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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:DENND1A-SLC26A7 (FusionGDB2 ID:22207)

Fusion Gene Summary for DENND1A-SLC26A7

check button Fusion gene summary
Fusion gene informationFusion gene name: DENND1A-SLC26A7
Fusion gene ID: 22207
HgeneTgene
Gene symbol

DENND1A

SLC26A7

Gene ID

57706

115111

Gene nameDENN domain containing 1Asolute carrier family 26 member 7
SynonymsFAM31A|KIAA1608SUT2
Cytomap

9q33.3

8q21.3

Type of geneprotein-codingprotein-coding
DescriptionDENN domain-containing protein 1ADENN/MADD domain containing 1Aconnecdenn 1anion exchange transportersolute carrier family 26 (anion exchanger), member 7solute carrier family 6 member 7sulfate anion transporter
Modification date2020032020200313
UniProtAcc

Q8TEH3

.
Ensembl transtripts involved in fusion geneENST00000373618, ENST00000373620, 
ENST00000373624, ENST00000394215, 
ENST00000394219, ENST00000473039, 
ENST00000542603, 
ENST00000523719, 
ENST00000276609, ENST00000309536, 
ENST00000520249, 
Fusion gene scores* DoF score18 X 18 X 14=45369 X 8 X 6=432
# samples 269
** MAII scorelog2(26/4536*10)=-4.12483711191377
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(9/432*10)=-2.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: DENND1A [Title/Abstract] AND SLC26A7 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointDENND1A(126519982)-SLC26A7(92231118), # samples:2
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
HgeneDENND1A

GO:0032483

regulation of Rab protein signal transduction

20937701

TgeneSLC26A7

GO:0006820

anion transport

11834742

TgeneSLC26A7

GO:0006821

chloride transport

1183472

TgeneSLC26A7

GO:0008272

sulfate transport

1183472

TgeneSLC26A7

GO:0019532

oxalate transport

1183472


check buttonFusion gene breakpoints across DENND1A (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 SLC26A7 (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
ChimerDB4BRCATCGA-A2-A0T1-01ADENND1Achr9

126519982

-SLC26A7chr8

92231118

+


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Fusion Gene ORF analysis for DENND1A-SLC26A7

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-5UTRENST00000373618ENST00000523719DENND1Achr9

126519982

-SLC26A7chr8

92231118

+
5CDS-5UTRENST00000373620ENST00000523719DENND1Achr9

126519982

-SLC26A7chr8

92231118

+
5CDS-5UTRENST00000373624ENST00000523719DENND1Achr9

126519982

-SLC26A7chr8

92231118

+
5CDS-5UTRENST00000394215ENST00000523719DENND1Achr9

126519982

-SLC26A7chr8

92231118

+
5CDS-5UTRENST00000394219ENST00000523719DENND1Achr9

126519982

-SLC26A7chr8

92231118

+
5CDS-intronENST00000373618ENST00000276609DENND1Achr9

126519982

-SLC26A7chr8

92231118

+
5CDS-intronENST00000373618ENST00000309536DENND1Achr9

126519982

-SLC26A7chr8

92231118

+
5CDS-intronENST00000373618ENST00000520249DENND1Achr9

126519982

-SLC26A7chr8

92231118

+
5CDS-intronENST00000373620ENST00000276609DENND1Achr9

126519982

-SLC26A7chr8

92231118

+
5CDS-intronENST00000373620ENST00000309536DENND1Achr9

126519982

-SLC26A7chr8

92231118

+
5CDS-intronENST00000373620ENST00000520249DENND1Achr9

126519982

-SLC26A7chr8

92231118

+
5CDS-intronENST00000373624ENST00000276609DENND1Achr9

126519982

-SLC26A7chr8

92231118

+
5CDS-intronENST00000373624ENST00000309536DENND1Achr9

126519982

-SLC26A7chr8

92231118

+
5CDS-intronENST00000373624ENST00000520249DENND1Achr9

126519982

-SLC26A7chr8

92231118

+
5CDS-intronENST00000394215ENST00000276609DENND1Achr9

126519982

-SLC26A7chr8

92231118

+
5CDS-intronENST00000394215ENST00000309536DENND1Achr9

126519982

-SLC26A7chr8

92231118

+
5CDS-intronENST00000394215ENST00000520249DENND1Achr9

126519982

-SLC26A7chr8

92231118

+
5CDS-intronENST00000394219ENST00000276609DENND1Achr9

126519982

-SLC26A7chr8

92231118

+
5CDS-intronENST00000394219ENST00000309536DENND1Achr9

126519982

-SLC26A7chr8

92231118

+
5CDS-intronENST00000394219ENST00000520249DENND1Achr9

126519982

-SLC26A7chr8

92231118

+
5UTR-5UTRENST00000473039ENST00000523719DENND1Achr9

126519982

-SLC26A7chr8

92231118

+
5UTR-intronENST00000473039ENST00000276609DENND1Achr9

126519982

-SLC26A7chr8

92231118

+
5UTR-intronENST00000473039ENST00000309536DENND1Achr9

126519982

-SLC26A7chr8

92231118

+
5UTR-intronENST00000473039ENST00000520249DENND1Achr9

126519982

-SLC26A7chr8

92231118

+
intron-5UTRENST00000542603ENST00000523719DENND1Achr9

126519982

-SLC26A7chr8

92231118

+
intron-intronENST00000542603ENST00000276609DENND1Achr9

126519982

-SLC26A7chr8

92231118

+
intron-intronENST00000542603ENST00000309536DENND1Achr9

126519982

-SLC26A7chr8

92231118

+
intron-intronENST00000542603ENST00000520249DENND1Achr9

126519982

-SLC26A7chr8

92231118

+

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 DENND1A-SLC26A7


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)
DENND1Achr9126519981-SLC26A7chr892231117+1.62E-050.9999838
DENND1Achr9126519981-SLC26A7chr892231117+1.62E-050.9999838

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 DENND1A-SLC26A7


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/:126519982/:92231118)
- 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
DENND1A

Q8TEH3

.
FUNCTION: Guanine nucleotide exchange factor (GEF) regulating clathrin-mediated endocytosis through RAB35 activation. Promotes the exchange of GDP to GTP, converting inactive GDP-bound RAB35 into its active GTP-bound form. Regulates clathrin-mediated endocytosis of synaptic vesicles and mediates exit from early endosomes (PubMed:20154091, PubMed:20937701). Binds phosphatidylinositol-phosphates (PtdInsPs), with some preference for PtdIns(3)P (By similarity). {ECO:0000250|UniProtKB:Q8K382, ECO:0000269|PubMed:20154091, ECO:0000269|PubMed:20937701}.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 DENND1A-SLC26A7


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 DENND1A-SLC26A7


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 DENND1A-SLC26A7


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 DENND1A-SLC26A7


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