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 PSMB8

Basic gene info.	Gene symbol	PSMB8
	Gene name	proteasome (prosome, macropain) subunit, beta type, 8
	Synonyms	ALDD\|D6S216\|D6S216E\|JMP\|LMP7\|NKJO\|PSMB5i\|RING10
	Cytomap	UCSC genome browser: 6p21.3
	Genomic location	chr6_qbl_hap6 :4040600-4044819
	Type of gene	protein-coding
	RefGenes	NM_004159.4, NM_148919.3,
	Ensembl id	ENSG00000204264
	Description	large multifunctional peptidase 7low molecular mass protein 7low molecular weight protein 7macropain subunit C13multicatalytic endopeptidase complex subunit C13protease component C13proteasome (prosome, macropain) subunit, beta type, 8 (large multif
	Modification date	20141207
dbXrefs	MIM : 177046
	HGNC : HGNC
	Ensembl : ENSG00000204264
	HPRD : 01515
	Vega : OTTHUMG00000031285
Protein	UniProt: go to UniProt's Cross Reference DB Table
Expression	CleanEX: HS_PSMB8
	BioGPS: 5696
	Gene Expression Atlas: ENSG00000204264
	The Human Protein Atlas: ENSG00000204264
Pathway	NCI Pathway Interaction Database: PSMB8
	KEGG: PSMB8
	REACTOME: PSMB8
	ConsensusPathDB
	Pathway Commons: PSMB8
Metabolism	MetaCyc: PSMB8
	HUMANCyc: PSMB8
Regulation	Ensembl's Regulation: ENSG00000204264
	miRBase: chr6_qbl_hap6 :4,040,600-4,044,819
	TargetScan: NM_004159
	cisRED: ENSG00000204264
Context	iHOP: PSMB8
	cancer metabolism search in PubMed: PSMB8
	UCL Cancer Institute: PSMB8
Assigned class in ccmGDB	C

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Phenotypic Information for PSMB8(metabolism pathway, cancer, disease, phenome)

Cancer Description
Cancer	CGAP: PSMB8
	Familial Cancer Database: PSMB8

* 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_AMINO_ACIDS_AND_DERIVATIVES REACTOME_METABOLISM_OF_MRNA REACTOME_METABOLISM_OF_RNA

Others
OMIM
Orphanet
Disease	KEGG Disease: PSMB8
	MedGen: PSMB8 (Human Medical Genetics with Condition)
	ClinVar: PSMB8
Phenotype	MGI: PSMB8 (International Mouse Phenotyping Consortium)
Phenotype	PhenomicDB: PSMB8

Mutations for PSMB8

* 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 PSMB8 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

AI280186

SERPINF1

1680762

1680857

PSMB8

472

4239280

4240152

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=19)	Stat. for Synonymous SNVs (# total SNVs=3)

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
chr6:32809494-32809494	p.V182M	3
chr6:32809404-32809404	p.R212W	3
chr6:32810002-32810002	p.S145L	2
chr6:32808790-32808790	p.V255V	1
chr6:32810860-32810860	p.E48K	1
chr6:32808814-32808814	p.M247I	1
chr6:32809941-32809941	p.M165I	1
chr6:32810867-32810867	p.?	1
chr6:32809342-32809342	p.T232T	1
chr6:32809961-32809961	p.R159W	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=2

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	1	2	7	2		1		1			1	1				6	3		3
# mutation	2	1	2	7	2		1		1			1	1				6	3		3
nonsynonymous SNV	1	1	2	6	2		1						1				4	2		2
synonymous SNV	1			1					1			1					2	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
chr6:32809404	p.R212W,PSMB8	2
chr6:32810842	p.G54S,PSMB8	2
chr6:32808814	p.P30R	1
chr6:32810026	p.G199G,PSMB8	1
chr6:32812058	p.G25W	1
chr6:32809342	p.G199E,PSMB8	1
chr6:32810470	p.L19L	1
chr6:32812093	p.T196T,PSMB8	1
chr6:32810726	p.A18T	1
chr6:32812187	p.M193V,PSMB8	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 PSMB8 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 PSMB8

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


APOL1,APOL2,APOL3,B2M,ETV7,HCG26,HCP5, HLA-A,HLA-B,HLA-C,HLA-E,HLA-F,HLA-H,PSMB10, PSMB8,PSMB9,PSME2,TAP1,TAP2,TAPBP,UBE2L6	ABI3,BAX,CD7,CSK,ETV7,HLA-A,HLA-B, HLA-C,HLA-DPB1,HLA-F,PSMB10,PSMB8,PSMB9,PSME1, PSME2,RGS19,SH3BP1,TAP1,TAPBP,TRIM47,UBE2L6

BAK1,BATF2,ETV7,FBXO6,HCP5,HLA-B,HLA-C, HLA-E,HLA-F,IL15RA,IRF1,NMI,PARP9,PSMB10, PSMB8,PSMB9,PSME1,PSME2,RARRES3,TAP1,UBE2L6	BATF2,CARD16,CASP1,EPSTI1,ETV7,FAM26F,FBXO6, IFI30,IFI35,IRF1,NMI,PSMB10,PSMB3,PSMB8, PSMB9,PSME1,RARRES3,RTP4,TAP1,TRIM21,UBE2L6

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 PSMB8

There's no related Drug.

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Cross referenced IDs for PSMB8

* 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