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 NUP88

Basic gene info.	Gene symbol	NUP88
	Gene name	nucleoporin 88kDa
	Synonyms	-
	Cytomap	UCSC genome browser: 17p13.2
	Genomic location	chr17 :5289345-5323059
	Type of gene	protein-coding
	RefGenes	NM_002532.4,
	Ensembl id	ENSG00000108559
	Description	88 kDa nucleoporinkaryoporinnuclear pore complex protein 88nuclear pore complex protein Nup88nucleoporin 88kDnucleoporin Nup88
	Modification date	20141207
dbXrefs	MIM : 602552
	HGNC : HGNC
	Ensembl : ENSG00000108559
	HPRD : 03974
	Vega : OTTHUMG00000099453
Protein	UniProt: Q99567 go to UniProt's Cross Reference DB Table
Expression	CleanEX: HS_NUP88
	BioGPS: 4927
	Gene Expression Atlas: ENSG00000108559
	The Human Protein Atlas: ENSG00000108559
Pathway	NCI Pathway Interaction Database: NUP88
	KEGG: NUP88
	REACTOME: NUP88
	ConsensusPathDB
	Pathway Commons: NUP88
Metabolism	MetaCyc: NUP88
	HUMANCyc: NUP88
Regulation	Ensembl's Regulation: ENSG00000108559
	miRBase: chr17 :5,289,345-5,323,059
	TargetScan: NM_002532
	cisRED: ENSG00000108559
Context	iHOP: NUP88
	cancer metabolism search in PubMed: NUP88
	UCL Cancer Institute: NUP88
Assigned class in ccmGDB	B - This gene belongs to cancer gene.

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Phenotypic Information for NUP88(metabolism pathway, cancer, disease, phenome)

Cancer Description
Cancer	CGAP: NUP88
	Familial Cancer Database: NUP88

* 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_NON_CODING_RNA REACTOME_METABOLISM_OF_RNA REACTOME_METABOLISM_OF_CARBOHYDRATES

Others
OMIM	602552; gene.
Orphanet
Disease	KEGG Disease: NUP88
	MedGen: NUP88 (Human Medical Genetics with Condition)
	ClinVar: NUP88
Phenotype	MGI: NUP88 (International Mouse Phenotyping Consortium)
Phenotype	PhenomicDB: NUP88

Mutations for NUP88

* 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 NUP88 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
DA165761	FRMD4B	1	126	3	69268374	69268499	NUP88	127	577	17	5319873	5322994
BE706779	SF3B3	44	157	16	70582572	70582685	NUP88	155	228	17	5319833	5319906

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=4

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Somatic Mutation Counts per Tissue in COSMIC data

Stat. for Non-Synonymous SNVs (# total SNVs=45)	Stat. for Synonymous SNVs (# total SNVs=14)

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
chr17:5289580-5289580	p.H724H	2
chr17:5290033-5290033	p.K719K	2
chr17:5308488-5308488	p.A311A	2
chr17:5322843-5322843	p.A43V	2
chr17:5308489-5308489	p.A311V	2
chr17:5308516-5308516	p.A302V	2
chr17:5294927-5294927	p.M480V	2
chr17:5302963-5302963	p.K400N	2
chr17:5322727-5322727	p.R82C	2
chr17:5307457-5307457	p.F385Y	2

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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		11	1		2		3	1		5					4	8		8
# mutation	3	1		10	1		2		3	1		5					4	8		9
nonsynonymous SNV	3	1		8	1		1		1	1		4					2	5		7
synonymous SNV				2			1		2			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
chr17:5289552	p.A302V	2
chr17:5308516	p.D734N	2
chr17:5290067	p.L654L	1
chr17:5317415	p.I326I	1
chr17:5298291	p.Q113E	1
chr17:5322820	p.S646R	1
chr17:5312067	p.A311E	1
chr17:5290080	p.F109L	1
chr17:5319923	p.R621H	1
chr17:5302881	p.E304D	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 NUP88 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 NUP88

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


C1QBP,COX10,DHX33,EIF4A1,FAM64A,GEMIN4,GSG2, MIS12,MYBBP1A,NUP88,PITPNA,PRPF8,RPA1,RPAIN, SCO1,SENP3,TSR1,UBE2G1,YWHAE,ZFP3,ZNF232	ATP5C1,CIRH1A,COPS3,EIF3J,FAF1,FARSB,FASTKD2, KCMF1,METAP2,NUP88,OXNAD1,PAIP1,PLAA,PMPCB, PRKRA,RABGGTB,SUPV3L1,TBCE,TCP1,TOMM70A,ZW10

AURKB,C1QBP,COPS3,COX10,EIF4A1,EIF5A,EIF5AL1, ELAC2,GEMIN4,GLOD4,MIS12,NUP88,PRPSAP2,RNMTL1, RPAIN,SCO1,SENP3,SLC25A11,TSR1,WRAP53,YWHAE	APOO,CCT2,DCAF13,EBNA1BP2,GNL3,HEATR3,HMBS, HSPA14,HSPE1,ILF2,MRPL3,NUP37,NUP88,PCNA, RAN,SLBP,TFDP1,TMX2,UBE2T,UTP6,VRK1

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 NUP88

There's no related Drug.

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Cross referenced IDs for NUP88

* 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