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PSMD11 (proteasome 26S subunit, non-ATPase 11)

Identity

Alias_namesproteasome (prosome
Alias_symbol (synonym)S9
p44.5
MGC3844
Rpn6
Other alias
HGNC (Hugo) PSMD11
LocusID (NCBI) 5717
Atlas_Id 41888
Location 17q11.2  [Link to chromosome band 17q11]
Location_base_pair Starts at 30771481 and ends at 30810337 bp from pter ( according to hg19-Feb_2009)
Fusion genes
(updated 2016)
AKAP10 (17p11.2) / PSMD11 (17q11.2)CASC15 (6p22.3) / PSMD11 (17q11.2)NF1 (17q11.2) / PSMD11 (17q11.2)
PSMD11 (17q11.2) / CEP112 (17q24.1)PSMD11 (17q11.2) / CTNND1 (11q12.1)PSMD11 (17q11.2) / PSMD11 (17q11.2)
TMED10 (14q24.3) / PSMD11 (17q11.2)WIPF2 (17q21.1) / PSMD11 (17q11.2)NF1 17q11.2 / PSMD11 17q11.2
PSMD11 17q11.2 / CEP112 17q24.1TMED10 14q24.3 / PSMD11 17q11.2WIPF2 17q21.1 / PSMD11 17q11.2

Note

Non-annotated gene. Preliminary data : if you are an author
who wish to write a full paper/card on this gene, go to  How to contribute

DNA/RNA

 


Other Solid tumors implicated (Data extracted from papers in the Atlas) [ 1 ]
  Lung: Translocations in Squamous Cell Carcinoma


