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GPR32 (G protein-coupled receptor 32)

Identity

Alias_symbol (synonym)RVDR1
Other alias
HGNC (Hugo) GPR32
LocusID (NCBI) 2854
Atlas_Id 63991
Location 19q13.33  [Link to chromosome band 19q13]
Location_base_pair Starts at 51273721 and ends at 51274989 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)GPR32   4487
Cards
Entrez_Gene (NCBI)GPR32  2854  G protein-coupled receptor 32
AliasesRVDR1
GeneCards (Weizmann)GPR32
Ensembl hg19 (Hinxton)ENSG00000142511 [Gene_View]  chr19:51273721-51274989 [Contig_View]  GPR32 [Vega]
Ensembl hg38 (Hinxton)ENSG00000142511 [Gene_View]  chr19:51273721-51274989 [Contig_View]  GPR32 [Vega]
ICGC DataPortalENSG00000142511
TCGA cBioPortalGPR32
AceView (NCBI)GPR32
Genatlas (Paris)GPR32
WikiGenes2854
SOURCE (Princeton)GPR32
Genetics Home Reference (NIH)GPR32
Genomic and cartography
GoldenPath hg19 (UCSC)GPR32  -     chr19:51273721-51274989 +  19q13.33   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)GPR32  -     19q13.33   [Description]    (hg38-Dec_2013)
EnsemblGPR32 - 19q13.33 [CytoView hg19]  GPR32 - 19q13.33 [CytoView hg38]
Mapping of homologs : NCBIGPR32 [Mapview hg19]  GPR32 [Mapview hg38]
OMIM603195   
Gene and transcription
Genbank (Entrez)BC067453 BC067454 BC095544
RefSeq transcript (Entrez)NM_001506
RefSeq genomic (Entrez)NC_000019 NC_018930 NT_011109 NW_004929415
Consensus coding sequences : CCDS (NCBI)GPR32
Cluster EST : UnigeneHs.515555 [ NCBI ]
CGAP (NCI)Hs.515555
Alternative Splicing GalleryENSG00000142511
Gene ExpressionGPR32 [ NCBI-GEO ]   GPR32 [ EBI - ARRAY_EXPRESS ]   GPR32 [ SEEK ]   GPR32 [ MEM ]
Gene Expression Viewer (FireBrowse)GPR32 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)2854
GTEX Portal (Tissue expression)GPR32
Protein : pattern, domain, 3D structure
UniProt/SwissProtO75388   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtO75388  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProO75388
Splice isoforms : SwissVarO75388
PhosPhoSitePlusO75388
Domaine pattern : Prosite (Expaxy)G_PROTEIN_RECEP_F1_1 (PS00237)    G_PROTEIN_RECEP_F1_2 (PS50262)   
Domains : Interpro (EBI)Formyl_rcpt-rel    GPCR_Rhodpsn    GPCR_Rhodpsn_7TM   
Domain families : Pfam (Sanger)7tm_1 (PF00001)   
Domain families : Pfam (NCBI)pfam00001   
Conserved Domain (NCBI)GPR32
DMDM Disease mutations2854
Blocks (Seattle)GPR32
SuperfamilyO75388
Human Protein AtlasENSG00000142511
Peptide AtlasO75388
HPRD04430
IPIIPI00025357   
Protein Interaction databases
DIP (DOE-UCLA)O75388
IntAct (EBI)O75388
FunCoupENSG00000142511
BioGRIDGPR32
STRING (EMBL)GPR32
ZODIACGPR32
Ontologies - Pathways
QuickGOO75388
Ontology : AmiGOG-protein coupled receptor activity  integral component of plasma membrane  G-protein coupled receptor signaling pathway  
Ontology : EGO-EBIG-protein coupled receptor activity  integral component of plasma membrane  G-protein coupled receptor signaling pathway  
NDEx NetworkGPR32
Atlas of Cancer Signalling NetworkGPR32
Wikipedia pathwaysGPR32
Orthology - Evolution
OrthoDB2854
GeneTree (enSembl)ENSG00000142511
Phylogenetic Trees/Animal Genes : TreeFamGPR32
HOVERGENO75388
HOGENOMO75388
Homologs : HomoloGeneGPR32
Homology/Alignments : Family Browser (UCSC)GPR32
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerGPR32 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)GPR32
dbVarGPR32
ClinVarGPR32
1000_GenomesGPR32 
Exome Variant ServerGPR32
ExAC (Exome Aggregation Consortium)GPR32 (select the gene name)
Genetic variants : HAPMAP2854
Genomic Variants (DGV)GPR32 [DGVbeta]
DECIPHER (Syndromes)19:51273721-51274989  ENSG00000142511
CONAN: Copy Number AnalysisGPR32 
Mutations
ICGC Data PortalGPR32 
TCGA Data PortalGPR32 
Broad Tumor PortalGPR32
OASIS PortalGPR32 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICGPR32  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDGPR32
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch GPR32
DgiDB (Drug Gene Interaction Database)GPR32
DoCM (Curated mutations)GPR32 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)GPR32 (select a term)
intoGenGPR32
Cancer3DGPR32(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM603195   
Orphanet
MedgenGPR32
Genetic Testing Registry GPR32
NextProtO75388 [Medical]
TSGene2854
GENETestsGPR32
Huge Navigator GPR32 [HugePedia]
snp3D : Map Gene to Disease2854
BioCentury BCIQGPR32
ClinGenGPR32
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD2854
Chemical/Pharm GKB GenePA28875
Clinical trialGPR32
Miscellaneous
canSAR (ICR)GPR32 (select the gene name)
Probes
Litterature
PubMed8 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineGPR32
EVEXGPR32
GoPubMedGPR32
iHOPGPR32
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 12:06:45 CET 2017

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