TissGeneSummary for FLRT3 |
Gene summary |
Basic gene information | Gene symbol | FLRT3 |
Gene name | fibronectin leucine rich transmembrane protein 3 | |
Synonyms | HH21 | |
Cytomap | UCSC genome browser: 20p11 | |
Type of gene | protein-coding | |
RefGenes | NM_013281.3, NM_198391.2, | |
Description | fibronectin-like domain-containing leucine-rich transmembrane protein 3leucine-rich repeat transmembrane protein FLRT3 | |
Modification date | 20141207 | |
dbXrefs | MIM : 604808 | |
HGNC : HGNC | ||
Ensembl : ENSG00000125848 | ||
HPRD : 05313 | ||
Vega : OTTHUMG00000031914 | ||
Protein | UniProt: go to UniProt's Cross Reference DB Table | |
Expression | CleanEX: HS_FLRT3 | |
BioGPS: 23767 | ||
Pathway | NCI Pathway Interaction Database: FLRT3 | |
KEGG: FLRT3 | ||
REACTOME: FLRT3 | ||
Pathway Commons: FLRT3 | ||
Context | iHOP: FLRT3 | |
ligand binding site mutation search in PubMed: FLRT3 | ||
UCL Cancer Institute: FLRT3 | ||
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) | KidneyLung | |
Cancer types related to the specific-tissues in cancer samples (assigned by TissGDB using TCGA) | KIRC,KIRP,KICHLUAD,LUSC | |
Reference showing the relevant tissue of FLRT3 | ||
Description by TissGene annotations | Risk TissGene in OS Have significant anti-correlated miRNA |
* 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 FLRT3 |
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 |
PRAD | 0.136394089 | 1.505699858 | -1.369305769 | 6.71E-06 | 3.94E-05 |
KIRC | 1.026560008 | 2.577097508 | -1.5505375 | 1.30E-08 | 3.89E-08 |
LUAD | 0.927301052 | 3.470782086 | -2.543481034 | 3.04E-14 | 2.85E-13 |
KICH | -2.822018603 | 2.372721397 | -5.19474 | 1.33E-14 | 2.36E-13 |
LIHC | -0.370668603 | 1.093281397 | -1.46395 | 4.44E-06 | 2.05E-05 |
LUSC | -0.239101348 | 3.205477083 | -3.444578431 | 2.64E-14 | 1.47E-13 |
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TissGene-miRNA for FLRT3 |
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 |
UCS | hsa-miR-9-5p | MIMAT0000441 | 0.014 | -0.33 | 56 |
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TissGeneMut for FLRT3 |
TissGeneSNV for FLRT3 |
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.G197C | LUAD | 2 |
p.E498K | LUAD | 2 |
p.V329M | LIHC | 1 |
p.R186H | BRCA | 1 |
p.I364T | SKCM | 1 |
p.C334Y | HNSC | 1 |
p.T373P | UCEC | 1 |
p.R261W | UCEC | 1 |
p.R637I | STAD | 1 |
p.L302V | BLCA | 1 |
p.R461H | BLCA | 1 |
p.L348F | SKCM | 1 |
p.P174S | UCEC | 1 |
p.E591K | SKCM | 1 |
p.N226H | COAD | 1 |
p.R261L | LUAD | 1 |
p.D122N | SKCM | 1 |
p.R303C | SKCM | 1 |
p.G640D | PAAD | 1 |
p.L83Q | LUSC | 1 |
p.M433V | SARC | 1 |
p.E577K | SKCM | 1 |
p.S560L | HNSC | 1 |
p.R634Q | READ | 1 |
p.R234W | BRCA | 1 |
p.Y636* | SKCM | 1 |
p.N265D | COAD | 1 |
p.S279Y | PRAD | 1 |
p.R203H | HNSC | 1 |
p.L206I | UCEC | 1 |
p.T373I | STAD | 1 |
p.R303S | CHOL | 1 |
p.A4T | STAD | 1 |
p.S593Y | COAD | 1 |
p.S77* | BRCA | 1 |
p.Y636X | SKCM | 1 |
p.A239T | BLCA | 1 |
p.E132K | SKCM | 1 |
p.C496S | HNSC | 1 |
p.N621D | STAD | 1 |
p.E460K | SKCM | 1 |
p.V34A | UCEC | 1 |
p.S560T | LIHC | 1 |
p.E113* | UCEC | 1 |
p.H400Q | COAD | 1 |
p.R157Q | STAD | 1 |
p.I614M | ESCA | 1 |
p.I301L | STAD | 1 |
p.R36H | THYM | 1 |
p.R515Q | UCEC | 1 |
p.N67S | SKCM | 1 |
p.Q69R | PAAD | 1 |
p.I56T | STAD | 1 |
p.T168A | STAD | 1 |
p.R181C | BLCA | 1 |
p.R261W | SKCM | 1 |
p.D218E | READ | 1 |
p.P376S | SKCM | 1 |
p.S593C | HNSC | 1 |
p.T367N | COAD | 1 |
p.R330H | BLCA | 1 |
p.P642Q | PRAD | 1 |
p.W440L | ESCA | 1 |
p.W550C | LUAD | 1 |
p.N526K | SKCM | 1 |
p.N260D | UCEC | 1 |
p.R341C | SKCM | 1 |
p.R203H | LUSC | 1 |
p.N213T | PAAD | 1 |
p.R634* | UCEC | 1 |
p.S426C | BLCA | 1 |
p.P193L | SKCM | 1 |
p.S628G | LGG | 1 |
p.P306L | SKCM | 1 |
p.R186H | UCEC | 1 |
p.P406L | SKCM | 1 |
p.T363I | SKCM | 1 |
p.E463Q | HNSC | 1 |
p.N81T | COAD | 1 |
p.P170S | SKCM | 1 |
p.Q272R | LUAD | 1 |
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TissGeneCNV for FLRT3 |
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 FLRT3 |
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 |
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TissGeneNet for FLRT3 |
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 FLRT3 |
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 FLRT3 |
TissGeneDrug for FLRT3 |
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 FLRT3 |
Disease information associated with TissGene (DisGeNet, 2016-06-01) |
Disease ID | Disease name | # pubmeds | Source |
umls:C0000786 | Spontaneous abortion | 1 | CTD_human |
umls:C0022735 | Klinefelter Syndrome | 1 | BeFree |
umls:C0271623 | Hypogonadotropic hypogonadism | 1 | BeFree |
umls:C3808986 | HYPOGONADOTROPIC HYPOGONADISM 21 WITH OR WITHOUT ANOSMIA | 1 | UNIPROT |
umls:C0162809 | Kallmann Syndrome | 0 | ORPHANET |