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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 APOH
check button Gene summary
Basic gene informationGene symbolAPOH
Gene nameapolipoprotein H (beta-2-glycoprotein I)
SynonymsB2G1|B2GP1|BG
CytomapUCSC genome browser: 17q24.2
Type of geneprotein-coding
RefGenesNM_000042.2,
DescriptionAPC inhibitorB2GPIactivated protein C-binding proteinanticardiolipin cofactorapo-Hbeta(2)GPIbeta-2-glycoprotein 1
Modification date20141207
dbXrefs MIM : 138700
HGNC : HGNC
Ensembl : ENSG00000091583
HPRD : 00728
Vega : OTTHUMG00000179530
ProteinUniProt:
go to UniProt's Cross Reference DB Table
ExpressionCleanEX: HS_APOH
BioGPS: 350
PathwayNCI Pathway Interaction Database: APOH
KEGG: APOH
REACTOME: APOH
Pathway Commons: APOH
ContextiHOP: APOH
ligand binding site mutation search in PubMed: APOH
UCL Cancer Institute: APOH
Assigned class in TissGDB*B
Included tissue-specific gene expression resourcesHPA,TiGER,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 APOH
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
GO:0001937negative regulation of endothelial cell proliferation17872974
GO:0006641triglyceride metabolic process7417307
GO:0007597blood coagulation, intrinsic pathway4052628
GO:0010596negative regulation of endothelial cell migration17872974
GO:0016525negative regulation of angiogenesis17872974
GO:0030195negative regulation of blood coagulation4052628
GO:0031639plasminogen activation16480936
GO:0033033negative regulation of myeloid cell apoptotic process15534879
GO:0034392negative regulation of smooth muscle cell apoptotic process15534879
GO:0051006positive regulation of lipoprotein lipase activity7417307
GO:0051917regulation of fibrinolysis16480936
GO:0051918negative regulation of fibrinolysis14726399
GO:0001937negative regulation of endothelial cell proliferation17872974
GO:0006641triglyceride metabolic process7417307
GO:0007597blood coagulation, intrinsic pathway4052628
GO:0010596negative regulation of endothelial cell migration17872974
GO:0016525negative regulation of angiogenesis17872974
GO:0030195negative regulation of blood coagulation4052628
GO:0031639plasminogen activation16480936
GO:0033033negative regulation of myeloid cell apoptotic process15534879
GO:0034392negative regulation of smooth muscle cell apoptotic process15534879
GO:0051006positive regulation of lipoprotein lipase activity7417307
GO:0051917regulation of fibrinolysis16480936
GO:0051918negative regulation of fibrinolysis14726399


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TissGeneExp for APOH

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
LIHC13.6082959415.53252594-1.924232.24E-058.74E-05
KICH-2.0978560622.160099938-4.2579565.63E-072.22E-06
LUSC-0.875299674.812990526-5.6882901962.57E-321.70E-30
LUAD2.5129906274.746061317-2.233070693.07E-081.30E-07
KIRP-0.2851206874.011973063-4.297093751.62E-081.20E-07
COAD-0.3771762160.920354553-1.2975307690.0002190.000737065
KIRC1.4621199383.303357438-1.84123750.0003380.000669724


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TissGene-miRNA for APOH

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 APOH
TissGeneSNV for APOH

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.S146FSKCM2
p.G161ESKCM2
p.P85SSKCM2
p.T149MSTAD1
p.G128ESKCM1
p.K269NSTAD1
p.W335SCOAD1
p.M1VSKCM1
p.P148TKIRC1
p.S239FSKCM1
p.E321KCOAD1
p.D341NSKCM1
p.G277RSKCM1
p.T223PKIRC1
p.E284KSKCM1
p.E45*UCEC1
p.C315*LUSC1
p.G113RKIRC1
p.G93ESKCM1
p.E245*UCEC1
p.M180ISTAD1
p.F286ICOAD1
p.D317EBRCA1
p.D317ALIHC1
p.C51XTHYM1
p.P43AHNSC1
p.Q314LLUSC1
p.G242CBLCA1
p.P208SSKCM1
p.E304KSKCM1
p.E311*LUAD1
p.E245KSKCM1
p.D184NSKCM1
p.D312ELUAD1
p.E284*UCEC1
p.S297FSKCM1
p.D184YUCEC1
p.C307YCESC1
p.G214ESKCM1
p.R58*UCEC1
p.W130RSTAD1
p.P53LESCA1
p.C205YTHYM1
p.A160DDLBC1
p.E91KPAAD1
p.E46KESCA1
p.S164FSKCM1
p.T152ICESC1
p.R21QSKCM1
p.P85SLIHC1
p.Y156*LUAD1
p.P176SSTAD1
p.R154CHNSC1
p.K229TCOAD1
p.R58QSTAD1


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TissGeneCNV for APOH

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 APOH

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
Chimerdb3.0ChiTaRsNABG469920MTMR3-APOHchr22:30279348chr17:64212981
Chimerdb3.0ChiTaRsNABG824141MTMR3-APOHchr22:30279348chr17:64216676


