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Bioinformatics and Systems Medicine Laboratory Bioinformatics and Systems Medicine Laboratory

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TissGeneSummary

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TissGeneExp

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TissGene-miRNA

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TissGeneMut: TissGeneSNV, TissGeneCNV, and TissGeneFusions

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TissGeneNet

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TissGeneProg

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TissGeneClin: TissGeneDrug and TissGeneDisease

TissGeneSummary for SLC26A8
check button Gene summary
Basic gene informationGene symbolSLC26A8
Gene namesolute carrier family 26 (anion exchanger), member 8
SynonymsSPGF3|TAT1
CytomapUCSC genome browser: 6p21
Type of geneprotein-coding
RefGenesNM_001193476.1,
NM_052961.3,NM_138718.2,
Descriptionanion transporter/exchanger-8testis anion transporter 1
Modification date20141207
dbXrefs MIM : 608480
HGNC : HGNC
Ensembl : ENSG00000112053
HPRD : 12241
Vega : OTTHUMG00000014586
ProteinUniProt:
go to UniProt's Cross Reference DB Table
ExpressionCleanEX: HS_SLC26A8
BioGPS: 116369
PathwayNCI Pathway Interaction Database: SLC26A8
KEGG: SLC26A8
REACTOME: SLC26A8
Pathway Commons: SLC26A8
ContextiHOP: SLC26A8
ligand binding site mutation search in PubMed: SLC26A8
UCL Cancer Institute: SLC26A8
Assigned class in TissGDB*B
Included tissue-specific gene expression resourcesHPA,TiGER,GTEx
Specific-tissues in normal samples (assigned by TissGDB using HPA, TiGER, and GTEx)Testis
Cancer types related to the specific-tissues in cancer samples (assigned by TissGDB using TCGA)TGCT
Reference showing the relevant tissue of SLC26A8
Description by TissGene annotations
* Class A consists of genes with literature evidence and is part of the cTissGenes. Class B consists of only cTissGenes without additional evidence. The remaining genes belong to Class C.

check button Gene ontology having evidence of Inferred from Direct Assay (IDA) from Entrez
GO IDGO termPubMed ID
GO:0006820anion transport11834742
GO:0006821chloride transport1183472
GO:0008272sulfate transport1183472
GO:0019532oxalate transport1183472
GO:1902358sulfate transmembrane transport1183472
GO:1902476chloride transmembrane transport1183472
GO:0006820anion transport11834742
GO:0006821chloride transport1183472
GO:0008272sulfate transport1183472
GO:0019532oxalate transport1183472
GO:1902358sulfate transmembrane transport1183472
GO:1902476chloride transmembrane transport1183472


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TissGeneExp for SLC26A8

check button Gene expressions across 28 cancer types (X-axis: cancer type and Y-axis: log2(norm_counts+1))
(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16)
gene exp


check button Gene isoform expressions across 28 cancer types (X-axis: cancer type and Y-axis: log2(norm_counts+1))
(TCGA pan-cancer tcga_rsem_isoform_tpm, version 2016-09-01)
gene isoform exp


check button Gene expressions across normal tissues of GTEx data
(GTEx GTEx_Analysis_v6_RNA-seq_RNA-SeQCv1.1.8_gene_rpkm.gct)
- Here, we shows the matched tissue types only among our 28 cancer types.
normal gene exp


check button Different expressions across 14 cancer types with more than 10 samples between matched tumors and normals (X-axis: cancer type and Y-axis: log2(norm_counts+1))
(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16)
DEG exp

- Significantly differentially expressed cancer types and information. (|Fold change|>1 and FDR<0.05)
Cancer typeMean(exp) in tumorMean(exp) in matched normalLog2FCP-val.FDR


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TissGene-miRNA for SLC26A8

check button Significantly anti-correlated miRNAs of TissGene across 28 cancer types
(Gene-miRNA relations from TargetScanHuman Relsease 7.1, Conserved_Site_Context_Scores.txt.zip, 06.01.2016)
(TCGA IlluminaHiSeq_miRNASeq, log2(RPM+1) data, version 2016-11-21)
(TCGA IlluminaHiSeq_RNASeqV2, log2(normalized_count+1) data, version 2016-08-16)
(Spearman’s Rank Correlation (p-value<0.05 and coefficient<-0.25))
Cancer typemiRNA idmiRNA accessionP-val.Coeff.# samples


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TissGeneMut for SLC26A8
TissGeneSNV for SLC26A8

check button nsSNV counts per each loci.
Different colors of circles represent different cancer types. Circle size denotes number of samples.
(TCGA somatic mutation (SNPs and small INDELs) data, version 2016-04-25)

* Click on the image to enlarge it in a new window.
SNV lollipop
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check button Somatic nucleotide variants of TissGene across 28 cancer types
(X-axis: cancer type and Y-axis: % of mutated samples)
The numbers in parentheses are numbers of samples with mutation (nsSNVs).
(TCGA somatic mutation (SNPs and small INDELs) data, version 2016-04-25)
SNV distribution

