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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 CLCNKB
check button Gene summary
Basic gene informationGene symbolCLCNKB
Gene namechloride channel, voltage-sensitive Kb
SynonymsCLCKB|ClC-K2|ClC-Kb
CytomapUCSC genome browser: 1p36
Type of geneprotein-coding
RefGenesNM_000085.4,
NM_001165945.2,
Descriptionchloride channel protein ClC-Kbchloride channel, kidney, B
Modification date20141207
dbXrefs MIM : 602023
HGNC : HGNC
Ensembl : ENSG00000184908
HPRD : 03607
Vega : OTTHUMG00000009530
ProteinUniProt:
go to UniProt's Cross Reference DB Table
ExpressionCleanEX: HS_CLCNKB
BioGPS: 1188
PathwayNCI Pathway Interaction Database: CLCNKB
KEGG: CLCNKB
REACTOME: CLCNKB
Pathway Commons: CLCNKB
ContextiHOP: CLCNKB
ligand binding site mutation search in PubMed: CLCNKB
UCL Cancer Institute: CLCNKB
Assigned class in TissGDB*C
Included tissue-specific gene expression resourcesTiGER,GTEx
Specific-tissues in normal samples (assigned by TissGDB using HPA, TiGER, and GTEx)Kidney
Cancer types related to the specific-tissues in cancer samples (assigned by TissGDB using TCGA)KIRC,KIRP,KICH
Reference showing the relevant tissue of CLCNKB
Description by TissGene annotationsProtective TissGene in OS
* 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


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TissGeneExp for CLCNKB

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
THCA3.9997128736.972382365-2.9726694921.48E-229.36E-21
COAD-1.473831520.24836848-1.72222.12E-058.95E-05
KIRC1.4048152749.992169441-8.5873541674.91E-483.67E-46
BRCA-0.9624860410.464547292-1.4270333332.52E-222.12E-21
PRAD-0.0663795971.94344348-2.0098230771.74E-141.67E-12
LUSC0.069480471.805447137-1.7359666673.27E-101.18E-09
KIRP2.60870069110.64908819-8.04038752.83E-161.01E-14
HNSC-1.1300988731.353149964-2.4832488372.91E-050.000148133


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TissGene-miRNA for CLCNKB

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 CLCNKB
TissGeneSNV for CLCNKB

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.P513LSKCM2
p.P683LSKCM2
p.G35SLUAD1
p.R438HMESO1
p.L402ILIHC1
p.W389XSTAD1
p.G139SSKCM1
p.R438CPRAD1
p.P422STHYM1
p.L558PSTAD1
p.E649QBLCA1
p.G308SSKCM1
p.F277CCOAD1
p.G625VUCEC1
p.P500SSTAD1
p.W27*BLCA1
p.P342LKIRC1
p.D68NUCEC1
p.L161FSKCM1
p.V98MUCEC1
p.R544CHNSC1
p.G189RLIHC1
p.S232CBLCA1
p.V376MCOAD1
p.R22KBLCA1
p.R595LSKCM1
p.D140NSKCM1
p.R534QSKCM1
p.P608SSKCM1
p.V576MSTAD1
p.P513LCOAD1
p.P394LSTAD1
p.A204TCOAD1
p.R272QBRCA1
p.F44IUCEC1
p.R538HPRAD1
p.H480YBLCA1
p.T244IHNSC1
p.E450DLUAD1
p.S232PLUAD1
p.S445YBLCA1
p.E225KBLCA1
p.C157FSTAD1
p.R27LCOAD1
p.D363NUCEC1
p.R438CHNSC1
p.C292YSTAD1
p.S475LHNSC1
p.R351QSTAD1
p.G264ESKCM1
p.E643KESCA1
p.W389*STAD1
p.L564RBLCA1
p.P26LSKCM1
p.R251WSTAD1
p.G57RLGG1
p.M427IHNSC1
p.R311WPRAD1
p.S105FSKCM1
p.V671ASTAD1
p.V134ILGG1
p.A131VSTAD1
p.R365QSKCM1
p.R92WSKCM1
p.E490GSTAD1
p.F231LUCEC1
p.P216SSKCM1
p.S584ILUAD1
p.A321VSARC1
p.V233ISTAD1
p.P124TLGG1
p.Q197*LUAD1
p.R184CPAAD1
p.S640YDLBC1
p.G662DESCA1


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TissGeneCNV for CLCNKB

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 CLCNKB

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
Chimerdb3.0ChiTaRsNADA377618TNKS2-CLCNKBchr10:93609803chr1:16372781
Chimerdb3.0ChiTaRsNABF822523CLCNKB-ABHD2chr1:16377433chr15:89742663


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TissGeneNet for CLCNKB

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)


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TissGeneProg for CLCNKB

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 CLCNKB
TissGeneDrug for CLCNKB

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 CLCNKB

check button Disease information associated with TissGene
(DisGeNet, 2016-06-01)
Disease IDDisease name# pubmedsSource
umls:C0004775Bartter Disease23BeFree,CTD_human,LHGDN
umls:C1846343Bartter syndrome, type 312BeFree,CLINVAR,CTD_human,ORPHANET,UNIPROT
umls:C0020538Hypertensive disease7BeFree,GAD,LHGDN
umls:C0085580Essential Hypertension6BeFree
umls:C0268450Gitelman Syndrome5BeFree,ORPHANET
umls:C0018784Sensorineural Hearing Loss (disorder)3BeFree
umls:C0022658Kidney Diseases3BeFree
umls:C0020599Hypocalciuria2BeFree
umls:C0022661Kidney Failure, Chronic2BeFree
umls:C0155552Hearing Loss, Mixed Conductive-Sensorineural2BeFree
umls:C0001126Renal tubular acidosis1BeFree
umls:C0020438Hypercalciuria1BeFree
umls:C0027709Nephrocalcinosis1BeFree
umls:C0085570Hypokalemic alkalosis1BeFree
umls:C0162283Nephrogenic Diabetes Insipidus1BeFree
umls:C0271561Somatotropin deficiency1BeFree
umls:C0339789Congenital deafness1BeFree
umls:C1384514Conn Syndrome1BeFree
umls:C3714796Isolated somatotropin deficiency1BeFree
umls:C1563705Nephrogenic Diabetes Insipidus, Type I0MGD
umls:C1846344Bartter Syndrome, Type 3, with Hypocalciuria0CLINVAR
umls:C1865270BARTTER SYNDROME, TYPE 4A0CTD_human
umls:C2751312BARTTER SYNDROME, TYPE 4B0CLINVAR