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 RPL35

Basic gene info.	Gene symbol	RPL35
	Gene name	ribosomal protein L35
	Synonyms	L35
	Cytomap	UCSC genome browser: 9q34.1
	Genomic location	chr9 :127620157-127624240
	Type of gene	protein-coding
	RefGenes	NM_007209.3,
	Ensembl id	ENSG00000136942
	Description	60S ribosomal protein L35
	Modification date	20141207
dbXrefs	HGNC : HGNC
	Ensembl : ENSG00000136942
	HPRD : 10200
	Vega : OTTHUMG00000020659
Protein	UniProt: go to UniProt's Cross Reference DB Table
Expression	CleanEX: HS_RPL35
	BioGPS: 11224
	Gene Expression Atlas: ENSG00000136942
	The Human Protein Atlas: ENSG00000136942
Pathway	NCI Pathway Interaction Database: RPL35
	KEGG: RPL35
	REACTOME: RPL35
	ConsensusPathDB
	Pathway Commons: RPL35
Metabolism	MetaCyc: RPL35
	HUMANCyc: RPL35
Regulation	Ensembl's Regulation: ENSG00000136942
	miRBase: chr9 :127,620,157-127,624,240
	TargetScan: NM_007209
	cisRED: ENSG00000136942
Context	iHOP: RPL35
	cancer metabolism search in PubMed: RPL35
	UCL Cancer Institute: RPL35
Assigned class in ccmGDB	C

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Phenotypic Information for RPL35(metabolism pathway, cancer, disease, phenome)

Cancer Description
Cancer	CGAP: RPL35
	Familial Cancer Database: RPL35

* 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: RPL35
	MedGen: RPL35 (Human Medical Genetics with Condition)
	ClinVar: RPL35
Phenotype	MGI: RPL35 (International Mouse Phenotyping Consortium)
Phenotype	PhenomicDB: RPL35

Mutations for RPL35

* 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 RPL35 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
CA433490	RPL35	16	136	9	127620162	127620282	NOC2L	134	542	1	892529	892937
BF802262	RPL35	26	252	9	127622505	127624236	DIAPH1	247	336	5	140896140	140896229
CN394906	RPL35	6	120	9	127620167	127620281	C1orf43	115	765	1	154184844	154193017
AI682966	IGFBP5	13	299	2	217536832	217537116	RPL35	300	541	9	127622461	127624210

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=7)	Stat. for Synonymous SNVs (# total SNVs=3)

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
chr9:127620293-127620293	p.R92R	1
chr9:127620295-127620295	p.R92C	1
chr9:127620299-127620299	p.A90A	1
chr9:127620318-127620318	p.R84Q	1
chr9:127620332-127620332	p.K79N	1
chr9:127620210-127620210	p.A120G	1
chr9:127620344-127620344	p.G75G	1
chr9:127620219-127620219	p.R117Q	1
chr9:127623766-127623766	p.L24L	1
chr9:127620225-127620225	p.P115L	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	1	2		4								1		1			1			1
# mutation	1	2		4								1		1			1			1
nonsynonymous SNV		2		4								1					1
synonymous SNV	1													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
chr9:127620293	p.R84Q	1
chr9:127620318	p.K79N	1
chr9:127620332	p.R56S	1
chr9:127622518	p.L24L	1
chr9:127623766	p.A120G	1
chr9:127620210	p.R117Q	1
chr9:127620219	p.P115L	1
chr9:127620225	p.R94R	1
chr9:127620287	p.R94P	1
chr9:127620288	p.R94W	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 RPL35 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 RPL35

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


LOC152217,POLR2H,RPL11,RPL24,RPL27A,RPL31,RPL32, RPL35A,RPL36,RPL37,RPL37A,RPL6,RPLP2,RPS10, RPS15A,RPS18,RPS19,RPS2,RPS27A,RPS7,RPS8	BTF3,RPL14,RPL22,RPL23A,RPL24,RPL30,RPL32, RPL34,RPL35A,RPL41,RPL5,RPL6,RPS15A,RPS23, RPS24,RPS27A,RPS29,RPS3A,RPS4X,RPS6,RPS7

EEF1B2,RPL10A,RPL14,RPL15,RPL24,RPL29,RPL31, RPL32,RPL35A,RPL37A,RPL7A,RPS10,RPS11,RPS13, RPS14,RPS15A,RPS17,RPS18,RPS25,RPS27A,RPS6	C12orf57,DPY30,EEF1A1,EEF1A1P9,FAU,PFDN5,RPL15, RPL24,RPL27A,RPL35,RPL35A,RPL41,RPL5,RPS10, RPS11,RPS13,RPS3A,RPS5,RPS6,RPS7,SNRPD2

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 RPL35

There's no related Drug.

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Cross referenced IDs for RPL35

* 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