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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 GGN
check button Gene summary
Basic gene informationGene symbolGGN
Gene namegametogenetin
Synonyms-
CytomapUCSC genome browser: 19q13.2
Type of geneprotein-coding
RefGenesNM_152657.3,
NM_182477.1,
Description-
Modification date20141207
dbXrefs MIM : 609966
HGNC : HGNC
Ensembl : ENSG00000179168
HPRD : 17036
Vega : OTTHUMG00000182080
ProteinUniProt:
go to UniProt's Cross Reference DB Table
ExpressionCleanEX: HS_GGN
BioGPS: 199720
PathwayNCI Pathway Interaction Database: GGN
KEGG: GGN
REACTOME: GGN
Pathway Commons: GGN
ContextiHOP: GGN
ligand binding site mutation search in PubMed: GGN
UCL Cancer Institute: GGN
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)Testis
Cancer types related to the specific-tissues in cancer samples (assigned by TissGDB using TCGA)TGCT
Reference showing the relevant tissue of GGN
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 GGN

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
COAD-1.576602104-2.7714328731.1948307693.75E-072.31E-06


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TissGene-miRNA for GGN

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 GGN
TissGeneSNV for GGN

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.A480PACC3
p.A513VSTAD2
p.S267LLUAD1
p.P439QCOAD1
p.N610TKIRC1
p.I631MCESC1
p.P96LSKCM1
p.R334WSTAD1
p.P293HLUAD1
p.L73PLIHC1
p.G275DHNSC1
p.R187KBLCA1
p.P175LSKCM1
p.P429QESCA1
p.Q492PCOAD1
p.A115VSTAD1
p.A196TLIHC1
p.E425KSTAD1
p.A382TACC1
p.A224VTHCA1
p.S508LSTAD1
p.R207HSTAD1
p.G214SLUAD1
p.P557SSTAD1
p.L239MHNSC1
p.G218RTHYM1
p.T538ICOAD1
p.P429QLUAD1
p.G368EHNSC1
p.A264VHNSC1
p.A552SUCEC1
p.A196TSARC1
p.P118SLUAD1
p.S6LBLCA1
p.G314ESKCM1
p.L543VLUAD1
p.C594XSKCM1
p.Q18KCOAD1
p.W353GUVM1
p.Q492PPAAD1
p.T577IUCEC1
p.A160TSKCM1
p.A552DSARC1
p.T555ASTAD1
p.D491NCESC1
p.S327LESCA1
p.P376LSTAD1
p.A356TUCEC1
p.P438LLUAD1
p.E320KDLBC1
p.A569DLIHC1
p.G563RSKCM1
p.N367SSKCM1
p.P507SACC1
p.V611IKIRC1
p.R300CSTAD1
p.R581CSARC1
p.R207HCOAD1
p.R606SLUSC1
p.G218RUCEC1
p.G368RLUAD1
p.M61TESCA1
p.A333DKIRP1
p.G314RKIRC1
p.G368RHNSC1
p.P158RLUAD1
p.G272RHNSC1
p.F586LHNSC1
p.C594*SKCM1


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TissGeneCNV for GGN

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 GGN

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 GGN

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)
GGN, FANCL, GGNBP2, OAZ3 (tumor)GGN, FANCL, GGNBP2, OAZ3 (normal)
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COAD (tumor)COAD (normal)
GGN, FANCL, GGNBP2, OAZ3 (tumor)GGN, FANCL, GGNBP2, OAZ3 (normal)
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HNSC (tumor)HNSC (normal)
GGN, FANCL, GGNBP2, OAZ3 (tumor)GGN, FANCL, GGNBP2, OAZ3 (normal)
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KICH (tumor)KICH (normal)
GGN, FANCL, GGNBP2, OAZ3 (tumor)GGN, FANCL, GGNBP2, OAZ3 (normal)
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KIRC (tumor)KIRC (normal)
GGN, FANCL, GGNBP2, OAZ3 (tumor)GGN, FANCL, GGNBP2, OAZ3 (normal)
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KIRP (tumor)KIRP (normal)
GGN, FANCL, GGNBP2, OAZ3 (tumor)GGN, FANCL, GGNBP2, OAZ3 (normal)
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LIHC (tumor)LIHC (normal)
GGN, FANCL, GGNBP2, OAZ3 (tumor)GGN, FANCL, GGNBP2, OAZ3 (normal)
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LUAD (tumor)LUAD (normal)
GGN, FANCL, GGNBP2, OAZ3 (tumor)GGN, FANCL, GGNBP2, OAZ3 (normal)
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LUSC (tumor)LUSC (normal)
GGN, FANCL, GGNBP2, OAZ3 (tumor)GGN, FANCL, GGNBP2, OAZ3 (normal)
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PRAD (tumor)PRAD (normal)
GGN, FANCL, GGNBP2, OAZ3 (tumor)GGN, FANCL, GGNBP2, OAZ3 (normal)
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STAD (tumor)STAD (normal)
GGN, FANCL, GGNBP2, OAZ3 (tumor)GGN, FANCL, GGNBP2, OAZ3 (normal)
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THCA (tumor)THCA (normal)
GGN, FANCL, GGNBP2, OAZ3 (tumor)GGN, FANCL, GGNBP2, OAZ3 (normal)
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TissGeneProg for GGN

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 GGN
TissGeneDrug for GGN

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 GGN

check button Disease information associated with TissGene
(DisGeNet, 2016-06-01)
Disease IDDisease name# pubmedsSource
umls:C0376358Malignant neoplasm of prostate10BeFree
umls:C0600139Prostate carcinoma10BeFree
umls:C0021364Male infertility5BeFree
umls:C0010417Cryptorchidism3BeFree
umls:C1691215Penile hypospadias3BeFree
umls:C0452147Hypospadias, penoscrotal2BeFree
umls:C0848558Hypospadias2BeFree
umls:C1704272Benign Prostatic Hyperplasia2BeFree
umls:C0000768Congenital Abnormality1BeFree
umls:C0006142Malignant neoplasm of breast1BeFree
umls:C0007103Malignant neoplasm of endometrium1BeFree
umls:C0007138Carcinoma, Transitional Cell1BeFree
umls:C0027627Neoplasm Metastasis1BeFree
umls:C0028754Obesity1BeFree
umls:C0039585Androgen-Insensitivity Syndrome1BeFree
umls:C0042755Virilism1BeFree
umls:C0242339Dyslipidemias1BeFree
umls:C0311277Obesity, Abdominal1BeFree
umls:C0476089Endometrial Carcinoma1BeFree
umls:C0678222Breast Carcinoma1BeFree
umls:C085265421-hydroxylase deficiency1BeFree
umls:C0855197Testicular malignant germ cell tumor1BeFree
umls:C0936016Testicular Feminization1BeFree
umls:C1883486Uterine Corpus Cancer1BeFree
umls:C2145472Urothelial Carcinoma1BeFree
umls:C2936858Congenital adrenal hyperplasia due to 21 hydroxylase deficiency1BeFree