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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 FCN2
check button Gene summary
Basic gene informationGene symbolFCN2
Gene nameficolin (collagen/fibrinogen domain containing lectin) 2
SynonymsEBP-37|FCNL|P35|ficolin-2
CytomapUCSC genome browser: 9q34.3
Type of geneprotein-coding
RefGenesNM_004108.2,
NM_015837.2,NM_015838.1,NM_015839.1,
Description37 kDa elastin-binding proteinL-ficolincollagen/fibrinogen domain-containing protein 2ficolin (collagen/fibrinogen domain containing lectin) 2 (hucolin)ficolin Bficolin-2ficolin-Bficolin-betaserum lectin p35
Modification date20141207
dbXrefs MIM : 601624
HGNC : HGNC
Ensembl : ENSG00000160339
HPRD : 03376
Vega : OTTHUMG00000020892
ProteinUniProt:
go to UniProt's Cross Reference DB Table
ExpressionCleanEX: HS_FCN2
BioGPS: 2220
PathwayNCI Pathway Interaction Database: FCN2
KEGG: FCN2
REACTOME: FCN2
Pathway Commons: FCN2
ContextiHOP: FCN2
ligand binding site mutation search in PubMed: FCN2
UCL Cancer Institute: FCN2
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)Liver
Cancer types related to the specific-tissues in cancer samples (assigned by TissGDB using TCGA)LIHC
Reference showing the relevant tissue of FCN2
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 FCN2

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
LIHC0.971797288.14463928-7.1728421.00E-252.94E-23
BRCA-0.5079401241.189686192-1.6976263164.58E-121.97E-11
KIRP-0.992759970.01139003-1.004150.002160.00547819


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TissGene-miRNA for FCN2

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 FCN2
TissGeneSNV for FCN2

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.A185TSTAD2
p.R103HUCEC2
p.Q165*SKCM1
p.E152KSKCM1
p.P79SSKCM1
p.P54SSKCM1
p.T198ATHCA1
p.T236ATHCA1
p.Q224PESCA1
p.C257FSTAD1
p.V174LLUAD1
p.A193GLUAD1
p.A147TSTAD1
p.E228VSTAD1
p.A288GLUAD1
p.K106XSKCM1
p.S248NSKCM1
p.E190KSKCM1
p.S286NDLBC1
p.G217RSKCM1
p.D100NPAAD1
p.T130NUCEC1
p.G21DESCA1
p.G255RSKCM1
p.G117SREAD1
p.A13SLUAD1
p.K68*SKCM1
p.L197MLUAD1
p.G167SCOAD1
p.Q146HLUAD1
p.Q146HESCA1
p.T236MCOAD1
p.Q203XSKCM1
p.L26PLUAD1
p.C52FCOAD1
p.N163KLUAD1
p.G11VLUSC1
p.R154LLUAD1
p.P41SSKCM1
p.M1IHNSC1
p.G176WLUAD1
p.A65SESCA1
p.E179KSKCM1
p.Q108HESCA1
p.G247SSKCM1
p.M260TCOAD1
p.Y124*HNSC1
p.L191ICOAD1
p.I83MLUAD1
p.R119LHNSC1
p.W104*SKCM1
p.G247SSARC1
p.G72ESKCM1
p.A213VSTAD1
p.Q262PESCA1
p.G101VKIRP1
p.Q108HLUAD1
p.L15MUCEC1
p.I48VLUAD1
p.D138NPAAD1
p.A216VSTAD1
p.D69NSKCM1
p.R71TBRCA1
p.G138WLUAD1
p.D194YREAD1
p.A250GLUAD1
p.A258SCOAD1
p.M37VOV1
p.A65TUCEC1
p.D107NSKCM1
p.A28VPAAD1
p.D30NBLCA1
p.G101RSKCM1


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TissGeneCNV for FCN2

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 FCN2

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 FCN2

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)
FCN2, PITX3, CRP, MASP2, PTX3, MASP1 (tumor)FCN2, PITX3, CRP, MASP2, PTX3, MASP1 (normal)
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COAD (tumor)COAD (normal)
FCN2, PITX3, CRP, MASP2, PTX3, MASP1 (tumor)FCN2, PITX3, CRP, MASP2, PTX3, MASP1 (normal)
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HNSC (tumor)HNSC (normal)
FCN2, PITX3, CRP, MASP2, PTX3, MASP1 (tumor)FCN2, PITX3, CRP, MASP2, PTX3, MASP1 (normal)
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KICH (tumor)KICH (normal)
FCN2, PITX3, CRP, MASP2, PTX3, MASP1 (tumor)FCN2, PITX3, CRP, MASP2, PTX3, MASP1 (normal)
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KIRC (tumor)KIRC (normal)
FCN2, PITX3, CRP, MASP2, PTX3, MASP1 (tumor)FCN2, PITX3, CRP, MASP2, PTX3, MASP1 (normal)
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KIRP (tumor)KIRP (normal)
FCN2, PITX3, CRP, MASP2, PTX3, MASP1 (tumor)FCN2, PITX3, CRP, MASP2, PTX3, MASP1 (normal)
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LIHC (tumor)LIHC (normal)
FCN2, PITX3, CRP, MASP2, PTX3, MASP1 (tumor)FCN2, PITX3, CRP, MASP2, PTX3, MASP1 (normal)
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LUAD (tumor)LUAD (normal)
FCN2, PITX3, CRP, MASP2, PTX3, MASP1 (tumor)FCN2, PITX3, CRP, MASP2, PTX3, MASP1 (normal)
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LUSC (tumor)LUSC (normal)
FCN2, PITX3, CRP, MASP2, PTX3, MASP1 (tumor)FCN2, PITX3, CRP, MASP2, PTX3, MASP1 (normal)
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PRAD (tumor)PRAD (normal)
FCN2, PITX3, CRP, MASP2, PTX3, MASP1 (tumor)FCN2, PITX3, CRP, MASP2, PTX3, MASP1 (normal)
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STAD (tumor)STAD (normal)
FCN2, PITX3, CRP, MASP2, PTX3, MASP1 (tumor)FCN2, PITX3, CRP, MASP2, PTX3, MASP1 (normal)
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THCA (tumor)THCA (normal)
FCN2, PITX3, CRP, MASP2, PTX3, MASP1 (tumor)FCN2, PITX3, CRP, MASP2, PTX3, MASP1 (normal)
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TissGeneProg for FCN2

