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 PHPT1

Basic gene info.	Gene symbol	PHPT1
	Gene name	phosphohistidine phosphatase 1
	Synonyms	CGI-202\|HEL-S-132P\|HSPC141\|PHP14
	Cytomap	UCSC genome browser: 9q34.3
	Genomic location	chr9 :139743255-139745490
	Type of gene	protein-coding
	RefGenes	NM_001135860.1, NM_001135861.2,NM_001287342.1,NM_001287343.1,NM_014172.5, NR_109807.1,NR_109808.1,
	Ensembl id	ENSG00000054148
	Description	14 kDa phosphohistidine phosphataseepididymis secretory sperm binding protein Li 132Pprotein janus-A homologsex-regulated protein janus-a
	Modification date	20141207
dbXrefs	MIM : 610167
	HGNC : HGNC
	HPRD : 17849
Protein	UniProt: go to UniProt's Cross Reference DB Table
Expression	CleanEX: HS_PHPT1
	BioGPS: 29085
	Gene Expression Atlas: ENSG00000054148
	The Human Protein Atlas: ENSG00000054148
Pathway	NCI Pathway Interaction Database: PHPT1
	KEGG: PHPT1
	REACTOME: PHPT1
	ConsensusPathDB
	Pathway Commons: PHPT1
Metabolism	MetaCyc: PHPT1
	HUMANCyc: PHPT1
Regulation	Ensembl's Regulation: ENSG00000054148
	miRBase: chr9 :139,743,255-139,745,490
	TargetScan: NM_001135860
	cisRED: ENSG00000054148
Context	iHOP: PHPT1
	cancer metabolism search in PubMed: PHPT1
	UCL Cancer Institute: PHPT1
Assigned class in ccmGDB	C

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Phenotypic Information for PHPT1(metabolism pathway, cancer, disease, phenome)

Cancer Description
Cancer	CGAP: PHPT1
	Familial Cancer Database: PHPT1

* 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_FRUCTOSE_AND_MANNOSE_METABOLISM KEGG_RIBOFLAVIN_METABOLISM

Others
OMIM
Orphanet
Disease	KEGG Disease: PHPT1
	MedGen: PHPT1 (Human Medical Genetics with Condition)
	ClinVar: PHPT1
Phenotype	MGI: PHPT1 (International Mouse Phenotyping Consortium)
Phenotype	PhenomicDB: PHPT1

Mutations for PHPT1

* 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 PHPT1 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
BP388129	PPAP2B	1	264	1	56960451	56960714	PHPT1	264	499	9	139745226	139745461
DB295254	PHPT1	1	180	9	139745297	139745476	DLK1	176	553	14	101200394	101200771

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=1

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Somatic Mutation Counts per Tissue in COSMIC data

Stat. for Non-Synonymous SNVs (# total SNVs=6)	Stat. for Synonymous SNVs (# total SNVs=2)

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
chr9:139743945-139743945	p.K21N	1
chr9:139745264-139745264	p.D115N	1
chr9:139743958-139743958	p.R26*	1
chr9:139745268-139745268	p.Y116F	1
chr9:139743963-139743963	p.V27V	1
chr9:139744014-139744014	p.V44V	1
chr9:139744466-139744466	p.A54A	1
chr9:139744479-139744480	p.K59fs*13	1
chr9:139744517-139744517	p.C71C	1
chr9:139744537-139744537	p.R78H	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=1

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					1						5		1
# mutation			1				1					1						5		1
nonsynonymous SNV			1				1					1						3		1
synonymous SNV																		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
chr9:139744466	p.V27V,PHPT1	1
chr9:139744530	p.A54A,PHPT1	1
chr9:139744537	p.G76S,PHPT1	1
chr9:139744542	p.R78H,PHPT1	1
chr9:139744960	p.S80P,PHPT1	1
chr9:139745229	p.M96I,PHPT1	1
chr9:139745268	p.A105V,PHPT1	1
chr9:139743896	p.Y118F,PHPT1	1
chr9:139743963	p.D5G,PHPT1	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 PHPT1 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 PHPT1

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


ALKBH7,ATP5D,BLOC1S1,C19orf24,C7orf50,LAMTOR4,C9orf142, DNLZ,EDF1,FIS1,FKBP2,JOSD2,MPG,MRPL41, MRPL53,MRPL54,NDUFA13,NUDT22,PHPT1,SSNA1,UQCR11	ANAPC11,ATP5D,COX8A,FAM195A,FAM89B,FAM96B,FASTK, NAA38,MRPL12,MRPL38,NDUFA13,NDUFB11,NDUFB7,NDUFS6, NDUFS7,NDUFS8,NOSIP,PHPT1,PTGES2,PAM16,TIMM17B

TMEM256,SMDT1,PTRHD1,COX7A2,EDF1,MIF,MRPL54, NDUFA13,NDUFA2,NDUFB1,NDUFB7,PHPT1,RPL35,RPL7A, RPS29,RPS9,RPSAP58,SF3B5,SSNA1,TMEM141,TRUB2	ANAPC11,OXLD1,BABAM1,URB1-AS1,C7orf55,CCDC71,DHPS, DPM3,ERI3,EXOSC4,HDAC3,KLHDC9,MRPL57,MRPL43, MUS81,NARFL,NUBP2,PHPT1,PMF1,SDHAF1,ZNF76

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 PHPT1

There's no related Drug.

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Cross referenced IDs for PHPT1

* 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