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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 IRX5
check button Gene summary
Basic gene informationGene symbolIRX5
Gene nameiroquois homeobox 5
SynonymsHMMS|IRX-2a|IRXB2
CytomapUCSC genome browser: 16q12.2
Type of geneprotein-coding
RefGenesNM_001252197.1,
NM_005853.5,
Descriptionhomeodomain protein IRX-2Ahomeodomain protein IRXB2iroquois-class homeodomain protein IRX-5
Modification date20141207
dbXrefs MIM : 606195
HGNC : HGNC
Ensembl : ENSG00000176842
HPRD : 08395
Vega : OTTHUMG00000133201
ProteinUniProt:
go to UniProt's Cross Reference DB Table
ExpressionCleanEX: HS_IRX5
BioGPS: 10265
PathwayNCI Pathway Interaction Database: IRX5
KEGG: IRX5
REACTOME: IRX5
Pathway Commons: IRX5
ContextiHOP: IRX5
ligand binding site mutation search in PubMed: IRX5
UCL Cancer Institute: IRX5
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)BreastLung
Cancer types related to the specific-tissues in cancer samples (assigned by TissGDB using TCGA)BRCALUAD,LUSC
Reference showing the relevant tissue of IRX5
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


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TissGeneExp for IRX5

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
THCA-3.993181003-5.0187555791.0255745762.20E-079.19E-07
BRCA3.4373360952.418922061.0184140352.12E-108.17E-10
KICH-3.9103102911.093929709-5.004249.82E-195.28E-17
COAD-2.977222137-5.4849567532.5077346153.44E-072.15E-06
LIHC-3.671166291-5.3043062911.633144.69E-062.15E-05


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TissGene-miRNA for IRX5

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 IRX5
TissGeneSNV for IRX5

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.P254TCOAD2
p.R117QSTAD1
p.A103VCOAD1
p.V327LREAD1
p.Y415CESCA1
p.T413MCESC1
p.P204SSTAD1
p.L157VLUAD1
p.V160ASTAD1
p.P391LLUSC1
p.A406SSARC1
p.A104VHNSC1
p.E186KUCEC1
p.G419EHNSC1
p.S344LSKCM1
p.L370PSKCM1
p.G441ABLCA1
p.K210ECOAD1
p.P390SSKCM1
p.A124TLUSC1
p.S437CBLCA1
p.L460SUCEC1
p.A94VESCA1
p.P391SSKCM1
p.H438YBLCA1
p.A77TSTAD1
p.R400WBLCA1
p.R182WUCEC1
p.L402VBLCA1
p.E217KBLCA1
p.L128VESCA1
p.A94SCOAD1
p.P254TREAD1
p.D70HHNSC1
p.S19LBLCA1
p.P358SSKCM1
p.M155VSKCM1
p.E188KESCA1
p.Q465*SKCM1
p.D187NBLCA1
p.E201KSTAD1
p.D471NHNSC1
p.E197QESCA1
p.P391ALUAD1
p.G441VKIRC1
p.Y23HSTAD1
p.H100YSKCM1
p.L371PSKCM1
p.D34NHNSC1
p.H438RUCEC1
p.P360LSTAD1
p.H419YCOAD1
p.P435LSTAD1
p.P213RLIHC1
p.G419VTHYM1
p.P213LLGG1
p.R136HSTAD1
p.T178PSKCM1
p.R384GLUAD1
p.K206RLIHC1
p.S29LBLCA1
p.Q464XSKCM1
p.T125MBLCA1
p.P15LSKCM1
p.G364ELGG1
p.P21SUCEC1


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TissGeneCNV for IRX5

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 IRX5

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 IRX5

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)
IRX5, APLF (tumor)IRX5, APLF (normal)
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COAD (tumor)COAD (normal)
IRX5, APLF (tumor)IRX5, APLF (normal)
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HNSC (tumor)HNSC (normal)
IRX5, APLF (tumor)IRX5, APLF (normal)
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KICH (tumor)KICH (normal)
IRX5, APLF (tumor)IRX5, APLF (normal)
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KIRC (tumor)KIRC (normal)
IRX5, APLF (tumor)IRX5, APLF (normal)
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KIRP (tumor)KIRP (normal)
IRX5, APLF (tumor)IRX5, APLF (normal)
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LIHC (tumor)LIHC (normal)
IRX5, APLF (tumor)IRX5, APLF (normal)
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LUAD (tumor)LUAD (normal)
IRX5, APLF (tumor)IRX5, APLF (normal)
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LUSC (tumor)LUSC (normal)
IRX5, APLF (tumor)IRX5, APLF (normal)
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PRAD (tumor)PRAD (normal)
IRX5, APLF (tumor)IRX5, APLF (normal)
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STAD (tumor)STAD (normal)
IRX5, APLF (tumor)IRX5, APLF (normal)
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THCA (tumor)THCA (normal)
IRX5, APLF (tumor)IRX5, APLF (normal)
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TissGeneProg for IRX5

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 IRX5
TissGeneDrug for IRX5

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 IRX5

check button Disease information associated with TissGene
(DisGeNet, 2016-06-01)
Disease IDDisease name# pubmedsSource
umls:C0000768Congenital Abnormality1BeFree
umls:C0001430Adenoma1BeFree
umls:C0007102Malignant tumor of colon1BeFree
umls:C0018784Sensorineural Hearing Loss (disorder)1CTD_human
umls:C0018798Congenital Heart Defects1CTD_human
umls:C0022904Lacrimal Apparatus Diseases1CTD_human
umls:C0024115Lung diseases1CTD_human
umls:C0027092Myopia1CTD_human
umls:C0033578Prostatic Neoplasms1LHGDN
umls:C0271901Microcytic hypochromic anemia (disorder)1CTD_human
umls:C0376358Malignant neoplasm of prostate1BeFree
umls:C0376634Craniofacial Abnormalities1CTD_human
umls:C0399352Developmental absence of tooth1CTD_human
umls:C0525041Neurobehavioral Manifestations1GAD
umls:C0600139Prostate carcinoma1BeFree
umls:C0699790Colon Carcinoma1BeFree
umls:C1876203Frontonasal dysplasia1CTD_human
umls:C1970027Hypertelorism, Severe, With Midface Prominence, Myopia, Mental Retardation, And Bone Fragility1CLINVAR,ORPHANET,UNIPROT