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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: 15600

FusionGeneSummary for GSTT1_SLC2A11

check button Fusion gene summary
Fusion gene informationFusion gene name: GSTT1_SLC2A11
Fusion gene ID: 15600
HgeneTgene
Gene symbol

GSTT1

SLC2A11

Gene ID

2952

66035

Gene nameglutathione S-transferase theta 1solute carrier family 2 member 11
Synonyms-GLUT10|GLUT11
Cytomap

22q11.23

22q11.23

Type of geneprotein-codingprotein-coding
Descriptionglutathione S-transferase theta-1GST class-theta-1glutathione transferase T1-1solute carrier family 2, facilitated glucose transporter member 11facilitative glucose transporter GLUT11glucose transporter protein 10glucose transporter protein 11glucose transporter type 10glucose transporter type 11glucose transporter-like prote
Modification date2018052720180329
UniProtAcc

P30711

Q9BYW1

Ensembl transtripts involved in fusion geneENST00000248935, ENST00000439996, 
ENST00000345044, ENST00000403208, 
ENST00000398356, ENST00000405847, 
ENST00000467660, ENST00000316185, 
Fusion gene scores* DoF score1 X 1 X 1=12 X 2 X 2=8
# samples 12
** MAII scorelog2(1/1*10)=3.32192809488736log2(2/8*10)=1.32192809488736
Context

PubMed: GSTT1 [Title/Abstract] AND SLC2A11 [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotationTumor suppressor gene involved fusion gene, retained protein feature but frameshift.
DDR (DNA damage repair) gene involved fusion gene, in-frame but not retained their domain.
* 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
HgeneGSTT1

GO:0006749

glutathione metabolic process

9307035|9434735|20097269


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
ChiTaRS3.1CN352897GSTT1chr22

24384119

-SLC2A11chr22

24217301

+
* 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
Frame-shiftENST00000248935ENST00000345044GSTT1chr22

24384119

-SLC2A11chr22

24217301

+
5CDS-intronENST00000248935ENST00000403208GSTT1chr22

24384119

-SLC2A11chr22

24217301

+
5CDS-intronENST00000248935ENST00000398356GSTT1chr22

24384119

-SLC2A11chr22

24217301

+
5CDS-intronENST00000248935ENST00000405847GSTT1chr22

24384119

-SLC2A11chr22

24217301

+
5CDS-3UTRENST00000248935ENST00000467660GSTT1chr22

24384119

-SLC2A11chr22

24217301

+
5CDS-3UTRENST00000248935ENST00000316185GSTT1chr22

24384119

-SLC2A11chr22

24217301

+
5UTR-3CDSENST00000439996ENST00000345044GSTT1chr22

24384119

-SLC2A11chr22

24217301

+
5UTR-intronENST00000439996ENST00000403208GSTT1chr22

24384119

-SLC2A11chr22

24217301

+
5UTR-intronENST00000439996ENST00000398356GSTT1chr22

24384119

-SLC2A11chr22

24217301

+
5UTR-intronENST00000439996ENST00000405847GSTT1chr22

24384119

-SLC2A11chr22

24217301

+
5UTR-3UTRENST00000439996ENST00000467660GSTT1chr22

24384119

-SLC2A11chr22

24217301

+
5UTR-3UTRENST00000439996ENST00000316185GSTT1chr22

24384119

-SLC2A11chr22

24217301

+

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FusionProtFeatures for GSTT1_SLC2A11


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
GSTT1

P30711

SLC2A11

Q9BYW1

Conjugation of reduced glutathione to a wide number ofexogenous and endogenous hydrophobic electrophiles. Acts on 1,2-epoxy-3-(4-nitrophenoxy)propane, phenethylisothiocyanate 4-nitrobenzyl chloride and 4-nitrophenethyl bromide. Displaysglutathione peroxidase activity with cumene hydroperoxide.{ECO:0000269|PubMed:16298388, ECO:0000269|PubMed:20097269}. Facilitative glucose transporter.{ECO:0000269|PubMed:12175779}.

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 GSTT1_SLC2A11


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 GSTT1_SLC2A11


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
GSTT1GSTO1, ATOX1, CSTB, FKBP1A, HINT1, EGFR, MID1, MYLK2, HBB, SIRT2, PRSS2, SPRTN, LRP2BP, HBA2, LURAP1, ZMAT5SLC2A11


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 GSTT1_SLC2A11


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneGSTT1P30711DB00143GlutathioneGlutathione S-transferase theta-1small moleculeapproved|investigational|nutraceutical

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RelatedDiseases for GSTT1_SLC2A11


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneGSTT1C0036341Schizophrenia5PSYGENET
HgeneGSTT1C0033578Prostatic Neoplasms4CTD_human
HgeneGSTT1C0008625Chromosome Aberrations3CTD_human
HgeneGSTT1C4277682Chemical and Drug Induced Liver Injury3CTD_human
HgeneGSTT1C0236733Amphetamine-Related Disorders2CTD_human
HgeneGSTT1C0003949Asbestosis1CTD_human
HgeneGSTT1C0005586Bipolar Disorder1PSYGENET
HgeneGSTT1C0007134Renal Cell Carcinoma1CTD_human
HgeneGSTT1C0011570Mental Depression1PSYGENET
HgeneGSTT1C0011581Depressive disorder1PSYGENET
HgeneGSTT1C0017636Glioblastoma1CTD_human
HgeneGSTT1C0020538Hypertensive disease1CTD_human
HgeneGSTT1C0022665Kidney Neoplasm1CTD_human
HgeneGSTT1C0024121Lung Neoplasms1CTD_human
HgeneGSTT1C0026764Multiple Myeloma1CTD_human
HgeneGSTT1C0034734Raynaud Disease1CTD_human
HgeneGSTT1C0037286Skin Neoplasms1CTD_human
HgeneGSTT1C0279626Squamous cell carcinoma of esophagus1CTD_human
HgeneGSTT1C0400966Non-alcoholic Fatty Liver Disease1CTD_human
HgeneGSTT1C0403823Asthenozoospermia1CTD_human
HgeneGSTT1C1449861Micronuclei, Chromosome-Defective1CTD_human