TissGeneSummary for RFX2 |
Gene summary |
Basic gene information | Gene symbol | RFX2 |
Gene name | ||
Synonyms | ||
Cytomap | UCSC genome browser: | |
Type of gene | ||
RefGenes | ||
Description | ||
Modification date | ||
dbXrefs | ||
Protein | UniProt: go to UniProt's Cross Reference DB Table | |
Expression | CleanEX: HS_RFX2 | |
BioGPS: 101928900 | ||
Pathway | NCI Pathway Interaction Database: RFX2 | |
KEGG: RFX2 | ||
REACTOME: RFX2 | ||
Pathway Commons: RFX2 | ||
Context | iHOP: RFX2 | |
ligand binding site mutation search in PubMed: RFX2 | ||
UCL Cancer Institute: RFX2 | ||
Assigned class in TissGDB* | C | |
Included tissue-specific gene expression resources | TiGER,GTEx | |
Specific-tissues in normal samples (assigned by TissGDB using HPA, TiGER, and GTEx) | Bone marrowTestisThymus | |
Cancer types related to the specific-tissues in cancer samples (assigned by TissGDB using TCGA) | LAMLTGCTTHYM | |
Reference showing the relevant tissue of RFX2 | ||
Description by TissGene annotations | Protective TissGene in OS Cancer gene TissgsLTS |
* 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. |
Gene ontology having evidence of Inferred from Direct Assay (IDA) from Entrez |
GO ID | GO term | PubMed ID |
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TissGeneExp for RFX2 |
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 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 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. |
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) |
- Significantly differentially expressed cancer types and information. (|Fold change|>1 and FDR<0.05) |
Cancer type | Mean(exp) in tumor | Mean(exp) in matched normal | Log2FC | P-val. | FDR |
BRCA | 0.08166694 | 1.664214309 | -1.582547368 | 2.34E-28 | 2.79E-27 |
KICH | -1.275757937 | 0.200782063 | -1.47654 | 6.51E-07 | 2.51E-06 |
LUSC | 1.332742534 | 2.969271946 | -1.636529412 | 4.93E-12 | 2.14E-11 |
KIRC | 0.87743273 | -0.201920048 | 1.079352778 | 4.85E-12 | 1.94E-11 |
LUAD | 0.917835029 | 2.846364339 | -1.92852931 | 1.11E-16 | 1.33E-15 |
ESCA | 1.65393879 | 3.01953879 | -1.3656 | 0.00119 | 0.016541 |
BLCA | 1.194939747 | 2.601687116 | -1.406747368 | 5.08E-05 | 0.000649306 |
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TissGene-miRNA for RFX2 |
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 type | miRNA id | miRNA accession | P-val. | Coeff. | # samples |
ACC | hsa-miR-30e-5p | MIMAT0000692 | 0.02 | -0.27 | 78 |
ACC | hsa-miR-30e-5p | MIMAT0000692 | 0.02 | -0.27 | 78 |
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TissGeneMut for RFX2 |
TissGeneSNV for RFX2 |
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. |
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) |
- nsSNVs sorted by frequency. |
AAchange | Cancer type | # samples |
p.R169H | COAD | 1 |
p.T254M | STAD | 1 |
p.W202* | SKCM | 1 |
p.P467S | SKCM | 1 |
p.S621F | SKCM | 1 |
p.R693H | BLCA | 1 |
p.S219Y | STAD | 1 |
p.N237S | COAD | 1 |
p.E421K | HNSC | 1 |
p.E706K | BLCA | 1 |
p.R255W | DLBC | 1 |
p.Q472R | PRAD | 1 |
p.S219Y | READ | 1 |
p.E96K | BLCA | 1 |
p.W442* | BLCA | 1 |
p.M157V | THYM | 1 |
p.E671K | SKCM | 1 |
p.M288V | UCEC | 1 |
p.R291W | PAAD | 1 |
p.G156V | BRCA | 1 |
p.M177I | STAD | 1 |
p.A12V | ACC | 1 |
p.H599Y | THYM | 1 |
p.T515M | PRAD | 1 |
p.A473V | STAD | 1 |
p.R280Q | DLBC | 1 |
p.N487S | KICH | 1 |
p.A600D | BRCA | 1 |
p.R513H | STAD | 1 |
p.L581V | ESCA | 1 |
p.P63S | CESC | 1 |
p.P128S | SKCM | 1 |
p.K479* | HNSC | 1 |
p.D700N | ESCA | 1 |
p.A126V | HNSC | 1 |
p.S219Y | UCEC | 1 |
p.V564M | HNSC | 1 |
p.M290I | KIRP | 1 |
p.A239V | UCEC | 1 |
p.W202X | SKCM | 1 |
p.V72A | STAD | 1 |
p.E211K | SKCM | 1 |
p.V366I | HNSC | 1 |
p.Y645H | SKCM | 1 |
p.H639L | LUAD | 1 |
p.D674N | UCEC | 1 |
p.P603S | SKCM | 1 |
p.S505N | SKCM | 1 |
p.V549L | OV | 1 |
p.S4Y | CESC | 1 |
p.R566Q | STAD | 1 |
p.T307M | ESCA | 1 |
p.E421K | STAD | 1 |
p.S621Y | ESCA | 1 |
p.A423T | GBM | 1 |
p.Q498L | STAD | 1 |
p.R656H | PRAD | 1 |
p.S142R | LUSC | 1 |
p.R255W | SKCM | 1 |
p.G636S | STAD | 1 |
p.Q509R | STAD | 1 |
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TissGeneCNV for RFX2 |
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) |
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TissGeneFusions for RFX2 |
Fusion genes including TissGene (ChimerDB 3.0, 2016-12-01 and TCGA fusion Portal 2015-12-01) |
Database | Src | Cancer type | Sample | Fusion gene | ORF | 5'-gene BP | 3'-gene BP |
Chimerdb3.0 | ChiTaRs | NA | BF365469 | RFX2-RFX2 | chr19:6024327 | chr19:6024313 | |
Chimerdb3.0 | ChiTaRs | NA | BF902834 | RFX2-RFX2 | chr19:6039842 | chr19:6013055 | |
Chimerdb3.0 | FusionScan | ESCA | TCGA-Z6-A8JD-01A | RFX2-MLLT1 | 5'UTR-CDS | chr19:6110403 | chr19:6230724 |
Chimerdb3.0 | FusionScan | LUAD | TCGA-50-5946-01A | RFX2-EPOR | 5'UTR-CDS | chr19:6110403 | chr19:11489454 |
TCGAfusionPortal | PRADA | LUAD | TCGA-50-5946-01A | RFX2-EPOR | 5UTR-CDS | Chr19:6110404 | Chr19:11489454 |
TCGAfusionPortal | PRADA | LUAD | TCGA-78-7220-01A | RANBP3-RFX2 | Out-of-frame | Chr19:5978072 | Chr19:6016282 |
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TissGeneNet for RFX2 |
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 RFX2 |
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. |
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. |
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. |
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. |
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TissGeneClin for RFX2 |
TissGeneDrug for RFX2 |
Drug information targeting TissGene (DrugBank Version 5.0.6, 2017-04-01) |
DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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TissGeneDisease for RFX2 |
Disease information associated with TissGene (DisGeNet, 2016-06-01) |
Disease ID | Disease name | # pubmeds | Source |
umls:C0004936 | Mental disorders | 1 | GAD |
umls:C0031511 | Pheochromocytoma | 1 | BeFree |