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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: 29092

FusionGeneSummary for PSG3_PSG6

check button Fusion gene summary
Fusion gene informationFusion gene name: PSG3_PSG6
Fusion gene ID: 29092
HgeneTgene
Gene symbol

PSG3

PSG6

Gene ID

5671

5675

Gene namepregnancy specific beta-1-glycoprotein 3pregnancy specific beta-1-glycoprotein 6
Synonyms-PSBG-10|PSBG-12|PSBG-6|PSG10|PSGGB
Cytomap

19q13.2

19q13.31

Type of geneprotein-codingprotein-coding
Descriptionpregnancy-specific beta-1-glycoprotein 3PS-beta-G-3PSBG-3carcinoembryonic antigen SG5pregnancy-specific glycoprotein 3pregnancy-specific beta-1-glycoprotein 6PS-beta-G-10PS-beta-G-12PS-beta-G-6pregnancy-specific beta-1-glycoprotein 10pregnancy-specific beta-1-glycoprotein 12
Modification date2018051920180519
UniProtAcc

Q16557

Q00889

Ensembl transtripts involved in fusion geneENST00000327495, ENST00000595140, 
ENST00000490592, 
ENST00000187910, 
ENST00000402603, ENST00000292125, 
ENST00000601833, 
Fusion gene scores* DoF score1 X 1 X 1=12 X 2 X 1=4
# samples 23
** MAII scorelog2(2/1*10)=4.32192809488736log2(3/4*10)=2.90689059560852
Context

PubMed: PSG3 [Title/Abstract] AND PSG6 [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
ChiTaRS3.1BE928986PSG3chr19

43233410

+PSG6chr19

43519369

-
ChiTaRS3.1BE928953PSG3chr19

43233410

+PSG6chr19

43519369

-
* 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-intronENST00000327495ENST00000187910PSG3chr19

43233410

+PSG6chr19

43519369

-
intron-intronENST00000327495ENST00000402603PSG3chr19

43233410

+PSG6chr19

43519369

-
intron-intronENST00000327495ENST00000292125PSG3chr19

43233410

+PSG6chr19

43519369

-
intron-intronENST00000327495ENST00000601833PSG3chr19

43233410

+PSG6chr19

43519369

-
intron-intronENST00000595140ENST00000187910PSG3chr19

43233410

+PSG6chr19

43519369

-
intron-intronENST00000595140ENST00000402603PSG3chr19

43233410

+PSG6chr19

43519369

-
intron-intronENST00000595140ENST00000292125PSG3chr19

43233410

+PSG6chr19

43519369

-
intron-intronENST00000595140ENST00000601833PSG3chr19

43233410

+PSG6chr19

43519369

-
intron-intronENST00000490592ENST00000187910PSG3chr19

43233410

+PSG6chr19

43519369

-
intron-intronENST00000490592ENST00000402603PSG3chr19

43233410

+PSG6chr19

43519369

-
intron-intronENST00000490592ENST00000292125PSG3chr19

43233410

+PSG6chr19

43519369

-
intron-intronENST00000490592ENST00000601833PSG3chr19

43233410

+PSG6chr19

43519369

-

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FusionProtFeatures for PSG3_PSG6


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
PSG3

Q16557

PSG6

Q00889


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 PSG3_PSG6


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 PSG3_PSG6


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 PSG3_PSG6


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 PSG3_PSG6


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