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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:SPDL1-ANXA6 (FusionGDB2 ID:85646)

Fusion Gene Summary for SPDL1-ANXA6

check button Fusion gene summary
Fusion gene informationFusion gene name: SPDL1-ANXA6
Fusion gene ID: 85646
HgeneTgene
Gene symbol

SPDL1

ANXA6

Gene ID

54908

309

Gene namespindle apparatus coiled-coil protein 1annexin A6
SynonymsCCDC99ANX6|CBP68|CPB-II|p68|p70
Cytomap

5q35.1

5q33.1

Type of geneprotein-codingprotein-coding
Descriptionprotein Spindlyarsenite-related gene 1 proteincoiled-coil domain-containing protein 99rhabdomyosarcoma antigen MU-RMS-40.4Arrhabdomyosarcoma antigen protein MU-RMS-40.4Aannexin A667 kDa calelectrinannexin VI (p68)annexin-6calcium-binding protein p68calelectrincalphobindin IIchromobindin-20lipocortin VItestis secretory sperm-binding protein Li 198a
Modification date2020031320200313
UniProtAcc

Q96EA4

P08133

Ensembl transtripts involved in fusion geneENST00000510751, ENST00000265295, 
ENST00000354546, ENST00000356496, 
ENST00000377751, ENST00000521512, 
ENST00000523714, ENST00000519610, 
Fusion gene scores* DoF score5 X 5 X 2=508 X 8 X 5=320
# samples 510
** MAII scorelog2(5/50*10)=0log2(10/320*10)=-1.67807190511264
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SPDL1 [Title/Abstract] AND ANXA6 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointSPDL1(169010893)-ANXA6(150481068), # 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

check buttonFusion gene breakpoints across SPDL1 (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 ANXA6 (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
ChimerDB4SARCTCGA-3B-A9HS-01ASPDL1chr5

169010893

+ANXA6chr5

150481068

-


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Fusion Gene ORF analysis for SPDL1-ANXA6

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-3CDSENST00000510751ENST00000354546SPDL1chr5

169010893

+ANXA6chr5

150481068

-
3UTR-3CDSENST00000510751ENST00000356496SPDL1chr5

169010893

+ANXA6chr5

150481068

-
3UTR-3CDSENST00000510751ENST00000377751SPDL1chr5

169010893

+ANXA6chr5

150481068

-
3UTR-3CDSENST00000510751ENST00000521512SPDL1chr5

169010893

+ANXA6chr5

150481068

-
3UTR-3CDSENST00000510751ENST00000523714SPDL1chr5

169010893

+ANXA6chr5

150481068

-
3UTR-intronENST00000510751ENST00000519610SPDL1chr5

169010893

+ANXA6chr5

150481068

-
5UTR-3CDSENST00000265295ENST00000354546SPDL1chr5

169010893

+ANXA6chr5

150481068

-
5UTR-3CDSENST00000265295ENST00000356496SPDL1chr5

169010893

+ANXA6chr5

150481068

-
5UTR-3CDSENST00000265295ENST00000377751SPDL1chr5

169010893

+ANXA6chr5

150481068

-
5UTR-3CDSENST00000265295ENST00000521512SPDL1chr5

169010893

+ANXA6chr5

150481068

-
5UTR-3CDSENST00000265295ENST00000523714SPDL1chr5

169010893

+ANXA6chr5

150481068

-
5UTR-intronENST00000265295ENST00000519610SPDL1chr5

169010893

+ANXA6chr5

150481068

-

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 SPDL1-ANXA6


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 SPDL1-ANXA6


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/:169010893/:150481068)
- 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
SPDL1

Q96EA4

ANXA6

P08133

FUNCTION: Required for the localization of dynein and dynactin to the mitotic kintochore. Dynein is believed to control the initial lateral interaction between the kinetochore and spindle microtubules and to facilitate the subsequent formation of end-on kinetochore-microtubule attachments mediated by the NDC80 complex. Also required for correct spindle orientation. Does not appear to be required for the removal of spindle assembly checkpoint (SAC) proteins from the kinetochore upon bipolar spindle attachment (PubMed:17576797, PubMed:19468067). Acts as an adapter protein linking the dynein motor complex to various cargos and converts dynein from a non-processive to a highly processive motor in the presence of dynactin. Facilitates the interaction between dynein and dynactin and activates dynein processivity (the ability to move along a microtubule for a long distance without falling off the track) (PubMed:25035494). Plays a role in cell migration (PubMed:30258100). {ECO:0000255|HAMAP-Rule:MF_03041, ECO:0000269|PubMed:17576797, ECO:0000269|PubMed:19468067, ECO:0000269|PubMed:25035494, ECO:0000269|PubMed:30258100}.FUNCTION: May associate with CD21. May regulate the release of Ca(2+) from intracellular stores.

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 SPDL1-ANXA6


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 SPDL1-ANXA6


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 SPDL1-ANXA6


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 SPDL1-ANXA6


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