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TissGeneNet for APOH

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)
APOH, TP53, HNF4A, ONECUT1, GRB2, RBBP6, CDC42, GEM, ANXA2, PLG, AKT1, HNF1A, LRP8, LPA, F10, CLEC4G, LRP2, LDLR, F12 (tumor)APOH, TP53, HNF4A, ONECUT1, GRB2, RBBP6, CDC42, GEM, ANXA2, PLG, AKT1, HNF1A, LRP8, LPA, F10, CLEC4G, LRP2, LDLR, F12 (normal)
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COAD (tumor)COAD (normal)
APOH, TP53, HNF4A, ONECUT1, GRB2, RBBP6, CDC42, GEM, ANXA2, PLG, AKT1, HNF1A, LRP8, LPA, F10, CLEC4G, LRP2, LDLR, F12 (tumor)APOH, TP53, HNF4A, ONECUT1, GRB2, RBBP6, CDC42, GEM, ANXA2, PLG, AKT1, HNF1A, LRP8, LPA, F10, CLEC4G, LRP2, LDLR, F12 (normal)
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HNSC (tumor)HNSC (normal)
APOH, TP53, HNF4A, ONECUT1, GRB2, RBBP6, CDC42, GEM, ANXA2, PLG, AKT1, HNF1A, LRP8, LPA, F10, CLEC4G, LRP2, LDLR, F12 (tumor)APOH, TP53, HNF4A, ONECUT1, GRB2, RBBP6, CDC42, GEM, ANXA2, PLG, AKT1, HNF1A, LRP8, LPA, F10, CLEC4G, LRP2, LDLR, F12 (normal)
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KICH (tumor)KICH (normal)
APOH, TP53, HNF4A, ONECUT1, GRB2, RBBP6, CDC42, GEM, ANXA2, PLG, AKT1, HNF1A, LRP8, LPA, F10, CLEC4G, LRP2, LDLR, F12 (tumor)APOH, TP53, HNF4A, ONECUT1, GRB2, RBBP6, CDC42, GEM, ANXA2, PLG, AKT1, HNF1A, LRP8, LPA, F10, CLEC4G, LRP2, LDLR, F12 (normal)
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KIRC (tumor)KIRC (normal)
APOH, TP53, HNF4A, ONECUT1, GRB2, RBBP6, CDC42, GEM, ANXA2, PLG, AKT1, HNF1A, LRP8, LPA, F10, CLEC4G, LRP2, LDLR, F12 (tumor)APOH, TP53, HNF4A, ONECUT1, GRB2, RBBP6, CDC42, GEM, ANXA2, PLG, AKT1, HNF1A, LRP8, LPA, F10, CLEC4G, LRP2, LDLR, F12 (normal)
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KIRP (tumor)KIRP (normal)
APOH, TP53, HNF4A, ONECUT1, GRB2, RBBP6, CDC42, GEM, ANXA2, PLG, AKT1, HNF1A, LRP8, LPA, F10, CLEC4G, LRP2, LDLR, F12 (tumor)APOH, TP53, HNF4A, ONECUT1, GRB2, RBBP6, CDC42, GEM, ANXA2, PLG, AKT1, HNF1A, LRP8, LPA, F10, CLEC4G, LRP2, LDLR, F12 (normal)
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LIHC (tumor)LIHC (normal)
APOH, TP53, HNF4A, ONECUT1, GRB2, RBBP6, CDC42, GEM, ANXA2, PLG, AKT1, HNF1A, LRP8, LPA, F10, CLEC4G, LRP2, LDLR, F12 (tumor)APOH, TP53, HNF4A, ONECUT1, GRB2, RBBP6, CDC42, GEM, ANXA2, PLG, AKT1, HNF1A, LRP8, LPA, F10, CLEC4G, LRP2, LDLR, F12 (normal)
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LUAD (tumor)LUAD (normal)
APOH, TP53, HNF4A, ONECUT1, GRB2, RBBP6, CDC42, GEM, ANXA2, PLG, AKT1, HNF1A, LRP8, LPA, F10, CLEC4G, LRP2, LDLR, F12 (tumor)APOH, TP53, HNF4A, ONECUT1, GRB2, RBBP6, CDC42, GEM, ANXA2, PLG, AKT1, HNF1A, LRP8, LPA, F10, CLEC4G, LRP2, LDLR, F12 (normal)
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LUSC (tumor)LUSC (normal)
APOH, TP53, HNF4A, ONECUT1, GRB2, RBBP6, CDC42, GEM, ANXA2, PLG, AKT1, HNF1A, LRP8, LPA, F10, CLEC4G, LRP2, LDLR, F12 (tumor)APOH, TP53, HNF4A, ONECUT1, GRB2, RBBP6, CDC42, GEM, ANXA2, PLG, AKT1, HNF1A, LRP8, LPA, F10, CLEC4G, LRP2, LDLR, F12 (normal)
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PRAD (tumor)PRAD (normal)
APOH, TP53, HNF4A, ONECUT1, GRB2, RBBP6, CDC42, GEM, ANXA2, PLG, AKT1, HNF1A, LRP8, LPA, F10, CLEC4G, LRP2, LDLR, F12 (tumor)APOH, TP53, HNF4A, ONECUT1, GRB2, RBBP6, CDC42, GEM, ANXA2, PLG, AKT1, HNF1A, LRP8, LPA, F10, CLEC4G, LRP2, LDLR, F12 (normal)
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STAD (tumor)STAD (normal)
APOH, TP53, HNF4A, ONECUT1, GRB2, RBBP6, CDC42, GEM, ANXA2, PLG, AKT1, HNF1A, LRP8, LPA, F10, CLEC4G, LRP2, LDLR, F12 (tumor)APOH, TP53, HNF4A, ONECUT1, GRB2, RBBP6, CDC42, GEM, ANXA2, PLG, AKT1, HNF1A, LRP8, LPA, F10, CLEC4G, LRP2, LDLR, F12 (normal)
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THCA (tumor)THCA (normal)
APOH, TP53, HNF4A, ONECUT1, GRB2, RBBP6, CDC42, GEM, ANXA2, PLG, AKT1, HNF1A, LRP8, LPA, F10, CLEC4G, LRP2, LDLR, F12 (tumor)APOH, TP53, HNF4A, ONECUT1, GRB2, RBBP6, CDC42, GEM, ANXA2, PLG, AKT1, HNF1A, LRP8, LPA, F10, CLEC4G, LRP2, LDLR, F12 (normal)
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TissGeneProg for APOH

