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OR11H7 (olfactory receptor family 11 subfamily H member 7 (gene/pseudogene))

Identity

Alias_namesOR11H7P
olfactory receptor, family 11, subfamily H, member 7 pseudogene
olfactory receptor, family 11, subfamily H, member 7 (gene/pseudogene)
Other alias
HGNC (Hugo) OR11H7
LocusID (NCBI) 390441
Atlas_Id 79398
Location 14q11.2  [Link to chromosome band 14q11]
Location_base_pair Starts at 20228981 and ends at 20230749 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)OR11H7   15350
Cards
Entrez_Gene (NCBI)OR11H7  390441  olfactory receptor family 11 subfamily H member 7 (gene/pseudogene)
AliasesOR11H7P
GeneCards (Weizmann)OR11H7
Ensembl hg19 (Hinxton)ENSG00000258806 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000258806 [Gene_View]  chr14:20228981-20230749 [Contig_View]  OR11H7 [Vega]
ICGC DataPortalENSG00000258806
TCGA cBioPortalOR11H7
AceView (NCBI)OR11H7
Genatlas (Paris)OR11H7
WikiGenes390441
SOURCE (Princeton)OR11H7
Genetics Home Reference (NIH)OR11H7
Genomic and cartography
GoldenPath hg38 (UCSC)OR11H7  -     chr14:20228981-20230749 +  14q11.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)OR11H7  -     14q11.2   [Description]    (hg19-Feb_2009)
EnsemblOR11H7 - 14q11.2 [CytoView hg19]  OR11H7 - 14q11.2 [CytoView hg38]
Mapping of homologs : NCBIOR11H7 [Mapview hg19]  OR11H7 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)NM_001348273
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)OR11H7
Alternative Splicing GalleryENSG00000258806
Gene ExpressionOR11H7 [ NCBI-GEO ]   OR11H7 [ EBI - ARRAY_EXPRESS ]   OR11H7 [ SEEK ]   OR11H7 [ MEM ]
Gene Expression Viewer (FireBrowse)OR11H7 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)390441
GTEX Portal (Tissue expression)OR11H7
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8NGC8   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8NGC8  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8NGC8
Splice isoforms : SwissVarQ8NGC8
PhosPhoSitePlusQ8NGC8
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)OR11H7
DMDM Disease mutations390441
Blocks (Seattle)OR11H7
SuperfamilyQ8NGC8
Human Protein AtlasENSG00000258806
Peptide AtlasQ8NGC8
IPIIPI00168980   
Protein Interaction databases
DIP (DOE-UCLA)Q8NGC8
IntAct (EBI)Q8NGC8
FunCoupENSG00000258806
BioGRIDOR11H7
STRING (EMBL)OR11H7
ZODIACOR11H7
Ontologies - Pathways
QuickGOQ8NGC8
Ontology : AmiGOolfactory receptor activity  G-protein coupled serotonin receptor activity  plasma membrane  integral component of membrane  neurotransmitter receptor activity  detection of chemical stimulus involved in sensory perception of smell  G-protein coupled serotonin receptor signaling pathway  
Ontology : EGO-EBIolfactory receptor activity  G-protein coupled serotonin receptor activity  plasma membrane  integral component of membrane  neurotransmitter receptor activity  detection of chemical stimulus involved in sensory perception of smell  G-protein coupled serotonin receptor signaling pathway  
NDEx NetworkOR11H7
Atlas of Cancer Signalling NetworkOR11H7
Wikipedia pathwaysOR11H7
Orthology - Evolution
OrthoDB390441
GeneTree (enSembl)ENSG00000258806
Phylogenetic Trees/Animal Genes : TreeFamOR11H7
HOVERGENQ8NGC8
HOGENOMQ8NGC8
Homologs : HomoloGeneOR11H7
Homology/Alignments : Family Browser (UCSC)OR11H7
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerOR11H7 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)OR11H7
dbVarOR11H7
ClinVarOR11H7
1000_GenomesOR11H7 
Exome Variant ServerOR11H7
ExAC (Exome Aggregation Consortium)OR11H7 (select the gene name)
Genetic variants : HAPMAP390441
Genomic Variants (DGV)OR11H7 [DGVbeta]
DECIPHEROR11H7 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisOR11H7 
Mutations
ICGC Data PortalOR11H7 
TCGA Data PortalOR11H7 
Broad Tumor PortalOR11H7
OASIS PortalOR11H7 [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDOR11H7
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 OR11H7
DgiDB (Drug Gene Interaction Database)OR11H7
DoCM (Curated mutations)OR11H7 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)OR11H7 (select a term)
intoGenOR11H7
Cancer3DOR11H7(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenOR11H7
Genetic Testing Registry OR11H7
NextProtQ8NGC8 [Medical]
TSGene390441
GENETestsOR11H7
Target ValidationOR11H7
Huge Navigator OR11H7 [HugePedia]
snp3D : Map Gene to Disease390441
BioCentury BCIQOR11H7
ClinGenOR11H7
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD390441
Chemical/Pharm GKB GenePA32019
Clinical trialOR11H7
Miscellaneous
canSAR (ICR)OR11H7 (select the gene name)
Probes
Litterature
PubMed6 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineOR11H7
EVEXOR11H7
GoPubMedOR11H7
iHOPOR11H7
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 13:32:48 CEST 2017

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