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

Cancer Cell Metabolism Gene Database

Cancer Cell Metabolism Gene DB

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	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 GPX7

Basic gene info.	Gene symbol	GPX7
	Gene name	glutathione peroxidase 7
	Synonyms	CL683\|GPX6\|GPx-7\|GSHPx-7\|NPGPx
	Cytomap	UCSC genome browser: 1p32
	Genomic location	chr1 :53068042-53074723
	Type of gene	protein-coding
	RefGenes	NM_015696.4,
	Ensembl id	ENSG00000116157
	Description	glutathione peroxidase 6non-selenocysteine containing phospholipid hydroperoxide glutathione peroxidase
	Modification date	20141207
dbXrefs	MIM : 615784
	HGNC : HGNC
	Ensembl : ENSG00000116157
	HPRD : 13606
	Vega : OTTHUMG00000008322
Protein	UniProt: go to UniProt's Cross Reference DB Table
Expression	CleanEX: HS_GPX7
	BioGPS: 2882
	Gene Expression Atlas: ENSG00000116157
	The Human Protein Atlas: ENSG00000116157
Pathway	NCI Pathway Interaction Database: GPX7
	KEGG: GPX7
	REACTOME: GPX7
	ConsensusPathDB
	Pathway Commons: GPX7
Metabolism	MetaCyc: GPX7
	HUMANCyc: GPX7
Regulation	Ensembl's Regulation: ENSG00000116157
	miRBase: chr1 :53,068,042-53,074,723
	TargetScan: NM_015696
	cisRED: ENSG00000116157
Context	iHOP: GPX7
	cancer metabolism search in PubMed: GPX7
	UCL Cancer Institute: GPX7
Assigned class in ccmGDB	C

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Phenotypic Information for GPX7(metabolism pathway, cancer, disease, phenome)

Cancer Description
Cancer	CGAP: GPX7
	Familial Cancer Database: GPX7

* 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_ARACHIDONIC_ACID_METABOLISM

Others
OMIM
Orphanet
Disease	KEGG Disease: GPX7
	MedGen: GPX7 (Human Medical Genetics with Condition)
	ClinVar: GPX7
Phenotype	MGI: GPX7 (International Mouse Phenotyping Consortium)
Phenotype	PhenomicDB: GPX7

Mutations for GPX7

* 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 GPX7 related fusion information.

ID	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
CV329033	GPX7	1	289	1	53072428	53074032	CTGF	281	376	6	132270038	132270134
CV329008	GPX7	1	289	1	53072428	53074032	CTGF	281	376	6	132270038	132270134

Other DBs for Structural Variants

Structural Variants in Ensembl: go to Ensembl Structural variation

Structural Variants in dbVar: go to dbVar

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

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

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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=3

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Somatic Mutation Counts per Tissue in COSMIC data

Stat. for Non-Synonymous SNVs (# total SNVs=8)	Stat. for Synonymous SNVs (# total SNVs=6)

Stat. for Deletions (# total SNVs=2)	Stat. for Insertions (# total SNVs=0)
	There's no inserted snv.

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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
chr1:53073950-53073950	p.E139D	2
chr1:53068088-53068088	p.A3S	2
chr1:53068093-53068093	p.A4A	2
chr1:53072531-53072531	p.R105L	2
chr1:53072383-53072383	p.E56*	2
chr1:53073948-53073948	p.E139K	1
chr1:53072454-53072454	p.F79F	1
chr1:53072457-53072457	p.N80N	1
chr1:53073967-53073967	p.W145L	1
chr1:53072487-53072487	p.G90G	1

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SNV Counts per Each Loci in TCGA data

: non-synonymous mutation, : synonymous mutation, Circle size denotes number of samples.
maximum mutation count=2

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		1		1					1			3	1				2	3		3
# mutation		1		1					1			3	1				2	3		3
nonsynonymous SNV		1		1					1			3						3		1
synonymous SNV													1				2			2

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])

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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
chr1:53072531	p.A19V	1
chr1:53072533	p.R34Q	1
chr1:53072580	p.S55S	1
chr1:53068137	p.Q69R	1
chr1:53073948	p.N80N	1
chr1:53068182	p.G90G	1
chr1:53073967	p.S102C	1
chr1:53072382	p.S102N	1
chr1:53073986	p.R105H	1
chr1:53072423	p.R106S	1

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 GPX7 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]

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Gene Expression for GPX7

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))

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CNV vs Gene Expression Plot

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

: Open all plots for all cancer types

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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


APBA2,BCL11A,CDK2AP1,CLIP2,DZIP1,FAM171A1,FBLIM1, FHL3,GPX7,KDELC1,LDHB,MAGOH,MFAP2,OLFM2, RGMA,SERPINH1,SRSF12,SMO,TMEM39B,UBE2E3,UQCRH	FAM216A,CDK4,CGREF1,CRABP1,FAM57A,FKBP10,FSCN1, GPX7,KCNMB4,NPM3,NT5DC2,OSTC,PDE9A,RPLP0, RPS2,RPSAP58,S1PR2,SMO,STMN1,TSPAN33,XPNPEP1

CERCAM,CMTM3,CNRIP1,CTSK,DCN,EFEMP2,EFS, FKBP7,FSTL1,GPX7,IGFBP7,LGALS1,LUM,MAGEH1, PCOLCE,PRRX1,RAB31,RAB34,SDC2,SPARC,THY1	AP1S2,BLVRA,DNAJC18,DUSP22,FAHD2B,GNB5,GPX7, IGFBP7,LOC653653,MAGED2,MAGEH1,NRSN2,OAZ2,PKIA, PRKD3,RAB34,RPL23AP82,RPS2P32,SELM,SMARCD3,TMEM55A

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

: Open all plots for all cancer types

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Interacting Genes (from Pathway Commons)

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

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Pharmacological Information for GPX7

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
DB00143	glutathione peroxidase 7	approved; nutraceutical	Glutathione
DB00515	glutathione peroxidase 7	approved	Cisplatin

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Cross referenced IDs for GPX7

* 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