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 WDR77

Basic gene info.	Gene symbol	WDR77
	Gene name	WD repeat domain 77
	Synonyms	MEP-50\|MEP50\|Nbla10071\|p44\|p44/Mep50
	Cytomap	UCSC genome browser: 1p13.2
	Genomic location	chr1 :111982511-111991830
	Type of gene	protein-coding
	RefGenes	NM_024102.2,
	Ensembl id	ENSG00000116455
	Description	WD repeat-containing protein 77androgen receptor cofactor p44methylosome protein 50
	Modification date	20141207
dbXrefs	MIM : 611734
	HGNC : HGNC
	Ensembl : ENSG00000116455
	HPRD : 14387
	Vega : OTTHUMG00000011748
Protein	UniProt: go to UniProt's Cross Reference DB Table
Expression	CleanEX: HS_WDR77
	BioGPS: 79084
	Gene Expression Atlas: ENSG00000116455
	The Human Protein Atlas: ENSG00000116455
Pathway	NCI Pathway Interaction Database: WDR77
	KEGG: WDR77
	REACTOME: WDR77
	ConsensusPathDB
	Pathway Commons: WDR77
Metabolism	MetaCyc: WDR77
	HUMANCyc: WDR77
Regulation	Ensembl's Regulation: ENSG00000116455
	miRBase: chr1 :111,982,511-111,991,830
	TargetScan: NM_024102
	cisRED: ENSG00000116455
Context	iHOP: WDR77
	cancer metabolism search in PubMed: WDR77
	UCL Cancer Institute: WDR77
Assigned class in ccmGDB	C

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Phenotypic Information for WDR77(metabolism pathway, cancer, disease, phenome)

Cancer Description
Cancer	CGAP: WDR77
	Familial Cancer Database: WDR77

* 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_NON_CODING_RNA REACTOME_METABOLISM_OF_RNA

Others
OMIM
Orphanet
Disease	KEGG Disease: WDR77
	MedGen: WDR77 (Human Medical Genetics with Condition)
	ClinVar: WDR77
Phenotype	MGI: WDR77 (International Mouse Phenotyping Consortium)
Phenotype	PhenomicDB: WDR77

Mutations for WDR77

* 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 WDR77 related fusion information.

ID	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
AA428438	WDR77	1	126	1	111985296	111985982	WDR77	121	406	1	111983302	111984662
BE312794	WDR77	1	478	1	111983976	111990072	HERPUD1	478	735	16	56976109	56977254

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=12)	Stat. for Synonymous SNVs (# total SNVs=5)

Stat. for Deletions (# total SNVs=1)	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
chr1:111984672-111984672	p.V282M	2
chr1:111986535-111986535	p.R191S	1
chr1:111991375-111991375	p.G56A	1
chr1:111983900-111983900	p.V327V	1
chr1:111986713-111986713	p.S176F	1
chr1:111991767-111991767	p.L9fs*1	1
chr1:111983905-111983905	p.V326I	1
chr1:111989749-111989749	p.L154R	1
chr1:111991770-111991770	p.P8S	1
chr1:111983920-111983920	p.Q321*	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=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	2			1			3		2			4				1	2			6
# mutation	2			1			3		2			4				1	2			6
nonsynonymous SNV	1						2		1			3				1	2			3
synonymous SNV	1			1			1		1			1								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
chr1:111986535	p.V326I	1
chr1:111983905	p.L86P	1
chr1:111989719	p.Q321K	1
chr1:111983920	p.P64L	1
chr1:111989749	p.L312V	1
chr1:111983947	p.G56A	1
chr1:111989760	p.P307P	1
chr1:111983960	p.P8S	1
chr1:111990091	p.P307S	1
chr1:111983962	p.V282M	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 WDR77 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 WDR77

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


ATP5F1,CDC20,CDCA3,CDCA8,CENPA,ECE2,FAM136A, LSM2,LYAR,MAGOH,NDUFAF4,NOP58,PDSS1,PSMA5, PSMB2,PSMG1,PSRC1,SERBP1,SNRPC,UQCRH,WDR77	AIMP2,ATP5G3,PRADC1,TIMMDC1,COX5A,FH,HIGD2A, LACTB,LSM10,MRPS16,NDUFA4,NDUFA9,NDUFAB1,NDUFB2, NDUFB3,PGK1,UQCR10,UQCR11,UQCRFS1,WDR77,WSB2

ACOT8,C20orf24,CASP6,CSE1L,DNAJA3,EIF2B3,GPSM2, GSS,HSD17B10,LRRC8D,MAGOH,MAPKAPK5,MTCH2,PDHA1, POU5F1B,PSMA7,RPIA,RPP40,TINAG,TSPAN6,WDR77	ABCE1,BRIX1,CCT2,DKC1,FARSB,GART,KIAA0020, METTL1,MRPL3,MRTO4,NOC3L,NOP56,NOP58,PUS7, RRP9,SRFBP1,SRPRB,SUV39H2,TFDP1,UTP6,WDR77

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 WDR77

There's no related Drug.

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Cross referenced IDs for WDR77

* 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