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OR9G9 (olfactory receptor family 9 subfamily G member 9)

Identity

Alias_namesolfactory receptor, family 9, subfamily G, member 9
Other aliasOR9G1
HGNC (Hugo) OR9G9
LocusID (NCBI) 504191
Atlas_Id 71539
Location 11q12.1  [Link to chromosome band 11q12]
Location_base_pair Starts at 56700388 and ends at 56701305 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)OR9G9   31940
Cards
Entrez_Gene (NCBI)OR9G9  504191  olfactory receptor family 9 subfamily G member 9
AliasesOR9G1
GeneCards (Weizmann)OR9G9
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr11:56700388-56701305 [Contig_View]  OR9G9 [Vega]
TCGA cBioPortalOR9G9
AceView (NCBI)OR9G9
Genatlas (Paris)OR9G9
WikiGenes504191
SOURCE (Princeton)OR9G9
Genetics Home Reference (NIH)OR9G9
Genomic and cartography
GoldenPath hg38 (UCSC)OR9G9  -     chr11:56700388-56701305 +  11q12.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)OR9G9  -     11q12.1   [Description]    (hg19-Feb_2009)
EnsemblOR9G9 - 11q12.1 [CytoView hg19]  OR9G9 - 11q12.1 [CytoView hg38]
Mapping of homologs : NCBIOR9G9 [Mapview hg19]  OR9G9 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)NM_001013358
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)OR9G9
Gene ExpressionOR9G9 [ NCBI-GEO ]   OR9G9 [ EBI - ARRAY_EXPRESS ]   OR9G9 [ SEEK ]   OR9G9 [ MEM ]
Gene Expression Viewer (FireBrowse)OR9G9 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)504191
GTEX Portal (Tissue expression)OR9G9
Protein : pattern, domain, 3D structure
UniProt/SwissProtP0C7N8   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtP0C7N8  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProP0C7N8
Splice isoforms : SwissVarP0C7N8
PhosPhoSitePlusP0C7N8
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)OR9G9
DMDM Disease mutations504191
Blocks (Seattle)OR9G9
SuperfamilyP0C7N8
Peptide AtlasP0C7N8
HPRD18490
IPIIPI00554566   
Protein Interaction databases
DIP (DOE-UCLA)P0C7N8
IntAct (EBI)P0C7N8
BioGRIDOR9G9
STRING (EMBL)OR9G9
ZODIACOR9G9
Ontologies - Pathways
QuickGOP0C7N8
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 NetworkOR9G9
Atlas of Cancer Signalling NetworkOR9G9
Wikipedia pathwaysOR9G9
Orthology - Evolution
OrthoDB504191
Phylogenetic Trees/Animal Genes : TreeFamOR9G9
HOVERGENP0C7N8
HOGENOMP0C7N8
Homologs : HomoloGeneOR9G9
Homology/Alignments : Family Browser (UCSC)OR9G9
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerOR9G9 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)OR9G9
dbVarOR9G9
ClinVarOR9G9
1000_GenomesOR9G9 
Exome Variant ServerOR9G9
ExAC (Exome Aggregation Consortium)OR9G9 (select the gene name)
Genetic variants : HAPMAP504191
Genomic Variants (DGV)OR9G9 [DGVbeta]
DECIPHEROR9G9 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisOR9G9 
Mutations
ICGC Data PortalOR9G9 
TCGA Data PortalOR9G9 
Broad Tumor PortalOR9G9
OASIS PortalOR9G9 [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDOR9G9
BioMutasearch OR9G9
DgiDB (Drug Gene Interaction Database)OR9G9
DoCM (Curated mutations)OR9G9 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)OR9G9 (select a term)
intoGenOR9G9
Cancer3DOR9G9(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenOR9G9
Genetic Testing Registry OR9G9
NextProtP0C7N8 [Medical]
TSGene504191
GENETestsOR9G9
Target ValidationOR9G9
Huge Navigator OR9G9 [HugePedia]
snp3D : Map Gene to Disease504191
BioCentury BCIQOR9G9
ClinGenOR9G9
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD504191
Chemical/Pharm GKB GenePA142671224
Clinical trialOR9G9
Miscellaneous
canSAR (ICR)OR9G9 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineOR9G9
EVEXOR9G9
GoPubMedOR9G9
iHOPOR9G9
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Wed May 31 15:35:09 CEST 2017

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