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RGS11 (regulator of G-protein signaling 11)

Identity

Other namesRS11
HGNC (Hugo) RGS11
LocusID (NCBI) 8786
Location 16p13.3
Location_base_pair Starts at 318310 and ends at 325914 bp from pter ( according to hg19-Feb_2009)
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

 

External links

Nomenclature
HGNC (Hugo)RGS11   9993
Cards
Entrez_Gene (NCBI)RGS11  8786  regulator of G-protein signaling 11
GeneCards (Weizmann)RGS11
Ensembl (Hinxton)ENSG00000076344 [Gene_View]  chr16:318310-325914 [Contig_View]  RGS11 [Vega]
AceView (NCBI)RGS11
Genatlas (Paris)RGS11
WikiGenes8786
SOURCE (Princeton)NM_001286485 NM_001286486 NM_003834 NM_183337
Genomic and cartography
GoldenPath (UCSC)RGS11  -  16p13.3   chr16:318310-325914 -  16p13.3   [Description]    (hg19-Feb_2009)
EnsemblRGS11 - 16p13.3 [CytoView]
Mapping of homologs : NCBIRGS11 [Mapview]
OMIM603895   
Gene and transcription
Genbank (Entrez)AB016929 AB209582 AF035153 AF035154 AK091701
RefSeq transcript (Entrez)NM_001286485 NM_001286486 NM_003834 NM_183337
RefSeq genomic (Entrez)AC_000148 NC_000016 NC_018927 NT_010393 NW_001838339 NW_004929400
Consensus coding sequences : CCDS (NCBI)RGS11
Cluster EST : UnigeneHs.65756 [ NCBI ]
CGAP (NCI)Hs.65756
Alternative Splicing : Fast-db (Paris)GSHG0011488
Alternative Splicing GalleryENSG00000076344
Gene ExpressionRGS11 [ NCBI-GEO ]     RGS11 [ SEEK ]   RGS11 [ MEM ]
Protein : pattern, domain, 3D structure
UniProt/SwissProtO94810 (Uniprot)
NextProtO94810  [Medical]
With graphics : InterProO94810
Splice isoforms : SwissVarO94810 (Swissvar)
Domaine pattern : Prosite (Expaxy)DEP (PS50186)    G_PROTEIN_GAMMA (PS50058)    RGS (PS50132)   
Domains : Interpro (EBI)DEP_dom    G-protein_gamma-like_dom    Regulat_G_prot_signal_dom1    Regulat_G_prot_signal_superfam    RGS_dom    WHTH_DNA-bd_dom   
Related proteins : CluSTrO94810
Domain families : Pfam (Sanger)DEP (PF00610)    G-gamma (PF00631)    RGS (PF00615)   
Domain families : Pfam (NCBI)pfam00610    pfam00631    pfam00615   
Domain families : Smart (EMBL)DEP (SM00049)  GGL (SM00224)  RGS (SM00315)  
DMDM Disease mutations8786
Blocks (Seattle)O94810
Human Protein AtlasENSG00000076344
Peptide AtlasO94810
HPRD04872
IPIIPI00015558   IPI00642088   IPI00922446   IPI00922405   IPI00556312   IPI00383458   IPI00375014   IPI00855802   
Protein Interaction databases
DIP (DOE-UCLA)O94810
IntAct (EBI)O94810
FunCoupENSG00000076344
BioGRIDRGS11
InParanoidO94810
Interologous Interaction database O94810
IntegromeDBRGS11
STRING (EMBL)RGS11
Ontologies - Pathways
Ontology : AmiGOsignal transducer activity  GTPase activator activity  cytoplasm  heterotrimeric G-protein complex  plasma membrane  G-protein coupled receptor signaling pathway  regulation of G-protein coupled receptor protein signaling pathway  intracellular signal transduction  termination of G-protein coupled receptor signaling pathway  protein complex  positive regulation of GTPase activity  positive regulation of GTPase activity  dendrite terminus  
Ontology : EGO-EBIsignal transducer activity  GTPase activator activity  cytoplasm  heterotrimeric G-protein complex  plasma membrane  G-protein coupled receptor signaling pathway  regulation of G-protein coupled receptor protein signaling pathway  intracellular signal transduction  termination of G-protein coupled receptor signaling pathway  protein complex  positive regulation of GTPase activity  positive regulation of GTPase activity  dendrite terminus  
REACTOMERGS11
Protein Interaction DatabaseRGS11
Wikipedia pathwaysRGS11
Gene fusion - rearrangments
Polymorphisms : SNP, mutations, diseases
SNP Single Nucleotide Polymorphism (NCBI)RGS11
SNP (GeneSNP Utah)RGS11
SNP : HGBaseRGS11
Genetic variants : HAPMAPRGS11
1000_GenomesRGS11 
ICGC programENSG00000076344 
Somatic Mutations in Cancer : COSMICRGS11 
CONAN: Copy Number AnalysisRGS11 
Mutations and Diseases : HGMDRGS11
OMIM603895   
GENETestsRGS11
Disease Genetic AssociationRGS11
Huge Navigator RGS11 [HugePedia]  RGS11 [HugeCancerGEM]
Genomic VariantsRGS11  RGS11 [DGVbeta]
Exome VariantRGS11
dbVarRGS11
ClinVarRGS11
snp3D : Map Gene to Disease8786
General knowledge
Homologs : HomoloGeneRGS11
Homology/Alignments : Family Browser (UCSC)RGS11
Phylogenetic Trees/Animal Genes : TreeFamRGS11
Chemical/Protein Interactions : CTD8786
Chemical/Pharm GKB GenePA34363
Clinical trialRGS11
Cancer Resource (Charite)ENSG00000076344
Other databases
Probes
Litterature
PubMed16 Pubmed reference(s) in Entrez
CoreMineRGS11
iHOPRGS11
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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Contributor(s)

Written09-2002Dessen P, Le Minor S
Updated12-2013Dessen P

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Fri Apr 18 16:56:58 CEST 2014

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