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 CNOT4

Basic gene info.	Gene symbol	CNOT4
	Gene name	CCR4-NOT transcription complex, subunit 4
	Synonyms	CLONE243\|NOT4\|NOT4H
	Cytomap	UCSC genome browser: 7q33
	Genomic location	chr7 :135071821-135194875
	Type of gene	protein-coding
	RefGenes	NM_001008225.2, NM_001190847.1,NM_001190848.1,NM_001190849.1,NM_001190850.1, NM_013316.3,
	Ensembl id	ENSG00000080802
	Description	CCR4-NOT transcription complex subunit 4CCR4-associated factor 4E3 ubiquitin-protein ligase CNOT4NOT4 (negative regulator of transcription 4, yeast) homologpotential transcriptional repressor NOT4Hp
	Modification date	20141207
dbXrefs	MIM : 604911
	HGNC : HGNC
	Ensembl : ENSG00000080802
	HPRD : 05369
	Vega : OTTHUMG00000155568
Protein	UniProt: O95628 go to UniProt's Cross Reference DB Table
Expression	CleanEX: HS_CNOT4
	BioGPS: 4850
	Gene Expression Atlas: ENSG00000080802
	The Human Protein Atlas: ENSG00000080802
Pathway	NCI Pathway Interaction Database: CNOT4
	KEGG: CNOT4
	REACTOME: CNOT4
	ConsensusPathDB
	Pathway Commons: CNOT4
Metabolism	MetaCyc: CNOT4
	HUMANCyc: CNOT4
Regulation	Ensembl's Regulation: ENSG00000080802
	miRBase: chr7 :135,071,821-135,194,875
	TargetScan: NM_001008225
	cisRED: ENSG00000080802
Context	iHOP: CNOT4
	cancer metabolism search in PubMed: CNOT4
	UCL Cancer Institute: CNOT4
Assigned class in ccmGDB	B - This gene belongs to cancer gene.

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Phenotypic Information for CNOT4(metabolism pathway, cancer, disease, phenome)

Cancer Description
Cancer	CGAP: CNOT4
	Familial Cancer Database: CNOT4

* 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	604911; gene. 604911; gene.
Orphanet
Disease	KEGG Disease: CNOT4
	MedGen: CNOT4 (Human Medical Genetics with Condition)
	ClinVar: CNOT4
Phenotype	MGI: CNOT4 (International Mouse Phenotyping Consortium)
Phenotype	PhenomicDB: CNOT4

Mutations for CNOT4

* 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

- Statistics for Tissue and Mutation type

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- For Inter-chromosomal Variations

There's no inter-chromosomal structural variation.

- For Intra-chromosomal Variations

* Intra-chromosomal variantions includes 'intrachromosomal amplicon to amplicon', 'intrachromosomal amplicon to non-amplified dna', 'intrachromosomal deletion', 'intrachromosomal fold-back inversion', 'intrachromosomal inversion', 'intrachromosomal tandem duplication', 'Intrachromosomal unknown type', 'intrachromosomal with inverted orientation', 'intrachromosomal with non-inverted orientation'.

Sample	Symbol_a	Chr_a	Start_a	End_a	Symbol_b	Chr_b	Start_b	End_b
ovary	CNOT4	chr7	135101194	135101214	CNOT4	chr7	135078401	135078421
ovary	CNOT4	chr7	135138101	135138121	CNOT4	chr7	135051715	135051735
ovary	CNOT4	chr7	135159132	135159152	CNOT4	chr7	135159306	135159326
pancreas	CNOT4	chr7	135189205	135189225	CNOT4	chr7	135189524	135189544

cf) Tissue number; Tissue name (1;Breast, 2;Central_nervous_system, 3;Haematopoietic_and_lymphoid_tissue, 4;Large_intestine, 5;Liver, 6;Lung, 7;Ovary, 8;Pancreas, 9;Prostate, 10;Skin, 11;Soft_tissue, 12;Upper_aerodigestive_tract)

Related fusion transcripts : go to Chitars2.0

* From mRNA Sanger sequences, Chitars2.0 arranged chimeric transcripts. This table shows CNOT4 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

Mutation type/ Tissue ID

brca

cns

cerv

endome

haematopo

kidn

Lintest

liver

lung

ovary

pancre

prost

skin

stoma

thyro

urina

Total # sample

GAIN (# sample)

LOSS (# sample)

cf) Tissue ID; Tissue type (1; Breast, 2; Central_nervous_system, 3; Cervix, 4; Endometrium, 5; Haematopoietic_and_lymphoid_tissue, 6; Kidney, 7; Large_intestine, 8; Liver, 9; Lung, 10; NS, 11; Ovary, 12; Pancreas, 13; Prostate, 14; Skin, 15; Stomach, 16; Thyroid, 17; Urinary_tract)

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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=37)	Stat. for Synonymous SNVs (# total SNVs=12)

Stat. for Deletions (# total SNVs=2)	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
chr7:135079001-135079001	p.S429S	3
chr7:135098360-135098360	p.A188A	2
chr7:135047695-135047695	p.R621T	2
chr7:135122949-135122949	p.R44Q	2
chr7:135080547-135080547	p.R320Q	2
chr7:135047807-135047807	p.A584T	1
chr7:135080631-135080631	p.S292F	1
chr7:135123072-135123072	p.R3H	1
chr7:135078698-135078698	p.N530K	1
chr7:135047675-135047675	p.T628P	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	2			5			3		2			6	5			1	11	7		7
# mutation	2			7			3		2			6	5			1	11	6		9
nonsynonymous SNV	2			4			3		1			6	4				9	3		7
synonymous SNV				3					1				1			1	2	3		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
chr7:135079001	p.S429S,CNOT4	3
chr7:135048771	p.G556W,CNOT4	2
chr7:135106961	p.V106I,CNOT4	2
chr7:135048770	p.A587T,CNOT4	1
chr7:135106940	p.V378V,CNOT4	1
chr7:135079154	p.R165W,CNOT4	1
chr7:135047645	p.D574D,CNOT4	1
chr7:135098287	p.S373L,CNOT4	1
chr7:135080388	p.N144N,CNOT4	1
chr7:135047689	p.A569V,CNOT4	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 CNOT4 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 CNOT4

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


CBLL1,CNOT4,COG5,KRIT1,LUZP6,MKLN1,MKRN1, KMT2C,KMT2E,NAPEPLD,NUP205,RINT1,RSBN1L,TMEM209, TNPO3,TTC26,UBE2H,UBN2,WASL,ZNF398,ZNF800	ARIH1,ARMC8,ATAD1,TRMT1L,CNOT4,DNAJC24,FAM175B, CCSER2,FBXW11,POLR2M___GCOM1,KLHL24,LOC221710,NAA30,PCMTD1, PPM1A,RCOR3,RPRD1A,SOS2,TAB2,TRIM23,TTC33

ATXN7L1,BRAF,CBLL1,CNOT4,EXOC4,GCC1,KLHDC10, KRIT1,LUC7L2,LUZP6,MKLN1,KMT2C,KMT2E,RSBN1L, SRPK2,TNPO3,TRIM4,UBN2,ZNF398,ZSCAN25,ZNF800	ARIH1,ASH1L,BAZ1B,CNOT4,DYNLL2,KIAA1429,KIDINS220, KPNA6,LRCH3,KMT2A,KAT7,PIK3R4,RAB3GAP1,RSF1, SETD1B,SNX27,UBR1,UBR5,ZNF37A,ZNF609,ZNF638

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 CNOT4

There's no related Drug.

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Cross referenced IDs for CNOT4

* 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