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 DCP1A

Basic gene info.	Gene symbol	DCP1A
	Gene name	decapping mRNA 1A
	Synonyms	HSA275986\|Nbla00360\|SMAD4IP1\|SMIF
	Cytomap	UCSC genome browser: 3p21.1
	Genomic location	chr3 :53317444-53381654
	Type of gene	protein-coding
	RefGenes	NM_001290204.1, NM_001290205.1,NM_001290206.1,NM_001290207.1,NM_018403.6,
	Ensembl id	ENSG00000162290
	Description	DCP1 decapping enzyme homolog ASmad4-interacting transcriptional co-activatordecapping enzyme hDcp1amRNA-decapping enzyme 1Aputative protein product of Nbla00360transcription factor SMIF
	Modification date	20141207
dbXrefs	MIM : 607010
	HGNC : HGNC
	Ensembl : ENSG00000272886
	HPRD : 06113
	Vega : OTTHUMG00000158193
Protein	UniProt: go to UniProt's Cross Reference DB Table
Expression	CleanEX: HS_DCP1A
	BioGPS: 55802
	Gene Expression Atlas: ENSG00000162290
	The Human Protein Atlas: ENSG00000162290
Pathway	NCI Pathway Interaction Database: DCP1A
	KEGG: DCP1A
	REACTOME: DCP1A
	ConsensusPathDB
	Pathway Commons: DCP1A
Metabolism	MetaCyc: DCP1A
	HUMANCyc: DCP1A
Regulation	Ensembl's Regulation: ENSG00000162290
	miRBase: chr3 :53,317,444-53,381,654
	TargetScan: NM_001290204
	cisRED: ENSG00000162290
Context	iHOP: DCP1A
	cancer metabolism search in PubMed: DCP1A
	UCL Cancer Institute: DCP1A
Assigned class in ccmGDB	C

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Phenotypic Information for DCP1A(metabolism pathway, cancer, disease, phenome)

Cancer Description
Cancer	CGAP: DCP1A
	Familial Cancer Database: DCP1A

* 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_MRNA REACTOME_METABOLISM_OF_RNA

Others
OMIM
Orphanet
Disease	KEGG Disease: DCP1A
	MedGen: DCP1A (Human Medical Genetics with Condition)
	ClinVar: DCP1A
Phenotype	MGI: DCP1A (International Mouse Phenotyping Consortium)
Phenotype	PhenomicDB: DCP1A

Mutations for DCP1A

* 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 DCP1A 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
BQ277160	DCP1A	2	468	3	53326464	53381554	DCP1A	464	768	3	53353434	53381473
AA368822	DCP1A	1	82	3	53324327	53324408	CSH2	82	107	17	61949937	61949962

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=3

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Somatic Mutation Counts per Tissue in COSMIC data

Stat. for Non-Synonymous SNVs (# total SNVs=21)	Stat. for Synonymous SNVs (# total SNVs=15)

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
chr3:53376254-53376254	p.N74S	2
chr3:53353455-53353455	p.R117H	2
chr3:53326317-53326317	p.L389F	1
chr3:53381533-53381533	p.L4L	1
chr3:53326747-53326747	p.L245L	1
chr3:53321675-53321675	p.D558N	1
chr3:53353456-53353456	p.R117C	1
chr3:53326366-53326366	p.Q372H	1
chr3:53338202-53338202	p.?	1
chr3:53322146-53322146	p.Q535Q	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	2	4	2	4			2					4	1				3	3	1	5
# mutation	2	4	2	4			2					5	1				3	3	1	5
nonsynonymous SNV	1	2	2	2			2					4	1				1	1		3
synonymous SNV	1	2		2								1					2	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
chr3:53326488	p.Q305L,DCP1A	1
chr3:53346310	p.L86L,DCP1A	1
chr3:53324879	p.P264L,DCP1A	1
chr3:53326499	p.P52L,DCP1A	1
chr3:53346358	p.G254W,DCP1A	1
chr3:53326214	p.P81S,DCP1A	1
chr3:53326592	p.T250T,DCP1A	1
chr3:53346369	p.E46K,DCP1A	1
chr3:53326245	p.S232S,DCP1A	1
chr3:53326674	p.D45Y,DCP1A	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 DCP1A 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 DCP1A

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


ACTR8,APPL1,FAM208A,CREBRF,DCP1A,DENND6A,KIAA1109, KIAA1143,NEK4,PBRM1,PPP4R2,PRKAR2A,RAD54L2,SACM1L, SETD2,SLMAP,TMF1,TTBK2,VPRBP,WDR82,ZNF445	ANKRD12,ARID4A,ATRX,C16orf52,FAM208A,CAPN7,CEP120, CTDSPL2,DCP1A,DENND4C,DIS3,FAM135A,HACE1,MON2, MORC3,RUFY2,SCAF11,USP8,ZDHHC17,ZNF280D,ZNF451

ACTR8,ASXL2,CAPN7,CLASP2,DCP1A,EAF1,KIF2A, LATS1,NEK4,PBRM1,PPP4R2,PRKAR2A,QRICH1,RAD54L2, RAPGEF6,RIF1,RPP14,SMARCC1,VHL,VPRBP,WDR82	NSRP1,DCP1A,EIF5B,HNRNPA3,INTS6,ITPRIP,KIF5B, LUC7L2,MAP4K5,MED1,PBRM1,PNN,RBBP6,RPGR, NEMF,SEC63,SRRM1,TAF2,TCERG1,TUBGCP3,UPF2

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 DCP1A

There's no related Drug.

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Cross referenced IDs for DCP1A

* 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