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 PGM3

Basic gene info.	Gene symbol	PGM3
	Gene name	phosphoglucomutase 3
	Synonyms	AGM1\|IMD23\|PAGM\|PGM 3
	Cytomap	UCSC genome browser: 6q14.1-q15
	Genomic location	chr6 :83874592-83903012
	Type of gene	protein-coding
	RefGenes	NM_001199917.1, NM_001199918.1,NM_001199919.1,NM_015599.2,
	Ensembl id	ENSG00000013375
	Description	N-acetylglucosamine-phosphate mutase 1acetylglucosamine phosphomutasephosphoacetylglucosamine mutase
	Modification date	20141207
dbXrefs	MIM : 172100
	HGNC : HGNC
	Ensembl : ENSG00000013375
	HPRD : 01390
	Vega : OTTHUMG00000015110
Protein	UniProt: go to UniProt's Cross Reference DB Table
Expression	CleanEX: HS_PGM3
	BioGPS: 5238
	Gene Expression Atlas: ENSG00000013375
	The Human Protein Atlas: ENSG00000013375
Pathway	NCI Pathway Interaction Database: PGM3
	KEGG: PGM3
	REACTOME: PGM3
	ConsensusPathDB
	Pathway Commons: PGM3
Metabolism	MetaCyc: PGM3
	HUMANCyc: PGM3
Regulation	Ensembl's Regulation: ENSG00000013375
	miRBase: chr6 :83,874,592-83,903,012
	TargetScan: NM_001199917
	cisRED: ENSG00000013375
Context	iHOP: PGM3
	cancer metabolism search in PubMed: PGM3
	UCL Cancer Institute: PGM3
Assigned class in ccmGDB	C

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Phenotypic Information for PGM3(metabolism pathway, cancer, disease, phenome)

Cancer Description
Cancer	CGAP: PGM3
	Familial Cancer Database: PGM3

* 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_AMINO_SUGAR_AND_NUCLEOTIDE_SUGAR_METABOLISM REACTOME_METABOLISM_OF_PROTEINS

Others
OMIM
Orphanet
Disease	KEGG Disease: PGM3
	MedGen: PGM3 (Human Medical Genetics with Condition)
	ClinVar: PGM3
Phenotype	MGI: PGM3 (International Mouse Phenotyping Consortium)
Phenotype	PhenomicDB: PGM3

Mutations for PGM3

* 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 PGM3 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

BP314848

HIST1H2BE

468

26183989

26184456

PGM3

467

583

83900698

83902978

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=5

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Somatic Mutation Counts per Tissue in COSMIC data

Stat. for Non-Synonymous SNVs (# total SNVs=34)	Stat. for Synonymous SNVs (# total SNVs=6)

Stat. for Deletions (# total SNVs=0)	Stat. for Insertions (# total SNVs=0)
There's no deleted snv.	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
chr6:83892687-83892687	p.L156F	5
chr6:83898499-83898499	p.L75V	2
chr6:83892684-83892684	p.L157F	2
chr6:83898387-83898387	p.K112I	2
chr6:83891474-83891474	p.S256R	1
chr6:83881683-83881683	p.D446E	1
chr6:83892661-83892661	p.M165T	1
chr6:83885778-83885778	p.V344A	1
chr6:83891476-83891476	p.S256G	1
chr6:83881749-83881749	p.L424L	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		7			1		1		1	4				1	3	10		5
# mutation		1		8			1		1		1	5				1	3	11		6
nonsynonymous SNV		1		7			1				1	5				1	1	8		3
synonymous SNV				1					1								2	3		3

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
chr6:83898366	p.Y287H,PGM3	1
chr6:83884156	p.Q57P,PGM3	1
chr6:83889686	p.H276H,PGM3	1
chr6:83898411	p.G45D,PGM3	1
chr6:83884176	p.V263A,PGM3	1
chr6:83891476	p.Q38L,PGM3	1
chr6:83898457	p.A249T,PGM3	1
chr6:83884180	p.R23T,PGM3	1
chr6:83891504	p.L232P,PGM3	1
chr6:83900572	p.E8K,PGM3	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 PGM3 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 PGM3

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


ACBD3,ARCN1,ASCC3,CCNC,COPB2,DOPEY1,EIF2AK3, FUCA2,HCCS,IBTK,UFL1,ME1,PGM3,PHACTR2, PIGA,RARS2,RNGTT,RWDD2A,SEC24A,SNX14,SYNCRIP	ACADL,BNIP3L,COL4A3BP,CRYBG3,DDHD1,EHHADH,EYS, FNIP2,GFPT1,GNAI1,IGF1,KCTD20,LIMA1,PGM3, PREX2,PTENP1,PTPDC1,SLC25A16,TMEM135,TRHDE,TTLL7

AGR2,ARCN1,ARF4,TMEM263,SLC18B1,COPB2,FAM46A, GSTTP2,HSPA5,IBTK,KDELR3,NUCB2,NUS1,PGM3, RWDD2A,SEC24D,SLC30A7,SLC31A1,SLC39A7,SSR1,SSR3	C19orf10,CLINT1,COPB1,DDOST,GNPNAT1,KDELR3,MTHFD2, NEK6,NUDT5,PDIA6,PGM3,PPIB,PYCR1,RPL22L1, SEC22B,SLC10A7,SLC38A5,TMED2,TMEM39A,TSTA3,UBXN4

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 PGM3

There's no related Drug.

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Cross referenced IDs for PGM3

* 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