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 MGAT2

Basic gene info.	Gene symbol	MGAT2
	Gene name	mannosyl (alpha-1,6-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase
	Synonyms	CDG2A\|CDGS2\|GLCNACTII\|GNT-II\|GNT2
	Cytomap	UCSC genome browser: 14q21
	Genomic location	chr14 :50087488-50090199
	Type of gene	protein-coding
	RefGenes	NM_002408.3, NM_001015883.1,
	Ensembl id	ENSG00000168282
	Description	Beta-1,2-N-acetylglucosaminyltransferase IIN-glycosyl-oligosaccharide-glycoprotein N-acetylglucosaminyltransferase IIUDP-N-acetylglucosamine:alpha-6-D-mannoside beta-1,2-N-acetylglucosaminyltransferase IIalpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylg
	Modification date	20141219
dbXrefs	MIM : 602616
	HGNC : HGNC
	Ensembl : ENSG00000168282
	HPRD : 04013
	Vega : OTTHUMG00000140271
Protein	UniProt: go to UniProt's Cross Reference DB Table
Expression	CleanEX: HS_MGAT2
	BioGPS: 4247
	Gene Expression Atlas: ENSG00000168282
	The Human Protein Atlas: ENSG00000168282
Pathway	NCI Pathway Interaction Database: MGAT2
	KEGG: MGAT2
	REACTOME: MGAT2
	ConsensusPathDB
	Pathway Commons: MGAT2
Metabolism	MetaCyc: MGAT2
	HUMANCyc: MGAT2
Regulation	Ensembl's Regulation: ENSG00000168282
	miRBase: chr14 :50,087,488-50,090,199
	TargetScan: NM_002408
	cisRED: ENSG00000168282
Context	iHOP: MGAT2
	cancer metabolism search in PubMed: MGAT2
	UCL Cancer Institute: MGAT2
Assigned class in ccmGDB	C

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Phenotypic Information for MGAT2(metabolism pathway, cancer, disease, phenome)

Cancer Description
Cancer	CGAP: MGAT2
	Familial Cancer Database: MGAT2

* 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
REACTOME_METABOLISM_OF_PROTEINS

Others
OMIM
Orphanet
Disease	KEGG Disease: MGAT2
	MedGen: MGAT2 (Human Medical Genetics with Condition)
	ClinVar: MGAT2
Phenotype	MGI: MGAT2 (International Mouse Phenotyping Consortium)
Phenotype	PhenomicDB: MGAT2

Mutations for MGAT2

* 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 MGAT2 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

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=18)	Stat. for Synonymous SNVs (# total SNVs=6)

Stat. for Deletions (# total SNVs=1)	Stat. for Insertions (# total SNVs=1)

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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
chr14:50088560-50088560	p.D192N	2
chr14:50088598-50088598	p.A204A	2
chr14:50088619-50088619	p.I211I	2
chr14:50088514-50088514	p.F176L	1
chr14:50088690-50088690	p.W235*	1
chr14:50089047-50089047	p.T354I	1
chr14:50088545-50088545	p.E187Q	1
chr14:50088719-50088719	p.V245M	1
chr14:50089057-50089057	p.C357C	1
chr14:50088553-50088553	p.P189P	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		1	1								1	3				3	3	1	3
# mutation	1		1	1								1	3				3	3	1	4
nonsynonymous SNV	1		1										2				1	2	1	2
synonymous SNV				1								1	1				2	1		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
chr14:50088493	p.D192N	1
chr14:50089211	p.R194T	1
chr14:50088553	p.N212S	1
chr14:50089303	p.K226N	1
chr14:50088560	p.F257F	1
chr14:50088567	p.L291L	1
chr14:50088621	p.S297R	1
chr14:50088095	p.T354I	1
chr14:50088664	p.L37I	1
chr14:50088220	p.C357C	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 MGAT2 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 MGAT2

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


ARF6,ATP5S,DNAAF2,CNIH1,EXOC5,GCH1,L2HGDH, MAP4K5,MAPK1IP1L,MGAT2,AP5M1,LRR1,PSMC6,RP2, NEMF,SEC23A,SNX6,SOCS4,STYX,TMX1,TRAPPC6B	AP3S1,ARF4,ATP6AP2,CAPZA1,CCNY,COMMD8,ERI1, FKBP1A,GNG10,GOLT1B,KDELR2,LY96,MGAT2,PRCP, RAB1A,RALB,RAP1A,RAP1B,SDCBP,SGPP1,YWHAB

AP4S1,ARF6,DNAAF2,EXOC5,GOLGA5,MAPK1IP1L,MGAT2, MPP5,NUMB,PPM1A,PPP2R5E,PSEN1,SCFD1,SLC39A9, SRP54,STRN3,STYX,TINF2,TMX1,TRAPPC6B,WDR20	ARF6,MCU,CDC42SE2,EHD4,FAM104A,FAM105A,FUCA2, HOXA1,MAD2L1BP,MGAT2,MOB1A,NRAS,PRKCI,RNF138, SLC35B3,TOR2A,TPD52,TXNDC11,ZDHHC13,ZDHHC3,ZNRF2

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 MGAT2

There's no related Drug.

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Cross referenced IDs for MGAT2

* 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