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 ALDH1B1

Basic gene info.	Gene symbol	ALDH1B1
	Gene name	aldehyde dehydrogenase 1 family, member B1
	Synonyms	ALDH5\|ALDHX
	Cytomap	UCSC genome browser: 9p11.1
	Genomic location	chr9 :38392660-38398662
	Type of gene	protein-coding
	RefGenes	NM_000692.4,
	Ensembl id	ENSG00000137124
	Description	ALDH class 2acetaldehyde dehydrogenase 5aldehyde dehydrogenase 5aldehyde dehydrogenase X, mitochondrial
	Modification date	20141222
dbXrefs	MIM : 100670
	HGNC : HGNC
	Ensembl : ENSG00000137124
	HPRD : 00005
	Vega : OTTHUMG00000019938
Protein	UniProt: go to UniProt's Cross Reference DB Table
Expression	CleanEX: HS_ALDH1B1
	BioGPS: 219
	Gene Expression Atlas: ENSG00000137124
	The Human Protein Atlas: ENSG00000137124
Pathway	NCI Pathway Interaction Database: ALDH1B1
	KEGG: ALDH1B1
	REACTOME: ALDH1B1
	ConsensusPathDB
	Pathway Commons: ALDH1B1
Metabolism	MetaCyc: ALDH1B1
	HUMANCyc: ALDH1B1
Regulation	Ensembl's Regulation: ENSG00000137124
	miRBase: chr9 :38,392,660-38,398,662
	TargetScan: NM_000692
	cisRED: ENSG00000137124
Context	iHOP: ALDH1B1
	cancer metabolism search in PubMed: ALDH1B1
	UCL Cancer Institute: ALDH1B1
Assigned class in ccmGDB	C

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Phenotypic Information for ALDH1B1(metabolism pathway, cancer, disease, phenome)

Cancer Description
Cancer	CGAP: ALDH1B1
	Familial Cancer Database: ALDH1B1

* 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_GLYCOLYSIS_GLUCONEOGENESIS KEGG_ASCORBATE_AND_ALDARATE_METABOLISM KEGG_FATTY_ACID_METABOLISM KEGG_ARGININE_AND_PROLINE_METABOLISM KEGG_HISTIDINE_METABOLISM KEGG_TRYPTOPHAN_METABOLISM KEGG_BETA_ALANINE_METABOLISM KEGG_GLYCEROLIPID_METABOLISM KEGG_PYRUVATE_METABOLISM KEGG_PROPANOATE_METABOLISM KEGG_BUTANOATE_METABOLISM

Others
OMIM
Orphanet
Disease	KEGG Disease: ALDH1B1
	MedGen: ALDH1B1 (Human Medical Genetics with Condition)
	ClinVar: ALDH1B1
Phenotype	MGI: ALDH1B1 (International Mouse Phenotyping Consortium)
Phenotype	PhenomicDB: ALDH1B1

Mutations for ALDH1B1

* 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 ALDH1B1 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
BE856261	NDUFB7	1	173	19	14676892	14677064	ALDH1B1	174	474	9	38396300	38396600
AI422203	NDUFB7	1	173	19	14676892	14677064	ALDH1B1	174	466	9	38396308	38396600

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=4

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Somatic Mutation Counts per Tissue in COSMIC data

Stat. for Non-Synonymous SNVs (# total SNVs=40)	Stat. for Synonymous SNVs (# total SNVs=10)

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
chr9:38395753-38395753	p.R3H	4
chr9:38395928-38395928	p.T61T	3
chr9:38396065-38396065	p.R107L	3
chr9:38396397-38396397	p.A218S	3
chr9:38395797-38395797	p.R18S	2
chr9:38395809-38395809	p.A22T	2
chr9:38395994-38395994	p.A83A	2
chr9:38396624-38396624	p.I293I	2
chr9:38396134-38396134	p.P130H	2
chr9:38396762-38396762	p.T339T	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=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	1	1		9			3		1	1		8	2	1			11	7	1	7
# mutation	1	1		10			3		1	1		8	2	1			11	8	1	7
nonsynonymous SNV		1		9			1		1	1		7	2	1			7	6		6
synonymous SNV	1			1			2					1					4	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
chr9:38395753	p.R3H	4
chr9:38396762	p.T339T	2
chr9:38395768	p.R8Q	2
chr9:38396569	p.P130L	2
chr9:38396134	p.G405G	2
chr9:38396624	p.G275V	2
chr9:38396960	p.I293I	2
chr9:38395964	p.M1L	1
chr9:38396998	p.R114L	1
chr9:38396249	p.F485L	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 ALDH1B1 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 ALDH1B1

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


ACTN1,ALDH1B1,CALD1,CALU,CHST3,COL8A1,DPYSL3, FLNA,FNDC1,GLS,HEPH,MSN,MYH9,MYO1E, NEXN,NRP2,PLS3,RAB23,RAI14,TAGLN,TIMP2	ALDH1B1,CAMK2G,CASQ2,DGKG,DMPK,FZD9,INPP5A, ITLN1,KCNA5,LGI1,LOC401093,MT3,MUSTN1,PDE4C, PKNOX2,POU4F1,RCAN2,TGM2,TYRP1,WFDC1,ZNF536

ALDH1B1,TMEM261,CDHR1,CDX2,DAGLA,FAM171A1,GSPT2, IFT74,KANK1,LOC151009,MAT1A,NOTCH1,PMFBP1,PRDX5, RGMB,SMTN,STK38L,TDGF1,TDGF1P3,TTLL11,WNK2	ALDH1B1,FAM210A,DOLK,DUSP14,ERAL1,FASTKD2,FXN, G6PC3,GCDH,COLGALT1,H2AFY2,IPO11,NDUFAF4,NUFIP1, OGFOD1,PROCR,RCL1,RNMTL1,SMYD5,TIMM44,TANGO6

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 ALDH1B1

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
DB00157	aldehyde dehydrogenase 1 family, member B1	approved; nutraceutical	NADH

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Cross referenced IDs for ALDH1B1

* 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