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GPR137 (G protein-coupled receptor 137)

Identity

Alias_symbol (synonym)C11orf4
GPR137A
TM7SF1L1
Other alias
HGNC (Hugo) GPR137
LocusID (NCBI) 56834
Atlas_Id 55360
Location 11q13.1  [Link to chromosome band 11q13]
Location_base_pair Starts at 64051811 and ends at 64056972 bp from pter ( according to hg19-Feb_2009)
Fusion genes
(updated 2016)
GPR137 (11q13.1) / GPR137 (11q13.1)PAFAH1B2 (11q23.3) / GPR137 (11q13.1)USP32 (17q23.1) / GPR137 (11q13.1)
PAFAH1B2 11q23.3 / GPR137 11q13.1USP32 17q23.1 / GPR137 11q13.1

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)GPR137   24300
Cards
Entrez_Gene (NCBI)GPR137  56834  G protein-coupled receptor 137
AliasesC11orf4; GPR137A; TM7SF1L1
GeneCards (Weizmann)GPR137
Ensembl hg19 (Hinxton)ENSG00000173264 [Gene_View]  chr11:64051811-64056972 [Contig_View]  GPR137 [Vega]
Ensembl hg38 (Hinxton)ENSG00000173264 [Gene_View]  chr11:64051811-64056972 [Contig_View]  GPR137 [Vega]
ICGC DataPortalENSG00000173264
TCGA cBioPortalGPR137
AceView (NCBI)GPR137
Genatlas (Paris)GPR137
WikiGenes56834
SOURCE (Princeton)GPR137
Genetics Home Reference (NIH)GPR137
Genomic and cartography
GoldenPath hg19 (UCSC)GPR137  -     chr11:64051811-64056972 +  11q13.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)GPR137  -     11q13.1   [Description]    (hg38-Dec_2013)
EnsemblGPR137 - 11q13.1 [CytoView hg19]  GPR137 - 11q13.1 [CytoView hg38]
Mapping of homologs : NCBIGPR137 [Mapview hg19]  GPR137 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AJ250392 AK056094 AK300209 AK302256 BC020396
RefSeq transcript (Entrez)NM_001170726 NM_001170880 NM_001170881 NM_001177358 NM_020155
RefSeq genomic (Entrez)NC_000011 NC_018922 NT_167190 NW_004929380
Consensus coding sequences : CCDS (NCBI)GPR137
Cluster EST : UnigeneHs.523763 [ NCBI ]
CGAP (NCI)Hs.523763
Alternative Splicing GalleryENSG00000173264
Gene ExpressionGPR137 [ NCBI-GEO ]   GPR137 [ EBI - ARRAY_EXPRESS ]   GPR137 [ SEEK ]   GPR137 [ MEM ]
Gene Expression Viewer (FireBrowse)GPR137 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)56834
GTEX Portal (Tissue expression)GPR137
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ96N19   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ96N19  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ96N19
Splice isoforms : SwissVarQ96N19
PhosPhoSitePlusQ96N19
Domains : Interpro (EBI)GPR137   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)GPR137
DMDM Disease mutations56834
Blocks (Seattle)GPR137
SuperfamilyQ96N19
Human Protein AtlasENSG00000173264
Peptide AtlasQ96N19
HPRD12600
IPIIPI00941884   IPI00815937   IPI00645236   IPI01015943   IPI00956520   IPI01010347   IPI01009962   IPI00140138   IPI01010434   IPI00385378   IPI01015538   IPI01013206   IPI01012796   IPI01012556   IPI01011159   IPI01009956   
Protein Interaction databases
DIP (DOE-UCLA)Q96N19
IntAct (EBI)Q96N19
FunCoupENSG00000173264
BioGRIDGPR137
STRING (EMBL)GPR137
ZODIACGPR137
Ontologies - Pathways
QuickGOQ96N19
Ontology : AmiGOintegral component of membrane  
Ontology : EGO-EBIintegral component of membrane  
NDEx NetworkGPR137
Atlas of Cancer Signalling NetworkGPR137
Wikipedia pathwaysGPR137
Orthology - Evolution
OrthoDB56834
GeneTree (enSembl)ENSG00000173264
Phylogenetic Trees/Animal Genes : TreeFamGPR137
HOVERGENQ96N19
HOGENOMQ96N19
Homologs : HomoloGeneGPR137
Homology/Alignments : Family Browser (UCSC)GPR137
Gene fusions - Rearrangements
Fusion : MitelmanPAFAH1B2/GPR137 [11q23.3/11q13.1]  [t(11;11)(q13;q23)]  
Fusion : MitelmanUSP32/GPR137 [17q23.1/11q13.1]  [t(11;17)(q13;q23)]  
Fusion: TCGAPAFAH1B2 11q23.3 GPR137 11q13.1 LUAD
Fusion: TCGAUSP32 17q23.1 GPR137 11q13.1 BRCA
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerGPR137 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)GPR137
dbVarGPR137
ClinVarGPR137
1000_GenomesGPR137 
Exome Variant ServerGPR137
ExAC (Exome Aggregation Consortium)GPR137 (select the gene name)
Genetic variants : HAPMAP56834
Genomic Variants (DGV)GPR137 [DGVbeta]
DECIPHER (Syndromes)11:64051811-64056972  ENSG00000173264
CONAN: Copy Number AnalysisGPR137 
Mutations
ICGC Data PortalGPR137 
TCGA Data PortalGPR137 
Broad Tumor PortalGPR137
OASIS PortalGPR137 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICGPR137  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDGPR137
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch GPR137
DgiDB (Drug Gene Interaction Database)GPR137
DoCM (Curated mutations)GPR137 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)GPR137 (select a term)
intoGenGPR137
Cancer3DGPR137(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenGPR137
Genetic Testing Registry GPR137
NextProtQ96N19 [Medical]
TSGene56834
GENETestsGPR137
Huge Navigator GPR137 [HugePedia]
snp3D : Map Gene to Disease56834
BioCentury BCIQGPR137
ClinGenGPR137
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD56834
Chemical/Pharm GKB GenePA143485482
Clinical trialGPR137
Miscellaneous
canSAR (ICR)GPR137 (select the gene name)
Probes
Litterature
PubMed9 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineGPR137
EVEXGPR137
GoPubMedGPR137
iHOPGPR137
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 13:08:00 CET 2017

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