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 EIF5

Basic gene info.	Gene symbol	EIF5
	Gene name	eukaryotic translation initiation factor 5
	Synonyms	EIF-5\|EIF-5A
	Cytomap	UCSC genome browser: 14q32.32
	Genomic location	chr14 :103801235-103811361
	Type of gene	protein-coding
	RefGenes	NM_001969.4, NM_183004.4,
	Ensembl id	ENSG00000100664
	Description	-
	Modification date	20141207
dbXrefs	MIM : 601710
	HGNC : HGNC
	Ensembl : ENSG00000100664
	HPRD : 03417
	Vega : OTTHUMG00000171839
Protein	UniProt: go to UniProt's Cross Reference DB Table
Expression	CleanEX: HS_EIF5
	BioGPS: 1983
	Gene Expression Atlas: ENSG00000100664
	The Human Protein Atlas: ENSG00000100664
Pathway	NCI Pathway Interaction Database: EIF5
	KEGG: EIF5
	REACTOME: EIF5
	ConsensusPathDB
	Pathway Commons: EIF5
Metabolism	MetaCyc: EIF5
	HUMANCyc: EIF5
Regulation	Ensembl's Regulation: ENSG00000100664
	miRBase: chr14 :103,801,235-103,811,361
	TargetScan: NM_001969
	cisRED: ENSG00000100664
Context	iHOP: EIF5
	cancer metabolism search in PubMed: EIF5
	UCL Cancer Institute: EIF5
Assigned class in ccmGDB	C

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Phenotypic Information for EIF5(metabolism pathway, cancer, disease, phenome)

Cancer Description
Cancer	CGAP: EIF5
	Familial Cancer Database: EIF5

* 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: EIF5
	MedGen: EIF5 (Human Medical Genetics with Condition)
	ClinVar: EIF5
Phenotype	MGI: EIF5 (International Mouse Phenotyping Consortium)
Phenotype	PhenomicDB: EIF5

Mutations for EIF5

* 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	EIF5	chr14	103808265	103808285	CDC42BPB	chr14	103424659	103424679

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 EIF5 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
AI133642	ITPR2	1	83	12	26853999	26854081	EIF5	82	630	14	103800574	103802408
BM833559	REV1	1	280	2	100019515	100021011	EIF5	261	461	14	103804688	103805151
BI058894	AKIP1	8	206	11	8941010	8941208	EIF5	200	456	14	103810337	103810593
DB066453	EIF5	1	67	14	103804245	103804311	BOP1	68	534	8	145505145	145505610

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=33)	Stat. for Synonymous SNVs (# total SNVs=4)

Stat. for Deletions (# total SNVs=4)	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
chr14:103803541-103803541	p.T139I	2
chr14:103807346-103807346	p.K418M	2
chr14:103805130-103805130	p.R215Q	2
chr14:103807366-103807372	p.D425fs*>5	2
chr14:103805187-103805187	p.R234K	2
chr14:103802238-103802238	p.Y14F	2
chr14:103802241-103802241	p.R15H	1
chr14:103805576-103805576	p.D271G	1
chr14:103803484-103803484	p.N120I	1
chr14:103806856-103806856	p.E388D	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		3	1	3			2	1	3			2	3			1	5	5		2
# mutation		3	1	4			2	1	3			2	3			1	5	6		2
nonsynonymous SNV		2	1	4			1	1	3			1	2				2	5		2
synonymous SNV		1					1					1	1			1	3	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
chr14:103802243	p.V42I,EIF5	1
chr14:103804719	p.I352V,EIF5	1
chr14:103807325	p.T51T,EIF5	1
chr14:103802255	p.E388D,EIF5	1
chr14:103804740	p.H80Y,EIF5	1
chr14:103807346	p.E402K,EIF5	1
chr14:103802419	p.F96C,EIF5	1
chr14:103805183	p.V411A,EIF5	1
chr14:103807359	p.K115K,EIF5	1
chr14:103802424	p.K418R,EIF5	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 EIF5 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 EIF5

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


CCDC58,DNAJC2,EIF5B,FAM136A,GEMIN6,GNL2,MAGOH, MEMO1,MPHOSPH10,MRPS9,NDUFS5,NOL10,NOP58,NUTF2, PDCL3,PDSS1,RPP40,SNRPG,SSB,SSBP1,UTP11L	C6orf203,CWC27,DNAJC7,DNAJC8,EIF2S2,EIF4E2,EIF5B, FAM118B,HTATSF1,LSM1,PRPS1,PSMC2,PSMD1,PSMD7, RBM17,SBDS,TTC1,UBC,UBE2G2,XPA,ZCRB1

CCAR1,CWC22,EIF5B,HNRNPA2B1,HNRNPA3,HNRNPU,IWS1, LTV1,MPHOSPH10,MRPS5,MRPS9,NCL,NOP58,POU2F1, PPIG,PPM1G,RPF2,SSB,TARDBP,WDR75,WDR92	ADAMTS9,AKAP12,ARMCX3,CELF2,DDX19A,DDX24,DYX1C1, EIF5B,LBR,NAV2,NUCKS1,OXCT1,PBRM1,PRKAR1A, PTPN11,ROCK1,SEC63,SRP68,SUPT16H,TCOF1,ZC3H13

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 EIF5

There's no related Drug.

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Cross referenced IDs for EIF5

* 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