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Phenotypic Information (metabolism pathway, cancer, disease, phenome) | |
Gene-Gene Network Information: Co-Expression Network, Interacting Genes & KEGG | |
Gene Summary for PSMD7 |
Basic gene info. | Gene symbol | PSMD7 |
Gene name | proteasome (prosome, macropain) 26S subunit, non-ATPase, 7 | |
Synonyms | MOV34|P40|Rpn8|S12 | |
Cytomap | UCSC genome browser: 16q22.3 | |
Genomic location | chr16 :74330672-74340186 | |
Type of gene | protein-coding | |
RefGenes | NM_002811.4, | |
Ensembl id | ENSG00000103035 | |
Description | 26S proteasome non-ATPase regulatory subunit 726S proteasome regulatory subunit S1226S proteasome regulatory subunit rpn8Moloney leukemia virus-34 proviral integrationMov34 homologproteasome (prosome, macropain) 26S subunit, non-ATPase, 7 (Mov34 homo | |
Modification date | 20141207 | |
dbXrefs | MIM : 157970 | |
HGNC : HGNC | ||
Ensembl : ENSG00000103035 | ||
HPRD : 01147 | ||
Vega : OTTHUMG00000137601 | ||
Protein | UniProt: P51665 go to UniProt's Cross Reference DB Table | |
Expression | CleanEX: HS_PSMD7 | |
BioGPS: 5713 | ||
Gene Expression Atlas: ENSG00000103035 | ||
The Human Protein Atlas: ENSG00000103035 | ||
Pathway | NCI Pathway Interaction Database: PSMD7 | |
KEGG: PSMD7 | ||
REACTOME: PSMD7 | ||
ConsensusPathDB | ||
Pathway Commons: PSMD7 | ||
Metabolism | MetaCyc: PSMD7 | |
HUMANCyc: PSMD7 | ||
Regulation | Ensembl's Regulation: ENSG00000103035 | |
miRBase: chr16 :74,330,672-74,340,186 | ||
TargetScan: NM_002811 | ||
cisRED: ENSG00000103035 | ||
Context | iHOP: PSMD7 | |
cancer metabolism search in PubMed: PSMD7 | ||
UCL Cancer Institute: PSMD7 | ||
Assigned class in ccmGDB | B - This gene belongs to cancer gene. |
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Phenotypic Information for PSMD7(metabolism pathway, cancer, disease, phenome) |
Cancer Description | |
Cancer | CGAP: PSMD7 |
Familial Cancer Database: PSMD7 |
* This gene is included in those cancer gene databases. |
. | ||||||||||||||||||||
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/ |
Metabolic Pathway Description | |
REACTOME_METABOLISM_OF_AMINO_ACIDS_AND_DERIVATIVES REACTOME_METABOLISM_OF_MRNA REACTOME_METABOLISM_OF_RNA |
Others | |
OMIM | 157970; gene. |
Orphanet | |
Disease | KEGG Disease: PSMD7 |
MedGen: PSMD7 (Human Medical Genetics with Condition) | |
ClinVar: PSMD7 | |
Phenotype | MGI: PSMD7 (International Mouse Phenotyping Consortium) |
PhenomicDB: PSMD7 |
Mutations for PSMD7 |
* 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 |
- Statistics for Tissue and Mutation type | Top |
- For Inter-chromosomal Variations |
* Inter-chromosomal variantions includes 'interchromosomal amplicon to amplicon', 'interchromosomal amplicon to non-amplified dna', 'interchromosomal insertion', 'Interchromosomal unknown type'. |
- For Intra-chromosomal Variations |
There's no intra-chromosomal structural variation. |
Sample | Symbol_a | Chr_a | Start_a | End_a | Symbol_b | Chr_b | Start_b | End_b |
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) |
Related fusion transcripts : go to Chitars2.0 |
* From mRNA Sanger sequences, Chitars2.0 arranged chimeric transcripts. This table shows PSMD7 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 |