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 FCN2
TissGeneDrug for FCN2

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 FCN2

check button Disease information associated with TissGene
(DisGeNet, 2016-06-01)
Disease IDDisease name# pubmedsSource
umls:C0035243Respiratory Tract Infections4BeFree,GAD
umls:C0524851Neurodegenerative Disorders4BeFree
umls:C0004623Bacterial Infections2BeFree,GAD
umls:C0011854Diabetes Mellitus, Insulin-Dependent2BeFree
umls:C0019163Hepatitis B2BeFree
umls:C0023343Leprosy2BeFree,GAD
umls:C0024141Lupus Erythematosus, Systemic2BeFree
umls:C0024198Lyme Disease2BeFree
umls:C0024530Malaria2BeFree
umls:C0029925Ovarian Carcinoma2BeFree
umls:C0036323Schistosomiasis2BeFree
umls:C0042769Virus Diseases2BeFree
umls:C1140680Malignant neoplasm of ovary2BeFree
umls:C3280586Mannose-Binding Protein Deficiency2BeFree
umls:C0002395Alzheimer's Disease1BeFree
umls:C0003873Rheumatoid Arthritis1GAD
umls:C0004096Asthma1BeFree
umls:C0004114Astrocytoma1BeFree
umls:C0004943Behcet Syndrome1BeFree,GAD
umls:C0006111Brain Diseases1BeFree
umls:C0006267Bronchiectasis1BeFree
umls:C0009447Common Variable Immunodeficiency1BeFree
umls:C0010346Crohn Disease1BeFree
umls:C0010823Cytomegalovirus Infections1BeFree
umls:C0019196Hepatitis C1BeFree
umls:C0023281Leishmaniasis1BeFree
umls:C0023283Leishmaniasis, Cutaneous1BeFree
umls:C0023290Leishmaniasis, Visceral1BeFree
umls:C0025202melanoma1BeFree
umls:C0026847Spinal Muscular Atrophy1BeFree
umls:C0027765nervous system disorder1BeFree
umls:C0027819Neuroblastoma1BeFree
umls:C0029463Osteosarcoma1BeFree
umls:C0030524Paratuberculosis1BeFree
umls:C0031154Peritonitis1BeFree
umls:C0032269Pneumococcal Infections1BeFree
umls:C0032787Postoperative Complications1GAD
umls:C0035204Respiration Disorders1BeFree
umls:C0035242Respiratory Tract Diseases1BeFree
umls:C0035436Rheumatic Fever1BeFree,GAD
umls:C0035439Rheumatic Heart Disease1BeFree,GAD
umls:C0036341Schizophrenia1BeFree
umls:C0036916Sexually Transmitted Diseases1BeFree
umls:C0038395Streptococcal Infections1BeFree,GAD
umls:C0038454Cerebrovascular accident1BeFree
umls:C0041296Tuberculosis1BeFree
umls:C0041327Tuberculosis, Pulmonary1BeFree
umls:C0041341Tuberous Sclerosis1BeFree
umls:C0158944Infections specific to perinatal period1BeFree
umls:C0175708Chronic rheumatic heart disease1BeFree
umls:C0220756Niemann-Pick Disease, Type C1BeFree
umls:C0233794Memory impairment1BeFree
umls:C0276609Acute type B viral hepatitis1BeFree
umls:C0333186Restenosis1BeFree
umls:C0585442Osteosarcoma of bone1BeFree
umls:C0700095Central neuroblastoma1BeFree
umls:C0863094Recurrent respiratory tract infections1BeFree
umls:C0919267ovarian neoplasm1BeFree
umls:C1292769Precursor B-cell lymphoblastic leukemia1BeFree
umls:C1562908Leprosy, Paucibacillary1BeFree
umls:C1704430Urinary Schistosomiasis1BeFree
umls:C1846064Recurrent infections (sinusitis and bacterial pneumonia and meningitis)1BeFree
umls:C1848199X-Linked Lissencephaly1BeFree
umls:C2607914Allergic rhinitis (disorder)1BeFree
umls:C3665346Unspecified visual loss1BeFree