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 ANPEP

Basic gene info.	Gene symbol	ANPEP
	Gene name	alanyl (membrane) aminopeptidase
	Synonyms	APN\|CD13\|GP150\|LAP1\|P150\|PEPN
	Cytomap	UCSC genome browser: 15q25-q26
	Genomic location	chr15 :90328125-90358072
	Type of gene	protein-coding
	RefGenes	NM_001150.2,
	Ensembl id	ENSG00000166825
	Description	AP-MAP-Nalanyl aminopeptidaseaminopeptidase Maminopeptidase NhAPNmicrosomal aminopeptidasemyeloid plasma membrane glycoprotein CD13
	Modification date	20141211
dbXrefs	MIM : 151530
	HGNC : HGNC
	Ensembl : ENSG00000166825
	HPRD : 01055
	Vega : OTTHUMG00000149814
Protein	UniProt: go to UniProt's Cross Reference DB Table
Expression	CleanEX: HS_ANPEP
	BioGPS: 290
	Gene Expression Atlas: ENSG00000166825
	The Human Protein Atlas: ENSG00000166825
Pathway	NCI Pathway Interaction Database: ANPEP
	KEGG: ANPEP
	REACTOME: ANPEP
	ConsensusPathDB
	Pathway Commons: ANPEP
Metabolism	MetaCyc: ANPEP
	HUMANCyc: ANPEP
Regulation	Ensembl's Regulation: ENSG00000166825
	miRBase: chr15 :90,328,125-90,358,072
	TargetScan: NM_001150
	cisRED: ENSG00000166825
Context	iHOP: ANPEP
	cancer metabolism search in PubMed: ANPEP
	UCL Cancer Institute: ANPEP
Assigned class in ccmGDB	C

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

Cancer Description
Cancer	CGAP: ANPEP
	Familial Cancer Database: ANPEP

* 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
KEGG_GLUTATHIONE_METABOLISM

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

Mutations for ANPEP

* 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 ANPEP 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
CB157580	ANPEP	1	252	15	90346505	90347130	ANPEP	248	622	15	90340903	90344722
BQ882584	CUX1	20	216	7	101461708	101461904	ANPEP	206	819	15	90347120	90348048

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=5

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Somatic Mutation Counts per Tissue in COSMIC data

Stat. for Non-Synonymous SNVs (# total SNVs=98)	Stat. for Synonymous SNVs (# total SNVs=32)

Stat. for Deletions (# total SNVs=2)	Stat. for Insertions (# total SNVs=3)

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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
chr15:90344681-90344681	p.R576H	4
chr15:90347169-90347169	p.S415F	3
chr15:90347174-90347174	p.F413F	3
chr15:90342704-90342704	p.E636K	3
chr15:90349236-90349236	p.F193L	3
chr15:90342782-90342782	p.D610N	3
chr15:90349552-90349552	p.T88M	3
chr15:90349564-90349564	p.S84Y	2
chr15:90347724-90347724	p.S341L	2
chr15:90349346-90349346	p.E157Q	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=5

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	5	2	22	2		2		11	2		9	9	3			23	10		18
# mutation	4	5	2	21	2		2		10	2		9	9	3			29	11		20
nonsynonymous SNV	3	5	1	15	1				7	2		5	8	2			17	7		12
synonymous SNV	1		1	6	1		2		3			4	1	1			12	4		8

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
chr15:90342704	p.E636K	3
chr15:90349552	p.A425A	2
chr15:90347138	p.P95P	2
chr15:90328653	p.P95H	2
chr15:90340926	p.T944M	2
chr15:90342493	p.T88M	2
chr15:90349530	p.A679A	2
chr15:90349346	p.A669A	2
chr15:90349531	p.E157Q	2
chr15:90349755	p.T277T	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 ANPEP 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 ANPEP

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


ACOT11,ANKRD33,ANKRD55,ANPEP,ATP12A,CDR1,CNGA3, TXLNGY,EIF1AY,FAM41AY1,FOXI2,KDM5D,LDHAL6A,NCRNA00185, NETO2,PPARG,RAB40A,RGAG1,STC1,TTTY15,ZNF486	SOWAHB,ANPEP,BARX2,BBOX1,PLEKHS1,CMTM7,CXCL16, GPR56,IL34,KLK5,KLK6,KLK8,KRT23,KRT7, KRT80,PLD2,STAC2,TNFRSF19,TTC9,VGLL1,VPS37B

ABCG2,ACADS,ANPEP,B3GALT5,C11orf86,TMEM253,C1orf177, C1orf94,CAPN11,CYP3A4,HSD17B2,MARVELD3,NAT8,LINC00114, SULT1C2,TM4SF20,TM4SF4,TMEM92,TUBAL3,UGT1A4,UGT1A5	ABHD6,ACE2,ANPEP,CHN2,FLVCR1,GBA3,SLC52A1, HEBP1,MEP1B,MYO1A,NAT8B,OIT3,OTC,PCK2, PKLR,PRAP1,PTGR1,SLC23A1,SLC6A4,TM4SF20,AGMO

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 ANPEP

Cross-referenced pharmacological DB IDs from Uniprot

DB Category

DB Name

DB's ID and Url link

Drug-Gene Interaction Network

* Gene Centered Interaction Network.

* Drug Centered Interaction Network.

DrugBank ID	Target Name	Drug Groups	Generic Name	Drug Centered Network	Drug Structure
DB00973	alanyl (membrane) aminopeptidase	approved	Ezetimibe
DB06196	alanyl (membrane) aminopeptidase	approved; investigational	Icatibant
DB08506	alanyl (membrane) aminopeptidase	experimental	N-{(2S)-3-[(1R)-1-aminoethyl](hydroxy)phosphoryl-2-benzylpropanoyl}-L-phenylalanine
DB00563	alanyl (membrane) aminopeptidase	approved	Methotrexate
DB00987	alanyl (membrane) aminopeptidase	approved; investigational	Cytarabine

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Cross referenced IDs for ANPEP

* 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