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MRGPRD (MAS related GPR family member D)

Identity

Alias (NCBI)MRGD
TGR7
HGNC (Hugo) MRGPRD
HGNC Alias symbmrgD
HGNC Previous nameMAS-related GPR, member D
LocusID (NCBI) 116512
Atlas_Id 55074
Location 11q13.3  [Link to chromosome band 11q13]
Location_base_pair Starts at 68980021 and ends at 68980986 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)		Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)

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)MRGPRD   29626
Cards
Entrez_Gene (NCBI)MRGPRD    MAS related GPR family member D
AliasesMRGD; TGR7
GeneCards (Weizmann)MRGPRD
Ensembl hg19 (Hinxton)ENSG00000172938 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000172938 [Gene_View]  ENSG00000172938 [Sequence]  chr11:68980021-68980986 [Contig_View]  MRGPRD [Vega]
ICGC DataPortalENSG00000172938
TCGA cBioPortalMRGPRD
AceView (NCBI)MRGPRD
Genatlas (Paris)MRGPRD
SOURCE (Princeton)MRGPRD
Genetics Home Reference (NIH)MRGPRD
Genomic and cartography
GoldenPath hg38 (UCSC)MRGPRD  -     chr11:68980021-68980986 -  11q13.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MRGPRD  -     11q13.3   [Description]    (hg19-Feb_2009)
GoldenPathMRGPRD - 11q13.3 [CytoView hg19]  MRGPRD - 11q13.3 [CytoView hg38]
ImmunoBaseENSG00000172938
Genome Data Viewer NCBIMRGPRD [Mapview hg19]  
OMIM607231   
Gene and transcription
Genbank (Entrez)AB154410 AY427820
RefSeq transcript (Entrez)NM_198923
Consensus coding sequences : CCDS (NCBI)MRGPRD
Gene ExpressionMRGPRD [ NCBI-GEO ]   MRGPRD [ EBI - ARRAY_EXPRESS ]   MRGPRD [ SEEK ]   MRGPRD [ MEM ]
Gene Expression Viewer (FireBrowse)MRGPRD [ Firebrowse - Broad ]
GenevisibleExpression of MRGPRD in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)116512
GTEX Portal (Tissue expression)MRGPRD
Human Protein AtlasENSG00000172938-MRGPRD [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8TDS7   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8TDS7  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8TDS7
PhosPhoSitePlusQ8TDS7
Domaine pattern : Prosite (Expaxy)G_PROTEIN_RECEP_F1_2 (PS50262)   
Domains : Interpro (EBI)GPCR_Rhodpsn    GPCR_Rhodpsn_7TM    MRGPCRD    MRGPCRFAMILY   
Domain families : Pfam (Sanger)7tm_1 (PF00001)   
Domain families : Pfam (NCBI)pfam00001   
Conserved Domain (NCBI)MRGPRD
SuperfamilyQ8TDS7
AlphaFold pdb e-kbQ8TDS7   
Human Protein Atlas [tissue]ENSG00000172938-MRGPRD [tissue]
HPRD06250
Protein Interaction databases
DIP (DOE-UCLA)Q8TDS7
IntAct (EBI)Q8TDS7
BioGRIDMRGPRD
STRING (EMBL)MRGPRD
ZODIACMRGPRD
Ontologies - Pathways
QuickGOQ8TDS7
Ontology : AmiGOG protein-coupled receptor activity  extracellular space  plasma membrane  G protein-coupled receptor signaling pathway  integral component of membrane  
Ontology : EGO-EBIG protein-coupled receptor activity  extracellular space  plasma membrane  G protein-coupled receptor signaling pathway  integral component of membrane  
NDEx NetworkMRGPRD
Atlas of Cancer Signalling NetworkMRGPRD
Wikipedia pathwaysMRGPRD
Orthology - Evolution
OrthoDB116512
GeneTree (enSembl)ENSG00000172938
Phylogenetic Trees/Animal Genes : TreeFamMRGPRD
Homologs : HomoloGeneMRGPRD
Homology/Alignments : Family Browser (UCSC)MRGPRD
Gene fusions - Rearrangements
Fusion : QuiverMRGPRD
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMRGPRD [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MRGPRD
dbVarMRGPRD
ClinVarMRGPRD
MonarchMRGPRD
1000_GenomesMRGPRD 
Exome Variant ServerMRGPRD
GNOMAD BrowserENSG00000172938
Varsome BrowserMRGPRD
ACMGMRGPRD variants
VarityQ8TDS7
Genomic Variants (DGV)MRGPRD [DGVbeta]
DECIPHERMRGPRD [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisMRGPRD 
Mutations
ICGC Data PortalMRGPRD 
TCGA Data PortalMRGPRD 
Broad Tumor PortalMRGPRD
OASIS PortalMRGPRD [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICMRGPRD  [overview]  [genome browser]  [tissue]  [distribution]  
Somatic Mutations in Cancer : COSMIC3DMRGPRD
Mutations and Diseases : HGMDMRGPRD
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaMRGPRD
DgiDB (Drug Gene Interaction Database)MRGPRD
DoCM (Curated mutations)MRGPRD
CIViC (Clinical Interpretations of Variants in Cancer)MRGPRD
Cancer3DMRGPRD
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM607231   
Orphanet
DisGeNETMRGPRD
MedgenMRGPRD
Genetic Testing Registry MRGPRD
NextProtQ8TDS7 [Medical]
GENETestsMRGPRD
Target ValidationMRGPRD
Huge Navigator MRGPRD [HugePedia]
ClinGenMRGPRD
Clinical trials, drugs, therapy
MyCancerGenomeMRGPRD
Protein Interactions : CTDMRGPRD
Pharm GKB GenePA134978563
PharosQ8TDS7
Clinical trialMRGPRD
Miscellaneous
canSAR (ICR)MRGPRD
HarmonizomeMRGPRD
DataMed IndexMRGPRD
Probes
Litterature
PubMed9 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXMRGPRD
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Oct 4 15:21:15 CEST 2021
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