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 LPCAT2

Basic gene info.	Gene symbol	LPCAT2
	Gene name	lysophosphatidylcholine acyltransferase 2
	Synonyms	AYTL1\|LysoPAFAT
	Cytomap	UCSC genome browser: 16q12.2
	Genomic location	chr16 :55542912-55620582
	Type of gene	protein-coding
	RefGenes	NM_017839.4,
	Ensembl id	ENSG00000087253
	Description	1-AGP acyltransferase 111-AGPAT 111-acylglycerol-3-phosphate O-acyltransferase 111-acylglycerophosphocholine O-acyltransferase1-alkylglycerophosphocholine O-acetyltransferaseLPAAT-alphaLPC acyltransferase 2LPCAT-2acetyl-CoA:lyso-PAF acetyltransfer
	Modification date	20141207
dbXrefs	MIM : 612040
	HGNC : HGNC
	Ensembl : ENSG00000087253
	HPRD : 07913
	Vega : OTTHUMG00000133238
Protein	UniProt: go to UniProt's Cross Reference DB Table
Expression	CleanEX: HS_LPCAT2
	BioGPS: 54947
	Gene Expression Atlas: ENSG00000087253
	The Human Protein Atlas: ENSG00000087253
Pathway	NCI Pathway Interaction Database: LPCAT2
	KEGG: LPCAT2
	REACTOME: LPCAT2
	ConsensusPathDB
	Pathway Commons: LPCAT2
Metabolism	MetaCyc: LPCAT2
	HUMANCyc: LPCAT2
Regulation	Ensembl's Regulation: ENSG00000087253
	miRBase: chr16 :55,542,912-55,620,582
	TargetScan: NM_017839
	cisRED: ENSG00000087253
Context	iHOP: LPCAT2
	cancer metabolism search in PubMed: LPCAT2
	UCL Cancer Institute: LPCAT2
Assigned class in ccmGDB	C

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Phenotypic Information for LPCAT2(metabolism pathway, cancer, disease, phenome)

Cancer Description
Cancer	CGAP: LPCAT2
	Familial Cancer Database: LPCAT2

* 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_GLYCEROPHOSPHOLIPID_METABOLISM REACTOME_PHOSPHOLIPID_METABOLISM REACTOME_METABOLISM_OF_LIPIDS_AND_LIPOPROTEINS

Others
OMIM
Orphanet
Disease	KEGG Disease: LPCAT2
	MedGen: LPCAT2 (Human Medical Genetics with Condition)
	ClinVar: LPCAT2
Phenotype	MGI: LPCAT2 (International Mouse Phenotyping Consortium)
Phenotype	PhenomicDB: LPCAT2

Mutations for LPCAT2

* 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 LPCAT2 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
AJ420584	LPCAT2	25	1589	16	55565824	55617581	TXNDC5	1584	1900	6	8014214	8014530
AI333351	ATP6V1D	3	350	14	67804589	67804936	LPCAT2	348	462	16	55600700	55600814
AA602968	LPCAT2	8	107	16	55620028	55620127	LPCAT2	103	429	16	55619706	55620032
CN286009	LPCAT2	13	74	16	55618722	55618783	LPCAT2	55	426	16	55618734	55619115

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=3

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Somatic Mutation Counts per Tissue in COSMIC data

Stat. for Non-Synonymous SNVs (# total SNVs=32)	Stat. for Synonymous SNVs (# total SNVs=10)

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
chr16:55579721-55579721	p.L309L	3
chr16:55613030-55613030	p.V442I	2
chr16:55613052-55613052	p.T449M	2
chr16:55585003-55585003	p.L402F	2
chr16:55568366-55568366	p.T258T	2
chr16:55616885-55616885	p.L504L	1
chr16:55579714-55579714	p.R307Q	1
chr16:55559500-55559500	p.A84A	1
chr16:55584910-55584910	p.A371S	1
chr16:55562455-55562455	p.L160L	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=4

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				6	1		2		1			7	3				7	9		6
# mutation				6	1		2		1			7	3				7	10		7
nonsynonymous SNV				4	1		2		1			4	3				3	8		6
synonymous SNV				2								3					4	2		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
chr16:55613052	p.T449M	2
chr16:55584911	p.A371V	2
chr16:55583308	p.Q262Q	1
chr16:55559537	p.V422V	1
chr16:55613023	p.G20W	1
chr16:55565881	p.V306V	1
chr16:55583314	p.L423S	1
chr16:55562317	p.P41L	1
chr16:55613030	p.M310V	1
chr16:55566747	p.N428I	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 LPCAT2 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 LPCAT2

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


ARHGAP31,BICC1,EOGT,CARD6,DPYD,DSE,DST, FAM126A,KCTD12,LHFPL2,LPCAT2,LRCH1,LUZP1,PKD2, PLSCR4,PROS1,QKI,RBMS1,RCBTB2,SOCS5,TSHZ2	TMEM237,TDRP,COMMD2,DENND6A,FAM13B,ZC2HC1A,CCSER1, FEM1B,IL1RAP,LPCAT2,LZTFL1,MCTP2,NAP1L2,NUDT21, PRKCI,RBMXL1,SMEK1,TP63,USP31,ZNF10,ZNF136

RGCC,C15orf26,CSRNP3,DERL1,DPY19L4,EBAG9,FAM91A1, HPCAL1,UFL1,LPCAT2,MAL2,MBNL2,NEBL,OXR1, PCSK1,PLEKHB1,PTK2,RAB2A,TMEM67,VEZF1,ZBTB10	ASUN,TMA16,C4orf46,CLINT1,GPX2,GSTCD,LPCAT2, MRPS27,MTHFD2,PGA4,PM20D2,PPAT,PRPS2,RCN1, RNF183,SKP2,SLC10A7,SORD,TMEM173,WDR75,ZWILCH

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 LPCAT2

There's no related Drug.

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Cross referenced IDs for LPCAT2

* 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