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GPR137C (G protein-coupled receptor 137C)

Identity

Alias_symbol (synonym)DKFZp762F0713
TM7SF1L2
Other alias
HGNC (Hugo) GPR137C
LocusID (NCBI) 283554
Atlas_Id 63958
Location 14q22.1  [Link to chromosome band 14q22]
Location_base_pair Starts at 53019866 and ends at 53104431 bp from pter ( according to hg19-Feb_2009)
Fusion genes
(updated 2016)
GPR137C (14q22.1) / FERMT2 (14q22.1)TXNDC16 (14q22.1) / GPR137C (14q22.1)

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)GPR137C   25445
Cards
Entrez_Gene (NCBI)GPR137C  283554  G protein-coupled receptor 137C
AliasesTM7SF1L2
GeneCards (Weizmann)GPR137C
Ensembl hg19 (Hinxton)ENSG00000180998 [Gene_View]  chr14:53019866-53104431 [Contig_View]  GPR137C [Vega]
Ensembl hg38 (Hinxton)ENSG00000180998 [Gene_View]  chr14:53019866-53104431 [Contig_View]  GPR137C [Vega]
ICGC DataPortalENSG00000180998
TCGA cBioPortalGPR137C
AceView (NCBI)GPR137C
Genatlas (Paris)GPR137C
WikiGenes283554
SOURCE (Princeton)GPR137C
Genetics Home Reference (NIH)GPR137C
Genomic and cartography
GoldenPath hg19 (UCSC)GPR137C  -     chr14:53019866-53104431 +  14q22.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)GPR137C  -     14q22.1   [Description]    (hg38-Dec_2013)
EnsemblGPR137C - 14q22.1 [CytoView hg19]  GPR137C - 14q22.1 [CytoView hg38]
Mapping of homologs : NCBIGPR137C [Mapview hg19]  GPR137C [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK123953 AK293812 AL834372 AW470753 AY255590
RefSeq transcript (Entrez)NM_001099652
RefSeq genomic (Entrez)NC_000014 NC_018925 NT_026437 NW_004929393
Consensus coding sequences : CCDS (NCBI)GPR137C
Cluster EST : UnigeneHs.416214 [ NCBI ]
CGAP (NCI)Hs.416214
Alternative Splicing GalleryENSG00000180998
Gene ExpressionGPR137C [ NCBI-GEO ]   GPR137C [ EBI - ARRAY_EXPRESS ]   GPR137C [ SEEK ]   GPR137C [ MEM ]
Gene Expression Viewer (FireBrowse)GPR137C [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)283554
GTEX Portal (Tissue expression)GPR137C
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8N3F9   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8N3F9  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8N3F9
Splice isoforms : SwissVarQ8N3F9
PhosPhoSitePlusQ8N3F9
Domains : Interpro (EBI)GPR137   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)GPR137C
DMDM Disease mutations283554
Blocks (Seattle)GPR137C
SuperfamilyQ8N3F9
Human Protein AtlasENSG00000180998
Peptide AtlasQ8N3F9
IPIIPI00855960   IPI01026127   IPI01013711   
Protein Interaction databases
DIP (DOE-UCLA)Q8N3F9
IntAct (EBI)Q8N3F9
FunCoupENSG00000180998
BioGRIDGPR137C
STRING (EMBL)GPR137C
ZODIACGPR137C
Ontologies - Pathways
QuickGOQ8N3F9
Ontology : AmiGOintegral component of membrane  
Ontology : EGO-EBIintegral component of membrane  
NDEx NetworkGPR137C
Atlas of Cancer Signalling NetworkGPR137C
Wikipedia pathwaysGPR137C
Orthology - Evolution
OrthoDB283554
GeneTree (enSembl)ENSG00000180998
Phylogenetic Trees/Animal Genes : TreeFamGPR137C
HOVERGENQ8N3F9
HOGENOMQ8N3F9
Homologs : HomoloGeneGPR137C
Homology/Alignments : Family Browser (UCSC)GPR137C
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerGPR137C [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)GPR137C
dbVarGPR137C
ClinVarGPR137C
1000_GenomesGPR137C 
Exome Variant ServerGPR137C
ExAC (Exome Aggregation Consortium)GPR137C (select the gene name)
Genetic variants : HAPMAP283554
Genomic Variants (DGV)GPR137C [DGVbeta]
DECIPHER (Syndromes)14:53019866-53104431  ENSG00000180998
CONAN: Copy Number AnalysisGPR137C 
Mutations
ICGC Data PortalGPR137C 
TCGA Data PortalGPR137C 
Broad Tumor PortalGPR137C
OASIS PortalGPR137C [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICGPR137C  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDGPR137C
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 GPR137C
DgiDB (Drug Gene Interaction Database)GPR137C
DoCM (Curated mutations)GPR137C (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)GPR137C (select a term)
intoGenGPR137C
Cancer3DGPR137C(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenGPR137C
Genetic Testing Registry GPR137C
NextProtQ8N3F9 [Medical]
TSGene283554
GENETestsGPR137C
Huge Navigator GPR137C [HugePedia]
snp3D : Map Gene to Disease283554
BioCentury BCIQGPR137C
ClinGenGPR137C
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD283554
Chemical/Pharm GKB GenePA143485483
Clinical trialGPR137C
Miscellaneous
canSAR (ICR)GPR137C (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineGPR137C
EVEXGPR137C
GoPubMedGPR137C
iHOPGPR137C
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 12:06:38 CET 2017

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