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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: 15597

FusionGeneSummary for GSTP1_SLC26A4

check button Fusion gene summary
Fusion gene informationFusion gene name: GSTP1_SLC26A4
Fusion gene ID: 15597
HgeneTgene
Gene symbol

GSTP1

SLC26A4

Gene ID

2950

5172

Gene nameglutathione S-transferase pi 1solute carrier family 26 member 4
SynonymsDFN7|FAEES3|GST3|GSTP|HEL-S-22|PIDFNB4|EVA|PDS|TDH2B
Cytomap

11q13.2

7q22.3

Type of geneprotein-codingprotein-coding
Descriptionglutathione S-transferase PGST class-piGSTP1-1deafness, X-linked 7epididymis secretory protein Li 22fatty acid ethyl ester synthase IIIpendrinsodium-independent chloride/iodide transportersolute carrier family 26 (anion exchanger), member 4truncated solute carrier family 26
Modification date2018052720180523
UniProtAcc

P09211

O43511

Ensembl transtripts involved in fusion geneENST00000398606, ENST00000398603, 
ENST00000498765, 
ENST00000265715, 
ENST00000541474, ENST00000544569, 
ENST00000543100, ENST00000480841, 
Fusion gene scores* DoF score11 X 9 X 4=3965 X 4 X 5=100
# samples 125
** MAII scorelog2(12/396*10)=-1.72246602447109
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/100*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: GSTP1 [Title/Abstract] AND SLC26A4 [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
HgeneGSTP1

GO:0006469

negative regulation of protein kinase activity

16636664

HgeneGSTP1

GO:0006749

glutathione metabolic process

1540159

HgeneGSTP1

GO:0006805

xenobiotic metabolic process

1540159

HgeneGSTP1

GO:0009890

negative regulation of biosynthetic process

18962899

HgeneGSTP1

GO:0032691

negative regulation of interleukin-1 beta production

18962899

HgeneGSTP1

GO:0032720

negative regulation of tumor necrosis factor production

18962899

HgeneGSTP1

GO:0043407

negative regulation of MAP kinase activity

11408560

HgeneGSTP1

GO:0043508

negative regulation of JUN kinase activity

16636664

HgeneGSTP1

GO:0043651

linoleic acid metabolic process

16624487

HgeneGSTP1

GO:0051771

negative regulation of nitric-oxide synthase biosynthetic process

18962899

HgeneGSTP1

GO:0070373

negative regulation of ERK1 and ERK2 cascade

11408560

HgeneGSTP1

GO:0071638

negative regulation of monocyte chemotactic protein-1 production

18962899

HgeneGSTP1

GO:2001237

negative regulation of extrinsic apoptotic signaling pathway

16636664


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
ChiTaRS3.1BU527119GSTP1chr11

67354124

+SLC26A4chr7

107322541

+
* 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-intronENST00000398606ENST00000265715GSTP1chr11

67354124

+SLC26A4chr7

107322541

+
3UTR-intronENST00000398606ENST00000541474GSTP1chr11

67354124

+SLC26A4chr7

107322541

+
3UTR-intronENST00000398606ENST00000544569GSTP1chr11

67354124

+SLC26A4chr7

107322541

+
3UTR-intronENST00000398606ENST00000543100GSTP1chr11

67354124

+SLC26A4chr7

107322541

+
3UTR-intronENST00000398606ENST00000480841GSTP1chr11

67354124

+SLC26A4chr7

107322541

+
5CDS-intronENST00000398603ENST00000265715GSTP1chr11

67354124

+SLC26A4chr7

107322541

+
5CDS-intronENST00000398603ENST00000541474GSTP1chr11

67354124

+SLC26A4chr7

107322541

+
5CDS-intronENST00000398603ENST00000544569GSTP1chr11

67354124

+SLC26A4chr7

107322541

+
5CDS-intronENST00000398603ENST00000543100GSTP1chr11

67354124

+SLC26A4chr7

107322541

+
5CDS-intronENST00000398603ENST00000480841GSTP1chr11

67354124

+SLC26A4chr7

107322541

+
intron-intronENST00000498765ENST00000265715GSTP1chr11

67354124

+SLC26A4chr7

107322541

+
intron-intronENST00000498765ENST00000541474GSTP1chr11

67354124

+SLC26A4chr7

107322541

+
intron-intronENST00000498765ENST00000544569GSTP1chr11

67354124

+SLC26A4chr7

107322541

+
intron-intronENST00000498765ENST00000543100GSTP1chr11

67354124

+SLC26A4chr7

107322541

+
intron-intronENST00000498765ENST00000480841GSTP1chr11

67354124

+SLC26A4chr7

107322541

+

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FusionProtFeatures for GSTP1_SLC26A4


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
GSTP1

P09211

SLC26A4

O43511

Conjugation of reduced glutathione to a wide number ofexogenous and endogenous hydrophobic electrophiles. Regulatesnegatively CDK5 activity via p25/p35 translocation to preventneurodegeneration. {ECO:0000269|PubMed:21668448}. Sodium-independent transporter of chloride and iodide.{ECO:0000269|PubMed:10192399}.

