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 ST3GAL2

Basic gene info.	Gene symbol	ST3GAL2
	Gene name	ST3 beta-galactoside alpha-2,3-sialyltransferase 2
	Synonyms	Gal-NAc6S\|SIAT4B\|ST3GALII\|ST3GalA.2
	Cytomap	UCSC genome browser: 16q22.1
	Genomic location	chr16 :70413337-70472991
	Type of gene	protein-coding
	RefGenes	NM_006927.3,
	Ensembl id	ENSG00000157350
	Description	CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase 2Gal-beta-1,3-GalNAc-alpha-2,3-sialyltransferaseSIAT4-BST3Gal IIalpha 2,3-ST 2beta-galactoside alpha-2,3-sialyltransferase 2beta-galactoside alpha-2,3-sialytransferasesialyltran
	Modification date	20141207
dbXrefs	MIM : 607188
	HGNC : HGNC
	Ensembl : ENSG00000157350
	HPRD : 06220
Protein	UniProt: go to UniProt's Cross Reference DB Table
Expression	CleanEX: HS_ST3GAL2
	BioGPS: 6483
	Gene Expression Atlas: ENSG00000157350
	The Human Protein Atlas: ENSG00000157350
Pathway	NCI Pathway Interaction Database: ST3GAL2
	KEGG: ST3GAL2
	REACTOME: ST3GAL2
	ConsensusPathDB
	Pathway Commons: ST3GAL2
Metabolism	MetaCyc: ST3GAL2
	HUMANCyc: ST3GAL2
Regulation	Ensembl's Regulation: ENSG00000157350
	miRBase: chr16 :70,413,337-70,472,991
	TargetScan: NM_006927
	cisRED: ENSG00000157350
Context	iHOP: ST3GAL2
	cancer metabolism search in PubMed: ST3GAL2
	UCL Cancer Institute: ST3GAL2
Assigned class in ccmGDB	C

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Phenotypic Information for ST3GAL2(metabolism pathway, cancer, disease, phenome)

Cancer Description
Cancer	CGAP: ST3GAL2
	Familial Cancer Database: ST3GAL2

* 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_CARBOHYDRATES

Others
OMIM
Orphanet
Disease	KEGG Disease: ST3GAL2
	MedGen: ST3GAL2 (Human Medical Genetics with Condition)
	ClinVar: ST3GAL2
Phenotype	MGI: ST3GAL2 (International Mouse Phenotyping Consortium)
Phenotype	PhenomicDB: ST3GAL2

Mutations for ST3GAL2

* 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

- Statistics for Tissue and Mutation type

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- For Inter-chromosomal Variations

There's no inter-chromosomal structural variation.

- For Intra-chromosomal Variations

* Intra-chromosomal variantions includes 'intrachromosomal amplicon to amplicon', 'intrachromosomal amplicon to non-amplified dna', 'intrachromosomal deletion', 'intrachromosomal fold-back inversion', 'intrachromosomal inversion', 'intrachromosomal tandem duplication', 'Intrachromosomal unknown type', 'intrachromosomal with inverted orientation', 'intrachromosomal with non-inverted orientation'.

Sample	Symbol_a	Chr_a	Start_a	End_a	Symbol_b	Chr_b	Start_b	End_b
ovary	ST3GAL2	chr16	70414855	70414875	ST3GAL2	chr16	70414989	70415009
pancreas	ST3GAL2	chr16	70419577	70419597	ST3GAL2	chr16	70419764	70419784

cf) Tissue number; Tissue name (1;Breast, 2;Central_nervous_system, 3;Haematopoietic_and_lymphoid_tissue, 4;Large_intestine, 5;Liver, 6;Lung, 7;Ovary, 8;Pancreas, 9;Prostate, 10;Skin, 11;Soft_tissue, 12;Upper_aerodigestive_tract)

Related fusion transcripts : go to Chitars2.0

* From mRNA Sanger sequences, Chitars2.0 arranged chimeric transcripts. This table shows ST3GAL2 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
BC048338	CYBA	1	1415	16	88711495	88717438	ST3GAL2	1410	1577	16	70413415	70413581
AW895060	BASP1	8	150	5	17275736	17275879	ST3GAL2	148	236	16	70417611	70417699

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=2

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Somatic Mutation Counts per Tissue in COSMIC data

Stat. for Non-Synonymous SNVs (# total SNVs=17)	Stat. for Synonymous SNVs (# total SNVs=6)

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
chr16:70417119-70417119	p.S245P	2
chr16:70422341-70422341	p.F214F	1
chr16:70428956-70428956	p.V154V	1
chr16:70415734-70415734	p.R304Q	1
chr16:70422369-70422369	p.A205D	1
chr16:70428967-70428967	p.R151C	1
chr16:70416716-70416716	p.C291R	1
chr16:70422372-70422372	p.S204I	1
chr16:70429006-70429006	p.E138K	1
chr16:70416797-70416797	p.Y264H	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		3		2								5		2			3	5	1	5
# mutation		3		2								5		2			4	5	1	6
nonsynonymous SNV		1		1								3		2			1	5	1	6
synonymous SNV		2		1								2					3

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
chr16:70417119	p.S245A	2
chr16:70422379	p.L131M	1
chr16:70432269	p.R304Q	1
chr16:70415734	p.P117P	1
chr16:70422438	p.C291R	1
chr16:70432294	p.Q109H	1
chr16:70416716	p.H266H	1
chr16:70428923	p.S82S	1
chr16:70432295	p.A260T	1
chr16:70416789	p.F246F	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 ST3GAL2 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 ST3GAL2

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


ACVRL1,BMP1,CLIP2,CNRIP1,COL16A1,COL18A1,COL6A1, COL6A2,EMILIN1,FMNL3,GPR124,HIC1,HLX,IFFO1, LRP1,PDGFRB,PPAPDC3,SCARF1,SCARF2,ST3GAL2,TGFB1	ADAMTS7,BMP1,C1orf216,COL5A1,COL6A1,COL6A2,FAM43B, GALNT2,IFFO1,MRC2,OLFML2B,PACS2,PDGFRB,PDLIM2, PLEKHM2,RCN3,SERPINH1,SLC25A19,ST3GAL2,THY1,ZBTB47

ADAMTS7,AP1M1,ARHGEF17,IRF2BPL,CD248,CDYL2,COL18A1, GLI2,GLIS2,GNA12,HIC1,NCKAP5L,NOTCH3,ORAI2, PLEKHG2,SAMD14,ST3GAL2,SYDE1,ZFHX3,ZNF319,ZNF512B	ABCA3,ANO6,AP1M1,BOK,CCDC102A,FAM110B,ITPKB, CTIF,LRCH1,LRSAM1,MAPK8IP1,NAB2,NRXN3,PKN1, RNF216,SALL2,SESTD1,SNPH,ST3GAL2,WFS1,ZNF512B

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 ST3GAL2

There's no related Drug.

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Cross referenced IDs for ST3GAL2

* 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