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| Phenotypic Information (metabolism pathway, cancer, disease, phenome) |
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| Gene-Gene Network Information: Co-Expression Network, Interacting Genes & KEGG |
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| Gene Summary for PDHB |
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| Phenotypic Information for PDHB(metabolism pathway, cancer, disease, phenome) |
| Cancer | CGAP: PDHB |
| Familial Cancer Database: PDHB | |
| * This gene is included in those cancer gene databases. |
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Oncogene 1 | Significant driver gene in | |||||||||||||||||||
| 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/ |
| KEGG_GLYCOLYSIS_GLUCONEOGENESIS KEGG_PYRUVATE_METABOLISM KEGG_BUTANOATE_METABOLISM REACTOME_PYRUVATE_METABOLISM_AND_CITRIC_ACID_TCA_CYCLE REACTOME_PYRUVATE_METABOLISM | |
| OMIM | |
| Orphanet | |
| Disease | KEGG Disease: PDHB |
| MedGen: PDHB (Human Medical Genetics with Condition) | |
| ClinVar: PDHB | |
| Phenotype | MGI: PDHB (International Mouse Phenotyping Consortium) |
| PhenomicDB: PDHB | |
| Mutations for PDHB |
| * 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. |
| There's no structural variation information in COSMIC data for this gene. |
| * From mRNA Sanger sequences, Chitars2.0 arranged chimeric transcripts. This table shows PDHB 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 |
| BF747570 | PDHB | 16 | 83 | 3 | 58415887 | 58415954 | RUFY3 | 81 | 323 | 4 | 71671497 | 71671739 | |
| BF747731 | PDHB | 14 | 85 | 3 | 58415883 | 58415954 | RUFY3 | 83 | 143 | 4 | 71671497 | 71671612 | |
| BF930759 | PTPRS | 14 | 190 | 19 | 5205861 | 5206041 | PDHB | 184 | 514 | 3 | 58417832 | 58418162 | |
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| There's no copy number variation information in COSMIC data for this gene. |
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| Stat. for Non-Synonymous SNVs (# total SNVs=14) | (# total SNVs=7) |
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(# total SNVs=0) | (# total SNVs=0) |
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| * 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 |
| chr3:58413894-58413894 | p.N316T | 2 |
| chr3:58417485-58417485 | p.K80N | 2 |
| chr3:58414285-58414285 | p.V283V | 2 |
| chr3:58416535-58416535 | p.G146G | 2 |
| chr3:58419403-58419403 | p.G17G | 1 |
| chr3:58413882-58413882 | p.A320V | 1 |
| chr3:58416621-58416621 | p.Q118* | 1 |
| chr3:58419505-58419505 | p.P11L | 1 |
| chr3:58417332-58417332 | p.V97V | 1 |
| chr3:58419532-58419532 | p.A2E | 1 |
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| 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 |   | 7 |   |   |   |   |   |   |   |   |   | 1 |   |   |   | 4 |   | 5 |
| # mutation |   | 1 |   | 6 |   |   |   |   |   |   |   |   |   | 1 |   |   |   | 4 |   | 5 |
| nonsynonymous SNV |   | 1 |   | 3 |   |   |   |   |   |   |   |   |   |   |   |   |   | 2 |   | 3 |
| synonymous SNV |   |   |   | 3 |   |   |   |   |   |   |   |   |   | 1 |   |   |   | 2 |   | 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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| * 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 |
| chr3:58414285 | p.A320V,PDHB | 2 |
| chr3:58413882 | p.V283V,PDHB | 2 |
| chr3:58413899 | p.A96D,PDHB | 1 |
| chr3:58419403 | p.A66T,PDHB | 1 |
| chr3:58414286 | p.V53I,PDHB | 1 |
| chr3:58414314 | p.T34T,PDHB | 1 |
| chr3:58414340 | p.G17G,PDHB | 1 |
| chr3:58416535 | p.A352A,PDHB | 1 |
| chr3:58417332 | p.K347T,PDHB | 1 |
| chr3:58413785 | p.N316T,PDHB | 1 |
| * 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. |
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| 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 PDHB |
| * CCLE gene expression data were extracted from CCLE_Expression_Entrez_2012-10-18.res: Gene-centric RMA-normalized mRNA expression data. |
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| * 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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| * This plots show the correlation between CNV and gene expression. |
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| Gene-Gene Network Information |
| * 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 |
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| ABHD14A,ACOX2,BCDIN3D,CCDC51,CYB561D2,CYB5D2,GLT8D1, KCTD6,KIF9,LZTFL1,NPRL2,PDHB,PHF7,PSMD6, RPP14,SEC22C,SHQ1,SPCS1,SUCLG2,TEX264,TUSC2 | ACAT1,ACO2,ALPK3,ATP5B,ATP5G3,ATP5J,TIMM21, CHCHD3,COX5A,FH,GHITM,IMMT,NDUFAB1,NDUFB3, PDHB,GATB,PGM1,PHYH,SDHB,SLC2A4,UQCRFS1 | ||||
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| CCDC58,TMA7,CETN3,CHCHD4,CMC1,GNL3,KCTD6, KIF9,LSM3,MRPL1,MRPS22,OXSM,PDHB,PSMD6, TRMT10C,RPL14,RPP14,SPCS1,THOC7,UBA3,UQCRC1 | TIMM21,COMMD10,COMMD2,DAP3,DNAJC8,GBAS,GPN3, GTF3A,MED21,MED28,MRPL18,MRPL24,NDUFAF2,NSMCE2, PDHB,POLR2K,PRKAG1,RNF41,RWDD2B,SNAPIN,ZCCHC17 |
| * 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 |
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| Pharmacological Information for PDHB |
| DB Category | DB Name | DB's ID and Url link |
| * Gene Centered Interaction Network. |
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| * Drug Centered Interaction Network. |
| DrugBank ID | Target Name | Drug Groups | Generic Name | Drug Centered Network | Drug Structure |
| DB00119 | pyruvate dehydrogenase (lipoamide) beta | approved; nutraceutical | Pyruvic acid | ![]() | ![]() |
| DB00157 | pyruvate dehydrogenase (lipoamide) beta | approved; nutraceutical | NADH | ![]() | ![]() |
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| Cross referenced IDs for PDHB |
| * We obtained these cross-references from Uniprot database. It covers 150 different DBs, 18 categories. http://www.uniprot.org/help/cross_references_section |
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