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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: 26732

FusionGeneSummary for PEX7_PEX7

check button Fusion gene summary
Fusion gene informationFusion gene name: PEX7_PEX7
Fusion gene ID: 26732
HgeneTgene
Gene symbol

PEX7

PEX7

Gene ID

5191

5191

Gene nameperoxisomal biogenesis factor 7peroxisomal biogenesis factor 7
SynonymsPBD9B|PTS2R|RCDP1|RDPBD9B|PTS2R|RCDP1|RD
Cytomap

6q23.3

6q23.3

Type of geneprotein-codingprotein-coding
Descriptionperoxisomal biogenesis factor 7PTS2 receptorperoxin-7peroxisomal PTS2 receptorperoxisomal targeting signal 2 receptorperoxisome targeting signal 2 receptorperoxisomal biogenesis factor 7PTS2 receptorperoxin-7peroxisomal PTS2 receptorperoxisomal targeting signal 2 receptorperoxisome targeting signal 2 receptor
Modification date2018052220180522
UniProtAcc

O00628

O00628

Ensembl transtripts involved in fusion geneENST00000541292, ENST00000318471, 
ENST00000367756, 
ENST00000541292, 
ENST00000318471, ENST00000367756, 
Fusion gene scores* DoF score3 X 3 X 2=181 X 1 X 1=1
# samples 31
** MAII scorelog2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(1/1*10)=3.32192809488736
Context

PubMed: PEX7 [Title/Abstract] AND PEX7 [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
HgenePEX7

GO:0016558

protein import into peroxisome matrix

9090381

TgenePEX7

GO:0016558

protein import into peroxisome matrix

9090381


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
ChiTaRS3.1BQ640052PEX7chr6

137180879

+PEX7chr6

137176704

+
* 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-intronENST00000541292ENST00000541292PEX7chr6

137180879

+PEX7chr6

137176704

+
intron-intronENST00000541292ENST00000318471PEX7chr6

137180879

+PEX7chr6

137176704

+
intron-intronENST00000541292ENST00000367756PEX7chr6

137180879

+PEX7chr6

137176704

+
intron-intronENST00000318471ENST00000541292PEX7chr6

137180879

+PEX7chr6

137176704

+
intron-intronENST00000318471ENST00000318471PEX7chr6

137180879

+PEX7chr6

137176704

+
intron-intronENST00000318471ENST00000367756PEX7chr6

137180879

+PEX7chr6

137176704

+
intron-intronENST00000367756ENST00000541292PEX7chr6

137180879

+PEX7chr6

137176704

+
intron-intronENST00000367756ENST00000318471PEX7chr6

137180879

+PEX7chr6

137176704

+
intron-intronENST00000367756ENST00000367756PEX7chr6

137180879

+PEX7chr6

137176704

+

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FusionProtFeatures for PEX7_PEX7


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
PEX7

O00628

PEX7

O00628

Binds to the N-terminal PTS2-type peroxisomal targetingsignal and plays an essential role in peroxisomal protein import. Binds to the N-terminal PTS2-type peroxisomal targetingsignal and plays an essential role in peroxisomal protein import.

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 PEX7_PEX7


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 PEX7_PEX7


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 PEX7_PEX7


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 PEX7_PEX7


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePEX7C1859133RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 13CTD_human;ORPHANET;UNIPROT
HgenePEX7C0034960Refsum Disease1CTD_human;ORPHANET
HgenePEX7C0282529Chondrodysplasia Punctata, Rhizomelic1CTD_human
HgenePEX7C2749346Refsum Disease, Adult, 21UNIPROT
TgenePEX7C1859133RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 13CTD_human;ORPHANET;UNIPROT
TgenePEX7C0034960Refsum Disease1CTD_human;ORPHANET
TgenePEX7C0282529Chondrodysplasia Punctata, Rhizomelic1CTD_human
TgenePEX7C2749346Refsum Disease, Adult, 21UNIPROT