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GPR132 (G protein-coupled receptor 132)

Identity

Alias_symbol (synonym)G2A
Other alias
HGNC (Hugo) GPR132
LocusID (NCBI) 29933
Atlas_Id 40740
Location 14q32.33  [Link to chromosome band 14q32]
Location_base_pair Starts at 105515726 and ends at 105531887 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)GPR132   17482
Cards
Entrez_Gene (NCBI)GPR132  29933  G protein-coupled receptor 132
AliasesG2A
GeneCards (Weizmann)GPR132
Ensembl hg19 (Hinxton)ENSG00000183484 [Gene_View]  chr14:105515726-105531887 [Contig_View]  GPR132 [Vega]
Ensembl hg38 (Hinxton)ENSG00000183484 [Gene_View]  chr14:105515726-105531887 [Contig_View]  GPR132 [Vega]
ICGC DataPortalENSG00000183484
TCGA cBioPortalGPR132
AceView (NCBI)GPR132
Genatlas (Paris)GPR132
WikiGenes29933
SOURCE (Princeton)GPR132
Genetics Home Reference (NIH)GPR132
Genomic and cartography
GoldenPath hg19 (UCSC)GPR132  -     chr14:105515726-105531887 -  14q32.33   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)GPR132  -     14q32.33   [Description]    (hg38-Dec_2013)
EnsemblGPR132 - 14q32.33 [CytoView hg19]  GPR132 - 14q32.33 [CytoView hg38]
Mapping of homologs : NCBIGPR132 [Mapview hg19]  GPR132 [Mapview hg38]
OMIM606167   
Gene and transcription
Genbank (Entrez)AA714520 AB465599 AB465600 AF083955 AK292142
RefSeq transcript (Entrez)NM_001278694 NM_001278695 NM_001278696 NM_013345
RefSeq genomic (Entrez)NC_000014 NC_018925 NT_026437 NW_004929393
Consensus coding sequences : CCDS (NCBI)GPR132
Cluster EST : UnigeneHs.532504 [ NCBI ]
CGAP (NCI)Hs.532504
Alternative Splicing GalleryENSG00000183484
Gene ExpressionGPR132 [ NCBI-GEO ]   GPR132 [ EBI - ARRAY_EXPRESS ]   GPR132 [ SEEK ]   GPR132 [ MEM ]
Gene Expression Viewer (FireBrowse)GPR132 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)29933
GTEX Portal (Tissue expression)GPR132
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9UNW8   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9UNW8  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9UNW8
Splice isoforms : SwissVarQ9UNW8
PhosPhoSitePlusQ9UNW8
Domaine pattern : Prosite (Expaxy)G_PROTEIN_RECEP_F1_1 (PS00237)    G_PROTEIN_RECEP_F1_2 (PS50262)   
Domains : Interpro (EBI)G2A_lysphc_rcpt    GPCR_Rhodpsn    GPCR_Rhodpsn_7TM   
Domain families : Pfam (Sanger)7tm_1 (PF00001)   
Domain families : Pfam (NCBI)pfam00001   
Conserved Domain (NCBI)GPR132
DMDM Disease mutations29933
Blocks (Seattle)GPR132
SuperfamilyQ9UNW8
Human Protein AtlasENSG00000183484
Peptide AtlasQ9UNW8
HPRD06936
IPIIPI00002514   IPI00376712   IPI01020741   IPI01021844   
Protein Interaction databases
DIP (DOE-UCLA)Q9UNW8
IntAct (EBI)Q9UNW8
FunCoupENSG00000183484
BioGRIDGPR132
STRING (EMBL)GPR132
ZODIACGPR132
Ontologies - Pathways
QuickGOQ9UNW8
Ontology : AmiGOG1/S transition of mitotic cell cycle  G-protein coupled receptor activity  plasma membrane  G-protein coupled receptor signaling pathway  negative regulation of G2/M transition of mitotic cell cycle  integral component of membrane  
Ontology : EGO-EBIG1/S transition of mitotic cell cycle  G-protein coupled receptor activity  plasma membrane  G-protein coupled receptor signaling pathway  negative regulation of G2/M transition of mitotic cell cycle  integral component of membrane  
NDEx NetworkGPR132
Atlas of Cancer Signalling NetworkGPR132
Wikipedia pathwaysGPR132
Orthology - Evolution
OrthoDB29933
GeneTree (enSembl)ENSG00000183484
Phylogenetic Trees/Animal Genes : TreeFamGPR132
HOVERGENQ9UNW8
HOGENOMQ9UNW8
Homologs : HomoloGeneGPR132
Homology/Alignments : Family Browser (UCSC)GPR132
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerGPR132 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)GPR132
dbVarGPR132
ClinVarGPR132
1000_GenomesGPR132 
Exome Variant ServerGPR132
ExAC (Exome Aggregation Consortium)GPR132 (select the gene name)
Genetic variants : HAPMAP29933
Genomic Variants (DGV)GPR132 [DGVbeta]
DECIPHER (Syndromes)14:105515726-105531887  ENSG00000183484
CONAN: Copy Number AnalysisGPR132 
Mutations
ICGC Data PortalGPR132 
TCGA Data PortalGPR132 
Broad Tumor PortalGPR132
OASIS PortalGPR132 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICGPR132  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDGPR132
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 GPR132
DgiDB (Drug Gene Interaction Database)GPR132
DoCM (Curated mutations)GPR132 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)GPR132 (select a term)
intoGenGPR132
Cancer3DGPR132(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM606167   
Orphanet
MedgenGPR132
Genetic Testing Registry GPR132
NextProtQ9UNW8 [Medical]
TSGene29933
GENETestsGPR132
Huge Navigator GPR132 [HugePedia]
snp3D : Map Gene to Disease29933
BioCentury BCIQGPR132
ClinGenGPR132
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD29933
Chemical/Pharm GKB GenePA134940832
Clinical trialGPR132
Miscellaneous
canSAR (ICR)GPR132 (select the gene name)
Probes
Litterature
PubMed20 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineGPR132
EVEXGPR132
GoPubMedGPR132
iHOPGPR132
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 13:08:00 CET 2017

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