External links

Nomenclature
HGNC (Hugo)PSMD11   9556
Cards
Entrez_Gene (NCBI)PSMD11  5717  proteasome 26S subunit, non-ATPase 11
AliasesRpn6; S9; p44.5
GeneCards (Weizmann)PSMD11
Ensembl hg19 (Hinxton)ENSG00000108671 [Gene_View]  chr17:30771481-30810337 [Contig_View]  PSMD11 [Vega]
Ensembl hg38 (Hinxton)ENSG00000108671 [Gene_View]  chr17:30771481-30810337 [Contig_View]  PSMD11 [Vega]
ICGC DataPortalENSG00000108671
TCGA cBioPortalPSMD11
AceView (NCBI)PSMD11
Genatlas (Paris)PSMD11
WikiGenes5717
SOURCE (Princeton)PSMD11
Genetics Home Reference (NIH)PSMD11
Genomic and cartography
GoldenPath hg19 (UCSC)PSMD11  -     chr17:30771481-30810337 +  17q11.2   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)PSMD11  -     17q11.2   [Description]    (hg38-Dec_2013)
EnsemblPSMD11 - 17q11.2 [CytoView hg19]  PSMD11 - 17q11.2 [CytoView hg38]
Mapping of homologs : NCBIPSMD11 [Mapview hg19]  PSMD11 [Mapview hg38]
OMIM604449   
Gene and transcription
Genbank (Entrez)AB003102 AF001212 AK093602 AK223196 AK290602
RefSeq transcript (Entrez)NM_001270482 NM_002815
RefSeq genomic (Entrez)NC_000017 NC_018928 NT_010783 NW_004929407
Consensus coding sequences : CCDS (NCBI)PSMD11
Cluster EST : UnigeneHs.443379 [ NCBI ]
CGAP (NCI)Hs.443379
Alternative Splicing GalleryENSG00000108671
Gene ExpressionPSMD11 [ NCBI-GEO ]   PSMD11 [ EBI - ARRAY_EXPRESS ]   PSMD11 [ SEEK ]   PSMD11 [ MEM ]
Gene Expression Viewer (FireBrowse)PSMD11 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)5717
GTEX Portal (Tissue expression)PSMD11
Protein : pattern, domain, 3D structure
UniProt/SwissProtO00231   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtO00231  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProO00231
Splice isoforms : SwissVarO00231
PhosPhoSitePlusO00231
Domains : Interpro (EBI)PAM    PCI_dom    TPR-like_helical_dom    WHTH_DNA-bd_dom   
Domain families : Pfam (Sanger)PCI (PF01399)   
Domain families : Pfam (NCBI)pfam01399   
Domain families : Smart (EMBL)PAM (SM00753)  PINT (SM00088)  
Conserved Domain (NCBI)PSMD11
DMDM Disease mutations5717
Blocks (Seattle)PSMD11
SuperfamilyO00231
Human Protein AtlasENSG00000108671
Peptide AtlasO00231
HPRD05119
IPIIPI00105598   IPI00790498   
Protein Interaction databases
DIP (DOE-UCLA)O00231
IntAct (EBI)O00231
FunCoupENSG00000108671
BioGRIDPSMD11
STRING (EMBL)PSMD11
ZODIACPSMD11
Ontologies - Pathways
QuickGOO00231
Ontology : AmiGOMAPK cascade  protein polyubiquitination  proteasome complex  stimulatory C-type lectin receptor signaling pathway  antigen processing and presentation of exogenous peptide antigen via MHC class I, TAP-dependent  protein binding  nucleus  nucleoplasm  cytosol  proteasome regulatory particle  ubiquitin-dependent protein catabolic process  regulation of cellular amino acid metabolic process  membrane  proteasome accessory complex  anaphase-promoting complex-dependent proteasomal ubiquitin-dependent protein catabolic process  tumor necrosis factor-mediated signaling pathway  NIK/NF-kappaB signaling  Fc-epsilon receptor signaling pathway  proteasome-mediated ubiquitin-dependent protein catabolic process  proteasome assembly  regulation of mRNA stability  stem cell differentiation  T cell receptor signaling pathway  negative regulation of ubiquitin-protein ligase activity involved in mitotic cell cycle  positive regulation of ubiquitin-protein ligase activity involved in regulation of mitotic cell cycle transition  Wnt signaling pathway, planar cell polarity pathway  extracellular exosome  negative regulation of canonical Wnt signaling pathway  positive regulation of canonical Wnt signaling pathway  
Ontology : EGO-EBIMAPK cascade  protein polyubiquitination  proteasome complex  stimulatory C-type lectin receptor signaling pathway  antigen processing and presentation of exogenous peptide antigen via MHC class I, TAP-dependent  protein binding  nucleus  nucleoplasm  cytosol  proteasome regulatory particle  ubiquitin-dependent protein catabolic process  regulation of cellular amino acid metabolic process  membrane  proteasome accessory complex  anaphase-promoting complex-dependent proteasomal ubiquitin-dependent protein catabolic process  tumor necrosis factor-mediated signaling pathway  NIK/NF-kappaB signaling  Fc-epsilon receptor signaling pathway  proteasome-mediated ubiquitin-dependent protein catabolic process  proteasome assembly  regulation of mRNA stability  stem cell differentiation  T cell receptor signaling pathway  negative regulation of ubiquitin-protein ligase activity involved in mitotic cell cycle  positive regulation of ubiquitin-protein ligase activity involved in regulation of mitotic cell cycle transition  Wnt signaling pathway, planar cell polarity pathway  extracellular exosome  negative regulation of canonical Wnt signaling pathway  positive regulation of canonical Wnt signaling pathway  
Pathways : KEGGProteasome    Epstein-Barr virus infection   
NDEx NetworkPSMD11
Atlas of Cancer Signalling NetworkPSMD11
Wikipedia pathwaysPSMD11
Orthology - Evolution
OrthoDB5717
GeneTree (enSembl)ENSG00000108671
Phylogenetic Trees/Animal Genes : TreeFamPSMD11
HOVERGENO00231
HOGENOMO00231
Homologs : HomoloGenePSMD11
Homology/Alignments : Family Browser (UCSC)PSMD11
Gene fusions - Rearrangements
Fusion : MitelmanAKAP10/PSMD11 [17p11.2/17q11.2]  [t(17;17)(p11;q11)]  
Fusion : MitelmanNF1/PSMD11 [17q11.2/17q11.2]  [t(17;17)(q11;q11)]  
Fusion : MitelmanPSMD11/CEP112 [17q11.2/17q24.1]  [t(17;17)(q11;q24)]  
Fusion : MitelmanTMED10/PSMD11 [14q24.3/17q11.2]  [t(14;17)(q24;q11)]  
Fusion : MitelmanWIPF2/PSMD11 [17q21.1/17q11.2]  [t(17;17)(q11;q21)]  
Fusion: TCGANF1 17q11.2 PSMD11 17q11.2 LUAD
Fusion: TCGAPSMD11 17q11.2 CEP112 17q24.1 BRCA
Fusion: TCGATMED10 14q24.3 PSMD11 17q11.2 PRAD
Fusion: TCGAWIPF2 17q21.1 PSMD11 17q11.2 BRCA
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerPSMD11 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)PSMD11
dbVarPSMD11
ClinVarPSMD11
1000_GenomesPSMD11 
Exome Variant ServerPSMD11
ExAC (Exome Aggregation Consortium)PSMD11 (select the gene name)
Genetic variants : HAPMAP5717
Genomic Variants (DGV)PSMD11 [DGVbeta]
DECIPHER (Syndromes)17:30771481-30810337  ENSG00000108671
CONAN: Copy Number AnalysisPSMD11 
Mutations
ICGC Data PortalPSMD11 
TCGA Data PortalPSMD11 
Broad Tumor PortalPSMD11
OASIS PortalPSMD11 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICPSMD11  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDPSMD11
intOGen PortalPSMD11
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD - Leiden Open Variation Database
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch PSMD11
DgiDB (Drug Gene Interaction Database)PSMD11
DoCM (Curated mutations)PSMD11 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)PSMD11 (select a term)
intoGenPSMD11
Cancer3DPSMD11(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM604449   
Orphanet
MedgenPSMD11
Genetic Testing Registry PSMD11
NextProtO00231 [Medical]
TSGene5717
GENETestsPSMD11
Huge Navigator PSMD11 [HugePedia]
snp3D : Map Gene to Disease5717
BioCentury BCIQPSMD11
ClinGenPSMD11
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD5717
Chemical/Pharm GKB GenePA33902
Clinical trialPSMD11
Miscellaneous
canSAR (ICR)PSMD11 (select the gene name)
Probes
Litterature
PubMed96 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMinePSMD11
EVEXPSMD11
GoPubMedPSMD11
iHOPPSMD11
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Mar 14 13:23:23 CET 2017

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