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Phenotypic Information (metabolism pathway, cancer, disease, phenome) | |
Gene-Gene Network Information: Co-Expression Network, Interacting Genes & KEGG | |
Gene Summary for PSMB2 |
Basic gene info. | Gene symbol | PSMB2 |
Gene name | proteasome (prosome, macropain) subunit, beta type, 2 | |
Synonyms | HC7-I | |
Cytomap | UCSC genome browser: 1p34.2 | |
Genomic location | chr1 :36065142-36097138 | |
Type of gene | protein-coding | |
RefGenes | NM_001199779.1, NM_001199780.1,NM_002794.4, | |
Ensembl id | ENSG00000126067 | |
Description | macropain subunit C7-Imulticatalytic endopeptidase complex subunit C7-1multicatalytic endopeptidase complex subunit C7-Iproteasome beta 2 subunitproteasome component C7-Iproteasome subunit beta type-2proteasome subunit, beta type, 2 | |
Modification date | 20141207 | |
dbXrefs | MIM : 602175 | |
HGNC : HGNC | ||
Ensembl : ENSG00000126067 | ||
HPRD : 03708 | ||
Protein | UniProt: go to UniProt's Cross Reference DB Table | |
Expression | CleanEX: HS_PSMB2 | |
BioGPS: 5690 | ||
Gene Expression Atlas: ENSG00000126067 | ||
The Human Protein Atlas: ENSG00000126067 | ||
Pathway | NCI Pathway Interaction Database: PSMB2 | |
KEGG: PSMB2 | ||
REACTOME: PSMB2 | ||
ConsensusPathDB | ||
Pathway Commons: PSMB2 | ||
Metabolism | MetaCyc: PSMB2 | |
HUMANCyc: PSMB2 | ||
Regulation | Ensembl's Regulation: ENSG00000126067 | |
miRBase: chr1 :36,065,142-36,097,138 | ||
TargetScan: NM_001199779 | ||
cisRED: ENSG00000126067 | ||
Context | iHOP: PSMB2 | |
cancer metabolism search in PubMed: PSMB2 | ||
UCL Cancer Institute: PSMB2 | ||
Assigned class in ccmGDB | C |
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Phenotypic Information for PSMB2(metabolism pathway, cancer, disease, phenome) |
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Cancer | CGAP: PSMB2 |
Familial Cancer Database: PSMB2 |
* 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/ |
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REACTOME_METABOLISM_OF_AMINO_ACIDS_AND_DERIVATIVES REACTOME_METABOLISM_OF_MRNA REACTOME_METABOLISM_OF_RNA |
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OMIM | |
Orphanet | |
Disease | KEGG Disease: PSMB2 |
MedGen: PSMB2 (Human Medical Genetics with Condition) | |
ClinVar: PSMB2 | |
Phenotype | MGI: PSMB2 (International Mouse Phenotyping Consortium) |
PhenomicDB: PSMB2 |
Mutations for PSMB2 |
* 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. |
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- Statistics for Tissue and Mutation type | Top |
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- For Inter-chromosomal Variations |
* Inter-chromosomal variantions includes 'interchromosomal amplicon to amplicon', 'interchromosomal amplicon to non-amplified dna', 'interchromosomal insertion', 'Interchromosomal unknown type'. |
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- 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'. |
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Sample | Symbol_a | Chr_a | Start_a | End_a | Symbol_b | Chr_b | Start_b | End_b |
breast | PSMB2 | chr1 | 36085155 | 36085155 | chr10 | 15216835 | 15216835 | |
ovary | PSMB2 | chr1 | 36091530 | 36091550 | DLGAP3 | chr1 | 35335849 | 35335869 |
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) |
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* From mRNA Sanger sequences, Chitars2.0 arranged chimeric transcripts. This table shows PSMB2 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 |
BE908471 | SRC | 1 | 221 | 20 | 36031753 | 36031973 | PSMB2 | 208 | 478 | 1 | 36068745 | 36070873 | |
AA393815 | PSMB2 | 1 | 238 | 1 | 36068559 | 36068796 | PSMB2 | 234 | 518 | 1 | 36101927 | 36107120 | |
CB156087 | PSMB2 | 1 | 472 | 1 | 36067669 | 36068140 | SLC25A35 | 467 | 660 | 17 | 8193447 | 8193640 | |
AA393918 | PSMB2 | 1 | 350 | 1 | 36096896 | 36107120 | PSMB2 | 346 | 430 | 1 | 36068559 | 36068643 |
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Mutation type/ Tissue ID | brca | cns | cerv | endome | haematopo | kidn | Lintest | liver | lung | ns | ovary | pancre | prost | skin | stoma | thyro | urina | |||
