Cancer Cell Metabolism Gene Database

  Cancer Cell Metabolism Gene DB

Home

Search

Download

 Statistics

Help

About Us

Bioinformatics and Systems Medicine Laboratory Bioinformatics and Systems Medicine Laboratory

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 IDI2
Basic gene info.Gene symbolIDI2
Gene nameisopentenyl-diphosphate delta isomerase 2
SynonymsIPPI2
CytomapUCSC genome browser: 10p15.3
Genomic locationchr10 :1064846-1071799
Type of geneprotein-coding
RefGenesNM_033261.2,
Ensembl idENSG00000148377
DescriptionIPP isomerase 2diphosphate dimethylallyl diphosphate isomerase 2isopentenyl pyrophosphate isomerase 2isopentenyl-diphosphate Delta-isomerase 2isopentenyl-diphosphate delta-isomerase 2
Modification date20141207
dbXrefs MIM : 615389
HGNC : HGNC
Ensembl : ENSG00000148377
HPRD : 17127
Vega : OTTHUMG00000017537
ProteinUniProt:
go to UniProt's Cross Reference DB Table
ExpressionCleanEX: HS_IDI2
BioGPS: 91734
Gene Expression Atlas: ENSG00000148377
The Human Protein Atlas: ENSG00000148377
PathwayNCI Pathway Interaction Database: IDI2
KEGG: IDI2
REACTOME: IDI2
ConsensusPathDB
Pathway Commons: IDI2
MetabolismMetaCyc: IDI2
HUMANCyc: IDI2
RegulationEnsembl's Regulation: ENSG00000148377
miRBase: chr10 :1,064,846-1,071,799
TargetScan: NM_033261
cisRED: ENSG00000148377
ContextiHOP: IDI2
cancer metabolism search in PubMed: IDI2
UCL Cancer Institute: IDI2
Assigned class in ccmGDBC

Top
Phenotypic Information for IDI2(metabolism pathway, cancer, disease, phenome)
check002.gifCancer Description
Cancer CGAP: IDI2
Familial Cancer Database: IDI2
* 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/

check002.gifMetabolic Pathway Description
REACTOME_METABOLISM_OF_LIPIDS_AND_LIPOPROTEINS

check002.gifOthers
OMIM
Orphanet
DiseaseKEGG Disease: IDI2
MedGen: IDI2 (Human Medical Genetics with Condition)
ClinVar: IDI2
PhenotypeMGI: IDI2 (International Mouse Phenotyping Consortium)
PhenomicDB: IDI2

Mutations for IDI2
* 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.

check002.gifStructural Variants in COSMIC: go to COSMIC mutation histogram
There's no structural variation information in COSMIC data for this gene.

check002.gifRelated fusion transcripts : go to Chitars2.0
* From mRNA Sanger sequences, Chitars2.0 arranged chimeric transcripts. This table shows IDI2 related fusion information.
IDHead GeneTail Gene
AccessionGene_aqStart_aqEnd_aChromosome_atStart_atEnd_aGene_aqStart_aqEnd_aChromosome_atStart_atEnd_a

check002.gifOther DBs for Structural Variants
Structural Variants in Ensembl: go to Ensembl Structural variation
Structural Variants in dbVar: go to dbVar

Top
check002.gifCopy Number Variations in COSMIC: go to COSMIC mutation CNV/Expr
There's no copy number variation information in COSMIC data for this gene.

Top
check002.gifSNV 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

Top
check002.gifSomatic Mutation Counts per Tissue in COSMIC data
Stat. for Non-Synonymous SNVs
(# total SNVs=16)
Stat. for Synonymous SNVs
(# total SNVs=4)
Stat. for Deletions
(# total SNVs=1)
Stat. for Insertions
(# total SNVs=0)
There's no inserted snv.

Top
check002.gifTop 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 positionMutation(aa)Unique sampleID count
chr10:1068633-1068633p.V75V2
chr10:1066741-1066741p.R111H2
chr10:1065729-1065729p.A138T1
chr10:1068614-1068614p.?1
chr10:1065490-1065490p.P217P1
chr10:1065753-1065753p.F130I1
chr10:1065491-1065491p.P217Q1
chr10:1066710-1066710p.E121E1
chr10:1068668-1068668p.R64*1
chr10:1065499-1065499p.D214D1

Top
check002.gifSNV 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 ID1234567891011121314151617181920
# sample3 141   2  121  32 2
# mutation3 141   2  121  32 2
nonsynonymous SNV3  21   2   21  11 1
synonymous SNV  12       1    21 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])

Top
check002.gifTop 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 PositionMutation(aa)Unique sampleID count
chr10:1066741p.R111H2
chr10:1066834p.Q113P1
chr10:1065491p.G103R1
chr10:1066837p.K99K1
chr10:1065499p.Y80C1
chr10:1068645p.G79A1
chr10:1065637p.S71S1
chr10:1068692p.V56I1
chr10:1065705p.X228X1
chr10:1070526p.E46E1

check002.gifOther 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

check002.gifCopy Number for IDI2 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]

Top
Gene Expression for IDI2

check002.gifGene 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.

check002.gifDifferential 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))
Top
check002.gifCNV vs Gene Expression Plot
* This plots show the correlation between CNV and gene expression.

: Open all plots for all cancer types


Top
Gene-Gene Network Information
check002.gifCo-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

ATP5C1,SNHG15,CCT4,CDC123,DGUOK,FAM136A,GTPBP4,
IDI2,KIN,LARP4B,LOC388796,MRTO4,NDUFAF4,NOP58,
PDSS1,RANBP1,RBM17,RPIA,RPP38,RPS27A,SF3B14
ANKRD23,ASB12,ASB5,CACNG1,CAPN3,DUSP26,FITM1,
IDI2,JPH1,KCNA7,LRRC39,MB,MYADML2,MYBPH,
MYH8,RYR1,SRPK3,TMEM38A,TNNI1,TNNI2,YIPF7

AGAP4,AGAP6,ANKRD16,LINC00852,C6orf163,CDK10,COMMD6,
EBPL,IDI2,MSRB2,NANOS1,NSUN5P1,NSUN5P2,RPL11,
RPS24,SPRN,TCTE3,TIAF1,UPF3A,ZNF692,ZNF789
AKAP8,BCL3,BPY2,C6orf141,CHSY1,EGR4,EPHA2,
FOSL1,FUT4,FUT5,IDI2,KIAA0040,KRT78,MESDC1,
MMP13,OR2T12,OR52M1,PHLDA1,PNPLA5,SYCN,YTHDF1
check002.gifCo-Expressed gene's Protein-protein interaction 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

Top
check002.gifInteracting Genes (from Pathway Commons)

: Open all interacting genes' information including KEGG pathway for all interacting genes from DAVID

Top
Pharmacological Information for IDI2


There's no related Drug.
Top
Cross referenced IDs for IDI2
* 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



Copyright © 2016-Present - The Univsersity of Texas Health Science Center at Houston @
Site Policies | State of Texas