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P2RY11 (purinergic receptor P2Y11)

Identity

Alias_namespurinergic receptor P2Y
Alias_symbol (synonym)P2Y11
Other alias
HGNC (Hugo) P2RY11
LocusID (NCBI) 5032
Atlas_Id 54919
Location 19p13.2  [Link to chromosome band 19p13]
Location_base_pair Starts at 10111521 and ends at 10115388 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)
CMTM7 (3p22.3) / P2RY11 (19p13.2)PPAN (19p13.2) / P2RY11 (19p13.2)

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

 


External links

Nomenclature
HGNC (Hugo)P2RY11   8540
Cards
Entrez_Gene (NCBI)P2RY11  5032  purinergic receptor P2Y11
AliasesP2Y11
GeneCards (Weizmann)P2RY11
Ensembl hg19 (Hinxton)ENSG00000244165 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000244165 [Gene_View]  ENSG00000244165 [Sequence]  chr19:10111521-10115388 [Contig_View]  P2RY11 [Vega]
ICGC DataPortalENSG00000244165
TCGA cBioPortalP2RY11
AceView (NCBI)P2RY11
Genatlas (Paris)P2RY11
WikiGenes5032
SOURCE (Princeton)P2RY11
Genetics Home Reference (NIH)P2RY11
Genomic and cartography
GoldenPath hg38 (UCSC)P2RY11  -     chr19:10111521-10115388 +  19p13.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)P2RY11  -     19p13.2   [Description]    (hg19-Feb_2009)
EnsemblP2RY11 - 19p13.2 [CytoView hg19]  P2RY11 - 19p13.2 [CytoView hg38]
Mapping of homologs : NCBIP2RY11 [Mapview hg19]  P2RY11 [Mapview hg38]
OMIM602697   
Gene and transcription
Genbank (Entrez)AA310412 AF498921 AJ298334 AK313550 AY449733
RefSeq transcript (Entrez)NM_002566
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)P2RY11
Cluster EST : UnigeneHs.14468 [ NCBI ]
CGAP (NCI)Hs.14468
Alternative Splicing GalleryENSG00000244165
Gene ExpressionP2RY11 [ NCBI-GEO ]   P2RY11 [ EBI - ARRAY_EXPRESS ]   P2RY11 [ SEEK ]   P2RY11 [ MEM ]
Gene Expression Viewer (FireBrowse)P2RY11 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevestigatorExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)5032
GTEX Portal (Tissue expression)P2RY11
Human Protein AtlasENSG00000244165-P2RY11 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ96G91   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ96G91  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ96G91
Splice isoforms : SwissVarQ96G91
PhosPhoSitePlusQ96G91
Domaine pattern : Prosite (Expaxy)G_PROTEIN_RECEP_F1_1 (PS00237)    G_PROTEIN_RECEP_F1_2 (PS50262)   
Domains : Interpro (EBI)GPCR_Rhodpsn    GPCR_Rhodpsn_7TM    P2Y11_rcpt   
Domain families : Pfam (Sanger)7tm_1 (PF00001)   
Domain families : Pfam (NCBI)pfam00001   
Conserved Domain (NCBI)P2RY11
DMDM Disease mutations5032
Blocks (Seattle)P2RY11
PDB (SRS)2B6S   
PDB (PDBSum)2B6S   
PDB (IMB)2B6S   
PDB (RSDB)2B6S   
Structural Biology KnowledgeBase2B6S   
SCOP (Structural Classification of Proteins)2B6S   
CATH (Classification of proteins structures)2B6S   
SuperfamilyQ96G91
Human Protein Atlas [tissue]ENSG00000244165-P2RY11 [tissue]
Peptide AtlasQ96G91
HPRD04076
IPIIPI00101425   
Protein Interaction databases
DIP (DOE-UCLA)Q96G91
IntAct (EBI)Q96G91
FunCoupENSG00000244165
BioGRIDP2RY11
STRING (EMBL)P2RY11
ZODIACP2RY11
Ontologies - Pathways
QuickGOQ96G91
Ontology : AmiGOadenosine receptor signaling pathway  plasma membrane  integral component of plasma membrane  defense response  G protein-coupled receptor signaling pathway  G protein-coupled receptor signaling pathway  activation of adenylate cyclase activity  phospholipase C-activating G protein-coupled receptor signaling pathway  calcium-mediated signaling  neuronal signal transduction  neuronal signal transduction  neurotransmitter receptor activity  neurotransmitter receptor activity  G protein-coupled purinergic nucleotide receptor signaling pathway  signaling receptor activity  G protein-coupled purinergic nucleotide receptor activity  ATP-activated adenosine receptor activity  ATP-activated adenosine receptor activity  cellular response to ATP  
Ontology : EGO-EBIadenosine receptor signaling pathway  plasma membrane  integral component of plasma membrane  defense response  G protein-coupled receptor signaling pathway  G protein-coupled receptor signaling pathway  activation of adenylate cyclase activity  phospholipase C-activating G protein-coupled receptor signaling pathway  calcium-mediated signaling  neuronal signal transduction  neuronal signal transduction  neurotransmitter receptor activity  neurotransmitter receptor activity  G protein-coupled purinergic nucleotide receptor signaling pathway  signaling receptor activity  G protein-coupled purinergic nucleotide receptor activity  ATP-activated adenosine receptor activity  ATP-activated adenosine receptor activity  cellular response to ATP  
Pathways : KEGGNeuroactive ligand-receptor interaction   
NDEx NetworkP2RY11
Atlas of Cancer Signalling NetworkP2RY11
Wikipedia pathwaysP2RY11
Orthology - Evolution
OrthoDB5032
GeneTree (enSembl)ENSG00000244165
Phylogenetic Trees/Animal Genes : TreeFamP2RY11
HOGENOMQ96G91
Homologs : HomoloGeneP2RY11
Homology/Alignments : Family Browser (UCSC)P2RY11
Gene fusions - Rearrangements
Fusion : QuiverP2RY11
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerP2RY11 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)P2RY11
dbVarP2RY11
ClinVarP2RY11
1000_GenomesP2RY11 
Exome Variant ServerP2RY11
ExAC (Exome Aggregation Consortium)ENSG00000244165
GNOMAD BrowserENSG00000244165
Varsome BrowserP2RY11
Genetic variants : HAPMAP5032
Genomic Variants (DGV)P2RY11 [DGVbeta]
DECIPHERP2RY11 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisP2RY11 
Mutations
ICGC Data PortalP2RY11 
TCGA Data PortalP2RY11 
Broad Tumor PortalP2RY11
OASIS PortalP2RY11 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICP2RY11  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDP2RY11
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 P2RY11
DgiDB (Drug Gene Interaction Database)P2RY11
DoCM (Curated mutations)P2RY11 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)P2RY11 (select a term)
intoGenP2RY11
Cancer3DP2RY11(select the gene name)
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM602697   
Orphanet3637   
DisGeNETP2RY11
MedgenP2RY11
Genetic Testing Registry P2RY11
NextProtQ96G91 [Medical]
TSGene5032
GENETestsP2RY11
Target ValidationP2RY11
Huge Navigator P2RY11 [HugePedia]
snp3D : Map Gene to Disease5032
BioCentury BCIQP2RY11
ClinGenP2RY11
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD5032
Chemical/Pharm GKB GenePA32869
Clinical trialP2RY11
Miscellaneous
canSAR (ICR)P2RY11 (select the gene name)
Probes
Litterature
PubMed34 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineP2RY11
EVEXP2RY11
GoPubMedP2RY11
iHOPP2RY11
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Fri Dec 21 15:40:51 CET 2018

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