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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: 37749

FusionGeneSummary for TESC_PSMA7

check button Fusion gene summary
Fusion gene informationFusion gene name: TESC_PSMA7
Fusion gene ID: 37749
HgeneTgene
Gene symbol

TESC

PSMA7

Gene ID

54997

5688

Gene nametescalcinproteasome subunit alpha 7
SynonymsCHP3|TSCC6|HEL-S-276|HSPC|RC6-1|XAPC7
Cytomap

12q24.22

20q13.33

Type of geneprotein-codingprotein-coding
Descriptioncalcineurin B homologous protein 3calcineurin-like EF hand protein 3proteasome subunit alpha type-7epididymis secretory protein Li 276proteasome (prosome, macropain) subunit, alpha type, 7proteasome subunit RC6-1proteasome subunit XAPC7proteasome subunit alpha 4testicular tissue protein Li 151
Modification date2018051920180523
UniProtAcc

Q96BS2

O14818

Ensembl transtripts involved in fusion geneENST00000335209, ENST00000541210, 
ENST00000392545, ENST00000535198, 
ENST00000370873, ENST00000484488, 
ENST00000370861, ENST00000370858, 
Fusion gene scores* DoF score4 X 4 X 4=644 X 5 X 2=40
# samples 45
** MAII scorelog2(4/64*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/40*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: TESC [Title/Abstract] AND PSMA7 [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
HgeneTESC

GO:0030854

positive regulation of granulocyte differentiation

20060826

HgeneTESC

GO:0032417

positive regulation of sodium:proton antiporter activity

18321853

HgeneTESC

GO:0050821

protein stabilization

18321853

HgeneTESC

GO:0051604

protein maturation

18321853

HgeneTESC

GO:0071300

cellular response to retinoic acid

20060826

HgeneTESC

GO:0072659

protein localization to plasma membrane

18321853


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
ChiTaRS3.1BG474310TESCchr12

117476879

-PSMA7chr20

60714913

-
* 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-3CDSENST00000335209ENST00000370873TESCchr12

117476879

-PSMA7chr20

60714913

-
intron-5UTRENST00000335209ENST00000484488TESCchr12

117476879

-PSMA7chr20

60714913

-
intron-5UTRENST00000335209ENST00000370861TESCchr12

117476879

-PSMA7chr20

60714913

-
intron-5UTRENST00000335209ENST00000370858TESCchr12

117476879

-PSMA7chr20

60714913

-
intron-3CDSENST00000541210ENST00000370873TESCchr12

117476879

-PSMA7chr20

60714913

-
intron-5UTRENST00000541210ENST00000484488TESCchr12

117476879

-PSMA7chr20

60714913

-
intron-5UTRENST00000541210ENST00000370861TESCchr12

117476879

-PSMA7chr20

60714913

-
intron-5UTRENST00000541210ENST00000370858TESCchr12

117476879

-PSMA7chr20

60714913

-
intron-3CDSENST00000392545ENST00000370873TESCchr12

117476879

-PSMA7chr20

60714913

-
intron-5UTRENST00000392545ENST00000484488TESCchr12

117476879

-PSMA7chr20

60714913

-
intron-5UTRENST00000392545ENST00000370861TESCchr12

117476879

-PSMA7chr20

60714913

-
intron-5UTRENST00000392545ENST00000370858TESCchr12

117476879

-PSMA7chr20

60714913

-
intron-3CDSENST00000535198ENST00000370873TESCchr12

117476879

-PSMA7chr20

60714913

-
intron-5UTRENST00000535198ENST00000484488TESCchr12

117476879

-PSMA7chr20

60714913

-
intron-5UTRENST00000535198ENST00000370861TESCchr12

117476879

-PSMA7chr20

60714913

-
intron-5UTRENST00000535198ENST00000370858TESCchr12

117476879

-PSMA7chr20

60714913

-

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FusionProtFeatures for TESC_PSMA7


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

Q96BS2

PSMA7

O14818

Functions as an integral cofactor in cell pH regulationby controlling plasma membrane-type Na(+)/H(+) exchange activity.Promotes the maturation, transport, cell surface stability andexchange activity of SLC9A1/NHE1 at the plasma membrane. Promotesthe induction of hematopoietic stem cell differentiation towardmegakaryocytic lineage. Essential for the coupling of ERK cascadeactivation with the expression of ETS family genes inmegakaryocytic differentiation. Also involved in granulocyticdifferentiation in a ERK-dependent manner. Inhibits thephosphatase activity of calcineurin. {ECO:0000269|PubMed:17717601,ECO:0000269|PubMed:18321853, ECO:0000269|PubMed:20060826}. Component of the 20S core proteasome complex involved inthe proteolytic degradation of most intracellular proteins. Thiscomplex plays numerous essential roles within the cell byassociating with different regulatory particles. Associated withtwo 19S regulatory particles, forms the 26S proteasome and thusparticipates in the ATP-dependent degradation of ubiquitinatedproteins. The 26S proteasome plays a key role in the maintenanceof protein homeostasis by removing misfolded or damaged proteinsthat could impair cellular functions, and by removing proteinswhose functions are no longer required. Associated with the PA200or PA28, the 20S proteasome mediates ubiquitin-independent proteindegradation. This type of proteolysis is required in severalpathways including spermatogenesis (20S-PA200 complex) orgeneration of a subset of MHC class I-presented antigenic peptides(20S-PA28 complex). Inhibits the transactivation function of HIF-1A under both normoxic and hypoxia-mimicking conditions. Theinteraction with EMAP2 increases the proteasome-mediated HIF-1Adegradation under the hypoxic conditions. Plays a role inhepatitis C virus internal ribosome entry site-mediatedtranslation. Mediates nuclear translocation of the androgenreceptor (AR) and thereby enhances androgen-mediatedtransactivation. Promotes MAVS degradation and thereby negativelyregulates MAVS-mediated innate immune response.{ECO:0000269|PubMed:11389899, ECO:0000269|PubMed:11713272,ECO:0000269|PubMed:12119296, ECO:0000269|PubMed:15244466,ECO:0000269|PubMed:19442227, ECO:0000269|PubMed:19734229,ECO:0000269|PubMed:27176742, ECO:0000269|PubMed:8610016}.

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 TESC_PSMA7


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 TESC_PSMA7


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 TESC_PSMA7


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 TESC_PSMA7


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