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P2RY10 (purinergic receptor P2Y10)

Identity

Alias_namespurinergic receptor P2Y, G-protein coupled, 10
Alias_symbol (synonym)P2Y10
Other aliasLYPSR2
HGNC (Hugo) P2RY10
LocusID (NCBI) 27334
Atlas_Id 71605
Location Xq21.1  [Link to chromosome band Xq21]
Location_base_pair Starts at 78945332 and ends at 78963727 bp from pter ( according to hg38-Dec_2013)

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)P2RY10   19906
Cards
Entrez_Gene (NCBI)P2RY10  27334  purinergic receptor P2Y10
AliasesLYPSR2; P2Y10
GeneCards (Weizmann)P2RY10
Ensembl hg19 (Hinxton)ENSG00000078589 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000078589 [Gene_View]  chrX:78945332-78963727 [Contig_View]  P2RY10 [Vega]
ICGC DataPortalENSG00000078589
TCGA cBioPortalP2RY10
AceView (NCBI)P2RY10
Genatlas (Paris)P2RY10
WikiGenes27334
SOURCE (Princeton)P2RY10
Genetics Home Reference (NIH)P2RY10
Genomic and cartography
GoldenPath hg38 (UCSC)P2RY10  -     chrX:78945332-78963727 +  Xq21.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)P2RY10  -     Xq21.1   [Description]    (hg19-Feb_2009)
EnsemblP2RY10 - Xq21.1 [CytoView hg19]  P2RY10 - Xq21.1 [CytoView hg38]
Mapping of homologs : NCBIP2RY10 [Mapview hg19]  P2RY10 [Mapview hg38]
OMIM300529   
Gene and transcription
Genbank (Entrez)AK292138 AK313218 AW294346 BC051875 BC095498
RefSeq transcript (Entrez)NM_001324218 NM_001324221 NM_001324225 NM_014499 NM_198333
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)P2RY10
Cluster EST : UnigeneHs.445500 [ NCBI ]
CGAP (NCI)Hs.445500
Alternative Splicing GalleryENSG00000078589
Gene ExpressionP2RY10 [ NCBI-GEO ]   P2RY10 [ EBI - ARRAY_EXPRESS ]   P2RY10 [ SEEK ]   P2RY10 [ MEM ]
Gene Expression Viewer (FireBrowse)P2RY10 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)27334
GTEX Portal (Tissue expression)P2RY10
Protein : pattern, domain, 3D structure
UniProt/SwissProtO00398   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtO00398  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProO00398
Splice isoforms : SwissVarO00398
PhosPhoSitePlusO00398
Domaine pattern : Prosite (Expaxy)G_PROTEIN_RECEP_F1_2 (PS50262)   
Domains : Interpro (EBI)GPCR_Rhodpsn    GPCR_Rhodpsn_7TM    P2Y10_rcpt   
Domain families : Pfam (Sanger)7tm_1 (PF00001)   
Domain families : Pfam (NCBI)pfam00001   
Conserved Domain (NCBI)P2RY10
DMDM Disease mutations27334
Blocks (Seattle)P2RY10
SuperfamilyO00398
Human Protein AtlasENSG00000078589
Peptide AtlasO00398
HPRD06670
IPIIPI00004964   
Protein Interaction databases
DIP (DOE-UCLA)O00398
IntAct (EBI)O00398
FunCoupENSG00000078589
BioGRIDP2RY10
STRING (EMBL)P2RY10
ZODIACP2RY10
Ontologies - Pathways
QuickGOO00398
Ontology : AmiGOG-protein coupled receptor activity  plasma membrane  integral component of plasma membrane  positive regulation of Rho protein signal transduction  G-protein coupled purinergic nucleotide receptor signaling pathway  G-protein coupled purinergic nucleotide receptor activity  positive regulation of cytosolic calcium ion concentration involved in phospholipase C-activating G-protein coupled signaling pathway  
Ontology : EGO-EBIG-protein coupled receptor activity  plasma membrane  integral component of plasma membrane  positive regulation of Rho protein signal transduction  G-protein coupled purinergic nucleotide receptor signaling pathway  G-protein coupled purinergic nucleotide receptor activity  positive regulation of cytosolic calcium ion concentration involved in phospholipase C-activating G-protein coupled signaling pathway  
Pathways : KEGGNeuroactive ligand-receptor interaction   
NDEx NetworkP2RY10
Atlas of Cancer Signalling NetworkP2RY10
Wikipedia pathwaysP2RY10
Orthology - Evolution
OrthoDB27334
GeneTree (enSembl)ENSG00000078589
Phylogenetic Trees/Animal Genes : TreeFamP2RY10
HOVERGENO00398
HOGENOMO00398
Homologs : HomoloGeneP2RY10
Homology/Alignments : Family Browser (UCSC)P2RY10
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerP2RY10 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)P2RY10
dbVarP2RY10
ClinVarP2RY10
1000_GenomesP2RY10 
Exome Variant ServerP2RY10
ExAC (Exome Aggregation Consortium)P2RY10 (select the gene name)
Genetic variants : HAPMAP27334
Genomic Variants (DGV)P2RY10 [DGVbeta]
DECIPHERP2RY10 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisP2RY10 
Mutations
ICGC Data PortalP2RY10 
TCGA Data PortalP2RY10 
Broad Tumor PortalP2RY10
OASIS PortalP2RY10 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICP2RY10  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDP2RY10
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
LOVD (Leiden Open Variation Database)X-chromosome gene database
BioMutasearch P2RY10
DgiDB (Drug Gene Interaction Database)P2RY10
DoCM (Curated mutations)P2RY10 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)P2RY10 (select a term)
intoGenP2RY10
Cancer3DP2RY10(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM300529   
Orphanet
MedgenP2RY10
Genetic Testing Registry P2RY10
NextProtO00398 [Medical]
TSGene27334
GENETestsP2RY10
Target ValidationP2RY10
Huge Navigator P2RY10 [HugePedia]
snp3D : Map Gene to Disease27334
BioCentury BCIQP2RY10
ClinGenP2RY10
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD27334
Chemical/Pharm GKB GenePA134873055
Clinical trialP2RY10
Miscellaneous
canSAR (ICR)P2RY10 (select the gene name)
Probes
Litterature
PubMed12 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineP2RY10
EVEXP2RY10
GoPubMedP2RY10
iHOPP2RY10
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Wed May 31 15:35:20 CEST 2017

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