FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

FusionGeneSummary

leaf

FusionProtFeature

leaf

FusionGeneSequence

leaf

FusionGenePPI

leaf

RelatedDrugs

leaf

RelatedDiseases

Fusion gene ID: 39276

FusionGeneSummary for TPT1_PLEKHB2

check button Fusion gene summary
Fusion gene informationFusion gene name: TPT1_PLEKHB2
Fusion gene ID: 39276
HgeneTgene
Gene symbol

TPT1

PLEKHB2

Gene ID

7178

55041

Gene nametumor protein, translationally-controlled 1pleckstrin homology domain containing B2
SynonymsHRF|TCTP|p02|p23EVT2
Cytomap

13q14.13

2q21.1

Type of geneprotein-codingprotein-coding
Descriptiontranslationally-controlled tumor proteinfortilinhistamine-releasing factorpleckstrin homology domain-containing family B member 2PH domain-containing family B member 2evectin-2pleckstrin homology domain containing, family B (evectins) member 2
Modification date2018052320180523
UniProtAcc

P13693

Q96CS7

Ensembl transtripts involved in fusion geneENST00000379056, ENST00000529421, 
ENST00000530705, ENST00000379060, 
ENST00000379055, ENST00000309246, 
ENST00000404460, ENST00000303908, 
ENST00000409158, ENST00000403716, 
ENST00000234115, ENST00000439822, 
ENST00000487980, ENST00000438882, 
ENST00000538982, ENST00000409612, 
ENST00000409279, 
Fusion gene scores* DoF score13 X 6 X 11=85813 X 3 X 10=390
# samples 1715
** MAII scorelog2(17/858*10)=-2.33544290136184
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(15/390*10)=-1.37851162325373
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: TPT1 [Title/Abstract] AND PLEKHB2 [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

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
TCGARVPRADTCGA-HC-A6HY-01ATPT1chr13

45911008

-PLEKHB2chr2

131876464

+
* 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
5CDS-intronENST00000379056ENST00000404460TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
5CDS-intronENST00000379056ENST00000303908TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
5CDS-intronENST00000379056ENST00000409158TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
5CDS-intronENST00000379056ENST00000403716TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
5CDS-intronENST00000379056ENST00000234115TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
5CDS-intronENST00000379056ENST00000439822TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
5CDS-intronENST00000379056ENST00000487980TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
5CDS-intronENST00000379056ENST00000438882TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
5CDS-intronENST00000379056ENST00000538982TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
5CDS-intronENST00000379056ENST00000409612TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
5CDS-intronENST00000379056ENST00000409279TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000529421ENST00000404460TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000529421ENST00000303908TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000529421ENST00000409158TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000529421ENST00000403716TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000529421ENST00000234115TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000529421ENST00000439822TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000529421ENST00000487980TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000529421ENST00000438882TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000529421ENST00000538982TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000529421ENST00000409612TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000529421ENST00000409279TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000530705ENST00000404460TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000530705ENST00000303908TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000530705ENST00000409158TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000530705ENST00000403716TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000530705ENST00000234115TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000530705ENST00000439822TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000530705ENST00000487980TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000530705ENST00000438882TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000530705ENST00000538982TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000530705ENST00000409612TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000530705ENST00000409279TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000379060ENST00000404460TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000379060ENST00000303908TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000379060ENST00000409158TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000379060ENST00000403716TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000379060ENST00000234115TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000379060ENST00000439822TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000379060ENST00000487980TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000379060ENST00000438882TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000379060ENST00000538982TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000379060ENST00000409612TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000379060ENST00000409279TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000379055ENST00000404460TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000379055ENST00000303908TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000379055ENST00000409158TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000379055ENST00000403716TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000379055ENST00000234115TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000379055ENST00000439822TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000379055ENST00000487980TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000379055ENST00000438882TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000379055ENST00000538982TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000379055ENST00000409612TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000379055ENST00000409279TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000309246ENST00000404460TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000309246ENST00000303908TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000309246ENST00000409158TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000309246ENST00000403716TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000309246ENST00000234115TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000309246ENST00000439822TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000309246ENST00000487980TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000309246ENST00000438882TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000309246ENST00000538982TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000309246ENST00000409612TPT1chr13

45911008

-PLEKHB2chr2

131876464

+
intron-intronENST00000309246ENST00000409279TPT1chr13

45911008

-PLEKHB2chr2

131876464

+

Top

FusionProtFeatures for TPT1_PLEKHB2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
TPT1

P13693

PLEKHB2

Q96CS7

Involved in calcium binding and microtubulestabilization.

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


Top

FusionGeneSequence for TPT1_PLEKHB2


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).

Top

FusionGenePPI for TPT1_PLEKHB2


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
TPT1VHL, FANCA, IKBKG, CALM1, RBBP6, DBN1, RPLP1, TP53, SPP1, CDK2, MDM2, APP, TBCB, LIG4, NKX3-1, BAG3, PER2, BCL2L1, MCL1, TUBB2A, EEF1D, TRIP13, NOTCH3, HSPB1, CALR, NPEPL1, SAMD9, MSH2, MYCBP, LACC1, CST7, EEF1A2, EEF1B2, FOXA1, MCPH1PLEKHB2KRT85, KRT31, KRT82, KRT34, UPF1, CDA, BHLHE40, DAZAP2, STAM2, EPN1, C1orf94, MAP3K1, TMEM231, CST6, ITCH, NCCRP1, ALOXE3, CGRRF1, TRIM25


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


Top

RelatedDrugs for TPT1_PLEKHB2


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneTPT1P13693DB11093Calcium CitrateTranslationally-controlled tumor proteinsmall moleculeapproved
HgeneTPT1P13693DB11348Calcium PhosphateTranslationally-controlled tumor proteinsmall moleculeapproved

Top

RelatedDiseases for TPT1_PLEKHB2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneTPT1C0033578Prostatic Neoplasms1CTD_human
HgeneTPT1C0036341Schizophrenia1PSYGENET