BF858256 | KLK3 | 1 | 68 | 19 | 51361441 | 51361508 | PSMD7 | 63 | 146 | 16 | 74330845 | 74334055 |
Other DBs for Structural Variants |
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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 |
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Somatic Mutation Counts per Tissue in COSMIC data |
Stat. for Non-Synonymous SNVs (# total SNVs=20) | (# total SNVs=10) |
(# total SNVs=1) | (# total SNVs=0) |
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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 |
chr16:74334091-74334091 | p.S51S | 2 |
chr16:74339460-74339460 | p.S268S | 2 |
chr16:74339242-74339242 | p.H196Y | 2 |
chr16:74339301-74339301 | p.V215V | 2 |
chr16:74338218-74338218 | p.S152S | 1 |
chr16:74339317-74339317 | p.P221S | 1 |
chr16:74334086-74334086 | p.V50I | 1 |
chr16:74338233-74338233 | p.H157H | 1 |
chr16:74339345-74339345 | p.L230Q | 1 |
chr16:74334090-74334090 | p.S51L | 1 |
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SNV Counts per Each Loci in TCGA data |
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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 |   | 2 |   |   |   |   | 2 |   |   | 4 | 3 | 1 |   | 1 | 1 | 5 |   | 8 |
# mutation |   | 1 |   | 1 |   |   |   |   | 2 |   |   | 4 | 3 | 1 |   | 1 | 1 | 5 |   | 8 |
nonsynonymous SNV |   | 1 |   |   |   |   |   |   | 2 |   |   | 4 | 3 | 1 |   |   |   | 3 |   | 5 |
synonymous SNV |   |   |   | 1 |   |   |   |   |   |   |   |   |   |   |   | 1 | 1 | 2 |   | 3 |
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 |
chr16:74334091 | p.S51S | 2 |
chr16:74339391 | p.F245F | 2 |
chr16:74338270 | p.K127R | 1 |
chr16:74334090 | p.K297N | 1 |
chr16:74338292 | p.E302K | 1 |
chr16:74339275 | p.P128Q | 1 |
chr16:74334950 | p.E136K | 1 |
chr16:74339301 | p.A137A | 1 |
chr16:74336132 | p.V144D | 1 |
chr16:74339302 | p.S152S | 1 |
Other DBs for Point Mutations |
Copy Number for PSMD7 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 PSMD7 |
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. |
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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 |
AARS,CMC2,CFAP20,CENPN,CFDP1,CIAPIN1,CIRH1A, COG4,EMC8,DDX19A,DHX38,DUS2,EXOSC6,KARS, NAE1,NIP7,NUP93,PSMD7,SF3B3,VAC14,VPS4A | PRADC1,CHCHD3,FEZ2,FUNDC2,HSPB7,HTATSF1,MAP4, NDUFB3,OPTN,PGK1,PINK1,PSMC2,PSMD1,PSMD2, PSMD7,RNF10,SGCG,SNTA1,UBE2D4,WSB2,YBX1 |
CFDP1,CIRH1A,COG4,EMC8,DDX19A,DNAJA3,E2F4, HSBP1,KARS,MPHOSPH6,NAE1,NIP7,NUDT21,NUTF2, PDF,POLR2C,PSMA7,PSMD7,SLC7A6OS,USP10,VPS4A | CCDC167,EIF2B3,EIF2S2,ENSA,ERH,GOLT1B,HAT1, MORF4L2,PSMA1,PSMA3,PSMA4,PSMA7,PSMC2,PSMD14, PSMD6,PSMD7,SARNP,SNRPB2,SNRPE,SSBP1,TCEB1 |
Co-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 |
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Interacting Genes (from Pathway Commons) |
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Pharmacological Information for PSMD7 |
There's no related Drug. |
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Cross referenced IDs for PSMD7 |
* 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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