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GPR119 (G protein-coupled receptor 119)

Identity

Alias_symbol (synonym)hGPCR2
GPCR2
Other alias
HGNC (Hugo) GPR119
LocusID (NCBI) 139760
Atlas_Id 63949
Location Xq26.1  [Link to chromosome band Xq26]
Location_base_pair Starts at 130384345 and ends at 130385537 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)GPR119   19060
Cards
Entrez_Gene (NCBI)GPR119  139760  G protein-coupled receptor 119
AliasesGPCR2
GeneCards (Weizmann)GPR119
Ensembl hg19 (Hinxton)ENSG00000147262 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000147262 [Gene_View]  chrX:130384345-130385537 [Contig_View]  GPR119 [Vega]
ICGC DataPortalENSG00000147262
TCGA cBioPortalGPR119
AceView (NCBI)GPR119
Genatlas (Paris)GPR119
WikiGenes139760
SOURCE (Princeton)GPR119
Genetics Home Reference (NIH)GPR119
Genomic and cartography
GoldenPath hg38 (UCSC)GPR119  -     chrX:130384345-130385537 -  Xq26.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)GPR119  -     Xq26.1   [Description]    (hg19-Feb_2009)
EnsemblGPR119 - Xq26.1 [CytoView hg19]  GPR119 - Xq26.1 [CytoView hg38]
Mapping of homologs : NCBIGPR119 [Mapview hg19]  GPR119 [Mapview hg38]
OMIM300513   
Gene and transcription
Genbank (Entrez)AY288416 BC095502 BC101166 BC101167 BC101168
RefSeq transcript (Entrez)NM_178471
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)GPR119
Cluster EST : UnigeneHs.496762 [ NCBI ]
CGAP (NCI)Hs.496762
Alternative Splicing GalleryENSG00000147262
Gene ExpressionGPR119 [ NCBI-GEO ]   GPR119 [ EBI - ARRAY_EXPRESS ]   GPR119 [ SEEK ]   GPR119 [ MEM ]
Gene Expression Viewer (FireBrowse)GPR119 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)139760
GTEX Portal (Tissue expression)GPR119
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8TDV5   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8TDV5  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8TDV5
Splice isoforms : SwissVarQ8TDV5
PhosPhoSitePlusQ8TDV5
Domaine pattern : Prosite (Expaxy)G_PROTEIN_RECEP_F1_1 (PS00237)    G_PROTEIN_RECEP_F1_2 (PS50262)   
Domains : Interpro (EBI)GPCR_Rhodpsn    GPCR_Rhodpsn_7TM    GPR119   
Domain families : Pfam (Sanger)7tm_1 (PF00001)   
Domain families : Pfam (NCBI)pfam00001   
Conserved Domain (NCBI)GPR119
DMDM Disease mutations139760
Blocks (Seattle)GPR119
SuperfamilyQ8TDV5
Human Protein AtlasENSG00000147262
Peptide AtlasQ8TDV5
HPRD06579
IPIIPI00152634   
Protein Interaction databases
DIP (DOE-UCLA)Q8TDV5
IntAct (EBI)Q8TDV5
FunCoupENSG00000147262
BioGRIDGPR119
STRING (EMBL)GPR119
ZODIACGPR119
Ontologies - Pathways
QuickGOQ8TDV5
Ontology : AmiGOG-protein coupled receptor activity  plasma membrane  G-protein coupled receptor signaling pathway  integral component of membrane  insulin secretion  phosphatidylcholine binding  receptor complex  
Ontology : EGO-EBIG-protein coupled receptor activity  plasma membrane  G-protein coupled receptor signaling pathway  integral component of membrane  insulin secretion  phosphatidylcholine binding  receptor complex  
Pathways : KEGGInsulin secretion   
NDEx NetworkGPR119
Atlas of Cancer Signalling NetworkGPR119
Wikipedia pathwaysGPR119
Orthology - Evolution
OrthoDB139760
GeneTree (enSembl)ENSG00000147262
Phylogenetic Trees/Animal Genes : TreeFamGPR119
HOVERGENQ8TDV5
HOGENOMQ8TDV5
Homologs : HomoloGeneGPR119
Homology/Alignments : Family Browser (UCSC)GPR119
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerGPR119 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)GPR119
dbVarGPR119
ClinVarGPR119
1000_GenomesGPR119 
Exome Variant ServerGPR119
ExAC (Exome Aggregation Consortium)GPR119 (select the gene name)
Genetic variants : HAPMAP139760
Genomic Variants (DGV)GPR119 [DGVbeta]
DECIPHERGPR119 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisGPR119 
Mutations
ICGC Data PortalGPR119 
TCGA Data PortalGPR119 
Broad Tumor PortalGPR119
OASIS PortalGPR119 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICGPR119  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDGPR119
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
LOVD (Leiden Open Variation Database)X-chromosome gene database
BioMutasearch GPR119
DgiDB (Drug Gene Interaction Database)GPR119
DoCM (Curated mutations)GPR119 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)GPR119 (select a term)
intoGenGPR119
Cancer3DGPR119(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM300513   
Orphanet
MedgenGPR119
Genetic Testing Registry GPR119
NextProtQ8TDV5 [Medical]
TSGene139760
GENETestsGPR119
Huge Navigator GPR119 [HugePedia]
snp3D : Map Gene to Disease139760
BioCentury BCIQGPR119
ClinGenGPR119
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD139760
Chemical/Pharm GKB GenePA134928131
Clinical trialGPR119
Miscellaneous
canSAR (ICR)GPR119 (select the gene name)
Probes
Litterature
PubMed25 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineGPR119
EVEXGPR119
GoPubMedGPR119
iHOPGPR119
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Fri May 19 11:14:17 CEST 2017

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