Total # sample |   |   |   |   |   |   |   |   |   |   | 1 |   |   |   |   |   |   | |||
GAIN (# sample) |   |   |   |   |   |   |   |   |   |   | 1 |   |   |   |   |   |   | |||
LOSS (# sample) |   |   |   |   |   |   |   |   |   |   |   |   |   |   |   |   |   |
cf) Tissue ID; Tissue type (1; Breast, 2; Central_nervous_system, 3; Cervix, 4; Endometrium, 5; Haematopoietic_and_lymphoid_tissue, 6; Kidney, 7; Large_intestine, 8; Liver, 9; Lung, 10; NS, 11; Ovary, 12; Pancreas, 13; Prostate, 14; Skin, 15; Stomach, 16; Thyroid, 17; Urinary_tract) |
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Stat. for Non-Synonymous SNVs (# total SNVs=9) | (# total SNVs=1) |
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(# total SNVs=1) | (# 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 |
chr1:36101971-36101971 | p.D52H | 2 |
chr1:36074989-36074989 | p.L102L | 1 |
chr1:36096876-36096876 | p.R95L | 1 |
chr1:36101916-36101916 | p.R70Q | 1 |
chr1:36101917-36101917 | p.R70* | 1 |
chr1:36070882-36070882 | p.T150T | 1 |
chr1:36074873-36074873 | p.S141T | 1 |
chr1:36102023-36102023 | p.K34N | 1 |
chr1:36074881-36074891 | p.G135fs*16 | 1 |
chr1:36107026-36107026 | p.Y3C | 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 |   |   |   | 4 |   |   | 1 |   |   |   |   |   |   |   |   |   | 2 | 3 |   | 1 |
# mutation |   |   |   | 3 |   |   | 1 |   |   |   |   |   |   |   |   |   | 2 | 3 |   | 1 |
nonsynonymous SNV |   |   |   | 2 |   |   | 1 |   |   |   |   |   |   |   |   |   | 2 | 2 |   | 1 |
synonymous SNV |   |   |   | 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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* 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 |
chr1:36074882 | p.L21P,PSMB2 | 2 |
chr1:36096876 | p.Y3S,PSMB2 | 1 |
chr1:36096883 | p.S62T,PSMB2 | 1 |
chr1:36102014 | p.T60I,PSMB2 | 1 |
chr1:36107026 | p.T33T,PSMB2 | 1 |
chr1:36068938 | p.S24T,PSMB2 | 1 |
chr1:36068944 | p.A6T,PSMB2 | 1 |
chr1:36070882 | p.A89A,PSMB2 | 1 |
chr1:36074873 | p.R70L,PSMB2 | 1 |
chr1:36074928 | p.R68W,PSMB2 | 1 |
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* 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 PSMB2 |
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* 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 |
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* 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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ADPRHL2,AK2,AUNIP,CDC20,CDCA8,EIF2B3,ERI3, GNL2,KIF2C,MAGOH,MED8,MRPL37,PSMB2,PSMG1, PTTG1,TRAPPC3,TUBA1C,UQCRH,UQCRHL,UTP11L,YARS | CDC123,COX16,DYNLT1,GNG5,MRPL47,MYL12B,NOP10, NUTF2,PSMA1,PSMA3,PSMA4,PSMA5,PSMB2,RBX1, RRAGA,SDHAF2,SLC35B1,SNRPG,TOMM5,TOMM6,UCHL3 | ||||
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ACOT7,ADPRHL2,AK2,SMIM12,CDC20,EBNA1BP2,EIF3I, HDAC1,MRPL20,MRPL37,MRPS15,NOC2L,NUDC,PEF1, PRDX1,PSMA5,PSMB2,TRAPPC3,TUBA1C,UTP11L,YARS | ACTR3,ASS1,CALR,CRELD2,DDX39A,DNAJB11,EIF5AL1, ENO1,H2AFZ,MANF,NOS2,PDIA6,PPIB,PSMA3, PSMB2,PSMB5,PSMC4,RPN1,SDF2L1,SEC61B,SNRPF |
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* 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 PSMB2 |
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DB Category | DB Name | DB's ID and Url link |
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* 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 |
DB00188 | proteasome (prosome, macropain) subunit, beta type, 2 | approved; investigational | Bortezomib | ![]() | ![]() |
DB07475 | proteasome (prosome, macropain) subunit, beta type, 2 | experimental | N-[(1R)-1-(DIHYDROXYBORYL)-3-METHYLBUTYL]-N-(PYRAZIN-2-YLCARBONYL)-L-PHENYLALANINAMIDE | ![]() | ![]() |
DB08515 | proteasome (prosome, macropain) subunit, beta type, 2 | experimental | (3AR,6R,6AS)-6-((S)-((S)-CYCLOHEX-2-ENYL)(HYDROXY)METHYL)-6A-METHYL-4-OXO-HEXAHYDRO-2H-FURO[3,2-C]PYRROLE-6-CARBALDEHYDE | ![]() | ![]() |
DB00171 | proteasome (prosome, macropain) subunit, beta type, 2 | approved; nutraceutical | Adenosine triphosphate | ![]() | ![]() |
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Cross referenced IDs for PSMB2 |
* 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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