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 MUC7

Basic gene info.	Gene symbol	MUC7
	Gene name	mucin 7, secreted
	Synonyms	MG2
	Cytomap	UCSC genome browser: 4q13.3
	Genomic location	chr4 :71337833-71348714
	Type of gene	protein-coding
	RefGenes	NM_001145006.1, NM_001145007.1,NM_152291.2,
	Ensembl id	ENSG00000171195
	Description	MUC-7apo-MG2mucin 7, salivarymucin-7salivary mucin-7
	Modification date	20141207
dbXrefs	MIM : 158375
	HGNC : HGNC
	Ensembl : ENSG00000171195
	HPRD : 11759
	Vega : OTTHUMG00000129916
Protein	UniProt: go to UniProt's Cross Reference DB Table
Expression	CleanEX: HS_MUC7
	BioGPS: 4589
	Gene Expression Atlas: ENSG00000171195
	The Human Protein Atlas: ENSG00000171195
Pathway	NCI Pathway Interaction Database: MUC7
	KEGG: MUC7
	REACTOME: MUC7
	ConsensusPathDB
	Pathway Commons: MUC7
Metabolism	MetaCyc: MUC7
	HUMANCyc: MUC7
Regulation	Ensembl's Regulation: ENSG00000171195
	miRBase: chr4 :71,337,833-71,348,714
	TargetScan: NM_001145006
	cisRED: ENSG00000171195
Context	iHOP: MUC7
	cancer metabolism search in PubMed: MUC7
	UCL Cancer Institute: MUC7
Assigned class in ccmGDB	C

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Phenotypic Information for MUC7(metabolism pathway, cancer, disease, phenome)

Cancer Description
Cancer	CGAP: MUC7
	Familial Cancer Database: MUC7

* 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: MUC7
	MedGen: MUC7 (Human Medical Genetics with Condition)
	ClinVar: MUC7
Phenotype	MGI: MUC7 (International Mouse Phenotyping Consortium)
Phenotype	PhenomicDB: MUC7

Mutations for MUC7

* 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 MUC7 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
BX487918	MALAT1	2	320	11	65266516	65266834	MUC7	314	451	4	71346885	71347022
BX487700	MALAT1	2	379	11	65266516	65266893	MUC7	374	627	4	71339738	71346714
BX537739	CUL9	1	497	6	43149971	43150467	MUC7	490	2516	4	71346688	71348714

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=9

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Somatic Mutation Counts per Tissue in COSMIC data

Stat. for Non-Synonymous SNVs (# total SNVs=87)	Stat. for Synonymous SNVs (# total SNVs=17)

Stat. for Deletions (# total SNVs=0)	Stat. for Insertions (# total SNVs=1)
There's no deleted 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
chr4:71347185-71347185	p.S242P	9
chr4:71346978-71346978	p.S173P	9
chr4:71347138-71347138	p.P226L	4
chr4:71347033-71347033	p.A191V	4
chr4:71347047-71347047	p.S196P	4
chr4:71346646-71346646	p.S62F	3
chr4:71347171-71347171	p.A237V	3
chr4:71347291-71347291	p.P277L	3
chr4:71346827-71346827	p.K122K	3
chr4:71347468-71347468	p.S336L	3

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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=6

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	4		14	2		4		4			22	4	4			19	8	5	11
# mutation	4	4		11	2		4		4			24	4	4			17	9	5	9
nonsynonymous SNV	3	3		9	1		3		3			22	3	2			16	5	4	8
synonymous SNV	1	1		3	1		1		1			2	1	2			1	4	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
chr4:71347185	p.S242P,MUC7	6
chr4:71346978	p.S173P,MUC7	5
chr4:71347138	p.P226L,MUC7	4
chr4:71347351	p.S62F,MUC7	3
chr4:71347468	p.S297Y,MUC7	3
chr4:71346827	p.K122N,MUC7	3
chr4:71347033	p.S336L,MUC7	3
chr4:71346646	p.A191V,MUC7	3
chr4:71346820	p.R358Q,MUC7	2
chr4:71347020	p.S196P,MUC7	2

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 MUC7 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 MUC7

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


C15orf41,C1QL3,BPIFB3,CACNA1A,CAT,CD44,CYP7A1, DMBT1,GPR85,MROH2B,KCNS1,MEIS2,MRGPRG,MUC7, OR7E156P,PLA2R1,PRM3,RBM44,RHD,TNFRSF11B,UTS2	C1orf194,C20orf85,CACNG3,CDC20B,CDC6,EPGN,GABRA3, KRT12,KRT20,MAGEC1,MUC7,OR2T11,OR5M11,OR6C65, OR6C76,OR6N2,SOX11,TEKT1,TMIGD1,TTTY23,ZBBX

TRAPPC3L,BSND,CABP1,CCL25,CDK6,FAM99A,FOXI1, GOLGA7B,KRT74,MUC7,LINC00028,NEUROD6,ODAM,PHACTR1, PTPRO,RAG2,SPP2,SULT1E1,SYT8,TCF7,TNNI2	AGRP,C10orf91,C16orf92,CT45A5,FLJ46361,H2BFM,IL31, LHX1,LOC221122,LOC727924,MMP26,MUC7,LINC00112,OLIG2, OR51B2,OR6X1,PRAMEF16,PRM2,PSG7,SCARNA21,SNORA11E, TMPRSS12

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 MUC7

There's no related Drug.

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Cross referenced IDs for MUC7

* 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