Cancer Cell Metabolism Database ~~ Bioinformatics and Systems Medicine Laboratory ~~

Cancer Cell Metabolism Gene Database

Cancer Cell Metabolism Gene DB

Home

	Gene Summary
	Phenotypic Information (metabolism pathway, cancer, disease, phenome)
	Mutations : SVs, CNVs, SNVs
	Gene expression: GE, Protein, DEGE, CNV vs GE
	Gene-Gene Network Information: Co-Expression Network, Interacting Genes & KEGG
	Pharmacological Information: Drug-Gene Network
	Cross referenced IDs

Gene Summary for GSTT2

Basic gene info.	Gene symbol	GSTT2
	Gene name	glutathione S-transferase theta 2 (gene/pseudogene)
	Synonyms	-
	Cytomap	UCSC genome browser: 22q11.23
	Genomic location	chr22 :24299600-24303393
	Type of gene	protein-coding
	RefGenes	NM_000854.4, NM_001302670.1,NR_126442.1,NR_126445.1,NR_126446.1,
	Ensembl id	ENSG00000099984
	Description	GST class-theta-2glutathione S-transferase theta-2
	Modification date	20141207
dbXrefs	MIM : 600437
	HGNC : HGNC
	Ensembl : ENSG00000099984
	HPRD : 02701
Protein	UniProt: go to UniProt's Cross Reference DB Table
Expression	CleanEX: HS_GSTT2
	BioGPS: 2953
	Gene Expression Atlas: ENSG00000099984
	The Human Protein Atlas: ENSG00000099984
Pathway	NCI Pathway Interaction Database: GSTT2
	KEGG: GSTT2
	REACTOME: GSTT2
	ConsensusPathDB
	Pathway Commons: GSTT2
Metabolism	MetaCyc: GSTT2
	HUMANCyc: GSTT2
Regulation	Ensembl's Regulation: ENSG00000099984
	miRBase: chr22 :24,299,600-24,303,393
	TargetScan: NM_000854
	cisRED: ENSG00000099984
Context	iHOP: GSTT2
	cancer metabolism search in PubMed: GSTT2
	UCL Cancer Institute: GSTT2
Assigned class in ccmGDB	C

Top

Phenotypic Information for GSTT2(metabolism pathway, cancer, disease, phenome)

Cancer Description
Cancer	CGAP: GSTT2
	Familial Cancer Database: GSTT2

* This gene is included in those cancer gene databases.

						.
Oncogene ¹	Tumor Suppressor gene ²	Cancer Gene Census ³	CancerGenes ⁴	Network of Cancer Gene ⁵	Significant driver gene in	Therapeutic Vulnerabilities in Cancer¹

cf) number; DB name
1 Oncogene; http://nar.oxfordjournals.org/content/35/suppl_1/D721.long,
2 Tumor Suppressor gene; https://bioinfo.uth.edu/TSGene/,
3 Cancer Gene Census; http://www.nature.com/nrc/journal/v4/n3/abs/nrc1299.html,
4 CancerGenes; http://nar.oxfordjournals.org/content/35/suppl_1/D721.long,
5 Network of Cancer Gene; http://ncg.kcl.ac.uk/index.php,
1Therapeutic Vulnerabilities in Cancer; http://cbio.mskcc.org/cancergenomics/statius/

Metabolic Pathway Description
KEGG_GLUTATHIONE_METABOLISM KEGG_METABOLISM_OF_XENOBIOTICS_BY_CYTOCHROME_P450 KEGG_DRUG_METABOLISM_CYTOCHROME_P450

Others
OMIM
Orphanet
Disease	KEGG Disease: GSTT2
	MedGen: GSTT2 (Human Medical Genetics with Condition)
	ClinVar: GSTT2
Phenotype	MGI: GSTT2 (International Mouse Phenotyping Consortium)
Phenotype	PhenomicDB: GSTT2

Mutations for GSTT2

* Under tables are showing count per each tissue to give us broad intuition about tissue specific mutation patterns.You can go to the detailed page for each mutation database's web site.

Structural Variants in COSMIC : go to COSMIC mutation histogram

There's no structural variation information in COSMIC data for this gene.

Related fusion transcripts : go to Chitars2.0

* From mRNA Sanger sequences, Chitars2.0 arranged chimeric transcripts. This table shows GSTT2 related fusion information.

