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GPR135 (G protein-coupled receptor 135)

Identity

Alias_symbol (synonym)HUMNPIIY20
PAFR
Other alias
HGNC (Hugo) GPR135
LocusID (NCBI) 64582
Atlas_Id 63955
Location 14q23.1  [Link to chromosome band 14q23]
Location_base_pair Starts at 59463522 and ends at 59465341 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)GPR135   19991
Cards
Entrez_Gene (NCBI)GPR135  64582  G protein-coupled receptor 135
AliasesHUMNPIIY20
GeneCards (Weizmann)GPR135
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr14:59463522-59465341 [Contig_View]  GPR135 [Vega]
TCGA cBioPortalGPR135
AceView (NCBI)GPR135
Genatlas (Paris)GPR135
WikiGenes64582
SOURCE (Princeton)GPR135
Genetics Home Reference (NIH)GPR135
Genomic and cartography
GoldenPath hg38 (UCSC)GPR135  -     chr14:59463522-59465341 -  14q23.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)GPR135  -     14q23.1   [Description]    (hg19-Feb_2009)
EnsemblGPR135 - 14q23.1 [CytoView hg19]  GPR135 - 14q23.1 [CytoView hg38]
Mapping of homologs : NCBIGPR135 [Mapview hg19]  GPR135 [Mapview hg38]
OMIM607970   
Gene and transcription
Genbank (Entrez)AK124598 AY255588 AY288418 BC032831 BX094623
RefSeq transcript (Entrez)NM_022571
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)GPR135
Cluster EST : UnigeneHs.648823 [ NCBI ]
CGAP (NCI)Hs.648823
Gene ExpressionGPR135 [ NCBI-GEO ]   GPR135 [ EBI - ARRAY_EXPRESS ]   GPR135 [ SEEK ]   GPR135 [ MEM ]
Gene Expression Viewer (FireBrowse)GPR135 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)64582
GTEX Portal (Tissue expression)GPR135
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8IZ08   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8IZ08  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8IZ08
Splice isoforms : SwissVarQ8IZ08
PhosPhoSitePlusQ8IZ08
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)GPR135
DMDM Disease mutations64582
Blocks (Seattle)GPR135
SuperfamilyQ8IZ08
Peptide AtlasQ8IZ08
HPRD16263
IPIIPI00478110   IPI00383390   
Protein Interaction databases
DIP (DOE-UCLA)Q8IZ08
IntAct (EBI)Q8IZ08
BioGRIDGPR135
STRING (EMBL)GPR135
ZODIACGPR135
Ontologies - Pathways
QuickGOQ8IZ08
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 NetworkGPR135
Atlas of Cancer Signalling NetworkGPR135
Wikipedia pathwaysGPR135
Orthology - Evolution
OrthoDB64582
Phylogenetic Trees/Animal Genes : TreeFamGPR135
HOVERGENQ8IZ08
HOGENOMQ8IZ08
Homologs : HomoloGeneGPR135
Homology/Alignments : Family Browser (UCSC)GPR135
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerGPR135 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)GPR135
dbVarGPR135
ClinVarGPR135
1000_GenomesGPR135 
Exome Variant ServerGPR135
ExAC (Exome Aggregation Consortium)GPR135 (select the gene name)
Genetic variants : HAPMAP64582
Genomic Variants (DGV)GPR135 [DGVbeta]
DECIPHERGPR135 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisGPR135 
Mutations
ICGC Data PortalGPR135 
TCGA Data PortalGPR135 
Broad Tumor PortalGPR135
OASIS PortalGPR135 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICGPR135  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDGPR135
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
BioMutasearch GPR135
DgiDB (Drug Gene Interaction Database)GPR135
DoCM (Curated mutations)GPR135 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)GPR135 (select a term)
intoGenGPR135
Cancer3DGPR135(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM607970   
Orphanet
MedgenGPR135
Genetic Testing Registry GPR135
NextProtQ8IZ08 [Medical]
TSGene64582
GENETestsGPR135
Target ValidationGPR135
Huge Navigator GPR135 [HugePedia]
snp3D : Map Gene to Disease64582
BioCentury BCIQGPR135
ClinGenGPR135
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD64582
Chemical/Pharm GKB GenePA134863427
Clinical trialGPR135
Miscellaneous
canSAR (ICR)GPR135 (select the gene name)
Probes
Litterature
PubMed9 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineGPR135
EVEXGPR135
GoPubMedGPR135
iHOPGPR135
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 15:51:09 CEST 2017

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