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GPRASP2 (G protein-coupled receptor associated sorting protein 2)

Identity

Alias_symbol (synonym)GASP2
FLJ37327
Other alias
HGNC (Hugo) GPRASP2
LocusID (NCBI) 114928
Atlas_Id 64016
Location Xq22.1  [Link to chromosome band Xq22]
Location_base_pair Starts at 101967104 and ends at 101972661 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)GPRASP2   25169
Cards
Entrez_Gene (NCBI)GPRASP2  114928  G protein-coupled receptor associated sorting protein 2
AliasesGASP2
GeneCards (Weizmann)GPRASP2
Ensembl hg19 (Hinxton)ENSG00000158301 [Gene_View]  chrX:101967104-101972661 [Contig_View]  GPRASP2 [Vega]
Ensembl hg38 (Hinxton)ENSG00000158301 [Gene_View]  chrX:101967104-101972661 [Contig_View]  GPRASP2 [Vega]
ICGC DataPortalENSG00000158301
TCGA cBioPortalGPRASP2
AceView (NCBI)GPRASP2
Genatlas (Paris)GPRASP2
WikiGenes114928
SOURCE (Princeton)GPRASP2
Genetics Home Reference (NIH)GPRASP2
Genomic and cartography
GoldenPath hg19 (UCSC)GPRASP2  -     chrX:101967104-101972661 +  Xq22.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)GPRASP2  -     Xq22.1   [Description]    (hg38-Dec_2013)
EnsemblGPRASP2 - Xq22.1 [CytoView hg19]  GPRASP2 - Xq22.1 [CytoView hg38]
Mapping of homologs : NCBIGPRASP2 [Mapview hg19]  GPRASP2 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AA906216 AK092981 AK094646 AK096067 AK123832
RefSeq transcript (Entrez)NM_001004051 NM_001184874 NM_001184875 NM_001184876 NM_138437
RefSeq genomic (Entrez)NC_000023 NC_018934 NG_021322 NT_011651 NW_004929444
Consensus coding sequences : CCDS (NCBI)GPRASP2
Cluster EST : UnigeneHs.731996 [ NCBI ]
CGAP (NCI)Hs.731996
Alternative Splicing GalleryENSG00000158301
Gene ExpressionGPRASP2 [ NCBI-GEO ]   GPRASP2 [ EBI - ARRAY_EXPRESS ]   GPRASP2 [ SEEK ]   GPRASP2 [ MEM ]
Gene Expression Viewer (FireBrowse)GPRASP2 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)114928
GTEX Portal (Tissue expression)GPRASP2
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ96D09   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ96D09  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ96D09
Splice isoforms : SwissVarQ96D09
PhosPhoSitePlusQ96D09
Domains : Interpro (EBI)ARM-like    ARM-rpt_dom    ARM-type_fold   
Domain families : Pfam (Sanger)Arm_2 (PF04826)   
Domain families : Pfam (NCBI)pfam04826   
Conserved Domain (NCBI)GPRASP2
DMDM Disease mutations114928
Blocks (Seattle)GPRASP2
SuperfamilyQ96D09
Human Protein AtlasENSG00000158301
Peptide AtlasQ96D09
HPRD06612
Protein Interaction databases
DIP (DOE-UCLA)Q96D09
IntAct (EBI)Q96D09
FunCoupENSG00000158301
BioGRIDGPRASP2
STRING (EMBL)GPRASP2
ZODIACGPRASP2
Ontologies - Pathways
QuickGOQ96D09
Ontology : AmiGObeta-amyloid binding  protein binding  cytoplasm  
Ontology : EGO-EBIbeta-amyloid binding  protein binding  cytoplasm  
NDEx NetworkGPRASP2
Atlas of Cancer Signalling NetworkGPRASP2
Wikipedia pathwaysGPRASP2
Orthology - Evolution
OrthoDB114928
GeneTree (enSembl)ENSG00000158301
Phylogenetic Trees/Animal Genes : TreeFamGPRASP2
HOVERGENQ96D09
HOGENOMQ96D09
Homologs : HomoloGeneGPRASP2
Homology/Alignments : Family Browser (UCSC)GPRASP2
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerGPRASP2 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)GPRASP2
dbVarGPRASP2
ClinVarGPRASP2
1000_GenomesGPRASP2 
Exome Variant ServerGPRASP2
ExAC (Exome Aggregation Consortium)GPRASP2 (select the gene name)
Genetic variants : HAPMAP114928
Genomic Variants (DGV)GPRASP2 [DGVbeta]
DECIPHER (Syndromes)X:101967104-101972661  ENSG00000158301
CONAN: Copy Number AnalysisGPRASP2 
Mutations
ICGC Data PortalGPRASP2 
TCGA Data PortalGPRASP2 
Broad Tumor PortalGPRASP2
OASIS PortalGPRASP2 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICGPRASP2  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDGPRASP2
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 GPRASP2
DgiDB (Drug Gene Interaction Database)GPRASP2
DoCM (Curated mutations)GPRASP2 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)GPRASP2 (select a term)
intoGenGPRASP2
Cancer3DGPRASP2(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenGPRASP2
Genetic Testing Registry GPRASP2
NextProtQ96D09 [Medical]
TSGene114928
GENETestsGPRASP2
Huge Navigator GPRASP2 [HugePedia]
snp3D : Map Gene to Disease114928
BioCentury BCIQGPRASP2
ClinGenGPRASP2
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD114928
Chemical/Pharm GKB GenePA134976848
Clinical trialGPRASP2
Miscellaneous
canSAR (ICR)GPRASP2 (select the gene name)
Probes
Litterature
PubMed23 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineGPRASP2
EVEXGPRASP2
GoPubMedGPRASP2
iHOPGPRASP2
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 12:06:49 CET 2017

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