Head Gene

Tail Gene

Accession

Gene_a

qStart_a

qEnd_a

Chromosome_a

tStart_a

tEnd_a

Gene_a

qStart_a

qEnd_a

Chromosome_a

tStart_a

tEnd_a

Other DBs for Structural Variants

Structural Variants in Ensembl: go to Ensembl Structural variation

Structural Variants in dbVar: go to dbVar

Top

Copy Number Variations in COSMIC : go to COSMIC mutation CNV/Expr

There's no copy number variation information in COSMIC data for this gene.

Top

SNV Counts per Each Loci in COSMIC data : go to COSMIC point mutation

: Non-synonymous mutation, : Synonymous mutation, Circle size denotes number of samples.
Maximum mutation count=1

Top

Somatic Mutation Counts per Tissue in COSMIC data

Stat. for Non-Synonymous SNVs (# total SNVs=4)	Stat. for Synonymous SNVs (# total SNVs=3)

Stat. for Deletions (# total SNVs=0)	Stat. for Insertions (# total SNVs=0)
There's no deleted snv.	There's no inserted snv.

Top

Top 10 SNVs Having the Most Samples in COSMIC data

* When you move the cursor on each content, you can see more deailed mutation information on the Tooltip. Those are primary_site,primary_histology,mutation(aa),pubmedID.

GRCh37 position	Mutation(aa)	Unique sampleID count
chr22:24325605-24325605	p.Y181*	2
chr22:24323194-24323194	p.T56T	1
chr22:24323218-24323218	p.L64F	1
chr22:24323226-24323226	p.S67N	1
chr22:24323227-24323227	p.?	1
chr22:24324928-24324928	p.D104N	1
chr22:24325062-24325062	p.V118M	1
chr22:24325095-24325095	p.K129E	1
chr22:24323131-24323131	p.?	1
chr22:24325127-24325127	p.M139I	1

Top

SNV Counts per Each Loci in TCGA data

: non-synonymous mutation, : synonymous mutation, Circle size denotes number of samples.
maximum mutation count=0

Point Mutation/ Tissue ID	1	2	3	4	5	6	7	8	9	10	11	12	13	14	15	16	17	18	19	20
# sample
# mutation
nonsynonymous SNV
synonymous SNV

cf) Tissue ID; Tissue type (1; BLCA[Bladder Urothelial Carcinoma], 2; BRCA[Breast invasive carcinoma], 3; CESC[Cervical squamous cell carcinoma and endocervical adenocarcinoma], 4; COAD[Colon adenocarcinoma], 5; GBM[Glioblastoma multiforme], 6; Glioma Low Grade, 7; HNSC[Head and Neck squamous cell carcinoma], 8; KICH[Kidney Chromophobe], 9; KIRC[Kidney renal clear cell carcinoma], 10; KIRP[Kidney renal papillary cell carcinoma], 11; LAML[Acute Myeloid Leukemia], 12; LUAD[Lung adenocarcinoma], 13; LUSC[Lung squamous cell carcinoma], 14; OV[Ovarian serous cystadenocarcinoma ], 15; PAAD[Pancreatic adenocarcinoma], 16; PRAD[Prostate adenocarcinoma], 17; SKCM[Skin Cutaneous Melanoma], 18:STAD[Stomach adenocarcinoma], 19:THCA[Thyroid carcinoma], 20:UCEC[Uterine Corpus Endometrial Carcinoma])

Top

Top 10 SNVs Having the Most Samples in TCGA data

* We represented just top 10 SNVs. When you move the cursor on each content, you can see more deailed mutation information on the Tooltip. Those are primary_site, primary_histology, mutation(aa), pubmedID.