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 APOH
TissGeneDrug for APOH

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 APOH

check button Disease information associated with TissGene
(DisGeNet, 2016-06-01)
Disease IDDisease name# pubmedsSource
umls:C0085278Antiphospholipid Syndrome39BeFree,GAD,LHGDN
umls:C0085409Polyendocrinopathies, Autoimmune22BeFree
umls:C0024141Lupus Erythematosus, Systemic14BeFree,GAD
umls:C0040053Thrombosis7GAD,LHGDN,RGD
umls:C0004153Atherosclerosis5BeFree,LHGDN
umls:C0151942Arterial thrombosis4BeFree
umls:C0311370Lupus anticoagulant disorder4BeFree
umls:C0584960Factor V Leiden mutation4BeFree
umls:C0007785Cerebral Infarction3BeFree,GAD,LHGDN
umls:C0038454Cerebrovascular accident3BeFree,GAD
umls:C0003850Arteriosclerosis2BeFree
umls:C0004364Autoimmune Diseases2BeFree
umls:C0023434Chronic Lymphocytic Leukemia2BeFree
umls:C0023903Liver neoplasms2BeFree
umls:C0024131Lupus Vulgaris2BeFree
umls:C0024138Lupus Erythematosus, Discoid2BeFree
umls:C0027051Myocardial Infarction2BeFree,RGD
umls:C0398623Thrombophilia2BeFree
umls:C0409974Lupus Erythematosus2BeFree
umls:C0553692Brain hemorrhage2GAD
umls:C0860207Drug-Induced Liver Injury2CTD_human,RGD
umls:C1562585Leprosy, Multibacillary2BeFree,GAD
umls:C2239176Liver carcinoma2BeFree
umls:C0004943Behcet Syndrome1LHGDN
umls:C0005779Blood Coagulation Disorders1BeFree
umls:C0007222Cardiovascular Diseases1BeFree
umls:C0007282Carotid Stenosis1GAD
umls:C0009324Ulcerative Colitis1LHGDN
umls:C0011847Diabetes1BeFree
umls:C0011849Diabetes Mellitus1BeFree
umls:C0012739Disseminated Intravascular Coagulation1LHGDN
umls:C0019196Hepatitis C1BeFree
umls:C0020445Hypercholesterolemia, Familial1BeFree
umls:C0020538Hypertensive disease1BeFree
umls:C0022661Kidney Failure, Chronic1GAD
umls:C0023487Acute Promyelocytic Leukemia1BeFree
umls:C0023890Liver Cirrhosis1LHGDN
umls:C0024143Lupus Nephritis1GAD
umls:C0024305Lymphoma, Non-Hodgkin1LHGDN
umls:C0025202melanoma1BeFree
umls:C0036341Schizophrenia1BeFree
umls:C0039614Tetanus1BeFree
umls:C0042373Vascular Diseases1BeFree
umls:C0042769Virus Diseases1BeFree
umls:C0156149Gastrointestinal tract vascular insufficiency1BeFree
umls:C0242422Parkinsonian Disorders1LHGDN
umls:C0242666Protein S Deficiency1BeFree
umls:C0272285Heparin-induced thrombocytopenia1BeFree
umls:C0524620Metabolic Syndrome X1BeFree
umls:C0600433Activated Protein C Resistance1LHGDN
umls:C0836924Thrombocytosis1BeFree
umls:C0856169Endothelial dysfunction1BeFree
umls:C0948008Ischemic stroke1BeFree
umls:C1527336Sjogren's Syndrome1LHGDN
umls:C1562908Leprosy, Paucibacillary1GAD
umls:C1704436Peripheral Arterial Diseases1BeFree
umls:C2004435Vascular insufficiency of intestine1BeFree
umls:C2937358Cerebral Hemorrhage1LHGDN
umls:C3714514Infection1LHGDN