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GPR101 (G protein-coupled receptor 101)

Identity

Other aliasGPCR6
PAGH2
HGNC (Hugo) GPR101
LocusID (NCBI) 83550
Atlas_Id 55842
Location Xq26.3  [Link to chromosome band Xq26]
Location_base_pair Starts at 137030148 and ends at 137031674 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)GPR101   14963
LRG (Locus Reference Genomic)LRG_1000
Cards
Entrez_Gene (NCBI)GPR101  83550  G protein-coupled receptor 101
AliasesGPCR6; PAGH2
GeneCards (Weizmann)GPR101
Ensembl hg19 (Hinxton)ENSG00000165370 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000165370 [Gene_View]  chrX:137030148-137031674 [Contig_View]  GPR101 [Vega]
ICGC DataPortalENSG00000165370
TCGA cBioPortalGPR101
AceView (NCBI)GPR101
Genatlas (Paris)GPR101
WikiGenes83550
SOURCE (Princeton)GPR101
Genetics Home Reference (NIH)GPR101
Genomic and cartography
GoldenPath hg38 (UCSC)GPR101  -     chrX:137030148-137031674 -  Xq26.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)GPR101  -     Xq26.3   [Description]    (hg19-Feb_2009)
EnsemblGPR101 - Xq26.3 [CytoView hg19]  GPR101 - Xq26.3 [CytoView hg38]
Mapping of homologs : NCBIGPR101 [Mapview hg19]  GPR101 [Mapview hg38]
OMIM300393   300943   
Gene and transcription
Genbank (Entrez)BC069439
RefSeq transcript (Entrez)NM_054021
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)GPR101
Cluster EST : UnigeneHs.350569 [ NCBI ]
CGAP (NCI)Hs.350569
Alternative Splicing GalleryENSG00000165370
Gene ExpressionGPR101 [ NCBI-GEO ]   GPR101 [ EBI - ARRAY_EXPRESS ]   GPR101 [ SEEK ]   GPR101 [ MEM ]
Gene Expression Viewer (FireBrowse)GPR101 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)83550
GTEX Portal (Tissue expression)GPR101
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ96P66   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ96P66  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ96P66
Splice isoforms : SwissVarQ96P66
PhosPhoSitePlusQ96P66
Domaine pattern : Prosite (Expaxy)G_PROTEIN_RECEP_F1_1 (PS00237)    G_PROTEIN_RECEP_F1_2 (PS50262)   
Domains : Interpro (EBI)GPCR_Rhodpsn    GPCR_Rhodpsn_7TM   
Domain families : Pfam (Sanger)7tm_1 (PF00001)   
Domain families : Pfam (NCBI)pfam00001   
Conserved Domain (NCBI)GPR101
DMDM Disease mutations83550
Blocks (Seattle)GPR101
SuperfamilyQ96P66
Human Protein AtlasENSG00000165370
Peptide AtlasQ96P66
HPRD02315
IPIIPI00046715   
Protein Interaction databases
DIP (DOE-UCLA)Q96P66
IntAct (EBI)Q96P66
FunCoupENSG00000165370
BioGRIDGPR101
STRING (EMBL)GPR101
ZODIACGPR101
Ontologies - Pathways
QuickGOQ96P66
Ontology : AmiGOadrenergic receptor activity  integral component of plasma membrane  cell-cell signaling  receptor complex  adenylate cyclase-activating adrenergic receptor signaling pathway  
Ontology : EGO-EBIadrenergic receptor activity  integral component of plasma membrane  cell-cell signaling  receptor complex  adenylate cyclase-activating adrenergic receptor signaling pathway  
NDEx NetworkGPR101
Atlas of Cancer Signalling NetworkGPR101
Wikipedia pathwaysGPR101
Orthology - Evolution
OrthoDB83550
GeneTree (enSembl)ENSG00000165370
Phylogenetic Trees/Animal Genes : TreeFamGPR101
HOVERGENQ96P66
HOGENOMQ96P66
Homologs : HomoloGeneGPR101
Homology/Alignments : Family Browser (UCSC)GPR101
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerGPR101 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)GPR101
dbVarGPR101
ClinVarGPR101
1000_GenomesGPR101 
Exome Variant ServerGPR101
ExAC (Exome Aggregation Consortium)GPR101 (select the gene name)
Genetic variants : HAPMAP83550
Genomic Variants (DGV)GPR101 [DGVbeta]
DECIPHERGPR101 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisGPR101 
Mutations
ICGC Data PortalGPR101 
TCGA Data PortalGPR101 
Broad Tumor PortalGPR101
OASIS PortalGPR101 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICGPR101  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDGPR101
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD - Leiden Open Variation Database
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
LOVD (Leiden Open Variation Database)X-chromosome gene database
BioMutasearch GPR101
DgiDB (Drug Gene Interaction Database)GPR101
DoCM (Curated mutations)GPR101 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)GPR101 (select a term)
intoGenGPR101
Cancer3DGPR101(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM300393    300943   
Orphanet408    23573   
MedgenGPR101
Genetic Testing Registry GPR101
NextProtQ96P66 [Medical]
TSGene83550
GENETestsGPR101
Target ValidationGPR101
Huge Navigator GPR101 [HugePedia]
snp3D : Map Gene to Disease83550
BioCentury BCIQGPR101
ClinGenGPR101
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD83550
Chemical/Pharm GKB GenePA28849
Clinical trialGPR101
Miscellaneous
canSAR (ICR)GPR101 (select the gene name)
Probes
Litterature
PubMed14 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineGPR101
EVEXGPR101
GoPubMedGPR101
iHOPGPR101
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Wed Jun 7 12:35:48 CEST 2017

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