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 UGT2B15

Basic gene info.	Gene symbol	UGT2B15
	Gene name	UDP glucuronosyltransferase 2 family, polypeptide B15
	Synonyms	HLUG4\|UDPGT 2B8\|UDPGT2B15\|UDPGTH3\|UGT2B8
	Cytomap	UCSC genome browser: 4q13
	Genomic location	chr4_ctg9_hap1 :224913-249081
	Type of gene	protein-coding
	RefGenes	NM_001076.3,
	Ensembl id	ENSG00000196620
	Description	UDP glycosyltransferase 2B15UDP-glucuronosyltransferase 2B15UDP-glucuronosyltransferase 2B8UDP-glucuronosyltransferase UGT2B15UDP-glucuronyltransferase, family 2, beta-15UDPGT 2B15UDPGTh-3
	Modification date	20141207
dbXrefs	MIM : 600069
	HGNC : HGNC
	Ensembl : ENSG00000196620
	HPRD : 07192
	Vega : OTTHUMG00000161507
Protein	UniProt: go to UniProt's Cross Reference DB Table
Expression	CleanEX: HS_UGT2B15
	BioGPS: 7366
	Gene Expression Atlas: ENSG00000196620
	The Human Protein Atlas: ENSG00000196620
Pathway	NCI Pathway Interaction Database: UGT2B15
	KEGG: UGT2B15
	REACTOME: UGT2B15
	ConsensusPathDB
	Pathway Commons: UGT2B15
Metabolism	MetaCyc: UGT2B15
	HUMANCyc: UGT2B15
Regulation	Ensembl's Regulation: ENSG00000196620
	miRBase: chr4_ctg9_hap1 :224,913-249,081
	TargetScan: NM_001076
	cisRED: ENSG00000196620
Context	iHOP: UGT2B15
	cancer metabolism search in PubMed: UGT2B15
	UCL Cancer Institute: UGT2B15
Assigned class in ccmGDB	C

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Phenotypic Information for UGT2B15(metabolism pathway, cancer, disease, phenome)

Cancer Description
Cancer	CGAP: UGT2B15
	Familial Cancer Database: UGT2B15

* 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_ASCORBATE_AND_ALDARATE_METABOLISM KEGG_STARCH_AND_SUCROSE_METABOLISM KEGG_RETINOL_METABOLISM KEGG_PORPHYRIN_AND_CHLOROPHYLL_METABOLISM KEGG_METABOLISM_OF_XENOBIOTICS_BY_CYTOCHROME_P450 KEGG_DRUG_METABOLISM_CYTOCHROME_P450 KEGG_DRUG_METABOLISM_OTHER_ENZYMES

Others
OMIM
Orphanet
Disease	KEGG Disease: UGT2B15
	MedGen: UGT2B15 (Human Medical Genetics with Condition)
	ClinVar: UGT2B15
Phenotype	MGI: UGT2B15 (International Mouse Phenotyping Consortium)
Phenotype	PhenomicDB: UGT2B15

Mutations for UGT2B15

* 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 UGT2B15 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=1

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Somatic Mutation Counts per Tissue in COSMIC data

Stat. for Non-Synonymous SNVs (# total SNVs=1)	Stat. for Synonymous SNVs (# total SNVs=0)
	There's no s-snv.
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
chr4:69563451-69563451	p.E295D	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=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		3	1	1	1		4		1			13	4				24	3		13
# mutation		3	1	1	1		4		1			12	4				33	3		12
nonsynonymous SNV		2	1	1	1		2		1			7	3				22	2		8
synonymous SNV		1					2					5	1				11	1		4

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
chr4:69519925	p.I381I	3
chr4:69536328	p.L3L	2
chr4:69536055	p.D452N	2
chr4:69535816	p.M215I	2
chr4:69513061	p.L94L	2
chr4:69535692	p.R174Q	2
chr4:69535920	p.F248L	1
chr4:69519874	p.L170L	1
chr4:69536220	p.L11L	1
chr4:69512912	p.I487I	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 UGT2B15 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 UGT2B15

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


AP3M1,BAG5,BEST3,METTL25,CA2,FAM9A,FRG2B, LEO1,OR10J5,RPL3L,SPPL2A,TFF1,TRH,TSG1, TYRP1,UGT2B10,UGT2B11,UGT2B15,USP29,USP8,VSIG1	ALB,ANGPTL3,ANKFN1,BCO1,HNF1A-AS1,SMCO3,C5, FGL1,HABP2,HNF1A,IGFL2,KIF12,MIA2,MTNR1B, PKHD1,RHBG,SERPINA4,TMED6,TTLL6,UGT2B15,ZNF385B

ADH1C,AMPD1,B3GALT1,ADTRP,CA2,CA4,CASR, CEACAM7,GPR15,GUCA2A,HSD3B2,ITM2C,LDHD,MS4A12, NR3C2,PIGR,SCNN1B,SLC25A34,TMIGD1,UGT2B15,USP2	ACCSL,AGGF1,CDH20,CNOT6L,FMR1,IFNAR1,IL13RA1, IREB2,KDM3A,LOC148824,LRRC6,MAN1A1,PTEN,TLR3, TMEM229B,TSGA10IP,UGT2B15,VCPIP1,ZHX1,ZNF217,ZNF654

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 UGT2B15

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
DB00675	UDP glucuronosyltransferase 2 family, polypeptide B15	approved	Tamoxifen
DB00842	UDP glucuronosyltransferase 2 family, polypeptide B15	approved	Oxazepam
DB00973	UDP glucuronosyltransferase 2 family, polypeptide B15	approved	Ezetimibe
DB00184	UDP glucuronosyltransferase 2 family, polypeptide B15	approved	Nicotine
DB00313	UDP glucuronosyltransferase 2 family, polypeptide B15	approved; investigational	Valproic Acid
DB00186	UDP glucuronosyltransferase 2 family, polypeptide B15	approved	Lorazepam
DB01033	UDP glucuronosyltransferase 2 family, polypeptide B15	approved	Mercaptopurine
DB00563	UDP glucuronosyltransferase 2 family, polypeptide B15	approved	Methotrexate
DB00890	UDP glucuronosyltransferase 2 family, polypeptide B15	approved	Dienestrol
DB00252	UDP glucuronosyltransferase 2 family, polypeptide B15	approved	Phenytoin

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Cross referenced IDs for UGT2B15

* 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