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OR11G2 (olfactory receptor family 11 subfamily G member 2)

Identity

Alias_namesolfactory receptor, family 11, subfamily G, member 2
Other aliasOR14-34
HGNC (Hugo) OR11G2
LocusID (NCBI) 390439
Atlas_Id 71178
Location 14q11.2  [Link to chromosome band 14q11]
Location_base_pair Starts at 20197336 and ends at 20198373 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)OR11G2   15346
Cards
Entrez_Gene (NCBI)OR11G2  390439  olfactory receptor family 11 subfamily G member 2
AliasesOR14-34
GeneCards (Weizmann)OR11G2
Ensembl hg19 (Hinxton)ENSG00000196832 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000196832 [Gene_View]  chr14:20197336-20198373 [Contig_View]  OR11G2 [Vega]
ICGC DataPortalENSG00000196832
TCGA cBioPortalOR11G2
AceView (NCBI)OR11G2
Genatlas (Paris)OR11G2
WikiGenes390439
SOURCE (Princeton)OR11G2
Genetics Home Reference (NIH)OR11G2
Genomic and cartography
GoldenPath hg38 (UCSC)OR11G2  -     chr14:20197336-20198373 +  14q11.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)OR11G2  -     14q11.2   [Description]    (hg19-Feb_2009)
EnsemblOR11G2 - 14q11.2 [CytoView hg19]  OR11G2 - 14q11.2 [CytoView hg38]
Mapping of homologs : NCBIOR11G2 [Mapview hg19]  OR11G2 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC148504
RefSeq transcript (Entrez)NM_001005503
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)OR11G2
Cluster EST : UnigeneHs.554582 [ NCBI ]
CGAP (NCI)Hs.554582
Alternative Splicing GalleryENSG00000196832
Gene ExpressionOR11G2 [ NCBI-GEO ]   OR11G2 [ EBI - ARRAY_EXPRESS ]   OR11G2 [ SEEK ]   OR11G2 [ MEM ]
Gene Expression Viewer (FireBrowse)OR11G2 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)390439
GTEX Portal (Tissue expression)OR11G2
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8NGC1   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8NGC1  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8NGC1
Splice isoforms : SwissVarQ8NGC1
PhosPhoSitePlusQ8NGC1
Domaine pattern : Prosite (Expaxy)G_PROTEIN_RECEP_F1_1 (PS00237)    G_PROTEIN_RECEP_F1_2 (PS50262)   
Domains : Interpro (EBI)GPCR_Rhodpsn    GPCR_Rhodpsn_7TM    Olfact_rcpt   
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)OR11G2
DMDM Disease mutations390439
Blocks (Seattle)OR11G2
SuperfamilyQ8NGC1
Human Protein AtlasENSG00000196832
Peptide AtlasQ8NGC1
HPRD14900
IPIIPI00456726   
Protein Interaction databases
DIP (DOE-UCLA)Q8NGC1
IntAct (EBI)Q8NGC1
FunCoupENSG00000196832
BioGRIDOR11G2
STRING (EMBL)OR11G2
ZODIACOR11G2
Ontologies - Pathways
QuickGOQ8NGC1
Ontology : AmiGOG-protein coupled receptor activity  olfactory receptor activity  plasma membrane  G-protein coupled receptor signaling pathway  integral component of membrane  detection of chemical stimulus involved in sensory perception of smell  
Ontology : EGO-EBIG-protein coupled receptor activity  olfactory receptor activity  plasma membrane  G-protein coupled receptor signaling pathway  integral component of membrane  detection of chemical stimulus involved in sensory perception of smell  
Pathways : KEGGOlfactory transduction   
NDEx NetworkOR11G2
Atlas of Cancer Signalling NetworkOR11G2
Wikipedia pathwaysOR11G2
Orthology - Evolution
OrthoDB390439
GeneTree (enSembl)ENSG00000196832
Phylogenetic Trees/Animal Genes : TreeFamOR11G2
HOVERGENQ8NGC1
HOGENOMQ8NGC1
Homologs : HomoloGeneOR11G2
Homology/Alignments : Family Browser (UCSC)OR11G2
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerOR11G2 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)OR11G2
dbVarOR11G2
ClinVarOR11G2
1000_GenomesOR11G2 
Exome Variant ServerOR11G2
ExAC (Exome Aggregation Consortium)OR11G2 (select the gene name)
Genetic variants : HAPMAP390439
Genomic Variants (DGV)OR11G2 [DGVbeta]
DECIPHEROR11G2 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisOR11G2 
Mutations
ICGC Data PortalOR11G2 
TCGA Data PortalOR11G2 
Broad Tumor PortalOR11G2
OASIS PortalOR11G2 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICOR11G2  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDOR11G2
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 OR11G2
DgiDB (Drug Gene Interaction Database)OR11G2
DoCM (Curated mutations)OR11G2 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)OR11G2 (select a term)
intoGenOR11G2
Cancer3DOR11G2(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenOR11G2
Genetic Testing Registry OR11G2
NextProtQ8NGC1 [Medical]
TSGene390439
GENETestsOR11G2
Target ValidationOR11G2
Huge Navigator OR11G2 [HugePedia]
snp3D : Map Gene to Disease390439
BioCentury BCIQOR11G2
ClinGenOR11G2
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD390439
Chemical/Pharm GKB GenePA32012
Clinical trialOR11G2
Miscellaneous
canSAR (ICR)OR11G2 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineOR11G2
EVEXOR11G2
GoPubMedOR11G2
iHOPOR11G2
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Sep 18 13:32:47 CEST 2017

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