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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: 35435

FusionGeneSummary for SOX11_PGK1

check button Fusion gene summary
Fusion gene informationFusion gene name: SOX11_PGK1
Fusion gene ID: 35435
HgeneTgene
Gene symbol

SOX11

PGK1

Gene ID

6664

5230

Gene nameSRY-box 11phosphoglycerate kinase 1
SynonymsMRD27HEL-S-68p|MIG10|PGKA
Cytomap

2p25.2

Xq21.1

Type of geneprotein-codingprotein-coding
Descriptiontranscription factor SOX-11SRY (sex-determining region Y)-box 11SRY-related HMG-box gene 11phosphoglycerate kinase 1PRP 2cell migration-inducing gene 10 proteinepididymis secretory sperm binding protein Li 68pprimer recognition protein 2
Modification date2018052320180523
UniProtAcc

P35716

P00558

Ensembl transtripts involved in fusion geneENST00000322002, ENST00000373316, 
ENST00000442431, ENST00000537456, 
ENST00000476531, 
Fusion gene scores* DoF score3 X 3 X 1=95 X 5 X 3=75
# samples 35
** MAII scorelog2(3/9*10)=1.73696559416621
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(5/75*10)=-0.584962500721156
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SOX11 [Title/Abstract] AND PGK1 [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
HgeneSOX11

GO:0000122

negative regulation of transcription by RNA polymerase II

19808959

HgeneSOX11

GO:0045944

positive regulation of transcription by RNA polymerase II

21124928

TgenePGK1

GO:0071456

cellular response to hypoxia

11130727


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
ChiTaRS3.1AU142940SOX11chr2

5838208

+PGK1chrX

77359752

+
* 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
3UTR-5UTRENST00000322002ENST00000373316SOX11chr2

5838208

+PGK1chrX

77359752

+
3UTR-5UTRENST00000322002ENST00000442431SOX11chr2

5838208

+PGK1chrX

77359752

+
3UTR-intronENST00000322002ENST00000537456SOX11chr2

5838208

+PGK1chrX

77359752

+
3UTR-intronENST00000322002ENST00000476531SOX11chr2

5838208

+PGK1chrX

77359752

+

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FusionProtFeatures for SOX11_PGK1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
SOX11

P35716

PGK1

P00558

Transcriptional factor involved in the embryonicneurogenesis. May also have a role in tissue modeling duringdevelopment. {ECO:0000269|PubMed:24886874}. In addition to its role as a glycolytic enzyme, it seemsthat PGK-1 acts as a polymerase alpha cofactor protein (primerrecognition protein) (PubMed:2324090). May play a role in spermmotility (PubMed:26677959). {ECO:0000269|PubMed:2324090,ECO:0000269|PubMed:26677959}.

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 SOX11_PGK1


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 SOX11_PGK1


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 SOX11_PGK1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgenePGK1P00558DB11638ArtenimolPhosphoglycerate kinase 1small moleculeapproved|investigational

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RelatedDiseases for SOX11_PGK1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSOX11C0010606Adenoid Cystic Carcinoma1CTD_human
HgeneSOX11C0027626Neoplasm Invasiveness1CTD_human
HgeneSOX11C0036095Salivary Gland Neoplasms1CTD_human
HgeneSOX11C4014528MENTAL RETARDATION, AUTOSOMAL DOMINANT 271UNIPROT
TgenePGK1C1970848Phosphoglycerate Kinase 1 Deficiency8CTD_human;UNIPROT
TgenePGK1C0007134Renal Cell Carcinoma1CTD_human
TgenePGK1C2239176Liver carcinoma1CTD_human