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 MCEE

Basic gene info.	Gene symbol	MCEE
	Gene name	methylmalonyl CoA epimerase
	Synonyms	GLOD2
	Cytomap	UCSC genome browser: 2p13.3
	Genomic location	chr2 :71336805-71357394
	Type of gene	protein-coding
	RefGenes	NM_032601.3,
	Ensembl id	ENSG00000124370
	Description	DL-methylmalonyl-CoA racemaseglyoxalase domain containing 2methylmalonyl-CoA epimerase, mitochondrial
	Modification date	20141219
dbXrefs	MIM : 608419
	HGNC : HGNC
	Ensembl : ENSG00000124370
	HPRD : 12229
	Vega : OTTHUMG00000129709
Protein	UniProt: go to UniProt's Cross Reference DB Table
Expression	CleanEX: HS_MCEE
	BioGPS: 84693
	Gene Expression Atlas: ENSG00000124370
	The Human Protein Atlas: ENSG00000124370
Pathway	NCI Pathway Interaction Database: MCEE
	KEGG: MCEE
	REACTOME: MCEE
	ConsensusPathDB
	Pathway Commons: MCEE
Metabolism	MetaCyc: MCEE
	HUMANCyc: MCEE
Regulation	Ensembl's Regulation: ENSG00000124370
	miRBase: chr2 :71,336,805-71,357,394
	TargetScan: NM_032601
	cisRED: ENSG00000124370
Context	iHOP: MCEE
	cancer metabolism search in PubMed: MCEE
	UCL Cancer Institute: MCEE
Assigned class in ccmGDB	C

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

Cancer Description
Cancer	CGAP: MCEE
	Familial Cancer Database: MCEE

* 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_PROPANOATE_METABOLISM REACTOME_METABOLISM_OF_LIPIDS_AND_LIPOPROTEINS

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

Mutations for MCEE

* 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 MCEE 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

DR980649

MCEE

161

71351563

71357359

METTL8

157

217

172180339

172180849

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=2

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Somatic Mutation Counts per Tissue in COSMIC data

Stat. for Non-Synonymous SNVs (# total SNVs=15)	Stat. for Synonymous SNVs (# total SNVs=1)

Stat. for Deletions (# total SNVs=4)	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
chr2:71337212-71337212	p.K140fs*6	4
chr2:71351338-71351338	p.E126K	3
chr2:71351574-71351574	p.R47Q	2
chr2:71337226-71337226	p.M135I	1
chr2:71351487-71351487	p.A76V	1
chr2:71351507-71351508	p.L69>?	1
chr2:71351373-71351373	p.K114R	1
chr2:71351516-71351516	p.K66N	1
chr2:71351378-71351378	p.L112L	1
chr2:71351523-71351523	p.F64Y	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=1

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			2								2	1	1			2	3		1
# mutation	1			2								2	1	1			2	3		1
nonsynonymous SNV	1			2								2	1				1	2		1
synonymous SNV														1			1	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
chr2:71351415	p.H82Y	1
chr2:71351470	p.A76A	1
chr2:71351486	p.K66N	1
chr2:71351516	p.F64Y	1
chr2:71351523	p.S41Y	1
chr2:71337190	p.A8A	1
chr2:71351592	p.E147D	1
chr2:71337204	p.R143C	1
chr2:71357326	p.L137F	1
chr2:71337220	p.E126K	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 MCEE 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 MCEE

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


ANAPC13,C11orf1,ATRAID,COA5,NMRK1,CDNF,EIF4EBP3, FLJ36777,LYRM1,MCEE,MGST2,NDUFV2,NFU1,OCIAD1, PIGH,PIGV,REEP5,SPCS1,UNC50,VIPR1,ZCWPW2	ANAPC16,ATP5S,AUH,MPC1,GHITM,GPN3,KLHDC2, LACTB2,MCEE,MNAT1,MRPL39,MRPS10,MRPS22,MRPS36, NDUFB5,NDUFS4,PCCB,SDHD,SNRNP27,SUCLG2,TMEM14B

ACN9,C14orf142,COA5,PRADC1,PTRHD1,TMEM261,CHMP5, DUSP11,HSCB,IFT20,KBTBD3,MCEE,NDUFA6,NDUFB5, NDUFB6,NIPSNAP3A,NUDT2,OST4,OSTC,PIGF,SAR1B	KANSL2,C12orf57,TIMMDC1,C6orf57,COG6,DPY30,ERLEC1, HAUS1,HSCB,INTS10,LYRM2,MCEE,NSMCE4A,RPL41, RPSAP58,SNRPD2,SSR2,TGDS,TMEM216,ZNF511,ZNHIT3

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 MCEE

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
DB00121	methylmalonyl CoA epimerase	approved; nutraceutical	Biotin

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Cross referenced IDs for MCEE

* 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