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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: 29759

FusionGeneSummary for PXDN_PXDN

check button Fusion gene summary
Fusion gene informationFusion gene name: PXDN_PXDN
Fusion gene ID: 29759
HgeneTgene
Gene symbol

PXDN

PXDN

Gene ID

7837

7837

Gene nameperoxidasinperoxidasin
SynonymsASGD7|COPOA|D2S448|D2S448E|MG50|PRG2|PXN|VPOASGD7|COPOA|D2S448|D2S448E|MG50|PRG2|PXN|VPO
Cytomap

2p25.3

2p25.3

Type of geneprotein-codingprotein-coding
Descriptionperoxidasin homologmelanoma-associated antigen MG50p53-responsive gene 2 proteinvascular peroxidase 1peroxidasin homologmelanoma-associated antigen MG50p53-responsive gene 2 proteinvascular peroxidase 1
Modification date2018052320180523
UniProtAcc

Q92626

Q92626

Ensembl transtripts involved in fusion geneENST00000252804, ENST00000483018, 
ENST00000252804, ENST00000483018, 
Fusion gene scores* DoF score4 X 4 X 3=482 X 2 X 1=4
# samples 42
** MAII scorelog2(4/48*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/4*10)=2.32192809488736
Context

PubMed: PXDN [Title/Abstract] AND PXDN [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
HgenePXDN

GO:0030198

extracellular matrix organization

19590037

HgenePXDN

GO:0042744

hydrogen peroxide catabolic process

18929642

HgenePXDN

GO:0055114

oxidation-reduction process

18929642

TgenePXDN

GO:0030198

extracellular matrix organization

19590037

TgenePXDN

GO:0042744

hydrogen peroxide catabolic process

18929642

TgenePXDN

GO:0055114

oxidation-reduction process

18929642


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
ChiTaRS3.1AI799528PXDNchr2

1637110

+PXDNchr2

1637395

-
* 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-3UTRENST00000252804ENST00000252804PXDNchr2

1637110

+PXDNchr2

1637395

-
intron-intronENST00000252804ENST00000483018PXDNchr2

1637110

+PXDNchr2

1637395

-
intron-3UTRENST00000483018ENST00000252804PXDNchr2

1637110

+PXDNchr2

1637395

-
intron-intronENST00000483018ENST00000483018PXDNchr2

1637110

+PXDNchr2

1637395

-

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FusionProtFeatures for PXDN_PXDN


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

Q92626

PXDN

Q92626

Displays low peroxidase activity and is likely toparticipate in H(2)O(2) metabolism and peroxidative reactions inthe cardiovascular system. Plays a role in extracellular matrixformation. {ECO:0000269|PubMed:18929642,ECO:0000269|PubMed:19590037}. Displays low peroxidase activity and is likely toparticipate in H(2)O(2) metabolism and peroxidative reactions inthe cardiovascular system. Plays a role in extracellular matrixformation. {ECO:0000269|PubMed:18929642,ECO:0000269|PubMed:19590037}.

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 PXDN_PXDN


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 PXDN_PXDN


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 PXDN_PXDN


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 PXDN_PXDN


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePXDNC0023467Leukemia, Myelocytic, Acute1CTD_human
HgenePXDNC0023893Liver Cirrhosis, Experimental1CTD_human
HgenePXDNC3151617CORNEAL OPACIFICATION WITH OTHER OCULAR ANOMALIES1ORPHANET;UNIPROT
TgenePXDNC0023467Leukemia, Myelocytic, Acute1CTD_human
TgenePXDNC0023893Liver Cirrhosis, Experimental1CTD_human
TgenePXDNC3151617CORNEAL OPACIFICATION WITH OTHER OCULAR ANOMALIES1ORPHANET;UNIPROT