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 GGT1

Basic gene info.	Gene symbol	GGT1
	Gene name	gamma-glutamyltransferase 1
	Synonyms	CD224\|D22S672\|D22S732\|GGT\|GGT 1\|GTG
	Cytomap	UCSC genome browser: 22q11.23
	Genomic location	chr22 :24999123-25024972
	Type of gene	protein-coding
	RefGenes	NM_013421.2, NM_013430.2,NM_001032364.2,NM_001032365.2,NM_005265.3, NM_001288833.1,
	Ensembl id	ENSG00000100031
	Description	gamma-glutamyltranspeptidase 1glutathione hydrolase 1leukotriene-C4 hydrolase
	Modification date	20141215
dbXrefs	MIM : 612346
	HGNC : HGNC
	Ensembl : ENSG00000100031
	HPRD : 01980
	Vega : OTTHUMG00000030859
Protein	UniProt: go to UniProt's Cross Reference DB Table
Expression	CleanEX: HS_GGT1
	BioGPS: 2678
	Gene Expression Atlas: ENSG00000100031
	The Human Protein Atlas: ENSG00000100031
Pathway	NCI Pathway Interaction Database: GGT1
	KEGG: GGT1
	REACTOME: GGT1
	ConsensusPathDB
	Pathway Commons: GGT1
Metabolism	MetaCyc: GGT1
	HUMANCyc: GGT1
Regulation	Ensembl's Regulation: ENSG00000100031
	miRBase: chr22 :24,999,123-25,024,972
	TargetScan: NM_013421
	cisRED: ENSG00000100031
Context	iHOP: GGT1
	cancer metabolism search in PubMed: GGT1
	UCL Cancer Institute: GGT1
Assigned class in ccmGDB	C

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Phenotypic Information for GGT1(metabolism pathway, cancer, disease, phenome)

Cancer Description
Cancer	CGAP: GGT1
	Familial Cancer Database: GGT1

* 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_TAURINE_AND_HYPOTAURINE_METABOLISM KEGG_SELENOAMINO_ACID_METABOLISM KEGG_GLUTATHIONE_METABOLISM KEGG_ARACHIDONIC_ACID_METABOLISM

Others
OMIM
Orphanet
Disease	KEGG Disease: GGT1
	MedGen: GGT1 (Human Medical Genetics with Condition)
	ClinVar: GGT1
Phenotype	MGI: GGT1 (International Mouse Phenotyping Consortium)
Phenotype	PhenomicDB: GGT1

Mutations for GGT1

* 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

- Statistics for Tissue and Mutation type

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- For Inter-chromosomal Variations

There's no inter-chromosomal structural variation.

- For Intra-chromosomal Variations

* Intra-chromosomal variantions includes 'intrachromosomal amplicon to amplicon', 'intrachromosomal amplicon to non-amplified dna', 'intrachromosomal deletion', 'intrachromosomal fold-back inversion', 'intrachromosomal inversion', 'intrachromosomal tandem duplication', 'Intrachromosomal unknown type', 'intrachromosomal with inverted orientation', 'intrachromosomal with non-inverted orientation'.

Sample	Symbol_a	Chr_a	Start_a	End_a	Symbol_b	Chr_b	Start_b	End_b
pancreas	GGT1	chr22	25008512	25008532	GGT1	chr22	25008935	25008955

cf) Tissue number; Tissue name (1;Breast, 2;Central_nervous_system, 3;Haematopoietic_and_lymphoid_tissue, 4;Large_intestine, 5;Liver, 6;Lung, 7;Ovary, 8;Pancreas, 9;Prostate, 10;Skin, 11;Soft_tissue, 12;Upper_aerodigestive_tract)

Related fusion transcripts : go to Chitars2.0

* From mRNA Sanger sequences, Chitars2.0 arranged chimeric transcripts. This table shows GGT1 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

