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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: 39028

FusionGeneSummary for TNS4_GPRC5B

check button Fusion gene summary
Fusion gene informationFusion gene name: TNS4_GPRC5B
Fusion gene ID: 39028
HgeneTgene
Gene symbol

TNS4

GPRC5B

Gene ID

84951

51704

Gene nametensin 4G protein-coupled receptor class C group 5 member B
SynonymsCTEN|PP14434RAIG-2|RAIG2
Cytomap

17q21.2

16p12.3

Type of geneprotein-codingprotein-coding
Descriptiontensin-4C terminal tensin likeC-terminal tensin-like proteinG-protein coupled receptor family C group 5 member BG protein-coupled receptor, family C, group 1, member Bretinoic acid responsive gene proteinretinoic acid-induced gene 2 protein
Modification date2018051920180519
UniProtAcc

Q8IZW8

Q9NZH0

Ensembl transtripts involved in fusion geneENST00000254051, ENST00000300571, 
ENST00000569102, ENST00000535671, 
ENST00000569479, ENST00000537135, 
ENST00000569847, 
Fusion gene scores* DoF score4 X 5 X 4=804 X 4 X 2=32
# samples 54
** MAII scorelog2(5/80*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/32*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: TNS4 [Title/Abstract] AND GPRC5B [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
HgeneTNS4

GO:0008104

protein localization

17190795


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
ChiTaRS3.1BU754064TNS4chr17

38632145

+GPRC5Bchr16

19870553

+
* 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-3UTRENST00000254051ENST00000300571TNS4chr17

38632145

+GPRC5Bchr16

19870553

+
intron-intronENST00000254051ENST00000569102TNS4chr17

38632145

+GPRC5Bchr16

19870553

+
intron-intronENST00000254051ENST00000535671TNS4chr17

38632145

+GPRC5Bchr16

19870553

+
intron-3UTRENST00000254051ENST00000569479TNS4chr17

38632145

+GPRC5Bchr16

19870553

+
intron-intronENST00000254051ENST00000537135TNS4chr17

38632145

+GPRC5Bchr16

19870553

+
intron-intronENST00000254051ENST00000569847TNS4chr17

38632145

+GPRC5Bchr16

19870553

+

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FusionProtFeatures for TNS4_GPRC5B


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
TNS4

Q8IZW8

GPRC5B

Q9NZH0

May be involved in cell migration, cartilage developmentand in linking signal transduction pathways to the cytoskeleton(By similarity). May promote apoptosis, via its cleavage bycaspase-3. {ECO:0000250}. Unknown. This retinoic acid-inducible G-protein coupledreceptor provide evidence for a possible interaction betweenretinoid and G-protein signaling pathways.

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 TNS4_GPRC5B


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 TNS4_GPRC5B


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 TNS4_GPRC5B


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 TNS4_GPRC5B


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