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OR11H12 (olfactory receptor family 11 subfamily H member 12)

Identity

Alias_namesolfactory receptor, family 11, subfamily H, member 12
Other alias-
HGNC (Hugo) OR11H12
LocusID (NCBI) 440153
Atlas_Id 71180
Location 14q11.2  [Link to chromosome band 14q11]
Location_base_pair Starts at 18601117 and ends at 18602097 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)OR11H12   30738
Cards
Entrez_Gene (NCBI)OR11H12  440153  olfactory receptor family 11 subfamily H member 12
Aliases
GeneCards (Weizmann)OR11H12
Ensembl hg19 (Hinxton)ENSG00000257115 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000257115 [Gene_View]  chr14:18601117-18602097 [Contig_View]  OR11H12 [Vega]
ICGC DataPortalENSG00000257115
TCGA cBioPortalOR11H12
AceView (NCBI)OR11H12
Genatlas (Paris)OR11H12
WikiGenes440153
SOURCE (Princeton)OR11H12
Genetics Home Reference (NIH)OR11H12
Genomic and cartography
GoldenPath hg38 (UCSC)OR11H12  -     chr14:18601117-18602097 +  14q11.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)OR11H12  -     14q11.2   [Description]    (hg19-Feb_2009)
EnsemblOR11H12 - 14q11.2 [CytoView hg19]  OR11H12 - 14q11.2 [CytoView hg38]
Mapping of homologs : NCBIOR11H12 [Mapview hg19]  OR11H12 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC136730 BC136731
RefSeq transcript (Entrez)NM_001013354
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)OR11H12
Cluster EST : UnigeneHs.534880 [ NCBI ]
CGAP (NCI)Hs.534880
Alternative Splicing GalleryENSG00000257115
Gene ExpressionOR11H12 [ NCBI-GEO ]   OR11H12 [ EBI - ARRAY_EXPRESS ]   OR11H12 [ SEEK ]   OR11H12 [ MEM ]
Gene Expression Viewer (FireBrowse)OR11H12 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)440153
GTEX Portal (Tissue expression)OR11H12
Protein : pattern, domain, 3D structure
UniProt/SwissProtB2RN74   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtB2RN74  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProB2RN74
Splice isoforms : SwissVarB2RN74
PhosPhoSitePlusB2RN74
Domaine pattern : Prosite (Expaxy)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)OR11H12
DMDM Disease mutations440153
Blocks (Seattle)OR11H12
SuperfamilyB2RN74
Human Protein AtlasENSG00000257115
Peptide AtlasB2RN74
HPRD18633
IPIIPI00465379   
Protein Interaction databases
DIP (DOE-UCLA)B2RN74
IntAct (EBI)B2RN74
FunCoupENSG00000257115
BioGRIDOR11H12
STRING (EMBL)OR11H12
ZODIACOR11H12
Ontologies - Pathways
QuickGOB2RN74
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 NetworkOR11H12
Atlas of Cancer Signalling NetworkOR11H12
Wikipedia pathwaysOR11H12
Orthology - Evolution
OrthoDB440153
GeneTree (enSembl)ENSG00000257115
Phylogenetic Trees/Animal Genes : TreeFamOR11H12
HOVERGENB2RN74
HOGENOMB2RN74
Homologs : HomoloGeneOR11H12
Homology/Alignments : Family Browser (UCSC)OR11H12
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerOR11H12 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)OR11H12
dbVarOR11H12
ClinVarOR11H12
1000_GenomesOR11H12 
Exome Variant ServerOR11H12
ExAC (Exome Aggregation Consortium)OR11H12 (select the gene name)
Genetic variants : HAPMAP440153
Genomic Variants (DGV)OR11H12 [DGVbeta]
DECIPHEROR11H12 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisOR11H12 
Mutations
ICGC Data PortalOR11H12 
TCGA Data PortalOR11H12 
Broad Tumor PortalOR11H12
OASIS PortalOR11H12 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICOR11H12  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDOR11H12
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch OR11H12
DgiDB (Drug Gene Interaction Database)OR11H12
DoCM (Curated mutations)OR11H12 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)OR11H12 (select a term)
intoGenOR11H12
Cancer3DOR11H12(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenOR11H12
Genetic Testing Registry OR11H12
NextProtB2RN74 [Medical]
TSGene440153
GENETestsOR11H12
Target ValidationOR11H12
Huge Navigator OR11H12 [HugePedia]
snp3D : Map Gene to Disease440153
BioCentury BCIQOR11H12
ClinGenOR11H12
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD440153
Chemical/Pharm GKB GenePA142671220
Clinical trialOR11H12
Miscellaneous
canSAR (ICR)OR11H12 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineOR11H12
EVEXOR11H12
GoPubMedOR11H12
iHOPOR11H12
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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