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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 34273

FusionGeneSummary for SLC26A7_TDRD3

check button Fusion gene summary
Fusion gene informationFusion gene name: SLC26A7_TDRD3
Fusion gene ID: 34273
HgeneTgene
Gene symbol

SLC26A7

TDRD3

Gene ID

115111

81550

Gene namesolute carrier family 26 member 7tudor domain containing 3
SynonymsSUT2-
Cytomap

8q21.3

13q21.2

Type of geneprotein-codingprotein-coding
Descriptionanion exchange transportersolute carrier family 26 (anion exchanger), member 7sulfate anion transportertudor domain-containing protein 3
Modification date2018052320180522
UniProtAcc

Q8TE54

Q9H7E2

Ensembl transtripts involved in fusion geneENST00000523719, ENST00000276609, 
ENST00000309536, ENST00000520249, 
ENST00000196169, ENST00000377894, 
ENST00000535286, ENST00000377881, 
ENST00000463109, 
Fusion gene scores* DoF score1 X 1 X 1=15 X 4 X 3=60
# samples 26
** MAII scorelog2(2/1*10)=4.32192809488736log2(6/60*10)=0
Context

PubMed: SLC26A7 [Title/Abstract] AND TDRD3 [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotation
* 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
HgeneSLC26A7

GO:0006820

anion transport

11834742

HgeneSLC26A7

GO:0006821

chloride transport

1183472

HgeneSLC26A7

GO:0008272

sulfate transport

1183472

HgeneSLC26A7

GO:0019532

oxalate transport

1183472


check button Fusion gene information from three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* 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.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS3.1AU137042SLC26A7chr8

92337422

+TDRD3chr13

61146439

+
ChiTaRS3.1AK023578SLC26A7chr8

92337422

+TDRD3chr13

61146439

+
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

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
intron-intronENST00000523719ENST00000196169SLC26A7chr8

92337422

+TDRD3chr13

61146439

+
intron-intronENST00000523719ENST00000377894SLC26A7chr8

92337422

+TDRD3chr13

61146439

+
intron-intronENST00000523719ENST00000535286SLC26A7chr8

92337422

+TDRD3chr13

61146439

+
intron-intronENST00000523719ENST00000377881SLC26A7chr8

92337422

+TDRD3chr13

61146439

+
intron-intronENST00000523719ENST00000463109SLC26A7chr8

92337422

+TDRD3chr13

61146439

+
intron-intronENST00000276609ENST00000196169SLC26A7chr8

92337422

+TDRD3chr13

61146439

+
intron-intronENST00000276609ENST00000377894SLC26A7chr8

92337422

+TDRD3chr13

61146439

+
intron-intronENST00000276609ENST00000535286SLC26A7chr8

92337422

+TDRD3chr13

61146439

+
intron-intronENST00000276609ENST00000377881SLC26A7chr8

92337422

+TDRD3chr13

61146439

+
intron-intronENST00000276609ENST00000463109SLC26A7chr8

92337422

+TDRD3chr13

61146439

+
intron-intronENST00000309536ENST00000196169SLC26A7chr8

92337422

+TDRD3chr13

61146439

+
intron-intronENST00000309536ENST00000377894SLC26A7chr8

92337422

+TDRD3chr13

61146439

+
intron-intronENST00000309536ENST00000535286SLC26A7chr8

92337422

+TDRD3chr13

61146439

+
intron-intronENST00000309536ENST00000377881SLC26A7chr8

92337422

+TDRD3chr13

61146439

+
intron-intronENST00000309536ENST00000463109SLC26A7chr8

92337422

+TDRD3chr13

61146439

+
intron-intronENST00000520249ENST00000196169SLC26A7chr8

92337422

+TDRD3chr13

61146439

+
intron-intronENST00000520249ENST00000377894SLC26A7chr8

92337422

+TDRD3chr13

61146439

+
intron-intronENST00000520249ENST00000535286SLC26A7chr8

92337422

+TDRD3chr13

61146439

+
intron-intronENST00000520249ENST00000377881SLC26A7chr8

92337422

+TDRD3chr13

61146439

+
intron-intronENST00000520249ENST00000463109SLC26A7chr8

92337422

+TDRD3chr13

61146439

+

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FusionProtFeatures for SLC26A7_TDRD3


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
SLC26A7

Q8TE54

TDRD3

Q9H7E2

Acts as a sodium-independent DIDS-sensitive anionexchanger mediating bicarbonate, chloride, sulfate and oxalatetransport. May play a role in the maintenance of the electrolyteand acid-base homeostasis in the kidney, by acting as a distalexcretory segment-specific anion exchanger. Plays a major role ingastric acid secretion. {ECO:0000250|UniProtKB:Q8R2Z3,ECO:0000269|PubMed:11834742, ECO:0000269|PubMed:12736153}. Scaffolding protein that specifically recognizes andbinds dimethylarginine-containing proteins. In nucleus, acts as acoactivator: recognizes and binds asymmetric dimethylation on thecore histone tails associated with transcriptional activation(H3R17me2a and H4R3me2a) and recruits proteins at these arginine-methylated loci. In cytoplasm, may play a role in the assemblyand/or disassembly of mRNA stress granules and in the regulationof translation of target mRNAs by binding Arg/Gly-rich motifs(GAR) in dimethylarginine-containing proteins.{ECO:0000269|PubMed:15955813, ECO:0000269|PubMed:18632687,ECO:0000269|PubMed:21172665}.

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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FusionGeneSequence for SLC26A7_TDRD3


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

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FusionGenePPI for SLC26A7_TDRD3


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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RelatedDrugs for SLC26A7_TDRD3


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for SLC26A7_TDRD3


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSLC26A7C0036341Schizophrenia1CTD_human