AW182722

GGT1

24981603

24981689

CARS2

429

111353839

111358446

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

Mutation type/ Tissue ID

brca

cns

cerv

endome

haematopo

kidn

Lintest

liver

lung

ovary

pancre

prost

skin

stoma

thyro

urina

Total # sample

GAIN (# sample)

LOSS (# sample)

cf) Tissue ID; Tissue type (1; Breast, 2; Central_nervous_system, 3; Cervix, 4; Endometrium, 5; Haematopoietic_and_lymphoid_tissue, 6; Kidney, 7; Large_intestine, 8; Liver, 9; Lung, 10; NS, 11; Ovary, 12; Pancreas, 13; Prostate, 14; Skin, 15; Stomach, 16; Thyroid, 17; Urinary_tract)

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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=11

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Somatic Mutation Counts per Tissue in COSMIC data

Stat. for Non-Synonymous SNVs (# total SNVs=49)	Stat. for Synonymous SNVs (# total SNVs=10)

Stat. for Deletions (# total SNVs=9)	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
chr22:25023893-25023893	p.S428N	11
chr22:25011062-25011062	p.T117S	10
chr22:25010758-25010758	p.D60D	8
chr22:25023869-25023869	p.M421fs*75	7
chr22:25024072-25024072	p.C454F	6
chr22:25024076-25024076	p.P455P	6
chr22:25023903-25023903	p.N431N	6
chr22:25016296-25016296	p.G128G	5
chr22:25023513-25023513	p.G379R	4
chr22:25010828-25010828	p.G84S	4

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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=3

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	2	3	1	4	1		1		2	1		2	2	1	1	1	10	8	2	5
# mutation	2	2	1	2	1		1		2	1		2	2	1	1	1	10	8	2	6
nonsynonymous SNV		2		1	1		1		1	1		1	1	1		1	5	4	2	5
synonymous SNV	2		1	1					1			1	1		1		5	4		1

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
chr22:25010828	p.G84S,GGT1	3
chr22:25023893	p.D60D,GGT1	2
chr22:25010758	p.S428N,GGT1	2
chr22:25010801	p.V336V,GGT1	1
chr22:25019101	p.S451L,GGT1	1
chr22:25023444	p.T92T,GGT1	1
chr22:25010806	p.D337G,GGT1	1
chr22:25023936	p.S451S,GGT1	1
chr22:25019109	p.R107H,GGT1	1
chr22:25023476	p.A351T,GGT1	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 GGT1 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 GGT1

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


ACSM1,AFMID,AKR1C2,AKR1D1,C15orf43,LRRC75B,CLPSL1, C6orf223,DBI,GGT1,GGT3P,GGTLC1,GGTLC2,HAAO, LOC644165,MUCL1,OXER1,SERHL2,SERHL,SPINK8,SULT1C3	ACSL3,ADAM2,AFMID,ALOX15B,B3GAT1,C15orf43,DHCR7, DHRS2,FIBCD1,GGT1,GGTLC2,HIST1H3D,HMGCS2,MVK, NSUN2,PNLIPRP3,SERHL2,SERHL,SLC15A1,SPINK8,SRD5A1

ABCB9,ABCC2,ACOT11,AP1B1,BMP7,LRRC75B,CISD3, COMT,FGFR3,GGT1,GGT3P,GGTLC1,GGTLC2,ID1, PKLR,PLA2G4F,RAB11FIP4,SCARB1,SMAD6,STX3,ZNRF3	ADIRF,CDH16,CLDN15,CYP3A7,FAM109A,GGT1,GGT3P, GGTLC1,GGTLC2,HEBP1,KDM8,KCP,NAALADL1,NAT8B, PKLR,SEC16B,SLC17A8,SLC34A2,TBX3,AGMO,XPNPEP2

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 GGT1

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	gamma-glutamyltransferase 1	approved; nutraceutical	Glutathione

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Cross referenced IDs for GGT1

* 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