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 GSTP1_SLC26A4


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 GSTP1_SLC26A4


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 GSTP1_SLC26A4


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneGSTP1P09211DB00316AcetaminophenGlutathione S-transferase Psmall moleculeapproved
HgeneGSTP1P09211DB00363ClozapineGlutathione S-transferase Psmall moleculeapproved
HgeneGSTP1P09211DB01015SulfamethoxazoleGlutathione S-transferase Psmall moleculeapproved
HgeneGSTP1P09211DB00903Etacrynic acidGlutathione S-transferase Psmall moleculeapproved|investigational
HgeneGSTP1P09211DB04339CarbocisteineGlutathione S-transferase Psmall moleculeapproved|investigational
HgeneGSTP1P09211DB09462GlycerinGlutathione S-transferase Psmall moleculeapproved|investigational
HgeneGSTP1P09211DB00143GlutathioneGlutathione S-transferase Psmall moleculeapproved|investigational|nutraceutical
HgeneGSTP1P09211DB01242ClomipramineGlutathione S-transferase Psmall moleculeapproved|investigational|vet_approved

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RelatedDiseases for GSTP1_SLC26A4


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneGSTP1C0032927Precancerous Conditions5CTD_human
HgeneGSTP1C0033578Prostatic Neoplasms5CTD_human
HgeneGSTP1C0023904Liver Neoplasms, Experimental4CTD_human
HgeneGSTP1C0004096Asthma3CTD_human
HgeneGSTP1C0005695Bladder Neoplasm3CTD_human
HgeneGSTP1C0030567Parkinson Disease2CTD_human
HgeneGSTP1C0036341Schizophrenia2PSYGENET
HgeneGSTP1C0038356Stomach Neoplasms2CTD_human
HgeneGSTP1C4277682Chemical and Drug Induced Liver Injury2CTD_human
HgeneGSTP1C0002736Amyotrophic Lateral Sclerosis1CTD_human
HgeneGSTP1C0004352Autistic Disorder1CTD_human
HgeneGSTP1C0007131Non-Small Cell Lung Carcinoma1CTD_human
HgeneGSTP1C0007134Renal Cell Carcinoma1CTD_human
HgeneGSTP1C0007273Carotid Artery Diseases1CTD_human
HgeneGSTP1C0008625Chromosome Aberrations1CTD_human
HgeneGSTP1C0011616Contact Dermatitis1CTD_human
HgeneGSTP1C0013182Drug Allergy1CTD_human
HgeneGSTP1C0017638Glioma1CTD_human
HgeneGSTP1C0019829Hodgkin Disease1CTD_human
HgeneGSTP1C0022650Kidney Calculi1CTD_human
HgeneGSTP1C0022658Kidney Diseases1CTD_human
HgeneGSTP1C0023473Myeloid Leukemia, Chronic1CTD_human
HgeneGSTP1C0024121Lung Neoplasms1CTD_human
HgeneGSTP1C0027540Necrosis1CTD_human
HgeneGSTP1C0029463Osteosarcoma1CTD_human
HgeneGSTP1C0031117Peripheral Neuropathy1CTD_human
HgeneGSTP1C0033941Psychoses, Substance-Induced1CTD_human
HgeneGSTP1C0033975Psychotic Disorders1PSYGENET
HgeneGSTP1C0035234Respiratory Sounds1CTD_human
HgeneGSTP1C0036939Shared Paranoid Disorder1PSYGENET
HgeneGSTP1C0042594Vestibular Diseases1CTD_human
HgeneGSTP1C0151744Myocardial Ischemia1CTD_human
HgeneGSTP1C0236733Amphetamine-Related Disorders1CTD_human
HgeneGSTP1C0282612Prostatic Intraepithelial Neoplasias1CTD_human
HgeneGSTP1C0349204Nonorganic psychosis1PSYGENET
HgeneGSTP1C0400966Non-alcoholic Fatty Liver Disease1CTD_human
HgeneGSTP1C0600427Cocaine Dependence1PSYGENET
HgeneGSTP1C0948089Acute Coronary Syndrome1CTD_human
HgeneGSTP1C1261473Sarcoma1CTD_human
HgeneGSTP1C1456865Ureteral Calculi1CTD_human
HgeneGSTP1C1458155Mammary Neoplasms1CTD_human
HgeneGSTP1C2239176Liver carcinoma1CTD_human
HgeneGSTP1C2609414Acute kidney injury1CTD_human
TgeneSLC26A4C0271829Pendred's syndrome22CTD_human;ORPHANET;UNIPROT
TgeneSLC26A4C3538946DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT17CTD_human;UNIPROT
TgeneSLC26A4C0018021Goiter3CTD_human;HPO
TgeneSLC26A4C0018784Sensorineural Hearing Loss (disorder)3CTD_human;HPO
TgeneSLC26A4C0033578Prostatic Neoplasms1CTD_human
TgeneSLC26A4C1384666hearing impairment1CTD_human