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OR2M7 (olfactory receptor family 2 subfamily M member 7)

Identity

Alias_namesolfactory receptor, family 2, subfamily M, member 7
Other aliasOR1-58
HGNC (Hugo) OR2M7
LocusID (NCBI) 391196
Atlas_Id 71275
Location 1q44  [Link to chromosome band 1q44]
Location_base_pair Starts at 248323630 and ends at 248324568 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)OR2M7   19594
Cards
Entrez_Gene (NCBI)OR2M7  391196  olfactory receptor family 2 subfamily M member 7
AliasesOR1-58
GeneCards (Weizmann)OR2M7
Ensembl hg19 (Hinxton)ENSG00000177186 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000177186 [Gene_View]  chr1:248323630-248324568 [Contig_View]  OR2M7 [Vega]
ICGC DataPortalENSG00000177186
TCGA cBioPortalOR2M7
AceView (NCBI)OR2M7
Genatlas (Paris)OR2M7
WikiGenes391196
SOURCE (Princeton)OR2M7
Genetics Home Reference (NIH)OR2M7
Genomic and cartography
GoldenPath hg38 (UCSC)OR2M7  -     chr1:248323630-248324568 -  1q44   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)OR2M7  -     1q44   [Description]    (hg19-Feb_2009)
EnsemblOR2M7 - 1q44 [CytoView hg19]  OR2M7 - 1q44 [CytoView hg38]
Mapping of homologs : NCBIOR2M7 [Mapview hg19]  OR2M7 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC136944 BC136946
RefSeq transcript (Entrez)NM_001004691
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)OR2M7
Cluster EST : UnigeneHs.530570 [ NCBI ]
CGAP (NCI)Hs.530570
Alternative Splicing GalleryENSG00000177186
Gene ExpressionOR2M7 [ NCBI-GEO ]   OR2M7 [ EBI - ARRAY_EXPRESS ]   OR2M7 [ SEEK ]   OR2M7 [ MEM ]
Gene Expression Viewer (FireBrowse)OR2M7 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)391196
GTEX Portal (Tissue expression)OR2M7
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8NG81   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8NG81  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8NG81
Splice isoforms : SwissVarQ8NG81
PhosPhoSitePlusQ8NG81
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)OR2M7
DMDM Disease mutations391196
Blocks (Seattle)OR2M7
SuperfamilyQ8NG81
Human Protein AtlasENSG00000177186
Peptide AtlasQ8NG81
HPRD14948
IPIIPI00303203   
Protein Interaction databases
DIP (DOE-UCLA)Q8NG81
IntAct (EBI)Q8NG81
FunCoupENSG00000177186
BioGRIDOR2M7
STRING (EMBL)OR2M7
ZODIACOR2M7
Ontologies - Pathways
QuickGOQ8NG81
Ontology : AmiGOG-protein coupled receptor activity  olfactory receptor activity  plasma membrane  G-protein coupled receptor signaling pathway  sensory perception of smell  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  sensory perception of smell  integral component of membrane  detection of chemical stimulus involved in sensory perception of smell  
Pathways : KEGGOlfactory transduction   
NDEx NetworkOR2M7
Atlas of Cancer Signalling NetworkOR2M7
Wikipedia pathwaysOR2M7
Orthology - Evolution
OrthoDB391196
GeneTree (enSembl)ENSG00000177186
Phylogenetic Trees/Animal Genes : TreeFamOR2M7
HOVERGENQ8NG81
HOGENOMQ8NG81
Homologs : HomoloGeneOR2M7
Homology/Alignments : Family Browser (UCSC)OR2M7
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerOR2M7 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)OR2M7
dbVarOR2M7
ClinVarOR2M7
1000_GenomesOR2M7 
Exome Variant ServerOR2M7
ExAC (Exome Aggregation Consortium)OR2M7 (select the gene name)
Genetic variants : HAPMAP391196
Genomic Variants (DGV)OR2M7 [DGVbeta]
DECIPHEROR2M7 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisOR2M7 
Mutations
ICGC Data PortalOR2M7 
TCGA Data PortalOR2M7 
Broad Tumor PortalOR2M7
OASIS PortalOR2M7 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICOR2M7  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDOR2M7
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 OR2M7
DgiDB (Drug Gene Interaction Database)OR2M7
DoCM (Curated mutations)OR2M7 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)OR2M7 (select a term)
intoGenOR2M7
Cancer3DOR2M7(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenOR2M7
Genetic Testing Registry OR2M7
NextProtQ8NG81 [Medical]
TSGene391196
GENETestsOR2M7
Target ValidationOR2M7
Huge Navigator OR2M7 [HugePedia]
snp3D : Map Gene to Disease391196
BioCentury BCIQOR2M7
ClinGenOR2M7
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD391196
Chemical/Pharm GKB GenePA134874354
Clinical trialOR2M7
Miscellaneous
canSAR (ICR)OR2M7 (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineOR2M7
EVEXOR2M7
GoPubMedOR2M7
iHOPOR2M7
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Wed May 31 15:34:09 CEST 2017

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