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 EPHX2

Basic gene info.	Gene symbol	EPHX2
	Gene name	epoxide hydrolase 2, cytoplasmic
	Synonyms	CEH\|SEH
	Cytomap	UCSC genome browser: 8p21
	Genomic location	chr8 :27348684-27402439
	Type of gene	protein-coding
	RefGenes	NM_001256482.1, NM_001256483.1,NM_001256484.1,NM_001979.5,
	Ensembl id	ENSG00000120915
	Description	bifunctional epoxide hydrolase 2epoxide hydrataseepoxide hydrolase 2, cytosolicepoxide hydrolase, soluble
	Modification date	20141207
dbXrefs	MIM : 132811
	HGNC : HGNC
	Ensembl : ENSG00000120915
	HPRD : 00582
	Vega : OTTHUMG00000102115
Protein	UniProt: go to UniProt's Cross Reference DB Table
Expression	CleanEX: HS_EPHX2
	BioGPS: 2053
	Gene Expression Atlas: ENSG00000120915
	The Human Protein Atlas: ENSG00000120915
Pathway	NCI Pathway Interaction Database: EPHX2
	KEGG: EPHX2
	REACTOME: EPHX2
	ConsensusPathDB
	Pathway Commons: EPHX2
Metabolism	MetaCyc: EPHX2
	HUMANCyc: EPHX2
Regulation	Ensembl's Regulation: ENSG00000120915
	miRBase: chr8 :27,348,684-27,402,439
	TargetScan: NM_001256482
	cisRED: ENSG00000120915
Context	iHOP: EPHX2
	cancer metabolism search in PubMed: EPHX2
	UCL Cancer Institute: EPHX2
Assigned class in ccmGDB	C

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Phenotypic Information for EPHX2(metabolism pathway, cancer, disease, phenome)

Cancer Description
Cancer	CGAP: EPHX2
	Familial Cancer Database: EPHX2

* 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_ARACHIDONIC_ACID_METABOLISM

Others
OMIM
Orphanet
Disease	KEGG Disease: EPHX2
	MedGen: EPHX2 (Human Medical Genetics with Condition)
	ClinVar: EPHX2
Phenotype	MGI: EPHX2 (International Mouse Phenotyping Consortium)
Phenotype	PhenomicDB: EPHX2

Mutations for EPHX2

* 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

* Inter-chromosomal variantions includes 'interchromosomal amplicon to amplicon', 'interchromosomal amplicon to non-amplified dna', 'interchromosomal insertion', 'Interchromosomal unknown type'.

- 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
liver	EPHX2	chr8	27389859	27389859	SCARA5	chr8	27830910	27830910

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 EPHX2 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

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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=3

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Somatic Mutation Counts per Tissue in COSMIC data

Stat. for Non-Synonymous SNVs (# total SNVs=41)	Stat. for Synonymous SNVs (# total SNVs=19)

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
chr8:27382881-27382881	p.A354V	3
chr8:27382957-27382957	p.P379P	3
chr8:27382971-27382971	p.Q384L	3
chr8:27369368-27369368	p.A226T	2
chr8:27396186-27396186	p.S418F	2
chr8:27379945-27379945	p.L326L	2
chr8:27364393-27364393	p.L183fs*8	2
chr8:27398071-27398071	p.G426E	2
chr8:27398101-27398101	p.P436L	2
chr8:27398124-27398124	p.E444K	2

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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	3	1	1	2	1		4		1			4	4	3			9	5		12
# mutation	3	1	1	2	1		4		1			4	4	3			9	5		13
nonsynonymous SNV	2		1	2			4		1			1	3	3			5	4		8
synonymous SNV	1	1			1							3	1				4	1		5

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
chr8:27364474	p.T142M,EPHX2	2
chr8:27396186	p.S352F,EPHX2	2
chr8:27380005	p.L61L,EPHX2	1
chr8:27361273	p.A214S,EPHX2	1
chr8:27398124	p.K389E,EPHX2	1
chr8:27382881	p.F83S,EPHX2	1
chr8:27362496	p.A224D,EPHX2	1
chr8:27398141	p.Y400Y,EPHX2	1
chr8:27364508	p.S87L,EPHX2	1
chr8:27348760	p.F254L,EPHX2	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 EPHX2 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 EPHX2

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


ALDH6A1,BNIP3L,CCDC25,ELP3,EPHX2,FBXO16,FBXO25, HMGCL,INTS9,CCAR2,KIF13B,NEK11,NOSTRIN,NUDT18, PHYHD1,RORC,SH2D4A,SIAE,TMEM25,UBXN8,ZNF395	AGBL5,CIRBP,EPHX2,GNG7,HSD17B8,IL17RC,ING5, LGTN,LOC100286793,MKS1,POLR1E,RPL3,RPL4,RPL5, RPL7A,RPS18,RPS6,SNHG8,TMCO4,VIPR1,ZNF821

AGPAT5,BIN3,CCDC25,CNOT7,ELP3,DMTN,EPHX2, ERICH1,FBXO25,INTS10,INTS9,KBTBD11,CCAR2,LONRF1, MCPH1,NAT1,NAT2,TRIM35,TTC38,VPS37A,XPO7	ACY1,CCDC108,CHN2,CLDN15,CYP2J2,DAK,DDC, DEGS2,DGAT1,EPHX2,FBP1,IYD,MACC1,MMEL1, MARC2,MYO1A,PCK2,PKLR,SLC37A4,SLC39A5,TM4SF5

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 EPHX2

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
DB01248	epoxide hydrolase 2, cytoplasmic	approved; investigational	Docetaxel

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Cross referenced IDs for EPHX2

* 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