- nsSNVs sorted by frequency.
AAchangeCancer type# samples
p.R520CSKCM2
p.L717VBLCA2
p.R87*UCEC2
p.M832VSKCM1
p.K571EPRAD1
p.G738ELUSC1
p.V161IREAD1
p.E682KSKCM1
p.S916YUCEC1
p.P662QLUSC1
p.S227FSKCM1
p.E311KSKCM1
p.R63_spliceOV1
p.V578ASKCM1
p.P711SSKCM1
p.R880QESCA1
p.S183LBLCA1
p.S509*BLCA1
p.Q145XPAAD1
p.L393VREAD1
p.R71*UCEC1
p.P634SSKCM1
p.R18*UCEC1
p.R63HREAD1
p.L585VOV1
p.E635KSKCM1
p.R71*PRAD1
p.K356QUCEC1
p.V668MUCEC1
p.E33DCESC1
p.R545QLUAD1
p.R798MHNSC1
p.E658ASKCM1
p.E81QBLCA1
p.A2VSTAD1
p.H921YSKCM1
p.R298KBLCA1
p.K89NLGG1
p.D790NSTAD1
p.M252ILUAD1
p.Q421*SKCM1
p.Q851*LGG1
p.P551TBLCA1
p.F774LUCEC1
p.A701VGBM1
p.G425ESKCM1
p.V792MLUSC1
p.T202ALGG1
p.Q37RCOAD1
p.R927CUCEC1
p.P346SSKCM1
p.V138AUCEC1
p.G964SOV1
p.R954HCESC1
p.R87XCOAD1
p.R880WSKCM1
p.G696*UCEC1
p.K605NUCEC1
p.A791TUCEC1
p.D958NSKCM1
p.V519ICESC1
p.R6KSKCM1
p.Q145*PAAD1
p.P711TLUAD1
p.V740ASKCM1
p.P914SSKCM1
p.K841ISKCM1
p.G426ESKCM1
p.L717ISARC1
p.R87XREAD1
p.P185SESCA1
p.G552VPRAD1
p.V173ISTAD1
p.D337ABLCA1
p.S690*BLCA1
p.V741ICOAD1
p.P225LSTAD1
p.R71QHNSC1
p.F370VBLCA1
p.C72YLGG1
p.R292QSKCM1
p.E33KSKCM1
p.R41KSKCM1
p.G603RSKCM1
p.Y568DSTAD1
p.S509LBLCA1
p.E968*UCEC1
p.S666LSKCM1
p.A656PTHCA1
p.T34PLUSC1
p.Q171RSKCM1
p.Q171RSTAD1
p.V668ALUAD1
p.M730KGBM1
p.L755FBLCA1
p.D633NSKCM1
p.I51MHNSC1
p.S183LSKCM1
p.A701VESCA1
p.G110RHNSC1
p.A459VSTAD1
p.P912SDLBC1
p.S134LSTAD1
p.I639VCOAD1
p.G552ESKCM1
p.D579GPAAD1
p.K89QUCEC1
p.T334MLGG1
p.F556LHNSC1
p.G802CUCEC1
p.S183LSARC1
p.P620LSKCM1
p.G604*UCEC1
p.E33VKIRC1
p.L793QSTAD1
p.R621GCOAD1
p.R737QLGG1
p.P78LSKCM1
p.V60IUCEC1
p.R71*GBM1
p.V792MHNSC1
p.K586ICESC1
p.S820*LUAD1
p.Y30CLGG1
p.G103CTHYM1
p.D614NLUAD1
p.V214ILGG1
p.N687DHNSC1


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TissGeneCNV for SLC26A8

check button Copy number variations of TissGene across 28 cancer types (X-axis: cancer type and Y-axis: % of CNV samples)
(TCGA Gistic2_CopyNumber_Gistic2_all_data_by_genes, Gistic2 copy number data, version 2016-08-16)
CNV


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TissGeneFusions for SLC26A8

check button Fusion genes including TissGene
(ChimerDB 3.0, 2016-12-01 and TCGA fusion Portal 2015-12-01)
DatabaseSrcCancer typeSampleFusion geneORF5'-gene BP3'-gene BP