Genomic Position

Mutation(aa)

Unique sampleID count

Other DBs for Point Mutations

Point Mutation Table of Ensembl: go to Ensembl variation table

Mutation of cBioPortal: go to cBioPortal's Cross-cancer alteration summary

Copy Number for GSTT2 in TCGA

* Copy number data were extracted from TCGA using R package TCGA-Assembler. The URLs of all public data files on TCGA DCC data server were gathered on Jan-05-2015. Function ProcessCNAData in TCGA-Assembler package was used to obtain gene-level copy number value which is calculated as the average copy number of the genomic region of a gene.

cf) Tissue ID[Tissue type]: BLCA[Bladder Urothelial Carcinoma], BRCA[Breast invasive carcinoma], CESC[Cervical squamous cell carcinoma and endocervical adenocarcinoma], COAD[Colon adenocarcinoma], GBM[Glioblastoma multiforme], Glioma Low Grade, HNSC[Head and Neck squamous cell carcinoma], KICH[Kidney Chromophobe], KIRC[Kidney renal clear cell carcinoma], KIRP[Kidney renal papillary cell carcinoma], LAML[Acute Myeloid Leukemia], LUAD[Lung adenocarcinoma], LUSC[Lung squamous cell carcinoma], OV[Ovarian serous cystadenocarcinoma ], PAAD[Pancreatic adenocarcinoma], PRAD[Prostate adenocarcinoma], SKCM[Skin Cutaneous Melanoma], STAD[Stomach adenocarcinoma], THCA[Thyroid carcinoma], UCEC[Uterine Corpus Endometrial Carcinoma]

Top

Gene Expression for GSTT2

Gene Expression in Cancer Cell-lines (CCLE)

* CCLE gene expression data were extracted from CCLE_Expression_Entrez_2012-10-18.res: Gene-centric RMA-normalized mRNA expression data.

Differential Gene Expression in Primary Tumors (TCGA)

* Normalized gene expression data of RNASeqV2 was extracted from TCGA using R package TCGA-Assembler. The URLs of all public data files on TCGA DCC data server were gathered at Jan-05-2015. Only eight cancer types have enough normal control samples for differential expression analysis.
(t test, adjusted p<0.05 (using Benjamini-Hochberg FDR))

Top

CNV vs Gene Expression Plot

* This plots show the correlation between CNV and gene expression.

: Open all plots for all cancer types

Top

Gene-Gene Network Information

Co-Expressed gene's network Plot

* Co-Expression network figures were drawn using R package igraph. Only the top 20 genes with the highest correlations were shown.
Red circle: input gene, orange circle: cell metabolism gene, sky circle: other gene

: Open all plots for all cancer types


AACS,ACSBG1,AKR1D1,LINC01554,CLEC4C,FCN2,GSTM2P1, GSTM5,GSTT2,GUSB,HIST3H3,LOC91948,MAGEB3,MYOM2, NANOG,LINC00160,NR1H4,RNASE11,RNASE12,SLC6A3,TMPRSS9	ABCC11,ABCC2,AKR1D1,B3GAT1,C6orf223,CLDN14,CPB2, FIBCD1,GSTT2,HMGCR,HMGCS1,LOC255167,LRFN2,MVD, MSMO1,SLC5A11,SLCO1B1,SYCP1,TARP,TRPC7,ZP2

ANXA5,ARHGAP10,ARHGAP29,CORO6,ELOVL4,FAM124A,GLI3, GSTT2,HCG4,KIAA1462,NIM1K,NTNG1,PABPC4L,PALLD, PODXL,RAB34,RGS2,RNF144B,SCHIP1,SRPX,VEGFC	ATP2B3,BOC,SSR4P1,COL6A3,FZD4,GPIHBP1,GSTT2, HIST2H2BA,HMX1,LEFTY2,LRRC2,LYPD2,MAN1C1,MAP3K3, MYH10,OLFML3,SEZ6L,STC2,SV2B,THBS2,TSHZ2

Co-Expressed gene's Protein-protein interaction Network Plot

: Open all plots for all cancer types

Top

Interacting Genes (from Pathway Commons)

: Open all interacting genes' information including KEGG pathway for all interacting genes from DAVID

Top

Pharmacological Information for GSTT2

Cross-referenced pharmacological DB IDs from Uniprot

DB Category

DB Name

DB's ID and Url link

Drug-Gene Interaction Network

* Gene Centered Interaction Network.

* Drug Centered Interaction Network.

DrugBank ID	Target Name	Drug Groups	Generic Name	Drug Centered Network	Drug Structure
DB00515	glutathione S-transferase theta 2	approved	Cisplatin
DB01248	glutathione S-transferase theta 2	approved; investigational	Docetaxel

Top

Cross referenced IDs for GSTT2

* We obtained these cross-references from Uniprot database. It covers 150 different DBs, 18 categories. http://www.uniprot.org/help/cross_references_section

: Open all cross reference information