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OR9Q2 (olfactory receptor family 9 subfamily Q member 2)

Identity

Alias_namesOR9Q2P
olfactory receptor, family 9, subfamily Q, member 2
Other alias
HGNC (Hugo) OR9Q2
LocusID (NCBI) 219957
Atlas_Id 71543
Location 11q12.1  [Link to chromosome band 11q12]
Location_base_pair Starts at 58190434 and ends at 58191518 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)OR9Q2   15328
Cards
Entrez_Gene (NCBI)OR9Q2  219957  olfactory receptor family 9 subfamily Q member 2
AliasesOR9Q2P
GeneCards (Weizmann)OR9Q2
Ensembl hg19 (Hinxton)ENSG00000186513 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000186513 [Gene_View]  chr11:58190434-58191518 [Contig_View]  OR9Q2 [Vega]
ICGC DataPortalENSG00000186513
TCGA cBioPortalOR9Q2
AceView (NCBI)OR9Q2
Genatlas (Paris)OR9Q2
WikiGenes219957
SOURCE (Princeton)OR9Q2
Genetics Home Reference (NIH)OR9Q2
Genomic and cartography
GoldenPath hg38 (UCSC)OR9Q2  -     chr11:58190434-58191518 +  11q12.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)OR9Q2  -     11q12.1   [Description]    (hg19-Feb_2009)
EnsemblOR9Q2 - 11q12.1 [CytoView hg19]  OR9Q2 - 11q12.1 [CytoView hg38]
Mapping of homologs : NCBIOR9Q2 [Mapview hg19]  OR9Q2 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC140718
RefSeq transcript (Entrez)NM_001005283
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)OR9Q2
Cluster EST : UnigeneHs.553643 [ NCBI ]
CGAP (NCI)Hs.553643
Alternative Splicing GalleryENSG00000186513
Gene ExpressionOR9Q2 [ NCBI-GEO ]   OR9Q2 [ EBI - ARRAY_EXPRESS ]   OR9Q2 [ SEEK ]   OR9Q2 [ MEM ]
Gene Expression Viewer (FireBrowse)OR9Q2 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)219957
GTEX Portal (Tissue expression)OR9Q2
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8NGE9   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8NGE9  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8NGE9
Splice isoforms : SwissVarQ8NGE9
PhosPhoSitePlusQ8NGE9
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)OR9Q2
DMDM Disease mutations219957
Blocks (Seattle)OR9Q2
SuperfamilyQ8NGE9
Human Protein AtlasENSG00000186513
Peptide AtlasQ8NGE9
HPRD17801
IPIIPI00168996   
Protein Interaction databases
DIP (DOE-UCLA)Q8NGE9
IntAct (EBI)Q8NGE9
FunCoupENSG00000186513
BioGRIDOR9Q2
STRING (EMBL)OR9Q2
ZODIACOR9Q2
Ontologies - Pathways
QuickGOQ8NGE9
Ontology : AmiGOG-protein coupled receptor activity  olfactory receptor activity  odorant binding  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  odorant binding  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 NetworkOR9Q2
Atlas of Cancer Signalling NetworkOR9Q2
Wikipedia pathwaysOR9Q2
Orthology - Evolution
OrthoDB219957
GeneTree (enSembl)ENSG00000186513
Phylogenetic Trees/Animal Genes : TreeFamOR9Q2
HOVERGENQ8NGE9
HOGENOMQ8NGE9
Homologs : HomoloGeneOR9Q2
Homology/Alignments : Family Browser (UCSC)OR9Q2
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerOR9Q2 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)OR9Q2
dbVarOR9Q2
ClinVarOR9Q2
1000_GenomesOR9Q2 
Exome Variant ServerOR9Q2
ExAC (Exome Aggregation Consortium)OR9Q2 (select the gene name)
Genetic variants : HAPMAP219957
Genomic Variants (DGV)OR9Q2 [DGVbeta]
DECIPHEROR9Q2 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisOR9Q2 
Mutations
ICGC Data PortalOR9Q2 
TCGA Data PortalOR9Q2 
Broad Tumor PortalOR9Q2
OASIS PortalOR9Q2 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICOR9Q2  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDOR9Q2
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 OR9Q2
DgiDB (Drug Gene Interaction Database)OR9Q2
DoCM (Curated mutations)OR9Q2 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)OR9Q2 (select a term)
intoGenOR9Q2
Cancer3DOR9Q2(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenOR9Q2
Genetic Testing Registry OR9Q2
NextProtQ8NGE9 [Medical]
TSGene219957
GENETestsOR9Q2
Target ValidationOR9Q2
Huge Navigator OR9Q2 [HugePedia]
snp3D : Map Gene to Disease219957
BioCentury BCIQOR9Q2
ClinGenOR9Q2
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD219957
Chemical/Pharm GKB GenePA32806
Clinical trialOR9Q2
Miscellaneous
canSAR (ICR)OR9Q2 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineOR9Q2
EVEXOR9Q2
GoPubMedOR9Q2
iHOPOR9Q2
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 13:33:42 CEST 2017

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