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 RPS19

Basic gene info.	Gene symbol	RPS19
	Gene name	ribosomal protein S19
	Synonyms	DBA\|DBA1\|S19
	Cytomap	UCSC genome browser: 19q13.2
	Genomic location	chr19 :42363987-42375484
	Type of gene	protein-coding
	RefGenes	NM_001022.3,
	Ensembl id	ENSG00000105372
	Description	40S ribosomal protein S19
	Modification date	20141222
dbXrefs	MIM : 603474
	HGNC : HGNC
	HPRD : 04591
Protein	UniProt: go to UniProt's Cross Reference DB Table
Expression	CleanEX: HS_RPS19
	BioGPS: 6223
	Gene Expression Atlas: ENSG00000105372
	The Human Protein Atlas: ENSG00000105372
Pathway	NCI Pathway Interaction Database: RPS19
	KEGG: RPS19
	REACTOME: RPS19
	ConsensusPathDB
	Pathway Commons: RPS19
Metabolism	MetaCyc: RPS19
	HUMANCyc: RPS19
Regulation	Ensembl's Regulation: ENSG00000105372
	miRBase: chr19 :42,363,987-42,375,484
	TargetScan: NM_001022
	cisRED: ENSG00000105372
Context	iHOP: RPS19
	cancer metabolism search in PubMed: RPS19
	UCL Cancer Institute: RPS19
Assigned class in ccmGDB	C

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Phenotypic Information for RPS19(metabolism pathway, cancer, disease, phenome)

Cancer Description
Cancer	CGAP: RPS19
	Familial Cancer Database: RPS19

* 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 REACTOME_METABOLISM_OF_MRNA REACTOME_METABOLISM_OF_RNA

Others
OMIM
Orphanet
Disease	KEGG Disease: RPS19
	MedGen: RPS19 (Human Medical Genetics with Condition)
	ClinVar: RPS19
Phenotype	MGI: RPS19 (International Mouse Phenotyping Consortium)
Phenotype	PhenomicDB: RPS19

Mutations for RPS19

* 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

* Inter-chromosomal variantions includes 'interchromosomal amplicon to amplicon', 'interchromosomal amplicon to non-amplified dna', 'interchromosomal insertion', 'Interchromosomal unknown type'.

- For Intra-chromosomal Variations

There's no intra-chromosomal structural variation.

Sample

Symbol_a

Chr_a

Start_a

End_a

Symbol_b

Chr_b

Start_b

End_b

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 RPS19 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
BU602070	RPS14	4	348	5	149826368	149829300	RPS19	348	482	19	42373271	42375484
AW300778	RPS19	9	399	19	42364325	42373284	RPS4Y1	387	474	Y	2734859	2734946
BQ351523	PLD1	66	295	3	171510161	171510388	RPS19	290	517	19	42364898	42373208
DB116923	RPS19	1	147	19	42364327	42365223	DCAF8	144	558	1	160209269	160209683

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=4)	Stat. for Synonymous SNVs (# total SNVs=1)

Stat. for Deletions (# total SNVs=0)	Stat. for Insertions (# total SNVs=0)
There's no deleted snv.	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
chr19:42373137-42373137	p.A70V	2
chr19:42373280-42373280	p.D118N	1
chr19:42373788-42373788	p.Q126*	1
chr19:42373817-42373817	p.A135A	1
chr19:42364847-42364847	p.M1I	1
chr19:42364852-42364852	p.G3A	1
chr19:42364896-42364896	p.L18V	1
chr19:42364908-42364908	p.L22F	1
chr19:42373235-42373235	p.V103I	1
chr19:42373237-42373237	p.V103V	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			1				1					1					1			1
# mutation			1				1					1					1			1
nonsynonymous SNV			1				1					1
synonymous SNV																	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
chr19:42364896	p.L18V	1
chr19:42373137	p.A70V	1
chr19:42373230	p.R101H	1
chr19:42373237	p.V103V	1
chr19:42373817	p.A135A	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 RPS19 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 RPS19

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


EXOSC5,FAU,LSM7,RPL13,RPL18,RPL18A,RPL27A, RPL28,RPL35,RPL36,RPL37,RPL37A,RPLP2,RPS10, RPS11,RPS19,RPS8,RPS9,SNRPA,SNRPD2,UBA52	ALKBH2,VPS51___IFT46,EXOSC5,FBL,GLTSCR2,RPL10,RPL13, RPL13A,RPL18,RPL18A,RPL19,RPL3,RPL36,RPL7A, RPL8,RPS19,RPS21,RPS3,RPS5,RPS8,RPS9

LRRC75A-AS1,RPL10,RPL13A,RPL13AP3,RPL18,RPL28,RPL35, RPL36,RPLP0,RPLP1,RPS11,RPS15,RPS16,RPS19, RPS29,RPS3,RPS5,RPS9,SDHAF1,SNRPD2,ZNF581	EEF1G,GNB2L1,RPL13,RPL18,RPL18A,RPL19,RPL23A, RPL32,RPL36,RPL37,RPL37A,RPL38,RPL8,RPLP0, RPS15,RPS16,RPS19,RPS23,RPS3,RPS9,UBA52

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 RPS19

There's no related Drug.

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Cross referenced IDs for RPS19

* 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