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MRGPRG (MAS related GPR family member G)

Identity

Alias_namesGPR169
G protein-coupled receptor 169
MAS-related GPR, member G
Alias_symbol (synonym)mrgG
Other aliasMRGG
HGNC (Hugo) MRGPRG
LocusID (NCBI) 386746
Atlas_Id 70413
Location 11p15.4  [Link to chromosome band 11p15]
Location_base_pair Starts at 3217944 and ends at 3218813 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)MRGPRG   24829
Cards
Entrez_Gene (NCBI)MRGPRG  386746  MAS related GPR family member G
AliasesGPR169; MRGG
GeneCards (Weizmann)MRGPRG
Ensembl hg19 (Hinxton)ENSG00000182170 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000182170 [Gene_View]  chr11:3217944-3218813 [Contig_View]  MRGPRG [Vega]
ICGC DataPortalENSG00000182170
TCGA cBioPortalMRGPRG
AceView (NCBI)MRGPRG
Genatlas (Paris)MRGPRG
WikiGenes386746
SOURCE (Princeton)MRGPRG
Genetics Home Reference (NIH)MRGPRG
Genomic and cartography
GoldenPath hg38 (UCSC)MRGPRG  -     chr11:3217944-3218813 -  11p15.4   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MRGPRG  -     11p15.4   [Description]    (hg19-Feb_2009)
EnsemblMRGPRG - 11p15.4 [CytoView hg19]  MRGPRG - 11p15.4 [CytoView hg38]
Mapping of homologs : NCBIMRGPRG [Mapview hg19]  MRGPRG [Mapview hg38]
OMIM607234   
Gene and transcription
Genbank (Entrez)AY255583
RefSeq transcript (Entrez)NM_001164377
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MRGPRG
Cluster EST : UnigeneHs.730306 [ NCBI ]
CGAP (NCI)Hs.730306
Alternative Splicing GalleryENSG00000182170
Gene ExpressionMRGPRG [ NCBI-GEO ]   MRGPRG [ EBI - ARRAY_EXPRESS ]   MRGPRG [ SEEK ]   MRGPRG [ MEM ]
Gene Expression Viewer (FireBrowse)MRGPRG [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)386746
GTEX Portal (Tissue expression)MRGPRG
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ86SM5   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ86SM5  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ86SM5
Splice isoforms : SwissVarQ86SM5
PhosPhoSitePlusQ86SM5
Domaine pattern : Prosite (Expaxy)G_PROTEIN_RECEP_F1_2 (PS50262)   
Domains : Interpro (EBI)GPCR_Rhodpsn    GPCR_Rhodpsn_7TM    MRGPCRFAMILY    MRGPCRG   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MRGPRG
DMDM Disease mutations386746
Blocks (Seattle)MRGPRG
SuperfamilyQ86SM5
Human Protein AtlasENSG00000182170
Peptide AtlasQ86SM5
IPIIPI00333751   
Protein Interaction databases
DIP (DOE-UCLA)Q86SM5
IntAct (EBI)Q86SM5
FunCoupENSG00000182170
BioGRIDMRGPRG
STRING (EMBL)MRGPRG
ZODIACMRGPRG
Ontologies - Pathways
QuickGOQ86SM5
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 NetworkMRGPRG
Atlas of Cancer Signalling NetworkMRGPRG
Wikipedia pathwaysMRGPRG
Orthology - Evolution
OrthoDB386746
GeneTree (enSembl)ENSG00000182170
Phylogenetic Trees/Animal Genes : TreeFamMRGPRG
HOVERGENQ86SM5
HOGENOMQ86SM5
Homologs : HomoloGeneMRGPRG
Homology/Alignments : Family Browser (UCSC)MRGPRG
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMRGPRG [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MRGPRG
dbVarMRGPRG
ClinVarMRGPRG
1000_GenomesMRGPRG 
Exome Variant ServerMRGPRG
ExAC (Exome Aggregation Consortium)MRGPRG (select the gene name)
Genetic variants : HAPMAP386746
Genomic Variants (DGV)MRGPRG [DGVbeta]
DECIPHERMRGPRG [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisMRGPRG 
Mutations
ICGC Data PortalMRGPRG 
TCGA Data PortalMRGPRG 
Broad Tumor PortalMRGPRG
OASIS PortalMRGPRG [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICMRGPRG  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDMRGPRG
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch MRGPRG
DgiDB (Drug Gene Interaction Database)MRGPRG
DoCM (Curated mutations)MRGPRG (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)MRGPRG (select a term)
intoGenMRGPRG
Cancer3DMRGPRG(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM607234   
Orphanet
MedgenMRGPRG
Genetic Testing Registry MRGPRG
NextProtQ86SM5 [Medical]
TSGene386746
GENETestsMRGPRG
Target ValidationMRGPRG
Huge Navigator MRGPRG [HugePedia]
snp3D : Map Gene to Disease386746
BioCentury BCIQMRGPRG
ClinGenMRGPRG
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD386746
Chemical/Pharm GKB GenePA134953683
Clinical trialMRGPRG
Miscellaneous
canSAR (ICR)MRGPRG (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMRGPRG
EVEXMRGPRG
GoPubMedMRGPRG
iHOPMRGPRG
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 15:31:21 CEST 2017
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