
ENST00000447267, ENST00000520168, 
ENST00000522243, 		ENST00000274361, 
ENST00000504022, ENST00000506364, 
Fusion gene scores* DoF score10 X 10 X 3=3004 X 6 X 4=96
# samples 125
** MAII scorelog2(12/300*10)=-1.32192809488736
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0		log2(5/96*10)=-0.941106310946431
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SDCBP [Title/Abstract] AND ANKRD31 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointSDCBP(59494745)-ANKRD31(74401181), # 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
HgeneSDCBP

GO:0042327

positive regulation of phosphorylation

18256285


check buttonFusion gene breakpoints across SDCBP (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 ANKRD31 (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/AFN078794SDCBPchr8

59494745

+ANKRD31chr5

74401181

+


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Fusion Gene ORF analysis for SDCBP-ANKRD31

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
3UTR-intronENST00000260130ENST00000274361SDCBPchr8

59494745

+ANKRD31chr5

74401181

+
3UTR-intronENST00000260130ENST00000504022SDCBPchr8

59494745

+ANKRD31chr5

74401181

+
3UTR-intronENST00000260130ENST00000506364SDCBPchr8

59494745

+ANKRD31chr5

74401181

+
3UTR-intronENST00000413219ENST00000274361SDCBPchr8

59494745

+ANKRD31chr5

74401181

+
3UTR-intronENST00000413219ENST00000504022SDCBPchr8

59494745

+ANKRD31chr5

74401181

+
3UTR-intronENST00000413219ENST00000506364SDCBPchr8

59494745

+ANKRD31chr5

74401181

+
3UTR-intronENST00000422546ENST00000274361SDCBPchr8

59494745

+ANKRD31chr5

74401181

+
3UTR-intronENST00000422546ENST00000504022SDCBPchr8

59494745

+ANKRD31chr5

74401181

+
3UTR-intronENST00000422546ENST00000506364SDCBPchr8

59494745

+ANKRD31chr5

74401181

+
3UTR-intronENST00000447182ENST00000274361SDCBPchr8

59494745

+ANKRD31chr5

74401181

+
3UTR-intronENST00000447182ENST00000504022SDCBPchr8

59494745

+ANKRD31chr5

74401181

+
3UTR-intronENST00000447182ENST00000506364SDCBPchr8

59494745

+ANKRD31chr5

74401181

+
3UTR-intronENST00000523483ENST00000274361SDCBPchr8

59494745

+ANKRD31chr5

74401181

+
3UTR-intronENST00000523483ENST00000504022SDCBPchr8

59494745

+ANKRD31chr5

74401181

+
3UTR-intronENST00000523483ENST00000506364SDCBPchr8

59494745

+ANKRD31chr5

74401181

+
intron-intronENST00000424270ENST00000274361SDCBPchr8

59494745

+ANKRD31chr5

74401181

+
intron-intronENST00000424270ENST00000504022SDCBPchr8

59494745

+ANKRD31chr5

74401181

+
intron-intronENST00000424270ENST00000506364SDCBPchr8

59494745

+ANKRD31chr5

74401181

+
intron-intronENST00000447267ENST00000274361SDCBPchr8

59494745

+ANKRD31chr5

74401181

+
intron-intronENST00000447267ENST00000504022SDCBPchr8

59494745

+ANKRD31chr5

74401181

+
intron-intronENST00000447267ENST00000506364SDCBPchr8

59494745

+ANKRD31chr5

74401181

+
intron-intronENST00000520168ENST00000274361SDCBPchr8

59494745

+ANKRD31chr5

74401181

+
intron-intronENST00000520168ENST00000504022SDCBPchr8

59494745

+ANKRD31chr5

74401181

+
intron-intronENST00000520168ENST00000506364SDCBPchr8

59494745

+ANKRD31chr5

74401181

+
intron-intronENST00000522243ENST00000274361SDCBPchr8

59494745

+ANKRD31chr5

74401181

+
intron-intronENST00000522243ENST00000504022SDCBPchr8

59494745

+ANKRD31chr5

74401181

+
intron-intronENST00000522243ENST00000506364SDCBPchr8

59494745

+ANKRD31chr5

74401181

+

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 SDCBP-ANKRD31


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 SDCBP-ANKRD31


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/:59494745/:74401181)
- 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
.ANKRD31

Q8N7Z5

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: Required for DNA double-strand breaks (DSBs) formation during meiotic recombination. Regulates the spatial and temporal patterns of pre-DSB recombinosome assembly and recombination activity by acting as a scaffold that anchors REC114 and other factors to specific genomic locations, thereby regulating DSB formation. Plays a key role in recombination in the pseudoautosomal regions of sex chromosomes. {ECO:0000250|UniProtKB:A0A140LI88}.

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 SDCBP-ANKRD31


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 SDCBP-ANKRD31


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 SDCBP-ANKRD31


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 SDCBP-ANKRD31


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