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GPR152 (G protein-coupled receptor 152)

Identity

Alias_symbol (synonym)PGR5
Other alias
HGNC (Hugo) GPR152
LocusID (NCBI) 390212
Atlas_Id 63969
Location 11q13.2  [Link to chromosome band 11q13]
Location_base_pair Starts at 67451301 and ends at 67452729 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)GPR152   23622
Cards
Entrez_Gene (NCBI)GPR152  390212  G protein-coupled receptor 152
AliasesPGR5
GeneCards (Weizmann)GPR152
Ensembl hg19 (Hinxton)ENSG00000175514 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000175514 [Gene_View]  chr11:67451301-67452729 [Contig_View]  GPR152 [Vega]
ICGC DataPortalENSG00000175514
TCGA cBioPortalGPR152
AceView (NCBI)GPR152
Genatlas (Paris)GPR152
WikiGenes390212
SOURCE (Princeton)GPR152
Genetics Home Reference (NIH)GPR152
Genomic and cartography
GoldenPath hg38 (UCSC)GPR152  -     chr11:67451301-67452729 -  11q13.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)GPR152  -     11q13.2   [Description]    (hg19-Feb_2009)
EnsemblGPR152 - 11q13.2 [CytoView hg19]  GPR152 - 11q13.2 [CytoView hg38]
Mapping of homologs : NCBIGPR152 [Mapview hg19]  GPR152 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AY255600 AY569571 BC119779 BC122869 BK005423
RefSeq transcript (Entrez)NM_206997
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)GPR152
Cluster EST : UnigeneHs.567997 [ NCBI ]
CGAP (NCI)Hs.567997
Alternative Splicing GalleryENSG00000175514
Gene ExpressionGPR152 [ NCBI-GEO ]   GPR152 [ EBI - ARRAY_EXPRESS ]   GPR152 [ SEEK ]   GPR152 [ MEM ]
Gene Expression Viewer (FireBrowse)GPR152 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)390212
GTEX Portal (Tissue expression)GPR152
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8TDT2   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8TDT2  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8TDT2
Splice isoforms : SwissVarQ8TDT2
PhosPhoSitePlusQ8TDT2
Domaine pattern : Prosite (Expaxy)G_PROTEIN_RECEP_F1_2 (PS50262)   
Domains : Interpro (EBI)GPCR_Rhodpsn    GPCR_Rhodpsn_7TM    GPR152_orphan_prd    MRGPCRFAMILY   
Domain families : Pfam (Sanger)7tm_1 (PF00001)   
Domain families : Pfam (NCBI)pfam00001   
Conserved Domain (NCBI)GPR152
DMDM Disease mutations390212
Blocks (Seattle)GPR152
SuperfamilyQ8TDT2
Human Protein AtlasENSG00000175514
Peptide AtlasQ8TDT2
HPRD13599
IPIIPI00152604   
Protein Interaction databases
DIP (DOE-UCLA)Q8TDT2
IntAct (EBI)Q8TDT2
FunCoupENSG00000175514
BioGRIDGPR152
STRING (EMBL)GPR152
ZODIACGPR152
Ontologies - Pathways
QuickGOQ8TDT2
Ontology : AmiGOG-protein coupled receptor activity  plasma membrane  G-protein coupled receptor signaling pathway  integral component of membrane  
Ontology : EGO-EBIG-protein coupled receptor activity  plasma membrane  G-protein coupled receptor signaling pathway  integral component of membrane  
NDEx NetworkGPR152
Atlas of Cancer Signalling NetworkGPR152
Wikipedia pathwaysGPR152
Orthology - Evolution
OrthoDB390212
GeneTree (enSembl)ENSG00000175514
Phylogenetic Trees/Animal Genes : TreeFamGPR152
HOVERGENQ8TDT2
HOGENOMQ8TDT2
Homologs : HomoloGeneGPR152
Homology/Alignments : Family Browser (UCSC)GPR152
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerGPR152 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)GPR152
dbVarGPR152
ClinVarGPR152
1000_GenomesGPR152 
Exome Variant ServerGPR152
ExAC (Exome Aggregation Consortium)GPR152 (select the gene name)
Genetic variants : HAPMAP390212
Genomic Variants (DGV)GPR152 [DGVbeta]
DECIPHERGPR152 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisGPR152 
Mutations
ICGC Data PortalGPR152 
TCGA Data PortalGPR152 
Broad Tumor PortalGPR152
OASIS PortalGPR152 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICGPR152  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDGPR152
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 GPR152
DgiDB (Drug Gene Interaction Database)GPR152
DoCM (Curated mutations)GPR152 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)GPR152 (select a term)
intoGenGPR152
Cancer3DGPR152(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenGPR152
Genetic Testing Registry GPR152
NextProtQ8TDT2 [Medical]
TSGene390212
GENETestsGPR152
Target ValidationGPR152
Huge Navigator GPR152 [HugePedia]
snp3D : Map Gene to Disease390212
BioCentury BCIQGPR152
ClinGenGPR152
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD390212
Chemical/Pharm GKB GenePA134897297
Clinical trialGPR152
Miscellaneous
canSAR (ICR)GPR152 (select the gene name)
Probes
Litterature
PubMed5 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineGPR152
EVEXGPR152
GoPubMedGPR152
iHOPGPR152
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Wed Jun 7 15:51:12 CEST 2017

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