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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: 16772

FusionGeneSummary for HS2ST1_GBP6

check button Fusion gene summary
Fusion gene informationFusion gene name: HS2ST1_GBP6
Fusion gene ID: 16772
HgeneTgene
Gene symbol

HS2ST1

GBP6

Gene ID

9653

163351

Gene nameheparan sulfate 2-O-sulfotransferase 1guanylate binding protein family member 6
SynonymsdJ604K5.2-
Cytomap

1p22.3

1p22.2

Type of geneprotein-codingprotein-coding
Descriptionheparan sulfate 2-O-sulfotransferase 12-O-sulfotransferase2OSTguanylate-binding protein 6GBP-6GTP-binding protein 6guanine nucleotide-binding protein 6
Modification date2018052320180519
UniProtAcc

Q7LGA3

Q6ZN66

Ensembl transtripts involved in fusion geneENST00000370551, ENST00000370550, 
ENST00000356813, 
ENST00000370456, 
ENST00000535065, 
Fusion gene scores* DoF score9 X 5 X 5=2251 X 1 X 1=1
# samples 91
** MAII scorelog2(9/225*10)=-1.32192809488736
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Context

PubMed: HS2ST1 [Title/Abstract] AND GBP6 [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
TCGALDBRCATCGA-AN-A0FZ-01AHS2ST1chr1

87380843

+GBP6chr1

89834088

+
* 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
5CDS-5UTRENST00000370551ENST00000370456HS2ST1chr1

87380843

+GBP6chr1

89834088

+
5CDS-intronENST00000370551ENST00000535065HS2ST1chr1

87380843

+GBP6chr1

89834088

+
5CDS-5UTRENST00000370550ENST00000370456HS2ST1chr1

87380843

+GBP6chr1

89834088

+
5CDS-intronENST00000370550ENST00000535065HS2ST1chr1

87380843

+GBP6chr1

89834088

+
intron-5UTRENST00000356813ENST00000370456HS2ST1chr1

87380843

+GBP6chr1

89834088

+
intron-intronENST00000356813ENST00000535065HS2ST1chr1

87380843

+GBP6chr1

89834088

+

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FusionProtFeatures for HS2ST1_GBP6


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
HS2ST1

Q7LGA3

GBP6

Q6ZN66

Catalyzes the transfer of sulfate to the C2-position ofselected hexuronic acid residues within the maturing heparansulfate (HS). 2-O-sulfation within HS, particularly of iduronateresidues, is essential for HS to participate in a variety of high-affinity ligand-binding interactions and signaling processes.Mediates 2-O-sulfation of both L-iduronyl and D-glucuronylresidues (By similarity). {ECO:0000250}. Binds GTP, GDP and GMP. {ECO:0000250}.

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 HS2ST1_GBP6


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 HS2ST1_GBP6


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
HS2ST1ATP12A, NMNAT3, DIAPH3, CKAP4, HLA-A, TBC1D23, DYM, PIGU, PEX19, TSPAN17, P2RX4, TGOLN2, CHRNA9, TMEM258, SOGA3, P2RX2, USP9Y, UXS1, SLC7A1, APP, TRIM25GBP6FRMD1, GBP7, SIRT5


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 HS2ST1_GBP6


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 HS2ST1_GBP6


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