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ADGRD2 (adhesion G protein-coupled receptor D2)

Identity

Alias_namesGPR144
G protein-coupled receptor 144
Alias_symbol (synonym)PGR24
Other alias
HGNC (Hugo) ADGRD2
LocusID (NCBI) 347088
Atlas_Id 77443
Location 9q33.3  [Link to chromosome band 9q33]
Location_base_pair Starts at 124465210 and ends at 124467340 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


External links

Nomenclature
HGNC (Hugo)ADGRD2   18651
Cards
Entrez_Gene (NCBI)ADGRD2  347088  adhesion G protein-coupled receptor D2
AliasesGPR144; PGR24
GeneCards (Weizmann)ADGRD2
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr9:124465210-124467340 [Contig_View]  ADGRD2 [Vega]
TCGA cBioPortalADGRD2
AceView (NCBI)ADGRD2
Genatlas (Paris)ADGRD2
WikiGenes347088
SOURCE (Princeton)ADGRD2
Genetics Home Reference (NIH)ADGRD2
Genomic and cartography
GoldenPath hg38 (UCSC)ADGRD2  -     chr9:124465210-124467340 +  9q33.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ADGRD2  -     9q33.3   [Description]    (hg19-Feb_2009)
EnsemblADGRD2 - 9q33.3 [CytoView hg19]  ADGRD2 - 9q33.3 [CytoView hg38]
Mapping of homologs : NCBIADGRD2 [Mapview hg19]  ADGRD2 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK022431 AY255620 AY278562 EF107715 EF107716
RefSeq transcript (Entrez)NM_001161808 NM_182611
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)ADGRD2
Cluster EST : UnigeneHs.454099 [ NCBI ]
CGAP (NCI)Hs.454099
Gene ExpressionADGRD2 [ NCBI-GEO ]   ADGRD2 [ EBI - ARRAY_EXPRESS ]   ADGRD2 [ SEEK ]   ADGRD2 [ MEM ]
Gene Expression Viewer (FireBrowse)ADGRD2 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)347088
GTEX Portal (Tissue expression)ADGRD2
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ7Z7M1   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ7Z7M1  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ7Z7M1
Splice isoforms : SwissVarQ7Z7M1
PhosPhoSitePlusQ7Z7M1
Domaine pattern : Prosite (Expaxy)G_PROTEIN_RECEP_F2_4 (PS50261)    GPS (PS50221)    PTX_2 (PS51828)   
Domains : Interpro (EBI)ConA-like_dom    GPCR_2-like    GPCR_2_secretin-like    GPS    Pentraxin-related   
Domain families : Pfam (Sanger)7tm_2 (PF00002)    GPS (PF01825)    Pentaxin (PF00354)   
Domain families : Pfam (NCBI)pfam00002    pfam01825    pfam00354   
Domain families : Smart (EMBL)GPS (SM00303)  PTX (SM00159)  
Conserved Domain (NCBI)ADGRD2
DMDM Disease mutations347088
Blocks (Seattle)ADGRD2
SuperfamilyQ7Z7M1
Peptide AtlasQ7Z7M1
HPRD17063
IPIIPI00385573   IPI01010244   IPI00827983   IPI00827696   
Protein Interaction databases
DIP (DOE-UCLA)Q7Z7M1
IntAct (EBI)Q7Z7M1
BioGRIDADGRD2
STRING (EMBL)ADGRD2
ZODIACADGRD2
Ontologies - Pathways
QuickGOQ7Z7M1
Ontology : AmiGOG-protein coupled receptor activity  cell surface receptor signaling pathway  G-protein coupled receptor signaling pathway  integral component of membrane  
Ontology : EGO-EBIG-protein coupled receptor activity  cell surface receptor signaling pathway  G-protein coupled receptor signaling pathway  integral component of membrane  
NDEx NetworkADGRD2
Atlas of Cancer Signalling NetworkADGRD2
Wikipedia pathwaysADGRD2
Orthology - Evolution
OrthoDB347088
Phylogenetic Trees/Animal Genes : TreeFamADGRD2
HOVERGENQ7Z7M1
HOGENOMQ7Z7M1
Homologs : HomoloGeneADGRD2
Homology/Alignments : Family Browser (UCSC)ADGRD2
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerADGRD2 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ADGRD2
dbVarADGRD2
ClinVarADGRD2
1000_GenomesADGRD2 
Exome Variant ServerADGRD2
ExAC (Exome Aggregation Consortium)ADGRD2 (select the gene name)
Genetic variants : HAPMAP347088
Genomic Variants (DGV)ADGRD2 [DGVbeta]
DECIPHERADGRD2 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisADGRD2 
Mutations
ICGC Data PortalADGRD2 
TCGA Data PortalADGRD2 
Broad Tumor PortalADGRD2
OASIS PortalADGRD2 [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDADGRD2
BioMutasearch ADGRD2
DgiDB (Drug Gene Interaction Database)ADGRD2
DoCM (Curated mutations)ADGRD2 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ADGRD2 (select a term)
intoGenADGRD2
Cancer3DADGRD2(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenADGRD2
Genetic Testing Registry ADGRD2
NextProtQ7Z7M1 [Medical]
TSGene347088
GENETestsADGRD2
Target ValidationADGRD2
Huge Navigator ADGRD2 [HugePedia]
snp3D : Map Gene to Disease347088
BioCentury BCIQADGRD2
ClinGenADGRD2
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD347088
Chemical/Pharm GKB GenePA134882616
Clinical trialADGRD2
Miscellaneous
canSAR (ICR)ADGRD2 (select the gene name)
Probes
Litterature
PubMed7 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineADGRD2
EVEXADGRD2
GoPubMedADGRD2
iHOPADGRD2
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Sep 18 13:00:57 CEST 2017

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