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TissGeneNet for SLC26A8

check button Co-expressed gene networks based on protein-protein interaction data (CePIN)
(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16)
(PINA2 ppi data)
BRCA (tumor)BRCA (normal)
SLC26A8, CFTR, RACGAP1, NXF1 (tumor)SLC26A8, CFTR, RACGAP1, NXF1 (normal)
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COAD (tumor)COAD (normal)
SLC26A8, CFTR, RACGAP1, NXF1 (tumor)SLC26A8, CFTR, RACGAP1, NXF1 (normal)
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HNSC (tumor)HNSC (normal)
SLC26A8, CFTR, RACGAP1, NXF1 (tumor)SLC26A8, CFTR, RACGAP1, NXF1 (normal)
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KICH (tumor)KICH (normal)
SLC26A8, CFTR, RACGAP1, NXF1 (tumor)SLC26A8, CFTR, RACGAP1, NXF1 (normal)
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KIRC (tumor)KIRC (normal)
SLC26A8, CFTR, RACGAP1, NXF1 (tumor)SLC26A8, CFTR, RACGAP1, NXF1 (normal)
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KIRP (tumor)KIRP (normal)
SLC26A8, CFTR, RACGAP1, NXF1 (tumor)SLC26A8, CFTR, RACGAP1, NXF1 (normal)
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LIHC (tumor)LIHC (normal)
SLC26A8, CFTR, RACGAP1, NXF1 (tumor)SLC26A8, CFTR, RACGAP1, NXF1 (normal)
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LUAD (tumor)LUAD (normal)
SLC26A8, CFTR, RACGAP1, NXF1 (tumor)SLC26A8, CFTR, RACGAP1, NXF1 (normal)
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LUSC (tumor)LUSC (normal)
SLC26A8, CFTR, RACGAP1, NXF1 (tumor)SLC26A8, CFTR, RACGAP1, NXF1 (normal)
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PRAD (tumor)PRAD (normal)
SLC26A8, CFTR, RACGAP1, NXF1 (tumor)SLC26A8, CFTR, RACGAP1, NXF1 (normal)
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STAD (tumor)STAD (normal)
SLC26A8, CFTR, RACGAP1, NXF1 (tumor)SLC26A8, CFTR, RACGAP1, NXF1 (normal)
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THCA (tumor)THCA (normal)
SLC26A8, CFTR, RACGAP1, NXF1 (tumor)SLC26A8, CFTR, RACGAP1, NXF1 (normal)
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TissGeneProg for SLC26A8

check button Kaplan-Meier plots with logrank tests of overall survival (OS) using 28 cancer types
(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16)
(TCGA clinicalMatrix, phenotype data, version 2016-04-27)

* Click on the image to enlarge it in a new window.
survival 1

check button Kaplan-Meier plots with logrank test of relapse free survival (RFS) using 28 cancer types
(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16)
(TCGA clinicalMatrix, phenotype data, version 2016-04-27)

* Click on the image enlarge it in a new window.
survival 2

check button Forest plot of Cox proportional hazard ratio (HR) and 95% CI of overall survival (OS) using 28 cancer types
(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16)
(TCGA clinicalMatrix, phenotype data, version 2016-04-27)

* Click on the image enlarge it in a new window.
survival 3

check button Forest plot of Cox proportional hazard ratio (HR) and 95% CI of relapse free survival (RFS) using 28 cancer types
(TCGA IlluminaHiSeq_RNASeqV2, pan-cancer normalized log2(norm_counts+1) data, version 2016-08-16)
(TCGA clinicalMatrix, phenotype data, version 2016-04-27)

* Click on the image enlarge it in a new window.
survival 4

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TissGeneClin for SLC26A8
TissGeneDrug for SLC26A8

check button Drug information targeting TissGene
(DrugBank Version 5.0.6, 2017-04-01)
DrugBank IDDrug nameDrug activityDrug typeDrug status


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TissGeneDisease for SLC26A8

check button Disease information associated with TissGene
(DisGeNet, 2016-06-01)
Disease IDDisease name# pubmedsSource
umls:C0019693HIV Infections8BeFree
umls:C0005684Malignant neoplasm of urinary bladder2BeFree
umls:C0699885Carcinoma of bladder2BeFree
umls:C0005695Bladder Neoplasm1BeFree
umls:C0007222Cardiovascular Diseases1GAD
umls:C0007786Brain Ischemia1GAD
umls:C0010068Coronary heart disease1GAD
umls:C0013170Drug habituation1BeFree
umls:C0021364Male infertility1BeFree
umls:C0022661Kidney Failure, Chronic1GAD
umls:C0024301Lymphoma, Follicular1BeFree
umls:C0027765nervous system disorder1BeFree
umls:C0036341Schizophrenia1CTD_human
umls:C0036572Seizures1BeFree
umls:C0037889Hereditary spherocytosis1BeFree
umls:C0038454Cerebrovascular accident1GAD
umls:C0040336Tobacco Use Disorder1GAD
umls:C0302592Cervix carcinoma1BeFree
umls:C0376358Malignant neoplasm of prostate1BeFree
umls:C0403809Primary spermatogenic failure1BeFree
umls:C0600139Prostate carcinoma1BeFree
umls:C1847540Azoospermia, Nonobstructive1CLINVAR,UNIPROT
umls:C2674218SPHEROCYTOSIS, TYPE 1 (disorder)1BeFree