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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 PRSS27
check button Gene summary
Basic gene informationGene symbolPRSS27
Gene nameprotease, serine 27
SynonymsCAPH2|MPN
CytomapUCSC genome browser: 16p13.3
Type of geneprotein-coding
RefGenesNM_031948.3,
Descriptionchannel-activating protease 2marapsinpancreasinserine protease 27
Modification date20141207
dbXrefs MIM : 608018
HGNC : HGNC
HPRD : 07451
ProteinUniProt:
go to UniProt's Cross Reference DB Table
ExpressionCleanEX: HS_PRSS27
BioGPS: 83886
PathwayNCI Pathway Interaction Database: PRSS27
KEGG: PRSS27
REACTOME: PRSS27
Pathway Commons: PRSS27
ContextiHOP: PRSS27
ligand binding site mutation search in PubMed: PRSS27
UCL Cancer Institute: PRSS27
Assigned class in TissGDB*C
Included tissue-specific gene expression resourcesHPA,GTEx
Specific-tissues in normal samples (assigned by TissGDB using HPA, TiGER, and GTEx)Esophagus
Cancer types related to the specific-tissues in cancer samples (assigned by TissGDB using TCGA)ESCA
Reference showing the relevant tissue of PRSS27
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 PRSS27

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
HNSC2.188313455.780501822-3.5921883722.63E-093.79E-08
BRCA0.07300939-0.9488485051.0218578959.78E-082.94E-07
LUSC0.544322341-1.2274384431.7717607843.98E-091.29E-08


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TissGene-miRNA for PRSS27

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 PRSS27
TissGeneSNV for PRSS27

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.V246GACC3
p.V110GUCEC1
p.Y116*LUAD1
p.L286SDLBC1
p.V246GKIRP1
p.G216SPCPG1
p.Q179*UCEC1
p.P133AHNSC1
p.R34QUCEC1
p.V143MCOAD1
p.V246GLGG1
p.EL129*OV1
p.C214YSKCM1
p.V246GTGCT1
p.Y203CSTAD1
p.E218KACC1
p.R93KHNSC1
p.V110GKIRC1
p.S167NSKCM1


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TissGeneCNV for PRSS27

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 PRSS27

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
TCGAfusionPortalPRADABRCATCGA-LL-A5YP-01AADCY9-PRSS27Out-of-frameChr16:4038995Chr16:2766527


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TissGeneNet for PRSS27

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 PRSS27

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 PRSS27
TissGeneDrug for PRSS27

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 PRSS27

check button Disease information associated with TissGene
(DisGeNet, 2016-06-01)
Disease IDDisease name# pubmedsSource
umls:C0023467Leukemia, Myelocytic, Acute15BeFree
umls:C0032463Polycythemia Vera14BeFree
umls:C0001815Primary Myelofibrosis13BeFree
umls:C0040028Thrombocythemia, Essential10BeFree
umls:C0008626Congenital chromosomal disease7BeFree
umls:C0026987Myelofibrosis4BeFree
umls:C0027022Myeloproliferative disease4BeFree
umls:C1292778Chronic myeloproliferative disorder4BeFree
umls:C0023418leukemia3BeFree
umls:C0023480Leukemia, Myelomonocytic, Chronic3BeFree
umls:C0033027Preleukemia3BeFree
umls:C0039240Supraventricular tachycardia3BeFree
umls:C0346421Chronic eosinophilic leukemia3BeFree
umls:C0349639Juvenile Myelomonocytic Leukemia3BeFree
umls:C1292772Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative3BeFree
umls:C0005699Blast Phase2BeFree
umls:C0019154Hepatic Vein Thrombosis2BeFree
umls:C0023473Myeloid Leukemia, Chronic2BeFree
umls:C0032461Polycythemia2BeFree
umls:C0035334Retinitis Pigmentosa2BeFree
umls:C0836924Thrombocytosis2BeFree
umls:C0856761Budd-Chiari Syndrome2BeFree
umls:C3463824MYELODYSPLASTIC SYNDROME2BeFree
umls:C0002874Aplastic Anemia1BeFree
umls:C0020541Hypertension, Portal1BeFree
umls:C0023481Chronic Neutrophilic Leukemia1BeFree
umls:C0024790Paroxysmal nocturnal hemoglobinuria1BeFree
umls:C0026985Myelodysplasia1BeFree
umls:C0038587Substance Withdrawal Syndrome1BeFree
umls:C0040038Thromboembolism1BeFree
umls:C0149871Deep Vein Thrombosis1BeFree
umls:C0152128Drug withdrawal syndrome1BeFree
umls:C0221013Mastocytosis, Systemic1BeFree
umls:C0272285Heparin-induced thrombocytopenia1BeFree
umls:C0280449secondary acute myeloid leukemia1BeFree
umls:C0398623Thrombophilia1BeFree
umls:C0410000Overlap syndrome1BeFree
umls:C0745091Hypereosinophilia1BeFree
umls:C1301355Myelodysplastic-Myeloproliferative Diseases1BeFree
umls:C1328061Myelodysplastic/myeloproliferative neoplasm, unclassifiable1BeFree
umls:C1333046Myeloproliferative Neoplasm, Unclassifiable1BeFree
umls:C1336735Treatment related acute myeloid leukaemia1BeFree
umls:C1559271Non-Malignant Ascites Adverse Event1BeFree
umls:C2939461Myeloid neoplasm1BeFree